PubMed:
RevDate: 2026-02-26
CmpDate: 2026-02-26
Virus Biomimetic-Delivery Systems for the Production of Vaccines.
Biomimetics (Basel, Switzerland), 11(2):.
The persistent emergence of infectious diseases has underscored the critical demand for next-generation vaccine technologies that are safe, effective, and scalable. This review explores virus biomimetic delivery systems, focusing on virus-like particles (VLPs) and virosomes as promising platforms for vaccine and therapeutic development. VLPs are self-assembled nanostructures composed of viral structural proteins that mimic native virions without carrying genetic material, while virosomes are reconstituted viral envelopes that retain functional glycoproteins but lack a nucleocapsid. Both systems provide strong immunogenicity and safety by mimicking viral architecture while eliminating the risk of replication. The paper examines various expression platforms for VLP production, including bacterial, yeast, insect, mammalian, and plant-based systems, highlighting their respective advantages, challenges, and optimization strategies. Mechanistic insights into antigen presentation, immune activation, and cellular uptake pathways are discussed to explain their superior performance in eliciting humoral and cellular immune responses. Furthermore, current applications of VLPs and virosomes in vaccines against major pathogens such as SARS-CoV-2, influenza, Newcastle disease virus, malaria, hepatitis, and respiratory syncytial virus are reviewed, demonstrating their versatility and clinical potential. By integrating molecular engineering, nanotechnology, and biofabrication strategies, virus biomimetic systems represent a transformative frontier in vaccinology, immunotherapy, and targeted drug delivery.
Additional Links: PMID-41744596
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@article {pmid41744596,
year = {2026},
author = {Barbinta-Patrascu, ME and Negut, I and Bita, B},
title = {Virus Biomimetic-Delivery Systems for the Production of Vaccines.},
journal = {Biomimetics (Basel, Switzerland)},
volume = {11},
number = {2},
pages = {},
pmid = {41744596},
issn = {2313-7673},
abstract = {The persistent emergence of infectious diseases has underscored the critical demand for next-generation vaccine technologies that are safe, effective, and scalable. This review explores virus biomimetic delivery systems, focusing on virus-like particles (VLPs) and virosomes as promising platforms for vaccine and therapeutic development. VLPs are self-assembled nanostructures composed of viral structural proteins that mimic native virions without carrying genetic material, while virosomes are reconstituted viral envelopes that retain functional glycoproteins but lack a nucleocapsid. Both systems provide strong immunogenicity and safety by mimicking viral architecture while eliminating the risk of replication. The paper examines various expression platforms for VLP production, including bacterial, yeast, insect, mammalian, and plant-based systems, highlighting their respective advantages, challenges, and optimization strategies. Mechanistic insights into antigen presentation, immune activation, and cellular uptake pathways are discussed to explain their superior performance in eliciting humoral and cellular immune responses. Furthermore, current applications of VLPs and virosomes in vaccines against major pathogens such as SARS-CoV-2, influenza, Newcastle disease virus, malaria, hepatitis, and respiratory syncytial virus are reviewed, demonstrating their versatility and clinical potential. By integrating molecular engineering, nanotechnology, and biofabrication strategies, virus biomimetic systems represent a transformative frontier in vaccinology, immunotherapy, and targeted drug delivery.},
}
RevDate: 2026-02-26
Preventing COVID-19 in at-risk populations: moving towards next-generation mRNA-1283 COVID-19 vaccine to address current challenges.
Expert review of vaccines [Epub ahead of print].
INTRODUCTION: Next-generation COVID-19 vaccines hold promise to reduce severe outcomes in populations most at risk. While the original mRNA COVID-19 vaccine, mRNA-1273, targets the full-length SARS-CoV-2 spike protein, mRNA-1283 is a novel next-generation mRNA COVID-19 vaccine that specifically targets immunodominant domains within the spike protein.
AREAS COVERED: This review summarizes literature on the development of mRNA-1283, from its design and preclinical evaluation to phase 1-3 clinical trial findings, with a particular focus on immunogenicity and efficacy in at-risk populations, specifically older adults and adults with comorbidities. The potential public health impact of this next-generation vaccine is explored, along with ongoing challenges facing COVID-19 vaccination.
EXPERT OPINION: Phase 1-3 clinical trials demonstrated that mRNA-1283 was well-tolerated, with safety and reactogenicity profiles comparable to mRNA-1273. Furthermore, mRNA-1283 demonstrated higher point estimates of immunogenicity and relative vaccine efficacy than mRNA-1273, including among older adults and individuals with underlying conditions who are most susceptible to severe COVID-19. Initial modeling studies indicate that mRNA-1283 could prevent more hospitalizations than current COVID-19 vaccines. Evidence to date suggests that the novel next-generation mRNA-1283 vaccine holds promise to advance progress in reducing the ongoing burden of COVID-19 across vulnerable populations.
Additional Links: PMID-41744151
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@article {pmid41744151,
year = {2026},
author = {Domachowske, JB and Zimet, GD and Hanage, W and Beck, E and Sule, P and Wahid, R and Vicic, N},
title = {Preventing COVID-19 in at-risk populations: moving towards next-generation mRNA-1283 COVID-19 vaccine to address current challenges.},
journal = {Expert review of vaccines},
volume = {},
number = {},
pages = {2632657},
doi = {10.1080/14760584.2026.2632657},
pmid = {41744151},
issn = {1744-8395},
abstract = {INTRODUCTION: Next-generation COVID-19 vaccines hold promise to reduce severe outcomes in populations most at risk. While the original mRNA COVID-19 vaccine, mRNA-1273, targets the full-length SARS-CoV-2 spike protein, mRNA-1283 is a novel next-generation mRNA COVID-19 vaccine that specifically targets immunodominant domains within the spike protein.
AREAS COVERED: This review summarizes literature on the development of mRNA-1283, from its design and preclinical evaluation to phase 1-3 clinical trial findings, with a particular focus on immunogenicity and efficacy in at-risk populations, specifically older adults and adults with comorbidities. The potential public health impact of this next-generation vaccine is explored, along with ongoing challenges facing COVID-19 vaccination.
EXPERT OPINION: Phase 1-3 clinical trials demonstrated that mRNA-1283 was well-tolerated, with safety and reactogenicity profiles comparable to mRNA-1273. Furthermore, mRNA-1283 demonstrated higher point estimates of immunogenicity and relative vaccine efficacy than mRNA-1273, including among older adults and individuals with underlying conditions who are most susceptible to severe COVID-19. Initial modeling studies indicate that mRNA-1283 could prevent more hospitalizations than current COVID-19 vaccines. Evidence to date suggests that the novel next-generation mRNA-1283 vaccine holds promise to advance progress in reducing the ongoing burden of COVID-19 across vulnerable populations.},
}
RevDate: 2026-02-26
PhIP-Seq: unveiling the complexity of antibody repertoires in health and disease.
Frontiers in immunology, 17:1735735.
Phage-Immunoprecipitation Sequencing (PhIP-Seq) merges phage display with next-generation sequencing to enable high-throughput profiling of antibody repertoires. This review synthesizes the technical evolution of the PhIP-Seq platform, critically assessing the workflow from peptide library design and immunoprecipitation to bioinformatics analysis. We evaluate strategies for optimizing library diversity and minimizing non-specific binding, while addressing inherent limitations such as the detection of conformational epitopes and post-translational modifications. The clinical utility of PhIP-Seq is examined through its application in identifying novel autoantigens in systemic lupus erythematosus and multiple sclerosis, mapping viral epitopes in SARS-CoV-2 and Plasmodium falciparum, and detecting tumor-associated antigens. Finally, we discuss the trajectory of the field toward integration with multi-omics datasets and the development of point-of-care diagnostic tools.
Additional Links: PMID-41743708
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Citation:
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@article {pmid41743708,
year = {2026},
author = {Tang, W and Gai, Q and Yang, J and Chen, J and Lyu, Z},
title = {PhIP-Seq: unveiling the complexity of antibody repertoires in health and disease.},
journal = {Frontiers in immunology},
volume = {17},
number = {},
pages = {1735735},
pmid = {41743708},
issn = {1664-3224},
abstract = {Phage-Immunoprecipitation Sequencing (PhIP-Seq) merges phage display with next-generation sequencing to enable high-throughput profiling of antibody repertoires. This review synthesizes the technical evolution of the PhIP-Seq platform, critically assessing the workflow from peptide library design and immunoprecipitation to bioinformatics analysis. We evaluate strategies for optimizing library diversity and minimizing non-specific binding, while addressing inherent limitations such as the detection of conformational epitopes and post-translational modifications. The clinical utility of PhIP-Seq is examined through its application in identifying novel autoantigens in systemic lupus erythematosus and multiple sclerosis, mapping viral epitopes in SARS-CoV-2 and Plasmodium falciparum, and detecting tumor-associated antigens. Finally, we discuss the trajectory of the field toward integration with multi-omics datasets and the development of point-of-care diagnostic tools.},
}
RevDate: 2026-02-26
CmpDate: 2026-02-26
Remdesivir in COVID-19: A Focus on Pediatric Cardiac Patients.
The Canadian journal of infectious diseases & medical microbiology = Journal canadien des maladies infectieuses et de la microbiologie medicale, 2026:4700812.
The coronavirus disease 2019 (COVID-19) pandemic has presented a significant global health challenge that necessitated the immediate search for various therapeutic modalities. Remdesivir, an antiviral drug inhibiting RNA-dependent RNA polymerase (RdRp), was among the most heavily used drugs against COVID-19. Of the several randomized controlled trials studying the efficacy of remdesivir, the vast majority were studied on the adult population. Results remain contradictory, with some studies supporting the high efficacy of remdesivir while others highlighting the lack of significance of its antiviral effects. Given the lack of focus on the pediatric population, the antiviral effects of remdesivir in cardiac pediatric patients, who are particularly vulnerable, remain especially under-investigated. This literature review explores current literature on remdesivir's mechanism of action and efficacy against COVID-19, especially in the pediatric cardiac population. Therefore, by combining results of studies from randomized controlled trials and retrospective studies in the adult and pediatric populations, this literature review underlines current knowledge gaps and highlights the need for studies targeting specific ages and comorbidities to effectively treat patients at higher risk of adverse events.
Additional Links: PMID-41743408
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Citation:
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@article {pmid41743408,
year = {2026},
author = {Bsat, D and Safi, D and Arabi, M},
title = {Remdesivir in COVID-19: A Focus on Pediatric Cardiac Patients.},
journal = {The Canadian journal of infectious diseases & medical microbiology = Journal canadien des maladies infectieuses et de la microbiologie medicale},
volume = {2026},
number = {},
pages = {4700812},
pmid = {41743408},
issn = {1712-9532},
abstract = {The coronavirus disease 2019 (COVID-19) pandemic has presented a significant global health challenge that necessitated the immediate search for various therapeutic modalities. Remdesivir, an antiviral drug inhibiting RNA-dependent RNA polymerase (RdRp), was among the most heavily used drugs against COVID-19. Of the several randomized controlled trials studying the efficacy of remdesivir, the vast majority were studied on the adult population. Results remain contradictory, with some studies supporting the high efficacy of remdesivir while others highlighting the lack of significance of its antiviral effects. Given the lack of focus on the pediatric population, the antiviral effects of remdesivir in cardiac pediatric patients, who are particularly vulnerable, remain especially under-investigated. This literature review explores current literature on remdesivir's mechanism of action and efficacy against COVID-19, especially in the pediatric cardiac population. Therefore, by combining results of studies from randomized controlled trials and retrospective studies in the adult and pediatric populations, this literature review underlines current knowledge gaps and highlights the need for studies targeting specific ages and comorbidities to effectively treat patients at higher risk of adverse events.},
}
RevDate: 2026-02-26
CmpDate: 2026-02-26
Regional health security architecture in ASEAN countries: Lessons from regional CDC models and Japan's strategic partnership for ACPHEED development.
Global health & medicine, 8(1):1-7.
The COVID-19 pandemic exposed critical gaps in regional health security mechanisms, prompting ASEAN to establish the ASEAN Centre for Public Health Emergencies and Emerging Diseases (ACPHEED), with functions distributed across Indonesia, Thailand, and Vietnam. This policy analysis examines strategic development approaches for ACPHEED through comprehensive benchmarking of the European Centre for Disease Prevention and Control (ECDC), Africa Centres for Disease Control and Prevention (Africa CDC), and Gulf CDC, supported by consultations in Indonesia (2024) and Sweden (2025) involving ASEAN member states and international partners. A comparative analysis reveals distinct organizational models: the ECDC operates within European Union (EU) institutional frameworks emphasizing functional specialization; the Africa CDC employs decentralized Regional Coordination Centers; and the Gulf CDC implements hybrid governance via Permanent Communication Networks. Each model offers valuable lessons for ACPHEED's development, particularly concerning governance structures that balance regional coordination with national sovereignty. ACPHEED faces unique challenges due to ASEAN's consensus-based, nonlegislative institutional nature and its tri-country operational structure. Critical success factors include phased surveillance emphasizing a defined scope and capacity building; inclusive governance mechanisms ensuring equitable member-state ownership; and operational frameworks applying subsidiarity principles to complement existing ASEAN mechanisms. Sustainable financing remains paramount given ASEAN's limited budgetary authority. Japan's strategic partnership should capitalize on its technical expertise in laboratory systems, digital surveillance, and disaster preparedness through comprehensive institutional support. ACPHEED's success depends on sustained political commitment, realistic financial arrangements, and effective integration into global health security architectures. This analysis provides a strategic roadmap for ACPHEED's preparatory phase so that it can serve as a regional health security leader while addressing ASEAN-specific institutional constraints.
Additional Links: PMID-41743347
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Citation:
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@article {pmid41743347,
year = {2026},
author = {Miyano, S and Nozaki, I and Hachiya, M and Miyamoto, T and Takei, T},
title = {Regional health security architecture in ASEAN countries: Lessons from regional CDC models and Japan's strategic partnership for ACPHEED development.},
journal = {Global health & medicine},
volume = {8},
number = {1},
pages = {1-7},
pmid = {41743347},
issn = {2434-9194},
abstract = {The COVID-19 pandemic exposed critical gaps in regional health security mechanisms, prompting ASEAN to establish the ASEAN Centre for Public Health Emergencies and Emerging Diseases (ACPHEED), with functions distributed across Indonesia, Thailand, and Vietnam. This policy analysis examines strategic development approaches for ACPHEED through comprehensive benchmarking of the European Centre for Disease Prevention and Control (ECDC), Africa Centres for Disease Control and Prevention (Africa CDC), and Gulf CDC, supported by consultations in Indonesia (2024) and Sweden (2025) involving ASEAN member states and international partners. A comparative analysis reveals distinct organizational models: the ECDC operates within European Union (EU) institutional frameworks emphasizing functional specialization; the Africa CDC employs decentralized Regional Coordination Centers; and the Gulf CDC implements hybrid governance via Permanent Communication Networks. Each model offers valuable lessons for ACPHEED's development, particularly concerning governance structures that balance regional coordination with national sovereignty. ACPHEED faces unique challenges due to ASEAN's consensus-based, nonlegislative institutional nature and its tri-country operational structure. Critical success factors include phased surveillance emphasizing a defined scope and capacity building; inclusive governance mechanisms ensuring equitable member-state ownership; and operational frameworks applying subsidiarity principles to complement existing ASEAN mechanisms. Sustainable financing remains paramount given ASEAN's limited budgetary authority. Japan's strategic partnership should capitalize on its technical expertise in laboratory systems, digital surveillance, and disaster preparedness through comprehensive institutional support. ACPHEED's success depends on sustained political commitment, realistic financial arrangements, and effective integration into global health security architectures. This analysis provides a strategic roadmap for ACPHEED's preparatory phase so that it can serve as a regional health security leader while addressing ASEAN-specific institutional constraints.},
}
RevDate: 2026-02-26
CmpDate: 2026-02-26
Rewriting the viral script: post-translational modifications orchestrating SARS-CoV-2 pathogenesis and immune evasion.
Frontiers in microbiology, 17:1748470.
SARS-CoV-2 reprograms host cell biology not solely through its genomic content but also through a sophisticated arsenal of post-translational modifications (PTMs) that modulate viral protein function, host signaling networks, and immune responses. Despite increasing recognition of PTMs as dynamic regulators of infection, their full functional breadth and therapeutic potential remain incompletely defined. Here, we provide a comprehensive, PTM-centric synthesis of SARS-CoV-2 pathogenesis, detailing how phosphorylation, ubiquitination, SUMOylation, glycosylation, acetylation, succinylation, ISGylation, and ADP-ribosylation cooperatively shape virus-host interplay. We dissect the mechanistic roles of individual modifications, such as phosphorylation-mediated transitions in nucleocapsid function, ubiquitin-driven degradation of immune factors, and SUMOylation-guided viral assembly, while revealing higher-order regulatory circuits and crosstalk among PTMs. Additionally, we highlight emerging computational tools for PTM site prediction and identify shared enzymatic nodes exploitable for host-directed antiviral strategies. This integrative framework positions PTMs as not merely bystanders but as central modulators of viral fitness and host vulnerability, offering novel avenues for therapeutic intervention against SARS-CoV-2 and future pandemic threats.
Additional Links: PMID-41743132
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Citation:
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@article {pmid41743132,
year = {2026},
author = {Qu, J and Liu, M and Zhou, C},
title = {Rewriting the viral script: post-translational modifications orchestrating SARS-CoV-2 pathogenesis and immune evasion.},
journal = {Frontiers in microbiology},
volume = {17},
number = {},
pages = {1748470},
pmid = {41743132},
issn = {1664-302X},
abstract = {SARS-CoV-2 reprograms host cell biology not solely through its genomic content but also through a sophisticated arsenal of post-translational modifications (PTMs) that modulate viral protein function, host signaling networks, and immune responses. Despite increasing recognition of PTMs as dynamic regulators of infection, their full functional breadth and therapeutic potential remain incompletely defined. Here, we provide a comprehensive, PTM-centric synthesis of SARS-CoV-2 pathogenesis, detailing how phosphorylation, ubiquitination, SUMOylation, glycosylation, acetylation, succinylation, ISGylation, and ADP-ribosylation cooperatively shape virus-host interplay. We dissect the mechanistic roles of individual modifications, such as phosphorylation-mediated transitions in nucleocapsid function, ubiquitin-driven degradation of immune factors, and SUMOylation-guided viral assembly, while revealing higher-order regulatory circuits and crosstalk among PTMs. Additionally, we highlight emerging computational tools for PTM site prediction and identify shared enzymatic nodes exploitable for host-directed antiviral strategies. This integrative framework positions PTMs as not merely bystanders but as central modulators of viral fitness and host vulnerability, offering novel avenues for therapeutic intervention against SARS-CoV-2 and future pandemic threats.},
}
RevDate: 2026-02-26
Chronic hypoxia adaptation at high altitude: a perspective on Its potential role in mortality in viral pneumonia-associated ARDS and implications for personalized critical care.
Critical care (London, England) pii:10.1186/s13054-026-05927-9 [Epub ahead of print].
Additional Links: PMID-41742211
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PubMed:
Citation:
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@article {pmid41742211,
year = {2026},
author = {Ortiz-Prado, E and Cadena-Padilla, MP and Vélez-Páez, JL and Vasconez-Gonzalez, J and Izquierdo-Condoy, JS and Vergara, M and Viscor, G},
title = {Chronic hypoxia adaptation at high altitude: a perspective on Its potential role in mortality in viral pneumonia-associated ARDS and implications for personalized critical care.},
journal = {Critical care (London, England)},
volume = {},
number = {},
pages = {},
doi = {10.1186/s13054-026-05927-9},
pmid = {41742211},
issn = {1466-609X},
}
RevDate: 2026-02-25
Assessment and management of post-COVID-19 pulmonary complications: a rapid review.
European respiratory review : an official journal of the European Respiratory Society, 35(179):.
The rising global prevalence of post-COVID-19 condition (PCC) underscores the substantial and ongoing burden faced by individuals following severe acute respiratory syndrome coronavirus 2 infection. The volume of emerging evidence regarding pulmonary-related PCC complications highlights the urgent need for current, evidence-informed guidelines to ensure timely assessment and effective treatment for those affected by PCC. Thus, the aim of this review was to synthesise existing research on the management and treatment of pulmonary complications in individuals with PCC. A rapid review of published and grey literature focused on pulmonary-related PCC complications was completed in November 2023 and updated in June 2025, in accordance with PRISMA (preferred reporting items for systematic reviews and meta-analyses) guidelines. We identified 73 unique articles, including 12 guidance documents, 24 secondary studies (including 11 systematic reviews with meta-analyses, eight systematic reviews and three scoping reviews) and 37 primary research studies (13 randomised controlled trials) and narratively synthesised their findings. Guidance documents addressed workup and management for pulmonary-related PCC complications, recommending the use of pulmonary function testing with diffusing capacity and the importance of ruling out other conditions. Although evidence regarding the use of medical and pharmacological interventions for treatment of pulmonary-related PCC complications were limited and inconclusive, the current evidence base suggested potential effectiveness of a multidisciplinary rehabilitation approach for pulmonary-related PCC treatment, involving specialist consultations and tailored rehabilitation programmes. The heterogeneity in study quality and risk of bias warrants cautious interpretation of the findings. The current evidence and evolving healthcare landscape suggest the need for updated, evidence-informed clinical guidance.
Additional Links: PMID-41741003
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Citation:
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@article {pmid41741003,
year = {2026},
author = {Michaelchuk, W and Soril, LJJ and Chiarieri-Hirsch, D and Giroux, E and Shatto, J and Gershon, AS and Gupta, S and Stickland, MK and Lam, GY},
title = {Assessment and management of post-COVID-19 pulmonary complications: a rapid review.},
journal = {European respiratory review : an official journal of the European Respiratory Society},
volume = {35},
number = {179},
pages = {},
pmid = {41741003},
issn = {1600-0617},
abstract = {The rising global prevalence of post-COVID-19 condition (PCC) underscores the substantial and ongoing burden faced by individuals following severe acute respiratory syndrome coronavirus 2 infection. The volume of emerging evidence regarding pulmonary-related PCC complications highlights the urgent need for current, evidence-informed guidelines to ensure timely assessment and effective treatment for those affected by PCC. Thus, the aim of this review was to synthesise existing research on the management and treatment of pulmonary complications in individuals with PCC. A rapid review of published and grey literature focused on pulmonary-related PCC complications was completed in November 2023 and updated in June 2025, in accordance with PRISMA (preferred reporting items for systematic reviews and meta-analyses) guidelines. We identified 73 unique articles, including 12 guidance documents, 24 secondary studies (including 11 systematic reviews with meta-analyses, eight systematic reviews and three scoping reviews) and 37 primary research studies (13 randomised controlled trials) and narratively synthesised their findings. Guidance documents addressed workup and management for pulmonary-related PCC complications, recommending the use of pulmonary function testing with diffusing capacity and the importance of ruling out other conditions. Although evidence regarding the use of medical and pharmacological interventions for treatment of pulmonary-related PCC complications were limited and inconclusive, the current evidence base suggested potential effectiveness of a multidisciplinary rehabilitation approach for pulmonary-related PCC treatment, involving specialist consultations and tailored rehabilitation programmes. The heterogeneity in study quality and risk of bias warrants cautious interpretation of the findings. The current evidence and evolving healthcare landscape suggest the need for updated, evidence-informed clinical guidance.},
}
RevDate: 2026-02-25
Cancer Care Disruptions Among Vulnerable Populations During the COVID-19 Pandemic: A Scoping Review.
Journal of cancer policy pii:S2213-5383(26)00016-0 [Epub ahead of print].
BACKGROUND: Infectious disease outbreaks, particularly COVID-19, have disrupted cancer care worldwide and disproportionately affected vulnerable populations.
OBJECTIVE: To identify vulnerable groups and characterize patterns of disruption in cancer screening and treatment during the COVID-19 pandemic.
METHODS: Following the Arksey and O'Malley framework, we conducted a scoping review of studies published between 2002 and 2023. Searches were performed in MEDLINE, EMBASE, the Cochrane Library, and Google Scholar. Thirty-four studies were included and analyzed with a focus on healthcare utilization, screening delays, and treatment disruptions across the cancer care continuum.
RESULTS: Older adults, women, immigrant and ethnic minority populations, individuals with low income or education, and patients with comorbidities were most frequently identified as vulnerable. Screening disruptions were more commonly associated with lower educational attainment, whereas treatment delays were concentrated among low-income individuals, newly diagnosed patients, and those with comorbidities. Health system strain, mobility restrictions, fear of infection, and socioeconomic barriers were key contributing factors.
CONCLUSION: This review demonstrates that vulnerability in cancer care during the COVID-19 pandemic is stage-specific and shaped by both population-level and health system-level factors. Mapping these patterns provides evidence to inform stage-specific and population-sensitive strategies to protect cancer care continuity during future public health emergencies.
Additional Links: PMID-41740848
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@article {pmid41740848,
year = {2026},
author = {Lee, GM and Yun, S and Jung, YW and Kim, JH and Chae, YM},
title = {Cancer Care Disruptions Among Vulnerable Populations During the COVID-19 Pandemic: A Scoping Review.},
journal = {Journal of cancer policy},
volume = {},
number = {},
pages = {100716},
doi = {10.1016/j.jcpo.2026.100716},
pmid = {41740848},
issn = {2213-5383},
abstract = {BACKGROUND: Infectious disease outbreaks, particularly COVID-19, have disrupted cancer care worldwide and disproportionately affected vulnerable populations.
OBJECTIVE: To identify vulnerable groups and characterize patterns of disruption in cancer screening and treatment during the COVID-19 pandemic.
METHODS: Following the Arksey and O'Malley framework, we conducted a scoping review of studies published between 2002 and 2023. Searches were performed in MEDLINE, EMBASE, the Cochrane Library, and Google Scholar. Thirty-four studies were included and analyzed with a focus on healthcare utilization, screening delays, and treatment disruptions across the cancer care continuum.
RESULTS: Older adults, women, immigrant and ethnic minority populations, individuals with low income or education, and patients with comorbidities were most frequently identified as vulnerable. Screening disruptions were more commonly associated with lower educational attainment, whereas treatment delays were concentrated among low-income individuals, newly diagnosed patients, and those with comorbidities. Health system strain, mobility restrictions, fear of infection, and socioeconomic barriers were key contributing factors.
CONCLUSION: This review demonstrates that vulnerability in cancer care during the COVID-19 pandemic is stage-specific and shaped by both population-level and health system-level factors. Mapping these patterns provides evidence to inform stage-specific and population-sensitive strategies to protect cancer care continuity during future public health emergencies.},
}
RevDate: 2026-02-25
Evidence-based assessment of safety and mechanistic questions Related to mRNA COVID-19 Vaccines.
Vaccine, 77:128394 pii:S0264-410X(26)00202-1 [Epub ahead of print].
Messenger RNA (mRNA) COVID-19 vaccines have been administered globally at unprecedented scale and have demonstrated strong effectiveness against severe disease, hospitalization, and death. Extensive safety monitoring across randomized clinical trials, national surveillance systems, and global pharmacovigilance programs has consistently supported a favorable benefit-risk profile for these vaccines. Despite this evidence, a range of questions and mechanistic hypotheses continue to circulate, including assertions of increased risk of malignancies, autoimmune diseases, and all-cause mortality, as well as proposed mechanisms involving product-related impurities (e.g. DNA contamination), biodistribution and antigen persistence, non-canonical translation (e.g. ribosomal frame-shifting), and immune modulation. This targeted narrative review synthesizes nonclinical, clinical, pharmacoepidemiologic, and regulatory evidence relevant to these mechanistic and safety related questions. Published literature, regulatory assessments, and surveillance data were qualitatively evaluated in the context of biological plausibility, methodological rigor, and consistency across independent data sources. Across the body of evidence, findings do not support increased long-term mortality, malignancy, autoimmune disease, genotoxicity or other long-term safety issues attributable to mRNA COVID-19 vaccination. On the contrary, several large population-based studies have reported lower all-cause mortality among vaccinated individuals. Residual DNA levels are within established regulatory limits when measured using validated methods, and no credible mechanism supports genomic integration. Biodistribution studies demonstrate expected localization to the injection site and lymphoid tissues with no persistence. Immunologic findings, including IgG4 subclass responses, have not been associated with impaired protection in real-world vaccine effectiveness studies. Collectively, the evidence supports the safety and effectiveness of mRNA COVID-19 vaccines. Ongoing surveillance and rigorous evaluation remain essential to inform public health policy. Importantly, vaccine safety questions should be assessed using transparent, structured frameworks that systematically weigh benefits, harms, quality of evidence, values, and feasibility.
Additional Links: PMID-41740458
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PubMed:
Citation:
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@article {pmid41740458,
year = {2026},
author = {Sohn, WY and Goody, SMG and Reid, DW and Edwards, DK and Urdaneta, V and Doyle, BP and Straus, WL and Henry, C and Rizkalla, B},
title = {Evidence-based assessment of safety and mechanistic questions Related to mRNA COVID-19 Vaccines.},
journal = {Vaccine},
volume = {77},
number = {},
pages = {128394},
doi = {10.1016/j.vaccine.2026.128394},
pmid = {41740458},
issn = {1873-2518},
abstract = {Messenger RNA (mRNA) COVID-19 vaccines have been administered globally at unprecedented scale and have demonstrated strong effectiveness against severe disease, hospitalization, and death. Extensive safety monitoring across randomized clinical trials, national surveillance systems, and global pharmacovigilance programs has consistently supported a favorable benefit-risk profile for these vaccines. Despite this evidence, a range of questions and mechanistic hypotheses continue to circulate, including assertions of increased risk of malignancies, autoimmune diseases, and all-cause mortality, as well as proposed mechanisms involving product-related impurities (e.g. DNA contamination), biodistribution and antigen persistence, non-canonical translation (e.g. ribosomal frame-shifting), and immune modulation. This targeted narrative review synthesizes nonclinical, clinical, pharmacoepidemiologic, and regulatory evidence relevant to these mechanistic and safety related questions. Published literature, regulatory assessments, and surveillance data were qualitatively evaluated in the context of biological plausibility, methodological rigor, and consistency across independent data sources. Across the body of evidence, findings do not support increased long-term mortality, malignancy, autoimmune disease, genotoxicity or other long-term safety issues attributable to mRNA COVID-19 vaccination. On the contrary, several large population-based studies have reported lower all-cause mortality among vaccinated individuals. Residual DNA levels are within established regulatory limits when measured using validated methods, and no credible mechanism supports genomic integration. Biodistribution studies demonstrate expected localization to the injection site and lymphoid tissues with no persistence. Immunologic findings, including IgG4 subclass responses, have not been associated with impaired protection in real-world vaccine effectiveness studies. Collectively, the evidence supports the safety and effectiveness of mRNA COVID-19 vaccines. Ongoing surveillance and rigorous evaluation remain essential to inform public health policy. Importantly, vaccine safety questions should be assessed using transparent, structured frameworks that systematically weigh benefits, harms, quality of evidence, values, and feasibility.},
}
RevDate: 2026-02-25
Links between COVID-19, long COVID, and neurodegeneration: The role of glycosphingolipids.
Pharmacological reviews, 78(2):100113 pii:S0031-6997(26)00001-3 [Epub ahead of print].
Glycosphingolipids (GSLs) play major roles in viral infections by mediating viral entry and egress from cells in lipid rafts; however, GSLs are also important in neurodegenerative diseases. The role of GSLs in acute COVID-19 infection is critical but remains less-studied in the sequelae of long COVID (post-COVID condition); because the same enzymes that regulate GSL metabolism are critical for viral entry and exit, neuromuscular junctions, neurological function, and cellular metabolism, it is important to determine whether long COVID may increase the risk of subsequent neurodegeneration. SARS-CoV-2 infection alters lipid metabolism and oxygen use and can bind to and modify the expression of neurotrophic GSLs such as GM1 ganglioside. GM1 (N-acetylneuraminic acid) is human-specific and probably evolved as a result of a pandemic 3-2.5 million years ago that drove its selection. GM1 functions as a coreceptor with angiotensin-converting enzyme 2 for SARS-CoV-2 while also being a neurotrophin. Viral multiplication takes place in the endoplasmic reticulum/Golgi apparatus, where GSLs are synthesized. This review defines the complex interaction between viruses, GSLs, and neurodegeneration, which provides new perspectives on the interlinked metabolic changes. A European working group has been set up to assess the risks of neurodegeneration with long COVID, based on potential GSL-mediated mechanisms. SIGNIFICANCE STATEMENT: The SARS-CoV-2 pandemic has resulted in a large number of subjects living with long-term consequences (long COVID). Glycosphingolipids and gangliosides are involved in both viral infections and neurodegeneration; hence, it is important to evaluate whether long COVID may increase the risk of neurodegeneration via this route. This study is the result of a European consortium formed to evaluate this possibility.
Additional Links: PMID-41740316
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PubMed:
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@article {pmid41740316,
year = {2026},
author = {Spedding, M and Aerts, J and Alexander, S and Bellozzi Woestelandt, AG and Chiricozzi, E and Henriques, A and Lledo, PM and Loeffler, JP and Perera, R and Platt, FM and Pradat, PF and Rene, F and Schapira, A and St Clair, L and Talbot, K and Taquet, M and Toborek, M and Turner, B and Zandi, M and Gressens, P},
title = {Links between COVID-19, long COVID, and neurodegeneration: The role of glycosphingolipids.},
journal = {Pharmacological reviews},
volume = {78},
number = {2},
pages = {100113},
doi = {10.1016/j.pharmr.2026.100113},
pmid = {41740316},
issn = {1521-0081},
abstract = {Glycosphingolipids (GSLs) play major roles in viral infections by mediating viral entry and egress from cells in lipid rafts; however, GSLs are also important in neurodegenerative diseases. The role of GSLs in acute COVID-19 infection is critical but remains less-studied in the sequelae of long COVID (post-COVID condition); because the same enzymes that regulate GSL metabolism are critical for viral entry and exit, neuromuscular junctions, neurological function, and cellular metabolism, it is important to determine whether long COVID may increase the risk of subsequent neurodegeneration. SARS-CoV-2 infection alters lipid metabolism and oxygen use and can bind to and modify the expression of neurotrophic GSLs such as GM1 ganglioside. GM1 (N-acetylneuraminic acid) is human-specific and probably evolved as a result of a pandemic 3-2.5 million years ago that drove its selection. GM1 functions as a coreceptor with angiotensin-converting enzyme 2 for SARS-CoV-2 while also being a neurotrophin. Viral multiplication takes place in the endoplasmic reticulum/Golgi apparatus, where GSLs are synthesized. This review defines the complex interaction between viruses, GSLs, and neurodegeneration, which provides new perspectives on the interlinked metabolic changes. A European working group has been set up to assess the risks of neurodegeneration with long COVID, based on potential GSL-mediated mechanisms. SIGNIFICANCE STATEMENT: The SARS-CoV-2 pandemic has resulted in a large number of subjects living with long-term consequences (long COVID). Glycosphingolipids and gangliosides are involved in both viral infections and neurodegeneration; hence, it is important to evaluate whether long COVID may increase the risk of neurodegeneration via this route. This study is the result of a European consortium formed to evaluate this possibility.},
}
RevDate: 2026-02-25
Emerging roles of IL-9 and Th9 cells in respiratory viral illnesses.
Seminars in immunology, 81:102017 pii:S1044-5323(26)00004-7 [Epub ahead of print].
Upon antigenic stimulation and cytokine cues, CD4[+] T cells differentiate into specialized helper subsets, giving rise to Th1, Th2, Th9 and Th17 cell lineages. These subsets orchestrate distinct immune functions that protect the host but can also drive immunopathology when dysregulated. The classical Th1-Th2 paradigm expanded with the discovery of Th17 and Th9 cells, revealing greater diversity and complexity in Th cell biology. Th9 cells, generated under the influence of TGF-β and IL-4, are defined by robust production of interleukin-9 (IL-9). IL-9 is now recognized as a multifunctional mediator produced by Th9 cells, mast cells, ILC2s, Tregs and certain Th17 subsets. Fate-mapping and reporter mouse models have improved our understanding of IL-9-producing immunocytes, though limitations remain in defining temporal and tissue-specific dynamics. As shown earlier, IL-9 promotes mastcell proliferation, mucus hypersecretion, epithelial changes and airway remodelling in allergic inflammation and asthma. Genetic studies have linked IL-9/IL-9 receptor variants to increased susceptibility to allergic diseases such as asthma. Similarly, during respiratory viral infections, including RSV and COVID-19, IL-9 amplifies type 2 inflammation, granulocyte recruitment and mucus production, exacerbating airway obstruction. In fact, emerging evidence implicates a Foxo1-IL-9 axis in COVID-19, where IL-9 enhances lung inflammation and impairs antiviral interferon-stimulated gene responses. Collectively, IL-9 represents a context-dependent driver of virus-induced lung pathology and a promising therapeutic target requiring deeper mechanistic and translational investigation.
Additional Links: PMID-41740281
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PubMed:
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@article {pmid41740281,
year = {2026},
author = {Dandotiya, J and Sadhu, S and Chandwaskar, RR and Awasthi, A},
title = {Emerging roles of IL-9 and Th9 cells in respiratory viral illnesses.},
journal = {Seminars in immunology},
volume = {81},
number = {},
pages = {102017},
doi = {10.1016/j.smim.2026.102017},
pmid = {41740281},
issn = {1096-3618},
abstract = {Upon antigenic stimulation and cytokine cues, CD4[+] T cells differentiate into specialized helper subsets, giving rise to Th1, Th2, Th9 and Th17 cell lineages. These subsets orchestrate distinct immune functions that protect the host but can also drive immunopathology when dysregulated. The classical Th1-Th2 paradigm expanded with the discovery of Th17 and Th9 cells, revealing greater diversity and complexity in Th cell biology. Th9 cells, generated under the influence of TGF-β and IL-4, are defined by robust production of interleukin-9 (IL-9). IL-9 is now recognized as a multifunctional mediator produced by Th9 cells, mast cells, ILC2s, Tregs and certain Th17 subsets. Fate-mapping and reporter mouse models have improved our understanding of IL-9-producing immunocytes, though limitations remain in defining temporal and tissue-specific dynamics. As shown earlier, IL-9 promotes mastcell proliferation, mucus hypersecretion, epithelial changes and airway remodelling in allergic inflammation and asthma. Genetic studies have linked IL-9/IL-9 receptor variants to increased susceptibility to allergic diseases such as asthma. Similarly, during respiratory viral infections, including RSV and COVID-19, IL-9 amplifies type 2 inflammation, granulocyte recruitment and mucus production, exacerbating airway obstruction. In fact, emerging evidence implicates a Foxo1-IL-9 axis in COVID-19, where IL-9 enhances lung inflammation and impairs antiviral interferon-stimulated gene responses. Collectively, IL-9 represents a context-dependent driver of virus-induced lung pathology and a promising therapeutic target requiring deeper mechanistic and translational investigation.},
}
RevDate: 2026-02-25
CmpDate: 2026-02-25
Biomarker-guided use of corticosteroids in pneumonia.
Pneumonia (Nathan Qld.), 18(1):.
Community-acquired pneumonia (CAP) is one of the leading causes of death worldwide. Although corticosteroids have been proposed as immunomodulatory, controversies surrounding the results of clinical trials have limited their widespread use. This review aims to determine which biomarker-guided corticosteroid treatment for CAP is generally agreed upon in the latest published studies and to discuss the main aspects to be taken into consideration based on lessons learnt from patients with conditions such as influenza, SARS-CoV-2 infection or the recently identified subphenotypes in acute respiratory distress syndrome (ARDS). Most studies have demonstrated that high C-reactive protein concentrations at the time of admission are associated with a hyperinflammatory state and that patients are more likely to benefit from corticosteroid treatment if they have high concentrations. High levels of C-reactive protein (CRP) were used as an inclusion criterion in one clinical trial, demonstrating that treatment failure was reduced in the corticosteroid group. A post-hoc analysis of the results of several studies also showed that CRP levels above 200 mg/L were associated with benefits in patients receiving corticosteroids. Recent guidelines have proposed the use of corticosteroids in patients with severe CAP or septic shock. Corticosteroids could be more beneficial for patients with a hyperinflammatory subphenotype; however, there are currently no prospective studies evaluating this approach. Further studies are needed to clarify the role of biomarkers in personalised medicine for patients with CAP. In the meantime, patients with severe CAP or high CRP levels should be treated with corticosteroids.
Additional Links: PMID-41736159
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Citation:
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@article {pmid41736159,
year = {2026},
author = {Soriano Puig, A and Monforte, V and Camprubí-Rimblas, M and Artigas, A and Ceccato, A},
title = {Biomarker-guided use of corticosteroids in pneumonia.},
journal = {Pneumonia (Nathan Qld.)},
volume = {18},
number = {1},
pages = {},
pmid = {41736159},
issn = {2200-6133},
abstract = {Community-acquired pneumonia (CAP) is one of the leading causes of death worldwide. Although corticosteroids have been proposed as immunomodulatory, controversies surrounding the results of clinical trials have limited their widespread use. This review aims to determine which biomarker-guided corticosteroid treatment for CAP is generally agreed upon in the latest published studies and to discuss the main aspects to be taken into consideration based on lessons learnt from patients with conditions such as influenza, SARS-CoV-2 infection or the recently identified subphenotypes in acute respiratory distress syndrome (ARDS). Most studies have demonstrated that high C-reactive protein concentrations at the time of admission are associated with a hyperinflammatory state and that patients are more likely to benefit from corticosteroid treatment if they have high concentrations. High levels of C-reactive protein (CRP) were used as an inclusion criterion in one clinical trial, demonstrating that treatment failure was reduced in the corticosteroid group. A post-hoc analysis of the results of several studies also showed that CRP levels above 200 mg/L were associated with benefits in patients receiving corticosteroids. Recent guidelines have proposed the use of corticosteroids in patients with severe CAP or septic shock. Corticosteroids could be more beneficial for patients with a hyperinflammatory subphenotype; however, there are currently no prospective studies evaluating this approach. Further studies are needed to clarify the role of biomarkers in personalised medicine for patients with CAP. In the meantime, patients with severe CAP or high CRP levels should be treated with corticosteroids.},
}
RevDate: 2026-02-24
CmpDate: 2026-02-24
Antiviral drug discovery and development: challenges and future directions.
Signal transduction and targeted therapy, 11(1):.
The coronavirus disease 2019 (COVID-19) pandemic has stimulated extensive endeavors toward the development of therapeutic interventions targeting severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and human proteins for viral infection control, encompassing numerous potential drugs and thousands of patients participating in clinical trials. These concerted efforts have resulted in significant advancements in antiviral drug discovery and development. In this review, we present a comprehensive timeline detailing the development of antiviral drugs, tracing the progression from early viral inhibitors to modern broad-spectrum antiviral agents. We also outline the current status of advancements in antiviral drug discovery, encompassing target-based strategies, innovative mechanism-based approaches, and pharmacokinetic optimization. Furthermore, we discuss the challenges and future prospects gained from COVID-19 and other infectious diseases, covering knowledge of artificial intelligence strategies, the utilization of medicinal chemistry tools, and advancements in nanotechnology applications. The application of artificial intelligence in drug discovery is increasingly prevalent, particularly in the areas of protein structure prediction, drug target identification, and bioactivity forecasting. Nanotechnology has played a crucial role in the delivery of antiviral drugs and the development of vaccines, exemplified by the use of lipid nanoparticles in mRNA vaccines. Additionally, we highlight potential future directions for drug discovery, such as targeting membraneless organelles (liquid‒liquid phase separation).
Additional Links: PMID-41735249
PubMed:
Citation:
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@article {pmid41735249,
year = {2026},
author = {Du, S and Hu, X and Li, P and Xu, S and Kim, M and Liu, X and Zhan, P},
title = {Antiviral drug discovery and development: challenges and future directions.},
journal = {Signal transduction and targeted therapy},
volume = {11},
number = {1},
pages = {},
pmid = {41735249},
issn = {2059-3635},
mesh = {Humans ; *Antiviral Agents/therapeutic use/chemistry ; *Drug Discovery/trends/methods ; *SARS-CoV-2/drug effects ; *COVID-19 Drug Treatment ; *COVID-19/virology ; Artificial Intelligence ; *Drug Development ; },
abstract = {The coronavirus disease 2019 (COVID-19) pandemic has stimulated extensive endeavors toward the development of therapeutic interventions targeting severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and human proteins for viral infection control, encompassing numerous potential drugs and thousands of patients participating in clinical trials. These concerted efforts have resulted in significant advancements in antiviral drug discovery and development. In this review, we present a comprehensive timeline detailing the development of antiviral drugs, tracing the progression from early viral inhibitors to modern broad-spectrum antiviral agents. We also outline the current status of advancements in antiviral drug discovery, encompassing target-based strategies, innovative mechanism-based approaches, and pharmacokinetic optimization. Furthermore, we discuss the challenges and future prospects gained from COVID-19 and other infectious diseases, covering knowledge of artificial intelligence strategies, the utilization of medicinal chemistry tools, and advancements in nanotechnology applications. The application of artificial intelligence in drug discovery is increasingly prevalent, particularly in the areas of protein structure prediction, drug target identification, and bioactivity forecasting. Nanotechnology has played a crucial role in the delivery of antiviral drugs and the development of vaccines, exemplified by the use of lipid nanoparticles in mRNA vaccines. Additionally, we highlight potential future directions for drug discovery, such as targeting membraneless organelles (liquid‒liquid phase separation).},
}
MeSH Terms:
show MeSH Terms
hide MeSH Terms
Humans
*Antiviral Agents/therapeutic use/chemistry
*Drug Discovery/trends/methods
*SARS-CoV-2/drug effects
*COVID-19 Drug Treatment
*COVID-19/virology
Artificial Intelligence
*Drug Development
RevDate: 2026-02-24
CmpDate: 2026-02-24
Mental health impact of the COVID-19 pandemic on frontline healthcare workers in Ethiopia: a scoping review of associated mental health risk and protective factors.
BMJ open, 16(2):e107175.
OBJECTIVES: The mental health impacts of COVID-19 on frontline healthcare workers have been reported globally; however, there is limited evidence from low-income countries such as Ethiopia. We reviewed the literature to understand how COVID-19 impacted the mental health of frontline healthcare workers, including the associated risk and protective factors.
DESIGN: A scoping review of peer-reviewed research was conducted between 2020-2025 to explore the mental health and well-being of frontline healthcare workers in Ethiopia during COVID-19. The process adhered to the guidelines for data extraction outlined in the Preferred Reporting Items for Systematic Reviews and Meta-Analyses extension for Scoping Reviews. Our search identified 35 studies, of which 29 studies were included in the final synthesis.
DATA SOURCES: Three online databases, PubMed, Web of Science and PsycInfo, were systematically searched for data.
ELIGIBILITY CRITERIA: Studies were considered for inclusion in the review if they focused on mental health conditions and psychosocial well-being among healthcare workers during COVID-19 in Ethiopia. Studies were only included if published in English and excluded if they were conference abstracts, case studies, reviews, commentaries, contained incomplete data or lacked variables of interest.
DATA EXTRACTION AND SYNTHESIS: Data extraction was conducted manually by two reviewers by using a data extraction sheet created in Excel.
RESULTS: Most frontline healthcare workers experienced symptoms of insomnia, psychological distress, stress, anxiety, post-traumatic stress disorder and depression during COVID-19. Female frontline healthcare workers, nurses, midwives and laboratory technicians reported higher rates of adverse mental health outcomes. Our results found that being married, living together with a spouse and having a high educational level were risk factors for adverse mental health outcomes.
CONCLUSION: The mental health and well-being of frontline healthcare workers is at risk during a global health crisis; however, there is a limited understanding of how to protect the mental health of frontline healthcare workers in low-income countries, such as Ethiopia, at such a critical time. Additional research is needed to better inform mental health preparedness interventions for frontline healthcare workers in these contexts, particularly given predictions of another pandemic occurring within the next decade.
Additional Links: PMID-41734932
PubMed:
Citation:
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@article {pmid41734932,
year = {2026},
author = {Dræbel, TA and Birhanu, Z and Lien, L and Soerensen, JB and Andersen, LS and Terefe Tucho, G and Mekonnen, H},
title = {Mental health impact of the COVID-19 pandemic on frontline healthcare workers in Ethiopia: a scoping review of associated mental health risk and protective factors.},
journal = {BMJ open},
volume = {16},
number = {2},
pages = {e107175},
pmid = {41734932},
issn = {2044-6055},
mesh = {Humans ; Ethiopia/epidemiology ; *COVID-19/psychology/epidemiology ; *Health Personnel/psychology ; *Mental Health ; SARS-CoV-2 ; Risk Factors ; Protective Factors ; },
abstract = {OBJECTIVES: The mental health impacts of COVID-19 on frontline healthcare workers have been reported globally; however, there is limited evidence from low-income countries such as Ethiopia. We reviewed the literature to understand how COVID-19 impacted the mental health of frontline healthcare workers, including the associated risk and protective factors.
DESIGN: A scoping review of peer-reviewed research was conducted between 2020-2025 to explore the mental health and well-being of frontline healthcare workers in Ethiopia during COVID-19. The process adhered to the guidelines for data extraction outlined in the Preferred Reporting Items for Systematic Reviews and Meta-Analyses extension for Scoping Reviews. Our search identified 35 studies, of which 29 studies were included in the final synthesis.
DATA SOURCES: Three online databases, PubMed, Web of Science and PsycInfo, were systematically searched for data.
ELIGIBILITY CRITERIA: Studies were considered for inclusion in the review if they focused on mental health conditions and psychosocial well-being among healthcare workers during COVID-19 in Ethiopia. Studies were only included if published in English and excluded if they were conference abstracts, case studies, reviews, commentaries, contained incomplete data or lacked variables of interest.
DATA EXTRACTION AND SYNTHESIS: Data extraction was conducted manually by two reviewers by using a data extraction sheet created in Excel.
RESULTS: Most frontline healthcare workers experienced symptoms of insomnia, psychological distress, stress, anxiety, post-traumatic stress disorder and depression during COVID-19. Female frontline healthcare workers, nurses, midwives and laboratory technicians reported higher rates of adverse mental health outcomes. Our results found that being married, living together with a spouse and having a high educational level were risk factors for adverse mental health outcomes.
CONCLUSION: The mental health and well-being of frontline healthcare workers is at risk during a global health crisis; however, there is a limited understanding of how to protect the mental health of frontline healthcare workers in low-income countries, such as Ethiopia, at such a critical time. Additional research is needed to better inform mental health preparedness interventions for frontline healthcare workers in these contexts, particularly given predictions of another pandemic occurring within the next decade.},
}
MeSH Terms:
show MeSH Terms
hide MeSH Terms
Humans
Ethiopia/epidemiology
*COVID-19/psychology/epidemiology
*Health Personnel/psychology
*Mental Health
SARS-CoV-2
Risk Factors
Protective Factors
RevDate: 2026-02-25
Therapeutic Approaches to Treat SARS-CoV-2.
ChemMedChem, 21(4):e202500387.
Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2), also known as COVID-19, spread across the globe, leading to a pandemic. Initially, the drug remdesivir is approved by the FDA for the treatment of SARS-CoV-2. Significant efforts have been directed toward epidemiology of the SARS-CoV-2 virus to discover potential drug targets that may contribute to the development of effective prevention and treatment strategies. The structure and functions of SARS-CoV-2 proteins that may be potential drug targets, including the spike protein, main protease, papain-like protease, RNA-dependent RNA polymerase, host proteins like angiotensin-converting enzyme 2, and transmembrane protease and serine 2, have been thoroughly studied. Biological screening platforms and repurposing have resulted in the discovery of drugs such as nirmatrelvir-ritonavir (Paxlovid), remdesivir (Veklury), molnupiravir (Lagevrio), anakinra (Kineret), vilobelimab (Gohibic), baricitinib (Olumiant), and tocilizumab (Actemra). The present analysis provides details on the pathogenesis, prevention, diagnosis, clinical characteristics, and potential treatment options currently available worldwide.
Additional Links: PMID-41739653
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PubMed:
Citation:
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@article {pmid41739653,
year = {2026},
author = {Sharma, L and Maheshwari, N and Maheshwari, N and Teli, G and Chelvam, V},
title = {Therapeutic Approaches to Treat SARS-CoV-2.},
journal = {ChemMedChem},
volume = {21},
number = {4},
pages = {e202500387},
doi = {10.1002/cmdc.202500387},
pmid = {41739653},
issn = {1860-7187},
support = {IITI 2023-25//Indian Institute of Technology Indore/ ; },
abstract = {Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2), also known as COVID-19, spread across the globe, leading to a pandemic. Initially, the drug remdesivir is approved by the FDA for the treatment of SARS-CoV-2. Significant efforts have been directed toward epidemiology of the SARS-CoV-2 virus to discover potential drug targets that may contribute to the development of effective prevention and treatment strategies. The structure and functions of SARS-CoV-2 proteins that may be potential drug targets, including the spike protein, main protease, papain-like protease, RNA-dependent RNA polymerase, host proteins like angiotensin-converting enzyme 2, and transmembrane protease and serine 2, have been thoroughly studied. Biological screening platforms and repurposing have resulted in the discovery of drugs such as nirmatrelvir-ritonavir (Paxlovid), remdesivir (Veklury), molnupiravir (Lagevrio), anakinra (Kineret), vilobelimab (Gohibic), baricitinib (Olumiant), and tocilizumab (Actemra). The present analysis provides details on the pathogenesis, prevention, diagnosis, clinical characteristics, and potential treatment options currently available worldwide.},
}
RevDate: 2026-02-25
CmpDate: 2026-02-25
Exacerbations and Management of Asthma in Viral Lower Respiratory Tract Infections: The Significance of Immunoglobulin E.
Immunity, inflammation and disease, 14(2):e70386.
BACKGROUND: Viral-respiratory infections are the most prevalent illness among humans. A viral infection affecting lower respiratory tract infections (LRTI) is a critical health concern worldwide. The COVID-19 pandemic has significantly impacted respiratory health, particularly in individuals with asthma. Other viral respiratory infections and asthma are critical concerns, either. The current study aimed to discuss how elevated IgE levels can influence viral LRTI and potentially exacerbate asthma symptoms, as well as biological treatments targeting IgE in managing asthma.
MATERIALS AND METHODS: The search was conducted in electronical databases (including PubMed, Scopus, Google Scholar, and so on). all obtained documents were listed and reviewed by two independent authors. All relevant studies were included and used for final assessment and data collection.
RESULTS: IgE is a crucial mediator in the pathophysiology of asthma, particularly in type 2-high (T2-high) asthma, where it drives allergic responses and airway inflammation. The interaction between COVID-19 and asthma has illustrated that asthmatic patients may experience increased respiratory symptoms following COVID-19 infection. Interestingly, T2-high asthmatics may have had some protection against severe COVID-19 outcomes, highlighting the need for a nuanced understanding of asthma management during and after the pandemic.
CONCLUSION: Viral infections, particularly those caused by human rhinoviruses, are a significant trigger for asthma exacerbations. These infections can lead to heightened serum IgE levels, which play a vital role in the immune response and the worsening of asthma symptoms. The Th2 inflammatory pathway is frequently upregulated during these infections, associated with increased production of cytokines such as IL-4, IL-5, and IL-13, which aggravate asthma symptoms. Additionally, viral infections can compromise the airway epithelium, resulting in greater exposure to allergens and irritants, and disrupt the balance between Th1 and Th2 cytokines, leading to more severe exacerbations.
Additional Links: PMID-41738365
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Citation:
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@article {pmid41738365,
year = {2026},
author = {Akhavan, M and Yousefi, P and Tabibzadeh, A},
title = {Exacerbations and Management of Asthma in Viral Lower Respiratory Tract Infections: The Significance of Immunoglobulin E.},
journal = {Immunity, inflammation and disease},
volume = {14},
number = {2},
pages = {e70386},
pmid = {41738365},
issn = {2050-4527},
mesh = {Humans ; *Asthma/immunology/therapy ; *Immunoglobulin E/immunology/blood ; *COVID-19/immunology/complications ; SARS-CoV-2/immunology ; *Respiratory Tract Infections/immunology/virology/complications ; Disease Progression ; },
abstract = {BACKGROUND: Viral-respiratory infections are the most prevalent illness among humans. A viral infection affecting lower respiratory tract infections (LRTI) is a critical health concern worldwide. The COVID-19 pandemic has significantly impacted respiratory health, particularly in individuals with asthma. Other viral respiratory infections and asthma are critical concerns, either. The current study aimed to discuss how elevated IgE levels can influence viral LRTI and potentially exacerbate asthma symptoms, as well as biological treatments targeting IgE in managing asthma.
MATERIALS AND METHODS: The search was conducted in electronical databases (including PubMed, Scopus, Google Scholar, and so on). all obtained documents were listed and reviewed by two independent authors. All relevant studies were included and used for final assessment and data collection.
RESULTS: IgE is a crucial mediator in the pathophysiology of asthma, particularly in type 2-high (T2-high) asthma, where it drives allergic responses and airway inflammation. The interaction between COVID-19 and asthma has illustrated that asthmatic patients may experience increased respiratory symptoms following COVID-19 infection. Interestingly, T2-high asthmatics may have had some protection against severe COVID-19 outcomes, highlighting the need for a nuanced understanding of asthma management during and after the pandemic.
CONCLUSION: Viral infections, particularly those caused by human rhinoviruses, are a significant trigger for asthma exacerbations. These infections can lead to heightened serum IgE levels, which play a vital role in the immune response and the worsening of asthma symptoms. The Th2 inflammatory pathway is frequently upregulated during these infections, associated with increased production of cytokines such as IL-4, IL-5, and IL-13, which aggravate asthma symptoms. Additionally, viral infections can compromise the airway epithelium, resulting in greater exposure to allergens and irritants, and disrupt the balance between Th1 and Th2 cytokines, leading to more severe exacerbations.},
}
MeSH Terms:
show MeSH Terms
hide MeSH Terms
Humans
*Asthma/immunology/therapy
*Immunoglobulin E/immunology/blood
*COVID-19/immunology/complications
SARS-CoV-2/immunology
*Respiratory Tract Infections/immunology/virology/complications
Disease Progression
RevDate: 2026-02-25
CmpDate: 2026-02-25
Impact of nutrition on long COVID.
Sports medicine and health science, 8(2):128-144.
Long COVID is characterized by a group of persistent symptoms following the acute SARS-COV2 infection, which presented a multifaceted challenge to the healthcare systems all over the globe. The long COVID symptoms span various organ systems including the respiratory, cardiovascular, gastrointestinal, and neurological manifestations. Mitochondrial dysfunction and immune dysregulation play crucial roles in the long COVID pathophysiology. Recently nutritional intervention gained much attention in managing post-viral syndromes. Effective interventions like supplementation of omega-3 fatty acid, macro and micro nutrients, and vitamins help to reduce systemic inflammation and counteract muscle wasting. Other approaches like nutritional recovery, dietetic interventions, continuous nutritional care post-hospital discharge, nutritional rehabilitation programs, whole-diet approaches like Mediterranean diet, plant-based diet, and caloric optimization, improve overall functional recovery. Physical activity and exercise regimes have been shown to improve fatigue, dyspnea, and cognitive function. Tailored exercise regimes may promote safe rehabilitation. Certain ineffective interventions, such as non-personalized approaches, high dose of antioxidants, use of herbal products that are not clinically validated need to be addressed. Dietary interventions such as personalized nutritional counseling have been demonstrated to improve physical performance in long COVID patients. Further research is needed to refine protocols and identify optimal combinations of dietary and movement-based therapies to support the recovery of long-COVID patients. This narrative review focuses on the ongoing researches that reveals the intricate relationship between nutrition and long COVID recovery and also establishes effective protocols for nutritional care.
Additional Links: PMID-41737593
PubMed:
Citation:
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@article {pmid41737593,
year = {2026},
author = {Thangaleela, S and Wang, CK},
title = {Impact of nutrition on long COVID.},
journal = {Sports medicine and health science},
volume = {8},
number = {2},
pages = {128-144},
pmid = {41737593},
issn = {2666-3376},
abstract = {Long COVID is characterized by a group of persistent symptoms following the acute SARS-COV2 infection, which presented a multifaceted challenge to the healthcare systems all over the globe. The long COVID symptoms span various organ systems including the respiratory, cardiovascular, gastrointestinal, and neurological manifestations. Mitochondrial dysfunction and immune dysregulation play crucial roles in the long COVID pathophysiology. Recently nutritional intervention gained much attention in managing post-viral syndromes. Effective interventions like supplementation of omega-3 fatty acid, macro and micro nutrients, and vitamins help to reduce systemic inflammation and counteract muscle wasting. Other approaches like nutritional recovery, dietetic interventions, continuous nutritional care post-hospital discharge, nutritional rehabilitation programs, whole-diet approaches like Mediterranean diet, plant-based diet, and caloric optimization, improve overall functional recovery. Physical activity and exercise regimes have been shown to improve fatigue, dyspnea, and cognitive function. Tailored exercise regimes may promote safe rehabilitation. Certain ineffective interventions, such as non-personalized approaches, high dose of antioxidants, use of herbal products that are not clinically validated need to be addressed. Dietary interventions such as personalized nutritional counseling have been demonstrated to improve physical performance in long COVID patients. Further research is needed to refine protocols and identify optimal combinations of dietary and movement-based therapies to support the recovery of long-COVID patients. This narrative review focuses on the ongoing researches that reveals the intricate relationship between nutrition and long COVID recovery and also establishes effective protocols for nutritional care.},
}
RevDate: 2026-02-25
CmpDate: 2026-02-25
Relationship Between COVID-19 and Retinal Artery Occlusions.
Journal of ophthalmology, 2026:5545707.
The relationship between coronavirus disease 2019 (COVID-19) infection or vaccination and retinal artery occlusions (RAOs) remains controversial. COVID-19 infection or vaccination can sometimes cause thrombin formation. RAOs occur due to thrombin in the retinal artery. The average age of occurrence after COVID-19 infection was 48.7 ± 17.2 years in central RAO (CRAO) and 41.3 ± 17.8 years in branch RAO (BRAO). After COVID-19 vaccination, the average age was 54.7 ± 17.1 years in CRAO and 62.3 ± 21.2 years in BRAO. The mean time from COVID-19 diagnosis to symptom onset was 10.5 ± 9.3 days in CRAO and 48.3 ± 39.6 days in BRAO. After vaccination, the mean time was 7.3 ± 6.8 days in CRAO and 21.0 ± 24.9 days in BRAO. Initial visual acuity (VA) after COVID-19 infection was 2.53 ± 0.65 in CRAO and 0.09 ± 0.07 in BRAO. Final VA was 2.73 ± 0.12 in CRAO, but data for BRAO were unavailable. After vaccination, initial VA was 2.28 ± 0.97 in CRAO and -0.02 ± 0.16 in BRAO. Final VA was 2.12 ± 1.24 in CRAO and could not be calculated in BRAO. The relationship between COVID-19 or its vaccination and RAOs was investigated through past case reports. Two types of reports existed regarding RAO incidence after the COVID-19 pandemic-some indicated an increase, while others found no change. No reports suggested a decrease in RAO occurrence. The current evidence does not clarify the relationship between COVID-19 or its vaccine and RAOs. However, this relationship cannot be ruled out. Further investigations are necessary, as future infectious disease pandemics may occur.
Additional Links: PMID-41737288
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@article {pmid41737288,
year = {2026},
author = {Muto, T and Machida, S and Imaizumi, S and Kamoi, K},
title = {Relationship Between COVID-19 and Retinal Artery Occlusions.},
journal = {Journal of ophthalmology},
volume = {2026},
number = {},
pages = {5545707},
pmid = {41737288},
issn = {2090-004X},
abstract = {The relationship between coronavirus disease 2019 (COVID-19) infection or vaccination and retinal artery occlusions (RAOs) remains controversial. COVID-19 infection or vaccination can sometimes cause thrombin formation. RAOs occur due to thrombin in the retinal artery. The average age of occurrence after COVID-19 infection was 48.7 ± 17.2 years in central RAO (CRAO) and 41.3 ± 17.8 years in branch RAO (BRAO). After COVID-19 vaccination, the average age was 54.7 ± 17.1 years in CRAO and 62.3 ± 21.2 years in BRAO. The mean time from COVID-19 diagnosis to symptom onset was 10.5 ± 9.3 days in CRAO and 48.3 ± 39.6 days in BRAO. After vaccination, the mean time was 7.3 ± 6.8 days in CRAO and 21.0 ± 24.9 days in BRAO. Initial visual acuity (VA) after COVID-19 infection was 2.53 ± 0.65 in CRAO and 0.09 ± 0.07 in BRAO. Final VA was 2.73 ± 0.12 in CRAO, but data for BRAO were unavailable. After vaccination, initial VA was 2.28 ± 0.97 in CRAO and -0.02 ± 0.16 in BRAO. Final VA was 2.12 ± 1.24 in CRAO and could not be calculated in BRAO. The relationship between COVID-19 or its vaccination and RAOs was investigated through past case reports. Two types of reports existed regarding RAO incidence after the COVID-19 pandemic-some indicated an increase, while others found no change. No reports suggested a decrease in RAO occurrence. The current evidence does not clarify the relationship between COVID-19 or its vaccine and RAOs. However, this relationship cannot be ruled out. Further investigations are necessary, as future infectious disease pandemics may occur.},
}
RevDate: 2026-02-25
CmpDate: 2026-02-25
Use of Artificial Intelligence in Public Health Education for Pandemic Preparedness and Response.
Annals of global health, 92(1):21.
Background: The rapid evolution of artificial intelligence (AI) has enabled new approaches for health education, particularly during public health emergencies. However, evidence remains fragmented on how AI-based educational strategies support preparedness, response, and recovery phases of pandemics and epidemics. Objective: To map the use of AI-based technologies in health education strategies addressing preparedness, response, and recovery during public health emergencies, identifying target populations, intervention characteristics, outcomes, scalability, and knowledge gaps. Methods: This scoping review followed Joanna Briggs Institute methodology and PRISMA-ScR guidelines. Searches were conducted in PubMed/MEDLINE, Scopus, Web of Science, Embase, IEEE Xplore, and LILACS, complemented by gray literature from Google Scholar. Studies published from 2010 onward in English, Portuguese, or Spanish were included. Eligible designs comprised primary studies, methodological or implementation research, and reviews with explicit educational components. Data extraction covered context, populations, AI modalities, educational purposes, delivery channels, supervision requirements, pandemic-cycle phase, scalability, outcomes, and evidence gaps. Results: Forty-one studies met the inclusion criteria. Conversational AI (chatbots and large language models) and algorithmic curation tools using machine learning and natural language processing predominated. Most interventions supported health literacy, risk communication, and misinformation management; others addressed personalized learning, microtraining, and clinical simulation for students and health professionals. Delivery channels included mobile applications, messaging platforms, websites/YouTube, and clinical AI systems. Human oversight (expert validation and curation) was consistently reported as essential for safety and reliability. Interventions mainly targeted the response phase, with emerging applications for preparedness. Major gaps included standardized learning measures, cost-effectiveness evaluations, equity analyses, and governance frameworks ensuring privacy, transparency, and bias control. Conclusions: AI-enabled educational technologies can strengthen rapid, scalable, and personalized learning during health emergencies. Future research should prioritize multicenter studies using standardized indicators, economic and equity assessments, and robust governance frameworks to ensure ethical, safe, and inclusive adoption.
Additional Links: PMID-41736834
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@article {pmid41736834,
year = {2026},
author = {Souza, ECSG and Dos Santos Junior, AG and Félix, AMS and Borges, JPA and de Oliveira, LB and Carneiro, LM and de Sousa, AFL},
title = {Use of Artificial Intelligence in Public Health Education for Pandemic Preparedness and Response.},
journal = {Annals of global health},
volume = {92},
number = {1},
pages = {21},
pmid = {41736834},
issn = {2214-9996},
mesh = {Humans ; *Artificial Intelligence ; *Pandemics/prevention & control ; *Public Health/education ; *Health Education/methods ; COVID-19 ; *Disaster Planning ; Civil Defense/education ; Pandemic Preparedness ; },
abstract = {Background: The rapid evolution of artificial intelligence (AI) has enabled new approaches for health education, particularly during public health emergencies. However, evidence remains fragmented on how AI-based educational strategies support preparedness, response, and recovery phases of pandemics and epidemics. Objective: To map the use of AI-based technologies in health education strategies addressing preparedness, response, and recovery during public health emergencies, identifying target populations, intervention characteristics, outcomes, scalability, and knowledge gaps. Methods: This scoping review followed Joanna Briggs Institute methodology and PRISMA-ScR guidelines. Searches were conducted in PubMed/MEDLINE, Scopus, Web of Science, Embase, IEEE Xplore, and LILACS, complemented by gray literature from Google Scholar. Studies published from 2010 onward in English, Portuguese, or Spanish were included. Eligible designs comprised primary studies, methodological or implementation research, and reviews with explicit educational components. Data extraction covered context, populations, AI modalities, educational purposes, delivery channels, supervision requirements, pandemic-cycle phase, scalability, outcomes, and evidence gaps. Results: Forty-one studies met the inclusion criteria. Conversational AI (chatbots and large language models) and algorithmic curation tools using machine learning and natural language processing predominated. Most interventions supported health literacy, risk communication, and misinformation management; others addressed personalized learning, microtraining, and clinical simulation for students and health professionals. Delivery channels included mobile applications, messaging platforms, websites/YouTube, and clinical AI systems. Human oversight (expert validation and curation) was consistently reported as essential for safety and reliability. Interventions mainly targeted the response phase, with emerging applications for preparedness. Major gaps included standardized learning measures, cost-effectiveness evaluations, equity analyses, and governance frameworks ensuring privacy, transparency, and bias control. Conclusions: AI-enabled educational technologies can strengthen rapid, scalable, and personalized learning during health emergencies. Future research should prioritize multicenter studies using standardized indicators, economic and equity assessments, and robust governance frameworks to ensure ethical, safe, and inclusive adoption.},
}
MeSH Terms:
show MeSH Terms
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Humans
*Artificial Intelligence
*Pandemics/prevention & control
*Public Health/education
*Health Education/methods
COVID-19
*Disaster Planning
Civil Defense/education
Pandemic Preparedness
RevDate: 2026-02-25
CmpDate: 2026-02-25
Security and privacy in e-health technologies: a scoping review of challenges and strategies in primary care.
Family practice, 43(2):.
BACKGROUND: The rapid integration of e-health technologies-such as telehealth, mobile health (mHealth), and electronic health records-has transformed primary care delivery, especially during the COVID-19 pandemic. However, this transformation has revealed significant vulnerabilities in data privacy and security, particularly in decentralized and resource-limited primary care settings. This scoping review aims to map current evidence on privacy and security concerns related to e-health technologies in primary care and to identify mitigation strategies and research gaps.
METHODS: A systematic search was conducted in PubMed, ACM, Scopus, and Web of Science for studies published between 2019 and 2024. Eligible studies addressed both privacy/security issues and e-health technology use in primary care. A two-stage screening process and full-text review were applied. Data were extracted and thematically synthesized.
RESULTS: Fifty-two studies were included. E-health technologies examined included teleconsultations, patient portals, digital decision support tools, and artificial intelligence (AI)-based systems. Among included studies, telehealth accounted for 28%, mHealth and wearables 20%, electronic health records 16%, and AI applications 6%. Common concerns involved data breaches, insufficient encryption, lack of interoperability, consent ambiguity, and challenges in securing virtual consultations. Vulnerable groups-such as older adults and low-literacy populations-faced higher risks. Recommended strategies included privacy-by-design principles, secure infrastructure, user-centered design, clearer governance policies, provider training, and hybrid care models.
CONCLUSION: Addressing privacy and security in e-health requires more than technical solutions. Equitable, safe, and trustworthy systems must incorporate legal, ethical, and human-centered approaches. In primary care, privacy must be positioned as a core element of digital health equity, not an optional enhancement.
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PubMed:
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@article {pmid41736688,
year = {2026},
author = {İşcan, G and Çöme, O},
title = {Security and privacy in e-health technologies: a scoping review of challenges and strategies in primary care.},
journal = {Family practice},
volume = {43},
number = {2},
pages = {},
doi = {10.1093/fampra/cmag006},
pmid = {41736688},
issn = {1460-2229},
mesh = {Humans ; *Primary Health Care ; *Telemedicine ; *Computer Security/standards ; *Confidentiality ; COVID-19/epidemiology ; Electronic Health Records ; *Privacy ; SARS-CoV-2 ; },
abstract = {BACKGROUND: The rapid integration of e-health technologies-such as telehealth, mobile health (mHealth), and electronic health records-has transformed primary care delivery, especially during the COVID-19 pandemic. However, this transformation has revealed significant vulnerabilities in data privacy and security, particularly in decentralized and resource-limited primary care settings. This scoping review aims to map current evidence on privacy and security concerns related to e-health technologies in primary care and to identify mitigation strategies and research gaps.
METHODS: A systematic search was conducted in PubMed, ACM, Scopus, and Web of Science for studies published between 2019 and 2024. Eligible studies addressed both privacy/security issues and e-health technology use in primary care. A two-stage screening process and full-text review were applied. Data were extracted and thematically synthesized.
RESULTS: Fifty-two studies were included. E-health technologies examined included teleconsultations, patient portals, digital decision support tools, and artificial intelligence (AI)-based systems. Among included studies, telehealth accounted for 28%, mHealth and wearables 20%, electronic health records 16%, and AI applications 6%. Common concerns involved data breaches, insufficient encryption, lack of interoperability, consent ambiguity, and challenges in securing virtual consultations. Vulnerable groups-such as older adults and low-literacy populations-faced higher risks. Recommended strategies included privacy-by-design principles, secure infrastructure, user-centered design, clearer governance policies, provider training, and hybrid care models.
CONCLUSION: Addressing privacy and security in e-health requires more than technical solutions. Equitable, safe, and trustworthy systems must incorporate legal, ethical, and human-centered approaches. In primary care, privacy must be positioned as a core element of digital health equity, not an optional enhancement.},
}
MeSH Terms:
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Humans
*Primary Health Care
*Telemedicine
*Computer Security/standards
*Confidentiality
COVID-19/epidemiology
Electronic Health Records
*Privacy
SARS-CoV-2
RevDate: 2026-02-25
CmpDate: 2026-02-25
Telerehabilitation for the Evaluation and Management of a Dizzy Patient: A Mini-Review.
JPMA. The Journal of the Pakistan Medical Association, 76(1):118-120.
Dizziness and vertigo are common, disabling symptoms, especially in older adults. They can negatively affect quality of life and independence of the person. Vestibular rehabilitation is a key treatment, but access is often limited by physical, geographic, and socioeconomic factors. Telerehabilitation has emerged as a viable alternative, particularly during the COVID-19 pandemic. This mini review synthesizes available evidence on vestibular telerehabilitation, focussing on feasibility, delivery methods, outcomes, and future directions. We have included commonly used outcomes measures like balance, gait, gaze stability, dizziness, psychological health, and quality of life. Findings suggest telerehabilitation is an effective alternative to in-person therapy. However, further research is needed to standardize protocols, evaluate cognitive outcomes, and ensure inclusivity across diverse populations. Digital innovations are a promising options for more accessible, patient-centered vestibular care.
Additional Links: PMID-41736351
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PubMed:
Citation:
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@article {pmid41736351,
year = {2026},
author = {V Rey-Matias, BM and S Ignacio, ML and D Leochico, CF and Rathore, FA},
title = {Telerehabilitation for the Evaluation and Management of a Dizzy Patient: A Mini-Review.},
journal = {JPMA. The Journal of the Pakistan Medical Association},
volume = {76},
number = {1},
pages = {118-120},
doi = {10.47391/JPMA.26-08},
pmid = {41736351},
issn = {0030-9982},
mesh = {Humans ; *Dizziness/rehabilitation/diagnosis ; *Telerehabilitation ; COVID-19/epidemiology ; Quality of Life ; *Vertigo/rehabilitation ; },
abstract = {Dizziness and vertigo are common, disabling symptoms, especially in older adults. They can negatively affect quality of life and independence of the person. Vestibular rehabilitation is a key treatment, but access is often limited by physical, geographic, and socioeconomic factors. Telerehabilitation has emerged as a viable alternative, particularly during the COVID-19 pandemic. This mini review synthesizes available evidence on vestibular telerehabilitation, focussing on feasibility, delivery methods, outcomes, and future directions. We have included commonly used outcomes measures like balance, gait, gaze stability, dizziness, psychological health, and quality of life. Findings suggest telerehabilitation is an effective alternative to in-person therapy. However, further research is needed to standardize protocols, evaluate cognitive outcomes, and ensure inclusivity across diverse populations. Digital innovations are a promising options for more accessible, patient-centered vestibular care.},
}
MeSH Terms:
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Humans
*Dizziness/rehabilitation/diagnosis
*Telerehabilitation
COVID-19/epidemiology
Quality of Life
*Vertigo/rehabilitation
RevDate: 2026-02-24
Global prevalence of dry Eye: A systematic review and meta-analysis.
Contact lens & anterior eye : the journal of the British Contact Lens Association, 49(2):102627 pii:S1367-0484(26)00023-8 [Epub ahead of print].
OBJECTIVE: Dry eye significantly impacts global quality of life and productivity, yet existing epidemiological data remain fragmented and outdated, hindering effective prevention and management strategies. This study aimed to estimate the global prevalence of dry eye and examine variations across regions, demographics, diagnostic criteria, study settings, and the COVID-19 pandemic.
METHODS: A systematic search of PubMed, Web of Science, Embase, and Cochrane Library identified 119 cohort or cross-sectional studies involving 15,251,528 participants. Two reviewers independently screened records, extracted data, and assessed study quality using the Joanna Briggs Institute checklist. A random-effects model pooled prevalence estimates, with subgroup analyses exploring heterogeneity.
RESULTS: The global pooled prevalence of dry eye was 34.6% (95% CI: 30.2%-39.4%). Regional disparities were pronounced, with the highest prevalence in Africa 43.9% (95% CI: 31.5%-57.2%) and the lowest in North America 20.9% (95% CI: 8.2%-43.8%). Higher rates were observed in females 39.1% (95% CI: 32.8%-45.8%) vs. males 30.8% (95% CI: 24.8%-37.7%), individuals aged > 40 years 37.0% (95% CI: 29.1%-45.7%) vs. ≤ 40 years 35.0% (95% CI: 25.4%-46.0%), institutional settings 45.2% (95% CI: 36.2%-54.5%), and during COVID-19 44.5% (95% CI: 28.0%-62.2%). Diagnostic criteria significantly influenced estimates, ranging from 6.9% (95% CI: 1.9%-21.7%) (ICD-9-based) to 53.8% (95% CI: 46.7%-60.8%) (OSDI ≥ 13).
CONCLUSIONS: Dry eye represents a major global public health challenge, with prevalence shaped by geographic, demographic, environmental, and methodological factors. The pandemic exacerbated dry eye burden, underscoring the urgency for standardized diagnostic protocols and targeted interventions to mitigate its growing impact.
Additional Links: PMID-41734553
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PubMed:
Citation:
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@article {pmid41734553,
year = {2026},
author = {Xiao, K and Li, L and Zhang, X and Ye, Y and Yao, Y and Liu, Y and Chen, W and Wang, X and Gu, C and He, M and Liang, L and Liu, YC and Zhu, Z},
title = {Global prevalence of dry Eye: A systematic review and meta-analysis.},
journal = {Contact lens & anterior eye : the journal of the British Contact Lens Association},
volume = {49},
number = {2},
pages = {102627},
doi = {10.1016/j.clae.2026.102627},
pmid = {41734553},
issn = {1476-5411},
abstract = {OBJECTIVE: Dry eye significantly impacts global quality of life and productivity, yet existing epidemiological data remain fragmented and outdated, hindering effective prevention and management strategies. This study aimed to estimate the global prevalence of dry eye and examine variations across regions, demographics, diagnostic criteria, study settings, and the COVID-19 pandemic.
METHODS: A systematic search of PubMed, Web of Science, Embase, and Cochrane Library identified 119 cohort or cross-sectional studies involving 15,251,528 participants. Two reviewers independently screened records, extracted data, and assessed study quality using the Joanna Briggs Institute checklist. A random-effects model pooled prevalence estimates, with subgroup analyses exploring heterogeneity.
RESULTS: The global pooled prevalence of dry eye was 34.6% (95% CI: 30.2%-39.4%). Regional disparities were pronounced, with the highest prevalence in Africa 43.9% (95% CI: 31.5%-57.2%) and the lowest in North America 20.9% (95% CI: 8.2%-43.8%). Higher rates were observed in females 39.1% (95% CI: 32.8%-45.8%) vs. males 30.8% (95% CI: 24.8%-37.7%), individuals aged > 40 years 37.0% (95% CI: 29.1%-45.7%) vs. ≤ 40 years 35.0% (95% CI: 25.4%-46.0%), institutional settings 45.2% (95% CI: 36.2%-54.5%), and during COVID-19 44.5% (95% CI: 28.0%-62.2%). Diagnostic criteria significantly influenced estimates, ranging from 6.9% (95% CI: 1.9%-21.7%) (ICD-9-based) to 53.8% (95% CI: 46.7%-60.8%) (OSDI ≥ 13).
CONCLUSIONS: Dry eye represents a major global public health challenge, with prevalence shaped by geographic, demographic, environmental, and methodological factors. The pandemic exacerbated dry eye burden, underscoring the urgency for standardized diagnostic protocols and targeted interventions to mitigate its growing impact.},
}
RevDate: 2026-02-24
CmpDate: 2026-02-24
Mucosal Wound Repair: Reinforcement of Respiratory Mucus Barrier Function by Inorganic Polyphosphate.
Progress in molecular and subcellular biology, 63:175-207.
Epithelial cell damage affects not only the skin, which covers the external surface of the human body, but also the non-keratinized epithelia, the mucosa, that lines the surfaces of internal organs, including the nasopharynx and lungs. This mucosa is characterized by a moist surface formed by the mucus overlying the epithelial cells. In the respiratory tract in particular, mucosa cells are constantly exposed to large amounts of environmental pathogens and stressors, including bacteria and viruses inhaled as aerosols. Therefore, mucins, a group of glycoproteins that constitute a major component of the mucus, play an important role in the innate immune defense provided by the protective mucus shield. This barrier function of the mucus can be disrupted by a number of agents, such as fine dust (particulate matter). Recent results have shown that inorganic polyphosphate (polyP), which can be administered, for example, in the form of a nasopharyngeal spray, offers a promising way to strengthen or repair impaired mucus function. This chapter describes the structure and formation of the mucus and its mucin building blocks, as well as the mode of action of polyP and drug-loaded polyP nanoparticles in restoring the mucus barrier, particularly with regard to their protective function against coronavirus infection.
Additional Links: PMID-41733677
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@article {pmid41733677,
year = {2026},
author = {Wang, X and Schröder, HC and Neufurth, M and Müller, WEG},
title = {Mucosal Wound Repair: Reinforcement of Respiratory Mucus Barrier Function by Inorganic Polyphosphate.},
journal = {Progress in molecular and subcellular biology},
volume = {63},
number = {},
pages = {175-207},
pmid = {41733677},
issn = {0079-6484},
mesh = {Humans ; *Polyphosphates/pharmacology ; *Respiratory Mucosa/drug effects/metabolism/pathology ; *Mucus/metabolism/drug effects ; *Wound Healing/drug effects ; Mucins/metabolism ; Animals ; COVID-19 ; Nanoparticles/chemistry ; },
abstract = {Epithelial cell damage affects not only the skin, which covers the external surface of the human body, but also the non-keratinized epithelia, the mucosa, that lines the surfaces of internal organs, including the nasopharynx and lungs. This mucosa is characterized by a moist surface formed by the mucus overlying the epithelial cells. In the respiratory tract in particular, mucosa cells are constantly exposed to large amounts of environmental pathogens and stressors, including bacteria and viruses inhaled as aerosols. Therefore, mucins, a group of glycoproteins that constitute a major component of the mucus, play an important role in the innate immune defense provided by the protective mucus shield. This barrier function of the mucus can be disrupted by a number of agents, such as fine dust (particulate matter). Recent results have shown that inorganic polyphosphate (polyP), which can be administered, for example, in the form of a nasopharyngeal spray, offers a promising way to strengthen or repair impaired mucus function. This chapter describes the structure and formation of the mucus and its mucin building blocks, as well as the mode of action of polyP and drug-loaded polyP nanoparticles in restoring the mucus barrier, particularly with regard to their protective function against coronavirus infection.},
}
MeSH Terms:
show MeSH Terms
hide MeSH Terms
Humans
*Polyphosphates/pharmacology
*Respiratory Mucosa/drug effects/metabolism/pathology
*Mucus/metabolism/drug effects
*Wound Healing/drug effects
Mucins/metabolism
Animals
COVID-19
Nanoparticles/chemistry
RevDate: 2026-02-24
CmpDate: 2026-02-24
Neutrophils in Coronavirus Disease 2019: Guardians or Triggers of Immunopathology?.
Cell biochemistry and function, 44(2):e70186.
COVID-19 (coronavirus disease 2019) is a respiratory viral disease with a wide range of clinical symptoms that emerged in December 2019. Innate immunity serves as a rapid immune system that can fight off pathogens before they can spread and cause an active infection. Neutrophils, the most abundant innate immune cells, are the first cells to migrate to the site of infection, where they defend against invading pathogens. Once activated at the inflammatory site, neutrophils mediate host protection through multiple mechanisms, including the phagocytosis of pathogens, the release of antimicrobial and pro-inflammatory enzymes, the production of reactive oxygen species (ROS), and the extrusion of their chromatin to form neutrophil extracellular traps (NETs) that bind to extracellular pathogens. Furthermore, neutrophils can move toward the source of the stimulus through a mechanism called chemotaxis, which is mediated by adhesion molecules and chemokine-chemokine receptor axes. However, neutrophil overactivation can have deleterious effects on various organs through the induction of cytokine storms, ROS production, and NET formation. Moreover, the contribution of distinct neutrophil subsets and their plasticity over the course of infection and recovery remain poorly understood. This review summarizes the current knowledge of the interplay between neutrophils and SARS-CoV-2, highlighting the most important mechanisms involved in the pathogenesis of COVID-19, to advance our understanding of this disease.
Additional Links: PMID-41733396
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Citation:
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@article {pmid41733396,
year = {2026},
author = {Henjeroei, FM and Nosratabadi, N and Pourghadamyari, H and Anaeigoudari, A and Sedghy, F and Nosratabadi, R},
title = {Neutrophils in Coronavirus Disease 2019: Guardians or Triggers of Immunopathology?.},
journal = {Cell biochemistry and function},
volume = {44},
number = {2},
pages = {e70186},
doi = {10.1002/cbf.70186},
pmid = {41733396},
issn = {1099-0844},
mesh = {Humans ; *COVID-19/immunology/pathology ; *Neutrophils/immunology/pathology ; *SARS-CoV-2/immunology ; Extracellular Traps/immunology ; Immunity, Innate ; Reactive Oxygen Species/metabolism/immunology ; },
abstract = {COVID-19 (coronavirus disease 2019) is a respiratory viral disease with a wide range of clinical symptoms that emerged in December 2019. Innate immunity serves as a rapid immune system that can fight off pathogens before they can spread and cause an active infection. Neutrophils, the most abundant innate immune cells, are the first cells to migrate to the site of infection, where they defend against invading pathogens. Once activated at the inflammatory site, neutrophils mediate host protection through multiple mechanisms, including the phagocytosis of pathogens, the release of antimicrobial and pro-inflammatory enzymes, the production of reactive oxygen species (ROS), and the extrusion of their chromatin to form neutrophil extracellular traps (NETs) that bind to extracellular pathogens. Furthermore, neutrophils can move toward the source of the stimulus through a mechanism called chemotaxis, which is mediated by adhesion molecules and chemokine-chemokine receptor axes. However, neutrophil overactivation can have deleterious effects on various organs through the induction of cytokine storms, ROS production, and NET formation. Moreover, the contribution of distinct neutrophil subsets and their plasticity over the course of infection and recovery remain poorly understood. This review summarizes the current knowledge of the interplay between neutrophils and SARS-CoV-2, highlighting the most important mechanisms involved in the pathogenesis of COVID-19, to advance our understanding of this disease.},
}
MeSH Terms:
show MeSH Terms
hide MeSH Terms
Humans
*COVID-19/immunology/pathology
*Neutrophils/immunology/pathology
*SARS-CoV-2/immunology
Extracellular Traps/immunology
Immunity, Innate
Reactive Oxygen Species/metabolism/immunology
RevDate: 2026-02-24
CmpDate: 2026-02-24
Post-COVID Syndrome in Patients With Comorbid Hypertension or Diabetes: A Narrative Review of Long-Term Outcomes.
Cureus, 18(1):e102117.
Post-COVID syndrome (PCS), or long COVID, refers to a cluster of enduring symptoms that extend beyond the acute phase of the initial SARS-CoV-2 infection. Acute infection predominantly impacts the respiratory tract, but there is growing evidence for the multisystem involvement, such as cardiovascular, metabolic, and neurological, to be responsible for the prolonged presentation in PCS. Underlying cardiometabolic vulnerability may contribute to a high degree of susceptibility in patients with comorbidities like hypertension (HTN) and diabetes mellitus (DM). This narrative review summarizes current literature regarding PCS in patients with HTN and/or DM, focusing on proposed pathophysiological mechanisms, clinical manifestations, and reported long-term outcomes. In these populations, PCS has been linked across studies to processes including endothelial dysfunction, chronic low-grade inflammation, autonomic imbalance, and potential dysregulation of the renin-angiotensin-aldosterone system (RAAS). Persistent cardiovascular, metabolic, and neurocognitive symptoms are reported, but the magnitude and patterns of risk vary across studies, while comparative findings across HTN and DM remain heterogeneous. Symptoms reported frequently include fatigue, cognitive impairment ("brain fog"), and psychological distress, supporting the multisystem complexity of PCS. Although, previous work has indicated that cardiometabolic comorbidities could interact and moderate PCS severity and persistence, there is an important shortfall of both causality and prognosis, as well as the management of PCS. Longitudinal studies are needed for future research regarding risk stratification, disease course, and targeted interventions in individuals with PCS with comorbid high blood pressure and diabetes.
Additional Links: PMID-41732619
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Citation:
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@article {pmid41732619,
year = {2026},
author = {Manoukian, G and Kundukulam, S and Asatorian, G and Johnson, DM and Masood, MH and Venugopal, A and Manoukian, M and Aswathappa, S},
title = {Post-COVID Syndrome in Patients With Comorbid Hypertension or Diabetes: A Narrative Review of Long-Term Outcomes.},
journal = {Cureus},
volume = {18},
number = {1},
pages = {e102117},
pmid = {41732619},
issn = {2168-8184},
abstract = {Post-COVID syndrome (PCS), or long COVID, refers to a cluster of enduring symptoms that extend beyond the acute phase of the initial SARS-CoV-2 infection. Acute infection predominantly impacts the respiratory tract, but there is growing evidence for the multisystem involvement, such as cardiovascular, metabolic, and neurological, to be responsible for the prolonged presentation in PCS. Underlying cardiometabolic vulnerability may contribute to a high degree of susceptibility in patients with comorbidities like hypertension (HTN) and diabetes mellitus (DM). This narrative review summarizes current literature regarding PCS in patients with HTN and/or DM, focusing on proposed pathophysiological mechanisms, clinical manifestations, and reported long-term outcomes. In these populations, PCS has been linked across studies to processes including endothelial dysfunction, chronic low-grade inflammation, autonomic imbalance, and potential dysregulation of the renin-angiotensin-aldosterone system (RAAS). Persistent cardiovascular, metabolic, and neurocognitive symptoms are reported, but the magnitude and patterns of risk vary across studies, while comparative findings across HTN and DM remain heterogeneous. Symptoms reported frequently include fatigue, cognitive impairment ("brain fog"), and psychological distress, supporting the multisystem complexity of PCS. Although, previous work has indicated that cardiometabolic comorbidities could interact and moderate PCS severity and persistence, there is an important shortfall of both causality and prognosis, as well as the management of PCS. Longitudinal studies are needed for future research regarding risk stratification, disease course, and targeted interventions in individuals with PCS with comorbid high blood pressure and diabetes.},
}
RevDate: 2026-02-23
CmpDate: 2026-02-23
A qualitative analysis of the barriers and facilitators to physicians and trainees seeking help for suicidality.
CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne, 198(7):E238-E248 pii:198/7/E238.
BACKGROUND: Suicidal thoughts among physicians are common and increased during the COVID-19 pandemic, yet many hesitate to seek mental health support. We sought to examine factors influencing seeking help for suicidality among physicians and trainees, their narrative descriptions of suicidality, and the impacts of losing a physician in their lives to suicide.
METHODS: We conducted a qualitative analysis of published narratives from physicians and trainees describing experiences in seeking help for suicidality. We systematically searched MEDLINE and PsycInfo (March 2000 to March 2023) and manually reviewed reference lists of included articles. We analyzed narratives and generated themes using reflexive thematic analysis.
RESULTS: Across 52 narratives, authors commonly described preceding pressures, ways of coping, and intense emotional distress and altered self-perceptions. Barriers to seeking help were rooted in pressures that contributed to suicidality, including a medical culture that values achievement and stoicism, the growing severity of illness, stigma regarding mental health, fears about losing one's license, reluctance to burden others, and limited access to timely, confidential care. In contrast, facilitators to seeking help included access to confidential services, mental health literacy and, most notably, the care and role modelling of seeking help by others. Narratives advocated for cultural and systemic changes within the profession.
INTERPRETATION: Intense pressures to achieve in medicine discourage physicians from acknowledging distress and seeking help, but role modelling of seeking help can attenuate the stigma. Understanding these intersecting factors can inform changes needed to develop targeted suicide prevention strategies for physicians and promote physician well-being.
Additional Links: PMID-41730537
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PubMed:
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@article {pmid41730537,
year = {2026},
author = {Yu, AYA and Stergiopoulos, E and Sukhera, J and Goldbloom, D and Martimianakis, MAT and Smith, S and Zaheer, J},
title = {A qualitative analysis of the barriers and facilitators to physicians and trainees seeking help for suicidality.},
journal = {CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne},
volume = {198},
number = {7},
pages = {E238-E248},
doi = {10.1503/cmaj.250200},
pmid = {41730537},
issn = {1488-2329},
mesh = {Humans ; *Physicians/psychology ; *COVID-19/psychology/epidemiology ; *Suicidal Ideation ; Qualitative Research ; *Suicide/psychology ; *Patient Acceptance of Health Care/psychology ; *Help-Seeking Behavior ; Social Stigma ; SARS-CoV-2 ; Suicide Prevention ; Adaptation, Psychological ; },
abstract = {BACKGROUND: Suicidal thoughts among physicians are common and increased during the COVID-19 pandemic, yet many hesitate to seek mental health support. We sought to examine factors influencing seeking help for suicidality among physicians and trainees, their narrative descriptions of suicidality, and the impacts of losing a physician in their lives to suicide.
METHODS: We conducted a qualitative analysis of published narratives from physicians and trainees describing experiences in seeking help for suicidality. We systematically searched MEDLINE and PsycInfo (March 2000 to March 2023) and manually reviewed reference lists of included articles. We analyzed narratives and generated themes using reflexive thematic analysis.
RESULTS: Across 52 narratives, authors commonly described preceding pressures, ways of coping, and intense emotional distress and altered self-perceptions. Barriers to seeking help were rooted in pressures that contributed to suicidality, including a medical culture that values achievement and stoicism, the growing severity of illness, stigma regarding mental health, fears about losing one's license, reluctance to burden others, and limited access to timely, confidential care. In contrast, facilitators to seeking help included access to confidential services, mental health literacy and, most notably, the care and role modelling of seeking help by others. Narratives advocated for cultural and systemic changes within the profession.
INTERPRETATION: Intense pressures to achieve in medicine discourage physicians from acknowledging distress and seeking help, but role modelling of seeking help can attenuate the stigma. Understanding these intersecting factors can inform changes needed to develop targeted suicide prevention strategies for physicians and promote physician well-being.},
}
MeSH Terms:
show MeSH Terms
hide MeSH Terms
Humans
*Physicians/psychology
*COVID-19/psychology/epidemiology
*Suicidal Ideation
Qualitative Research
*Suicide/psychology
*Patient Acceptance of Health Care/psychology
*Help-Seeking Behavior
Social Stigma
SARS-CoV-2
Suicide Prevention
Adaptation, Psychological
RevDate: 2026-02-23
Effectiveness, Comparative Effectiveness, and Harms of COVID-19 Vaccines in Adults Who Are Not Pregnant or Immunocompromised: A Rapid Review for the American College of Physicians.
Annals of internal medicine [Epub ahead of print].
BACKGROUND: The SARS-CoV-2 Omicron variant continues to pose a global health burden.
PURPOSE: To assess the effectiveness, comparative effectiveness, and harms of COVID-19 vaccines in nonpregnant, nonimmunocompromised adults.
DATA SOURCES: Medline via Ovid and DynaMedex from January 2022 to September 2025.
STUDY SELECTION: Two reviewers independently selected English-language randomized controlled trials (RCTs) and nonrandomized studies of interventions (NRSIs).
DATA EXTRACTION: One reviewer extracted data and assessed the certainty of evidence (CoE), and a second reviewer verified; 2 reviewers independently assessed risk of bias.
DATA SYNTHESIS: Five RCTs and 18 NRSIs were included. In adults of all ages, Omicron-adapted vaccination probably reduces all-cause mortality (vaccine effectiveness [VE] ranged from 26.6% [95% CI, 5.5% to 42.3%] to 75.2% [CI, 70.6% to 79.9%]; moderate CoE) and COVID-19-related hospitalization (VE ranged from 16.6% [CI, 6.5% to 25.8%] to 67.8% [CI, 63.1% to 72.5%]; moderate CoE) compared with no Omicron-adapted vaccination. When administered more than 365 days after the prior vaccine, it probably reduces all-cause mortality (VE, 36.1% [CI, 14.8% to 54.1%]; moderate CoE) and COVID-19-related hospitalization (VE, 22.2% [CI, 11.4% to 32.0%]; moderate CoE). When administered earlier, it may result in no difference in COVID-19-related hospitalization. Omicron-adapted vaccination may increase myocarditis (incidence rate ratio, 2.7 [CI, 1.0 to 7.0]; low CoE) in adults aged 50 years or older. The mRNA-1283.222 bivalent vaccine probably results in no difference in all-cause mortality or serious adverse events compared with mRNA-1273.222 in adults of all ages.
LIMITATIONS: No RCTs assessed the effectiveness of Omicron-adapted versus no Omicron-adapted vaccination. Evidence on harms was limited.
CONCLUSION: Omicron-adapted vaccines improve protection compared with no Omicron-adapted vaccines, particularly when administered more than 365 days after the prior vaccination.
PRIMARY FUNDING SOURCE: American College of Physicians. (PROSPERO: CRD420251136017).
Additional Links: PMID-41730209
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PubMed:
Citation:
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@article {pmid41730209,
year = {2026},
author = {Dobrescu, A and Pinte, L and Sharifan, A and Gadinger, A and Moser, I and Cooper, C and Gartlehner, G},
title = {Effectiveness, Comparative Effectiveness, and Harms of COVID-19 Vaccines in Adults Who Are Not Pregnant or Immunocompromised: A Rapid Review for the American College of Physicians.},
journal = {Annals of internal medicine},
volume = {},
number = {},
pages = {},
doi = {10.7326/ANNALS-25-05044},
pmid = {41730209},
issn = {1539-3704},
abstract = {BACKGROUND: The SARS-CoV-2 Omicron variant continues to pose a global health burden.
PURPOSE: To assess the effectiveness, comparative effectiveness, and harms of COVID-19 vaccines in nonpregnant, nonimmunocompromised adults.
DATA SOURCES: Medline via Ovid and DynaMedex from January 2022 to September 2025.
STUDY SELECTION: Two reviewers independently selected English-language randomized controlled trials (RCTs) and nonrandomized studies of interventions (NRSIs).
DATA EXTRACTION: One reviewer extracted data and assessed the certainty of evidence (CoE), and a second reviewer verified; 2 reviewers independently assessed risk of bias.
DATA SYNTHESIS: Five RCTs and 18 NRSIs were included. In adults of all ages, Omicron-adapted vaccination probably reduces all-cause mortality (vaccine effectiveness [VE] ranged from 26.6% [95% CI, 5.5% to 42.3%] to 75.2% [CI, 70.6% to 79.9%]; moderate CoE) and COVID-19-related hospitalization (VE ranged from 16.6% [CI, 6.5% to 25.8%] to 67.8% [CI, 63.1% to 72.5%]; moderate CoE) compared with no Omicron-adapted vaccination. When administered more than 365 days after the prior vaccine, it probably reduces all-cause mortality (VE, 36.1% [CI, 14.8% to 54.1%]; moderate CoE) and COVID-19-related hospitalization (VE, 22.2% [CI, 11.4% to 32.0%]; moderate CoE). When administered earlier, it may result in no difference in COVID-19-related hospitalization. Omicron-adapted vaccination may increase myocarditis (incidence rate ratio, 2.7 [CI, 1.0 to 7.0]; low CoE) in adults aged 50 years or older. The mRNA-1283.222 bivalent vaccine probably results in no difference in all-cause mortality or serious adverse events compared with mRNA-1273.222 in adults of all ages.
LIMITATIONS: No RCTs assessed the effectiveness of Omicron-adapted versus no Omicron-adapted vaccination. Evidence on harms was limited.
CONCLUSION: Omicron-adapted vaccines improve protection compared with no Omicron-adapted vaccines, particularly when administered more than 365 days after the prior vaccination.
PRIMARY FUNDING SOURCE: American College of Physicians. (PROSPERO: CRD420251136017).},
}
RevDate: 2026-02-23
Accelerating Diagnostics for Pandemic Preparedness.
Annual review of analytical chemistry (Palo Alto, Calif.) [Epub ahead of print].
Diagnostics are central to pandemic preparedness, guiding surveillance, clinical care, and public health response. The COVID-19 pandemic exposed limitations in diagnostic infrastructure but also accelerated innovation across assay types, created accessible testing mechanisms, and demonstrated the value of public-private partnerships. This review outlines the critical roles diagnostics play across pandemic phases, from early detection to post recovery surveillance. We review the current diagnostic landscape for pandemic priority pathogens and unmet needs and challenges and examine recent advances in analytical technologies, including isothermal amplification, CRISPR-based methods, alternative sample types, and novel platforms, with a focus on their potential for rapid deployment and field use. We also explore the emergence of diagnostic accelerators and biorepositories that support assay validation and global test availability. For analytical chemists, pandemic preparedness presents a call to action: to develop, validate, and translate innovative tools that can adapt to meet urgent diagnostic needs during future health emergencies.
Additional Links: PMID-41729699
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PubMed:
Citation:
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@article {pmid41729699,
year = {2026},
author = {Hoy-Schulz, YE and Damhorst, GL and Lam, WA},
title = {Accelerating Diagnostics for Pandemic Preparedness.},
journal = {Annual review of analytical chemistry (Palo Alto, Calif.)},
volume = {},
number = {},
pages = {},
doi = {10.1146/annurev-anchem-082824-031734},
pmid = {41729699},
issn = {1936-1335},
abstract = {Diagnostics are central to pandemic preparedness, guiding surveillance, clinical care, and public health response. The COVID-19 pandemic exposed limitations in diagnostic infrastructure but also accelerated innovation across assay types, created accessible testing mechanisms, and demonstrated the value of public-private partnerships. This review outlines the critical roles diagnostics play across pandemic phases, from early detection to post recovery surveillance. We review the current diagnostic landscape for pandemic priority pathogens and unmet needs and challenges and examine recent advances in analytical technologies, including isothermal amplification, CRISPR-based methods, alternative sample types, and novel platforms, with a focus on their potential for rapid deployment and field use. We also explore the emergence of diagnostic accelerators and biorepositories that support assay validation and global test availability. For analytical chemists, pandemic preparedness presents a call to action: to develop, validate, and translate innovative tools that can adapt to meet urgent diagnostic needs during future health emergencies.},
}
RevDate: 2026-02-23
Serological and virological evidence of MERS-CoV infection among dromedary camels in Africa: a systematic review and Meta-analysis.
Veterinary research communications, 50(2):.
Additional Links: PMID-41729334
PubMed:
Citation:
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@article {pmid41729334,
year = {2026},
author = {Gaddafi, MS and Lawal, H and Musawa, IA and Garba, B and Goni, MD and Jolayemi, KO and El-Yakub, AU and Jibril, AH and Saeed, SI and Bitrus, AA and Salman, M and Fasina, FO and Yakubu, Y},
title = {Serological and virological evidence of MERS-CoV infection among dromedary camels in Africa: a systematic review and Meta-analysis.},
journal = {Veterinary research communications},
volume = {50},
number = {2},
pages = {},
pmid = {41729334},
issn = {1573-7446},
}
RevDate: 2026-02-23
CmpDate: 2026-02-23
The utilization of virtual reality in the training of de-escalation of aggression for both providers and users of public and healthcare services from the new millennium to the COVID-19 era: a systematic review.
Frontiers in medicine, 13:1657986.
INTRODUCTION: Virtual reality (VR) is a promising modality for the effective delivery of training in the de-escalation of aggression. This review aims to assess how VR has been utilized in training for the de-escalation of aggression among both providers and users of public and healthcare services from the new millennium to the COVID-19 era (2000-2022).
METHODS: A systematic review was conducted in accordance with a pre-registered protocol and adhered to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. Seven key databases were searched, yielding 2373 studies for screening, of which 15 were included. Quality appraisal was performed using the widely used Critical Appraisal Skills Programme (CASP) tool.
RESULTS: VR training for the de-escalation of aggression was implemented using a variety of approaches, ranging from verbal interaction and emotion-recognition tasks to selection from multiple-choice response menus. Most studies assessed participants' responses to the intervention, but none evaluated whether VR training had an impact at the organizational level. Overall, VR training content, modes of interaction, and reported improvements in participants' confidence were viewed positively. However, some studies reported limitations related to the emotional impact, realism of virtual characters, and learning effectiveness. Additional features that may enhance the VR experience were discussed, with personalized, context-specific scenarios identified as an important area for development.
CONCLUSION: Larger-scale studies are required to determine which specific training domains may benefit most from VR-based approaches, given the heterogeneity of populations and methodologies across studies conducted between 2000 and 2022.
https://www.crd.york.ac.uk/PROSPERO/view/CRD42022307138, identifier CRD42022307138.
Additional Links: PMID-41728596
PubMed:
Citation:
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@article {pmid41728596,
year = {2026},
author = {Tang, CT and Lim, LJH and Lee, CTM and Heah, AJE and Yeo, DST and Tan, SM},
title = {The utilization of virtual reality in the training of de-escalation of aggression for both providers and users of public and healthcare services from the new millennium to the COVID-19 era: a systematic review.},
journal = {Frontiers in medicine},
volume = {13},
number = {},
pages = {1657986},
pmid = {41728596},
issn = {2296-858X},
abstract = {INTRODUCTION: Virtual reality (VR) is a promising modality for the effective delivery of training in the de-escalation of aggression. This review aims to assess how VR has been utilized in training for the de-escalation of aggression among both providers and users of public and healthcare services from the new millennium to the COVID-19 era (2000-2022).
METHODS: A systematic review was conducted in accordance with a pre-registered protocol and adhered to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. Seven key databases were searched, yielding 2373 studies for screening, of which 15 were included. Quality appraisal was performed using the widely used Critical Appraisal Skills Programme (CASP) tool.
RESULTS: VR training for the de-escalation of aggression was implemented using a variety of approaches, ranging from verbal interaction and emotion-recognition tasks to selection from multiple-choice response menus. Most studies assessed participants' responses to the intervention, but none evaluated whether VR training had an impact at the organizational level. Overall, VR training content, modes of interaction, and reported improvements in participants' confidence were viewed positively. However, some studies reported limitations related to the emotional impact, realism of virtual characters, and learning effectiveness. Additional features that may enhance the VR experience were discussed, with personalized, context-specific scenarios identified as an important area for development.
CONCLUSION: Larger-scale studies are required to determine which specific training domains may benefit most from VR-based approaches, given the heterogeneity of populations and methodologies across studies conducted between 2000 and 2022.
https://www.crd.york.ac.uk/PROSPERO/view/CRD42022307138, identifier CRD42022307138.},
}
RevDate: 2026-02-23
CmpDate: 2026-02-23
Antimicrobial Resistance: The Answers.
British journal of biomedical science, 83:15559.
Antimicrobial resistance (AMR) has caused a global public health crisis, contributing to approximately five million deaths in 2019 and predicted deaths of approximately ten million annually by 2050. This equates to approximately 1.4-fold more deaths annually from AMR in 2050 than the entire COVID-19 pandemic to date. To tackle this AMR pandemic, regulatory and policy frameworks have been prepared at local, national and international levels with multi-faceted proposals and advances encompassing surveillance, diagnostics, infection prevention, antibiotic prescribing and variation of existing and novel treatment approaches. This narrative review primarily focuses on research and development which have been documented over the last five years in relation to therapeutic approaches at various stages in clinical development and the potential role that vaccines can play in the fight against AMR. This review provides an overview on antibacterial drugs, including novel classes of antibiotics, which have been recently approved, as well as combination antibiotic therapy and the potential of repurposed drugs. The potential role of novel antimicrobial, antibiofilm and quorum sensing inhibitors, such as antimicrobial peptides, nanomaterials and compounds from the extreme and natural environments, as well as ethnopharmacology including the antimicrobial effects of plants, spices, honey and venoms are explored. Novel therapeutic approaches are critically discussed in terms of their realistic clinical potential, detailing recent and ongoing trials to highlight the current interest of these approaches, including immunotherapy, bacteriophage therapy, antimicrobial photodynamic therapy (aPDT), antimicrobial sonodynamic therapy (aSDT), nitric oxide therapy and microbiome manipulation including faecal microbiota transplantation (FMT). The potential of predatory bacteria as living antimicrobial agents is also discussed. Importantly, there have been many technological developments which have enhanced bioprospecting and research and development of novel antimicrobials which this review draws attention to, including artificial intelligence, machine learning and Organ-on-a-Chip devices. Finally, key messages from the recent World Health Organization report into the role of vaccines against AMR provides an interesting perspective relating to prevention which can be of significance in tackling the AMR burden.
Additional Links: PMID-41727556
PubMed:
Citation:
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@article {pmid41727556,
year = {2026},
author = {Millar, BC and Cates, MJ and Torrisi, MS and Round, AJ and Warde, A and Lowery, CJ and Moore, JE},
title = {Antimicrobial Resistance: The Answers.},
journal = {British journal of biomedical science},
volume = {83},
number = {},
pages = {15559},
pmid = {41727556},
issn = {2474-0896},
mesh = {Humans ; *Anti-Bacterial Agents/therapeutic use/pharmacology ; *Drug Resistance, Bacterial ; COVID-19/epidemiology ; SARS-CoV-2 ; },
abstract = {Antimicrobial resistance (AMR) has caused a global public health crisis, contributing to approximately five million deaths in 2019 and predicted deaths of approximately ten million annually by 2050. This equates to approximately 1.4-fold more deaths annually from AMR in 2050 than the entire COVID-19 pandemic to date. To tackle this AMR pandemic, regulatory and policy frameworks have been prepared at local, national and international levels with multi-faceted proposals and advances encompassing surveillance, diagnostics, infection prevention, antibiotic prescribing and variation of existing and novel treatment approaches. This narrative review primarily focuses on research and development which have been documented over the last five years in relation to therapeutic approaches at various stages in clinical development and the potential role that vaccines can play in the fight against AMR. This review provides an overview on antibacterial drugs, including novel classes of antibiotics, which have been recently approved, as well as combination antibiotic therapy and the potential of repurposed drugs. The potential role of novel antimicrobial, antibiofilm and quorum sensing inhibitors, such as antimicrobial peptides, nanomaterials and compounds from the extreme and natural environments, as well as ethnopharmacology including the antimicrobial effects of plants, spices, honey and venoms are explored. Novel therapeutic approaches are critically discussed in terms of their realistic clinical potential, detailing recent and ongoing trials to highlight the current interest of these approaches, including immunotherapy, bacteriophage therapy, antimicrobial photodynamic therapy (aPDT), antimicrobial sonodynamic therapy (aSDT), nitric oxide therapy and microbiome manipulation including faecal microbiota transplantation (FMT). The potential of predatory bacteria as living antimicrobial agents is also discussed. Importantly, there have been many technological developments which have enhanced bioprospecting and research and development of novel antimicrobials which this review draws attention to, including artificial intelligence, machine learning and Organ-on-a-Chip devices. Finally, key messages from the recent World Health Organization report into the role of vaccines against AMR provides an interesting perspective relating to prevention which can be of significance in tackling the AMR burden.},
}
MeSH Terms:
show MeSH Terms
hide MeSH Terms
Humans
*Anti-Bacterial Agents/therapeutic use/pharmacology
*Drug Resistance, Bacterial
COVID-19/epidemiology
SARS-CoV-2
RevDate: 2026-02-23
CmpDate: 2026-02-23
Dengue-SARS-CoV-2 interactions: immune crosstalk, variant emergence, and clinical outcomes.
Frontiers in immunology, 17:1650425.
This review aims to provide an overview of dengue-COVID-19 co-infection, emphasizing recently described immunological, genomic, and eco-epidemiological interactions that may influence clinical outcomes and viral evolution. It brings together molecular evidence, immunological perspectives, and epidemiological insights to summarize current hypotheses and working models of these complex disease interactions. We summarize and critically discuss evidence on antibody-dependent enhancement (ADE), cross-reactive immune responses, and cytokine amplification pathways, and propose mechanisms that could underlie exacerbated disease severity. Published clinical data indicate heterogeneity in co-infection outcomes globally, from mild presentations to severe complications, such as hemorrhagic stroke, acute kidney injury, and increased mortality, particularly among populations with prior dengue exposure. Diagnostic complexities arising from serological cross-reactivity underscore the need for simultaneous molecular testing to ensure accurate pathogen identification. Additionally, we review current evidence on reciprocal selective pressures between SARS-CoV-2 variants and dengue serotypes, highlighting potential evolutionary impacts arising from their co-circulation. The available evidence suggests that co-infection may exacerbate inflammatory pathways, lead to increased vascular and organ damage, and complicate patient management. However, definitive clinical evidence for ADE remains inconclusive, underscoring an ongoing need for targeted mechanistic studies. By outlining significant knowledge gaps and summarizing proposed research directions, this review aims to provide a valuable reference for clinicians, immunologists, epidemiologists, and policymakers managing concurrent dengue and COVID-19 outbreaks.
Additional Links: PMID-41727479
PubMed:
Citation:
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@article {pmid41727479,
year = {2026},
author = {Parra-González, M and Nájera-Maldonado, L and Peralta-Cuevas, E and Gutierrez-Onofre, A and Jaimes-López, LA and Juarez-Antonio, JA and Degollado-Hernández, NY and Garcia-Atutxa, I and Villanueva-Flores, F},
title = {Dengue-SARS-CoV-2 interactions: immune crosstalk, variant emergence, and clinical outcomes.},
journal = {Frontiers in immunology},
volume = {17},
number = {},
pages = {1650425},
pmid = {41727479},
issn = {1664-3224},
mesh = {Humans ; *COVID-19/immunology/epidemiology/virology ; *SARS-CoV-2/immunology/genetics/physiology ; *Dengue/immunology/epidemiology/virology ; *Dengue Virus/immunology ; *Coinfection/immunology/virology ; Antibody-Dependent Enhancement ; Cross Reactions ; },
abstract = {This review aims to provide an overview of dengue-COVID-19 co-infection, emphasizing recently described immunological, genomic, and eco-epidemiological interactions that may influence clinical outcomes and viral evolution. It brings together molecular evidence, immunological perspectives, and epidemiological insights to summarize current hypotheses and working models of these complex disease interactions. We summarize and critically discuss evidence on antibody-dependent enhancement (ADE), cross-reactive immune responses, and cytokine amplification pathways, and propose mechanisms that could underlie exacerbated disease severity. Published clinical data indicate heterogeneity in co-infection outcomes globally, from mild presentations to severe complications, such as hemorrhagic stroke, acute kidney injury, and increased mortality, particularly among populations with prior dengue exposure. Diagnostic complexities arising from serological cross-reactivity underscore the need for simultaneous molecular testing to ensure accurate pathogen identification. Additionally, we review current evidence on reciprocal selective pressures between SARS-CoV-2 variants and dengue serotypes, highlighting potential evolutionary impacts arising from their co-circulation. The available evidence suggests that co-infection may exacerbate inflammatory pathways, lead to increased vascular and organ damage, and complicate patient management. However, definitive clinical evidence for ADE remains inconclusive, underscoring an ongoing need for targeted mechanistic studies. By outlining significant knowledge gaps and summarizing proposed research directions, this review aims to provide a valuable reference for clinicians, immunologists, epidemiologists, and policymakers managing concurrent dengue and COVID-19 outbreaks.},
}
MeSH Terms:
show MeSH Terms
hide MeSH Terms
Humans
*COVID-19/immunology/epidemiology/virology
*SARS-CoV-2/immunology/genetics/physiology
*Dengue/immunology/epidemiology/virology
*Dengue Virus/immunology
*Coinfection/immunology/virology
Antibody-Dependent Enhancement
Cross Reactions
RevDate: 2026-02-22
CmpDate: 2026-02-22
Global impact of COVID-19 on organized CRC screening programs: lessons learned.
Best practice & research. Clinical gastroenterology, 80:102047.
Using a standardized data template, this study retrospectively collected data about colorectal cancer (CRC) screening activity in 2020 and 2021 to estimate the impact of the COVID-19 pandemic compared to the pre-pandemic period (2018 or 2019). Data were collected from 17 programs in 14 countries of which 15 were population-based programs. Invitation coverage was decreased by up to 53.7 % in 2020. Participation among those invited was similar in both periods for all programs. The maximum backlog in invitations was less than 7.4 months in 2020 and 3.3 months for 2021. Nine out of 15 programs observed a decrease in the number of detected CRCs in 2020. Four programs showed a positive percentage change in CRCs detected in 2021 relative to the pre-pandemic period. Half of the countries observed a worse stage-distribution in 2020/2021. Overall, organized CRC screening programs operated at lower screening activity, but screening outcomes were similar compared to the pre-pandemic period.
Additional Links: PMID-41724540
Publisher:
PubMed:
Citation:
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@article {pmid41724540,
year = {2026},
author = {de Jonge, L and Lansdorp-Vogelaar, I and Doria-Rose, VP and Portillo, I and Novak Mlakar, D and Buron, A and Quintin, C and Espinàs, JA and Plaine, J and Škrjanec, AL and Kofol Bric, T and Binefa, G and Font, R and Bulliard, JL and Chubak, J and Ziebell, R and McCurdy, BR and Rabeneck, L and Senore, C and , },
title = {Global impact of COVID-19 on organized CRC screening programs: lessons learned.},
journal = {Best practice & research. Clinical gastroenterology},
volume = {80},
number = {},
pages = {102047},
doi = {10.1016/j.bpg.2025.102047},
pmid = {41724540},
issn = {1532-1916},
mesh = {Humans ; *COVID-19/epidemiology ; *Colorectal Neoplasms/diagnosis/epidemiology ; *Early Detection of Cancer/statistics & numerical data/trends/methods ; Retrospective Studies ; Global Health ; *Mass Screening/organization & administration/statistics & numerical data ; SARS-CoV-2 ; Male ; Middle Aged ; Pandemics ; Aged ; Female ; },
abstract = {Using a standardized data template, this study retrospectively collected data about colorectal cancer (CRC) screening activity in 2020 and 2021 to estimate the impact of the COVID-19 pandemic compared to the pre-pandemic period (2018 or 2019). Data were collected from 17 programs in 14 countries of which 15 were population-based programs. Invitation coverage was decreased by up to 53.7 % in 2020. Participation among those invited was similar in both periods for all programs. The maximum backlog in invitations was less than 7.4 months in 2020 and 3.3 months for 2021. Nine out of 15 programs observed a decrease in the number of detected CRCs in 2020. Four programs showed a positive percentage change in CRCs detected in 2021 relative to the pre-pandemic period. Half of the countries observed a worse stage-distribution in 2020/2021. Overall, organized CRC screening programs operated at lower screening activity, but screening outcomes were similar compared to the pre-pandemic period.},
}
MeSH Terms:
show MeSH Terms
hide MeSH Terms
Humans
*COVID-19/epidemiology
*Colorectal Neoplasms/diagnosis/epidemiology
*Early Detection of Cancer/statistics & numerical data/trends/methods
Retrospective Studies
Global Health
*Mass Screening/organization & administration/statistics & numerical data
SARS-CoV-2
Male
Middle Aged
Pandemics
Aged
Female
RevDate: 2026-02-22
CmpDate: 2026-02-22
Developments in the roll-out and performance of CRC screening in Europe.
Best practice & research. Clinical gastroenterology, 80:102043.
The heterogeneous implementation of colorectal cancer screening programs across Europe makes performance comparison challenging. This study computed and analyzed seven key indicators of screening performance for eighteen European programs between 2011 and 2022. Trends in colorectal cancer incidence and mortality were also examined in relation to when each screening program was introduced. Coverage indicators showed considerable variation across programs but generally increased until the onset of the COVID pandemic. Yield indicators remained stable overall, whereas jumps were associated to protocol changes. In most countries, a decline in incidence followed the introduction of the screening program, whereas the connection of screening with mortality was less evident. The analysis of comparable screening performance indicators over time allows for cross-country and longitudinal monitoring of the programs. The observed decline in incidence following the implementation of fully rolled-out programs highlights the importance and effectiveness of well-organized screening in reducing the burden of the disease.
Additional Links: PMID-41724536
Publisher:
PubMed:
Citation:
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@article {pmid41724536,
year = {2026},
author = {Carbotti, G and van den Berg, DM and Carvalho, AL and Senore, C and Heijnsdijk, EA and de Koning, HJ and Lansdorp-Vogelaar, I and , },
title = {Developments in the roll-out and performance of CRC screening in Europe.},
journal = {Best practice & research. Clinical gastroenterology},
volume = {80},
number = {},
pages = {102043},
doi = {10.1016/j.bpg.2025.102043},
pmid = {41724536},
issn = {1532-1916},
mesh = {Humans ; *Colorectal Neoplasms/diagnosis/epidemiology/mortality ; Europe/epidemiology ; *Early Detection of Cancer/trends/methods/standards ; *COVID-19/epidemiology ; Incidence ; *Mass Screening ; },
abstract = {The heterogeneous implementation of colorectal cancer screening programs across Europe makes performance comparison challenging. This study computed and analyzed seven key indicators of screening performance for eighteen European programs between 2011 and 2022. Trends in colorectal cancer incidence and mortality were also examined in relation to when each screening program was introduced. Coverage indicators showed considerable variation across programs but generally increased until the onset of the COVID pandemic. Yield indicators remained stable overall, whereas jumps were associated to protocol changes. In most countries, a decline in incidence followed the introduction of the screening program, whereas the connection of screening with mortality was less evident. The analysis of comparable screening performance indicators over time allows for cross-country and longitudinal monitoring of the programs. The observed decline in incidence following the implementation of fully rolled-out programs highlights the importance and effectiveness of well-organized screening in reducing the burden of the disease.},
}
MeSH Terms:
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Humans
*Colorectal Neoplasms/diagnosis/epidemiology/mortality
Europe/epidemiology
*Early Detection of Cancer/trends/methods/standards
*COVID-19/epidemiology
Incidence
*Mass Screening
RevDate: 2026-02-22
Biochemistry, physiology and implications in human diseases of mammalian aminopeptidase N: A review.
International journal of biological macromolecules pii:S0141-8130(26)00956-6 [Epub ahead of print].
Aminopeptidases are proteases that selectively hydrolyze an amino acid residue from the amino terminus of proteins and peptides, leading to their activation or inactivation. These enzymes are predominantly metallopeptidases. One of them, membrane alanyl aminopeptidase, also known as aminopeptidase N (APN, EC 3.4.11.2), a M1 family metallo-aminopeptidase, plays essential roles in mammals. APN regulates pain sensitivity, central nervous system control of blood pressure, the final steps of protein degradation, cell motility and adhesion, and coronavirus entry. Furthermore, upregulated expression of APN has been implicated in the pathogenesis of various human disorders, including cancers, inflammation, and pressure dysregulation. APN is a multifunctional protein, and its ligation or inhibition of enzymatic activity may have therapeutic applications. Here, we focus on human and porcine enzymes as models to review the most important structural and functional features of mammalian APN, its roles in mammalian physiology, and the pathophysiological aspects in humans, with particular emphasis on cancer. We illustrate how APN is a tool for diagnosing and monitoring cancer and other pathologies, and discuss the obstacles to the therapeutic use of its inhibitors.
Additional Links: PMID-41724302
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PubMed:
Citation:
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@article {pmid41724302,
year = {2026},
author = {Pascual-Alonso, I and Arrebola-Sánchez, Y and Almeida-García, F and Frómeta-Fuentes, T and Acén-Ravelo, T and Del Valle-Pelaiz, S and Escandel-Barreto, A and Del Sol, DO and Valdés-Tresanco, ME and Sánchez-Ramírez, B and Bergado, G and Chao, L and Barrios, TF and Melchy, E and Chipres-Naranjo, LE and Gutiérrez-Mariscal, M and Charli, JL and Rosenstein, Y},
title = {Biochemistry, physiology and implications in human diseases of mammalian aminopeptidase N: A review.},
journal = {International journal of biological macromolecules},
volume = {},
number = {},
pages = {151030},
doi = {10.1016/j.ijbiomac.2026.151030},
pmid = {41724302},
issn = {1879-0003},
abstract = {Aminopeptidases are proteases that selectively hydrolyze an amino acid residue from the amino terminus of proteins and peptides, leading to their activation or inactivation. These enzymes are predominantly metallopeptidases. One of them, membrane alanyl aminopeptidase, also known as aminopeptidase N (APN, EC 3.4.11.2), a M1 family metallo-aminopeptidase, plays essential roles in mammals. APN regulates pain sensitivity, central nervous system control of blood pressure, the final steps of protein degradation, cell motility and adhesion, and coronavirus entry. Furthermore, upregulated expression of APN has been implicated in the pathogenesis of various human disorders, including cancers, inflammation, and pressure dysregulation. APN is a multifunctional protein, and its ligation or inhibition of enzymatic activity may have therapeutic applications. Here, we focus on human and porcine enzymes as models to review the most important structural and functional features of mammalian APN, its roles in mammalian physiology, and the pathophysiological aspects in humans, with particular emphasis on cancer. We illustrate how APN is a tool for diagnosing and monitoring cancer and other pathologies, and discuss the obstacles to the therapeutic use of its inhibitors.},
}
RevDate: 2026-02-22
Prehospital early warning scores for predicting clinical deterioration of COVID-19 patients: An integrative review.
Enfermeria intensiva, 37(2):500584 pii:S2529-9840(26)00007-8 [Epub ahead of print].
INTRODUCTION: Triage, and in particular scales, are a tool that allows patients with clinical risk to be managed for early, effective and efficient care.
OBJECTIVE: To identify the most precise and specific prehospital score for the detection of clinical worsening risk in COVID19 patients.
METHODS: The protocol followed for the integrative review was the PRISMA method 2020. A literature search was performed in five databases: Scopus, Cochrane Library, Pubmed, Embase, Prospero and Lit covid-nih-nlm. Based on 19 keywords, 5 inclusion and 5 exclusion points. Finally, 22 articles were selected.
RESULTS: Twenty-two studies were identified that addressed effective outcomes for early measures such as telephone triage, web, protocols or tools such as scales. We compared the functionality of 12 scales in patients with Covid-19, showing that the most important variables for this early assessment of clinical worsening were systolic blood pressure, temperature, oxygen saturation and the need for oxygen supplementation. The best predictive value for clinical deterioration and mortality was obtained by NEWS score, with sensitivities and specificities ranging from 77% to 88%.
CONCLUSIONS: Prehospital scales are still under development, with few research studies and a relative confidence in their statistical values. Nonetheless, it has been observed that the scale that best fit the covid-19 was NEWS with an optimal prediction for patients. This could pave the way for its use under other relevant clinical scenarios, such as acute respiratory infections, exacerbations of chronic diseases or future health emergencies.
Additional Links: PMID-41724028
Publisher:
PubMed:
Citation:
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@article {pmid41724028,
year = {2026},
author = {Moreta-Gil, E and Rivera-Picón, C and Conty-Serrano, R and Polonio-López, B and Martín-Conty, JL and Martín-Rodríguez, F and Sanz-García, A},
title = {Prehospital early warning scores for predicting clinical deterioration of COVID-19 patients: An integrative review.},
journal = {Enfermeria intensiva},
volume = {37},
number = {2},
pages = {500584},
doi = {10.1016/j.enfie.2026.500584},
pmid = {41724028},
issn = {2529-9840},
abstract = {INTRODUCTION: Triage, and in particular scales, are a tool that allows patients with clinical risk to be managed for early, effective and efficient care.
OBJECTIVE: To identify the most precise and specific prehospital score for the detection of clinical worsening risk in COVID19 patients.
METHODS: The protocol followed for the integrative review was the PRISMA method 2020. A literature search was performed in five databases: Scopus, Cochrane Library, Pubmed, Embase, Prospero and Lit covid-nih-nlm. Based on 19 keywords, 5 inclusion and 5 exclusion points. Finally, 22 articles were selected.
RESULTS: Twenty-two studies were identified that addressed effective outcomes for early measures such as telephone triage, web, protocols or tools such as scales. We compared the functionality of 12 scales in patients with Covid-19, showing that the most important variables for this early assessment of clinical worsening were systolic blood pressure, temperature, oxygen saturation and the need for oxygen supplementation. The best predictive value for clinical deterioration and mortality was obtained by NEWS score, with sensitivities and specificities ranging from 77% to 88%.
CONCLUSIONS: Prehospital scales are still under development, with few research studies and a relative confidence in their statistical values. Nonetheless, it has been observed that the scale that best fit the covid-19 was NEWS with an optimal prediction for patients. This could pave the way for its use under other relevant clinical scenarios, such as acute respiratory infections, exacerbations of chronic diseases or future health emergencies.},
}
RevDate: 2026-02-23
Scoping review: Facilitators, barriers, and cultural adaptations in the caregiver skills training program for children with developmental concerns.
Autism : the international journal of research and practice, 30(3):13623613251406399 [Epub ahead of print].
Autism interventions are predominantly developed in high-income countries, limiting access for families in low- and middle-income countries due to systemic, cultural, and logistical barriers. The Caregiver Skills Training program aims to address this disparity by equipping caregivers with practical skills. This scoping review examines the cultural adaptations, facilitators, and barriers to the implementation of Caregiver Skills Training, focusing on its accessibility, feasibility, and acceptability. A comprehensive search of ERIC, PsycINFO, PubMed, and Web of Science identified eligible studies that reported cultural or linguistic adaptations of Caregiver Skills Training. Forward searches and manual reference checks supplemented the review. Data were extracted using the Cultural Adaptation Checklist framework and analyzed for patterns in adaptation, training, barriers, and facilitators. Seventeen studies across Asia, Africa, Europe, and North America highlighted diverse adaptations in language, content, and delivery methods. Facilitators included community partnerships and task-shifting with non-specialists, while barriers involved logistical challenges, stigma, and resource constraints. Caregiver Skills Training's flexible, culturally responsive framework makes it a viable model for scaling autism interventions globally. Tailored adaptations and strong support systems for facilitators are essential to overcoming systemic challenges and ensuring equitable access in low- and middle-income countries.Lay abstractHow the Caregiver Skills Training Program Helps Families WorldwideThe Caregiver Skills Training program was designed to help families of children with autism and other developmental challenges in low-resource settings. Caregiver Skills Training empowers parents and caregivers by teaching them practical strategies to improve their child's communication, social interaction, and daily living skills. This program is unique because it does not require a formal diagnosis and is designed to be delivered by trained non-specialists, such as community health workers. A review of 17 studies from different countries examined how the Caregiver Skills Training program was adapted to fit the cultural and practical needs of families in each region. For example, materials were translated, simplified, and paired with visual aids to help parents with lower literacy levels. Non-specialist facilitators helped make the program more accessible, and online or hybrid delivery methods increased participation during the COVID-19 pandemic. However, challenges remain. Families often face barriers like limited transportation, stigma, and lack of Internet access, which can prevent them from fully participating in the program. Facilitators also need more training and support to maintain program quality. Despite these obstacles, Caregiver Skills Training shows promise as a global solution to bridge the gap in autism care, especially in underserved communities. This review highlights the importance of adapting programs like Caregiver Skills Training to meet the unique needs of families worldwide, ensuring that every child has the opportunity to thrive, regardless of where they live.
Additional Links: PMID-41454648
PubMed:
Citation:
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@article {pmid41454648,
year = {2025},
author = {Montiel-Nava, C and Montenegro, MC and Ramirez, AC and Villarreal, V and Murillo Chacko, L and Dixon, P and Dababnah, S},
title = {Scoping review: Facilitators, barriers, and cultural adaptations in the caregiver skills training program for children with developmental concerns.},
journal = {Autism : the international journal of research and practice},
volume = {30},
number = {3},
pages = {13623613251406399},
pmid = {41454648},
issn = {1461-7005},
abstract = {Autism interventions are predominantly developed in high-income countries, limiting access for families in low- and middle-income countries due to systemic, cultural, and logistical barriers. The Caregiver Skills Training program aims to address this disparity by equipping caregivers with practical skills. This scoping review examines the cultural adaptations, facilitators, and barriers to the implementation of Caregiver Skills Training, focusing on its accessibility, feasibility, and acceptability. A comprehensive search of ERIC, PsycINFO, PubMed, and Web of Science identified eligible studies that reported cultural or linguistic adaptations of Caregiver Skills Training. Forward searches and manual reference checks supplemented the review. Data were extracted using the Cultural Adaptation Checklist framework and analyzed for patterns in adaptation, training, barriers, and facilitators. Seventeen studies across Asia, Africa, Europe, and North America highlighted diverse adaptations in language, content, and delivery methods. Facilitators included community partnerships and task-shifting with non-specialists, while barriers involved logistical challenges, stigma, and resource constraints. Caregiver Skills Training's flexible, culturally responsive framework makes it a viable model for scaling autism interventions globally. Tailored adaptations and strong support systems for facilitators are essential to overcoming systemic challenges and ensuring equitable access in low- and middle-income countries.Lay abstractHow the Caregiver Skills Training Program Helps Families WorldwideThe Caregiver Skills Training program was designed to help families of children with autism and other developmental challenges in low-resource settings. Caregiver Skills Training empowers parents and caregivers by teaching them practical strategies to improve their child's communication, social interaction, and daily living skills. This program is unique because it does not require a formal diagnosis and is designed to be delivered by trained non-specialists, such as community health workers. A review of 17 studies from different countries examined how the Caregiver Skills Training program was adapted to fit the cultural and practical needs of families in each region. For example, materials were translated, simplified, and paired with visual aids to help parents with lower literacy levels. Non-specialist facilitators helped make the program more accessible, and online or hybrid delivery methods increased participation during the COVID-19 pandemic. However, challenges remain. Families often face barriers like limited transportation, stigma, and lack of Internet access, which can prevent them from fully participating in the program. Facilitators also need more training and support to maintain program quality. Despite these obstacles, Caregiver Skills Training shows promise as a global solution to bridge the gap in autism care, especially in underserved communities. This review highlights the importance of adapting programs like Caregiver Skills Training to meet the unique needs of families worldwide, ensuring that every child has the opportunity to thrive, regardless of where they live.},
}
RevDate: 2024-10-03
Cardiology Consult for the General Pediatrician after Cardiac Manifestations from a SARS-CoV-2 Infection.
Current pediatric reviews pii:CPR-EPUB-143567 [Epub ahead of print].
The novel Coronavirus Disease 2019 (COVID-19), caused by the SARS-CoV-2 virus, created a need for evidence-based guidelines for the evaluation, management, and follow-up after infection. Data have become rapidly available, creating a challenge for medical providers to stay abreast of the ever-evolving recommendations. This document, written collaboratively by pediatric cardiovascular experts, pediatricians, and sports medicine specialists, is focused on SARS-- CoV-2-related pediatric cardiac manifestations. It aims to provide a systemic review of high-yield literature related to all cardiovascular entities as a tool for primary pediatric clinicians to utilize as they consider the cardiac consequences of acute SARS-CoV-2 infection, MIS-C, vaccine-related myocarditis, return-to-play, and long COVID-19 syndrome.
Additional Links: PMID-39360535
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PubMed:
Citation:
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@article {pmid39360535,
year = {2024},
author = {Amdani, S and Altman, CA and Chowdhury, D and Ronai, C and Soma, D and Archer, JM and Tierney, S and Renno, MS and Miller, J and Nguyen, QT and Glickstein, JS and Orr, WB},
title = {Cardiology Consult for the General Pediatrician after Cardiac Manifestations from a SARS-CoV-2 Infection.},
journal = {Current pediatric reviews},
volume = {},
number = {},
pages = {},
doi = {10.2174/0115733963314978240923110844},
pmid = {39360535},
issn = {1875-6336},
abstract = {The novel Coronavirus Disease 2019 (COVID-19), caused by the SARS-CoV-2 virus, created a need for evidence-based guidelines for the evaluation, management, and follow-up after infection. Data have become rapidly available, creating a challenge for medical providers to stay abreast of the ever-evolving recommendations. This document, written collaboratively by pediatric cardiovascular experts, pediatricians, and sports medicine specialists, is focused on SARS-- CoV-2-related pediatric cardiac manifestations. It aims to provide a systemic review of high-yield literature related to all cardiovascular entities as a tool for primary pediatric clinicians to utilize as they consider the cardiac consequences of acute SARS-CoV-2 infection, MIS-C, vaccine-related myocarditis, return-to-play, and long COVID-19 syndrome.},
}
RevDate: 2026-02-22
The role of health beliefs in COVID-19 vaccination acceptance: A Meta-analysis.
Vaccine, 77:128379 pii:S0264-410X(26)00187-8 [Epub ahead of print].
This study employed a meta-analytic approach to examine the relationships between the Health Belief Model (HBM) constructs and COVID-19 vaccination acceptance. A comprehensive literature search identified 77 eligible studies with a combined sample size of 83,995 participants. Quantitative synthesis of the extracted data revealed that perceived benefits (r = 0.40) was the strongest positive predictor of individuals' vaccine acceptance, indicating a medium-to-large effect. Perceived severity (r = 0.17) and susceptibility (r = 0.18) to COVID-19 were also significant positive predictors, each with small-to-medium effect sizes. Cues to action (r = 0.11) and self-efficacy (r = 0.10) were also positively associated with vaccine acceptance, although the effects were small. In contrast, perceived barriers to vaccination (r = -0.25) were negatively associated with vaccine acceptance, approaching a medium effect in size. Several of these associations were moderated by study characteristics, including how the variables were operationalized (intention, hesitancy, refusal, etc.), the vulnerability of the study sample, the respondent type (parents vaccinating children vs. adults vaccinating themselves), the vaccine development stage, and the variant phase. Overall, these findings contribute to a deeper understanding of the psychological mechanisms underlying vaccine acceptance and hesitancy, and offer practical implications for developing targeted communication strategies to promote COVID-19 and other vaccinations.
Additional Links: PMID-41723921
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PubMed:
Citation:
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@article {pmid41723921,
year = {2026},
author = {Li, R and Vafeiadis, M and Shen, F and Hou, Z},
title = {The role of health beliefs in COVID-19 vaccination acceptance: A Meta-analysis.},
journal = {Vaccine},
volume = {77},
number = {},
pages = {128379},
doi = {10.1016/j.vaccine.2026.128379},
pmid = {41723921},
issn = {1873-2518},
abstract = {This study employed a meta-analytic approach to examine the relationships between the Health Belief Model (HBM) constructs and COVID-19 vaccination acceptance. A comprehensive literature search identified 77 eligible studies with a combined sample size of 83,995 participants. Quantitative synthesis of the extracted data revealed that perceived benefits (r = 0.40) was the strongest positive predictor of individuals' vaccine acceptance, indicating a medium-to-large effect. Perceived severity (r = 0.17) and susceptibility (r = 0.18) to COVID-19 were also significant positive predictors, each with small-to-medium effect sizes. Cues to action (r = 0.11) and self-efficacy (r = 0.10) were also positively associated with vaccine acceptance, although the effects were small. In contrast, perceived barriers to vaccination (r = -0.25) were negatively associated with vaccine acceptance, approaching a medium effect in size. Several of these associations were moderated by study characteristics, including how the variables were operationalized (intention, hesitancy, refusal, etc.), the vulnerability of the study sample, the respondent type (parents vaccinating children vs. adults vaccinating themselves), the vaccine development stage, and the variant phase. Overall, these findings contribute to a deeper understanding of the psychological mechanisms underlying vaccine acceptance and hesitancy, and offer practical implications for developing targeted communication strategies to promote COVID-19 and other vaccinations.},
}
RevDate: 2026-02-21
Comparison of the efficacy and safety of selective COX-2 inhibitors and non-steroidal anti-inflammatory drugs in the treatment of COVID-19 patients: a systematic review and network meta-analysis.
BMC infectious diseases pii:10.1186/s12879-026-12883-w [Epub ahead of print].
Additional Links: PMID-41723349
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PubMed:
Citation:
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@article {pmid41723349,
year = {2026},
author = {Wu, D and Li, Y and Chen, P and Zhu, K and Cao, C},
title = {Comparison of the efficacy and safety of selective COX-2 inhibitors and non-steroidal anti-inflammatory drugs in the treatment of COVID-19 patients: a systematic review and network meta-analysis.},
journal = {BMC infectious diseases},
volume = {},
number = {},
pages = {},
doi = {10.1186/s12879-026-12883-w},
pmid = {41723349},
issn = {1471-2334},
}
RevDate: 2026-02-21
CmpDate: 2026-02-21
Prevalence, risk factors, and early prediction of refractory pneumonia caused by Mycoplasma pneumoniae in children: a systematic review and meta-analysis.
European journal of pediatrics, 185(3):.
UNLABELLED: Refractory Mycoplasma pneumoniae pneumonia (rMPP) poses significant challenges in pediatric care due to delayed recognition and limited systematic evidence. This meta-analysis evaluates the prevalence, risk factors, and predictive accuracy of models for rMPP. We systematically searched PubMed, Cochrane Library, and Web of Science until November 2024 for observational studies involving children aged 0-18 years with rMPP. Study quality was assessed using Newcastle-Ottawa and JBI scales. Data were analyzed via R4.4.2. Fifty-three studies (n = 35,275) revealed an overall rMPP prevalence of 37.8% (95% CI 30.5-45.5%), with significant temporal variation: 33.1% pre-COVID-19, 42.0% during, and 86.5% post-pandemic. Independent risk factors included elevated lactate dehydrogenase (OR = 1.018), C-reactive protein (OR = 1.106), procalcitonin (OR = 1.825), interleukin-6 (OR = 2.440), neutrophil count (OR = 2.955), pleural effusion (OR = 4.469), mucus plugs (OR = 5.456), and older age (OR = 1.188). Eleven prediction models demonstrated high accuracy, with ROC-AUCs of 0.913 (training) and 0.895 (validation).
CONCLUSION: The prevalence of rMPP in children is significant and has increased markedly since the COVID-19 pandemic. Key biomarkers and clinical features facilitate early risk stratification, and validated predictive models improve clinical decision-making. These findings highlight the urgent need for targeted surveillance and customized interventions for high-risk populations.
WHAT IS KNOWN: • Pneumonia caused by Mycoplasma pneumoniae in children can be effectively controlled by first-line macrolide therapy. • However, there is still a proportion of children who do not respond well to this treatment regimen and develop refractory Mycoplasma pneumoniae due to macrolide resistance.
WHAT IS NEW: • This review and meta-analysis show the incidence of refractory Mycoplasma pneumonia and its potential risk factors. • Finding the feasibility of constructing a predictive model that facilitates early prediction, to provide evidence-based evidence for further in-depth clinical understanding of this disease.
Additional Links: PMID-41723336
PubMed:
Citation:
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@article {pmid41723336,
year = {2026},
author = {Huang, X and Huang, D and Wang, W and Huang, Y and Huang, C and Wang, G},
title = {Prevalence, risk factors, and early prediction of refractory pneumonia caused by Mycoplasma pneumoniae in children: a systematic review and meta-analysis.},
journal = {European journal of pediatrics},
volume = {185},
number = {3},
pages = {},
pmid = {41723336},
issn = {1432-1076},
support = {2024B1020//Social Public Welfare and Basic Research Special Project of Zhongshan City, Guangdong Province, China/ ; },
mesh = {Humans ; *Pneumonia, Mycoplasma/epidemiology/diagnosis/drug therapy ; Risk Factors ; Child ; Prevalence ; Child, Preschool ; Infant ; *Mycoplasma pneumoniae ; Adolescent ; COVID-19/epidemiology ; Anti-Bacterial Agents/therapeutic use ; },
abstract = {UNLABELLED: Refractory Mycoplasma pneumoniae pneumonia (rMPP) poses significant challenges in pediatric care due to delayed recognition and limited systematic evidence. This meta-analysis evaluates the prevalence, risk factors, and predictive accuracy of models for rMPP. We systematically searched PubMed, Cochrane Library, and Web of Science until November 2024 for observational studies involving children aged 0-18 years with rMPP. Study quality was assessed using Newcastle-Ottawa and JBI scales. Data were analyzed via R4.4.2. Fifty-three studies (n = 35,275) revealed an overall rMPP prevalence of 37.8% (95% CI 30.5-45.5%), with significant temporal variation: 33.1% pre-COVID-19, 42.0% during, and 86.5% post-pandemic. Independent risk factors included elevated lactate dehydrogenase (OR = 1.018), C-reactive protein (OR = 1.106), procalcitonin (OR = 1.825), interleukin-6 (OR = 2.440), neutrophil count (OR = 2.955), pleural effusion (OR = 4.469), mucus plugs (OR = 5.456), and older age (OR = 1.188). Eleven prediction models demonstrated high accuracy, with ROC-AUCs of 0.913 (training) and 0.895 (validation).
CONCLUSION: The prevalence of rMPP in children is significant and has increased markedly since the COVID-19 pandemic. Key biomarkers and clinical features facilitate early risk stratification, and validated predictive models improve clinical decision-making. These findings highlight the urgent need for targeted surveillance and customized interventions for high-risk populations.
WHAT IS KNOWN: • Pneumonia caused by Mycoplasma pneumoniae in children can be effectively controlled by first-line macrolide therapy. • However, there is still a proportion of children who do not respond well to this treatment regimen and develop refractory Mycoplasma pneumoniae due to macrolide resistance.
WHAT IS NEW: • This review and meta-analysis show the incidence of refractory Mycoplasma pneumonia and its potential risk factors. • Finding the feasibility of constructing a predictive model that facilitates early prediction, to provide evidence-based evidence for further in-depth clinical understanding of this disease.},
}
MeSH Terms:
show MeSH Terms
hide MeSH Terms
Humans
*Pneumonia, Mycoplasma/epidemiology/diagnosis/drug therapy
Risk Factors
Child
Prevalence
Child, Preschool
Infant
*Mycoplasma pneumoniae
Adolescent
COVID-19/epidemiology
Anti-Bacterial Agents/therapeutic use
RevDate: 2026-02-21
CmpDate: 2026-02-21
Comparison of Azvudine and Nirmatrelvir-Ritonavir in Hospitalised Patients With COVID-19: A Systematic Review and Meta-Analysis.
Reviews in medical virology, 36(2):e70114.
Azvudine is a nucleoside reverse transcriptase inhibitor (NRTI) and belongs to the family of 2', 3'-dideoxynucleoside (ddNs) that can mimic natural nucleosides and block viral DNA or RNA chain synthesis and prevent viral replication. Since the beginning of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic, Azvudine has been used to treat patients with COVID-19. Therefore, the objective of this meta-analysis study was to compare Azvudine and Nirmatrelvir-Ritonavir in hospitalised patients. The global online databases were used to identify relevant studies published between January 2019 and October 2024. The quality of all articles was determined using the Newcastle-Ottawa Scale (NOS) checklist. In this study, heterogeneity assay was assessed using the Cochran's Q-test and the I2 index, and STATA software version.14 (StataCorp) was used for statistical analysis. Egger's test, Begg's test, and funnel plot were performed to estimate of the publication bias, and the impact of each study on the overall estimate was assessed using sensitivity analysis. In this study, 19 studies were included in this meta-analysis. The results of the meta-analysis showed that the relative risk of death in the Azvudine treatment group compared with the Nirmatrelvir-Ritonavir treatment group was 0.64 (95% CI: 0. 44, 0. 93). These results suggest that treatment with Azvudine may provide significant clinical benefit in patients hospitalised with COVID-19.
Additional Links: PMID-41722060
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PubMed:
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@article {pmid41722060,
year = {2026},
author = {Mousavi, T and Moosazadeh, M and Jalali, H},
title = {Comparison of Azvudine and Nirmatrelvir-Ritonavir in Hospitalised Patients With COVID-19: A Systematic Review and Meta-Analysis.},
journal = {Reviews in medical virology},
volume = {36},
number = {2},
pages = {e70114},
doi = {10.1002/rmv.70114},
pmid = {41722060},
issn = {1099-1654},
mesh = {Humans ; *Ritonavir/therapeutic use ; *COVID-19 Drug Treatment ; SARS-CoV-2/drug effects ; *Antiviral Agents/therapeutic use ; Hospitalization ; Drug Combinations ; COVID-19/virology ; Lactams ; Leucine ; Nitriles ; Proline ; },
abstract = {Azvudine is a nucleoside reverse transcriptase inhibitor (NRTI) and belongs to the family of 2', 3'-dideoxynucleoside (ddNs) that can mimic natural nucleosides and block viral DNA or RNA chain synthesis and prevent viral replication. Since the beginning of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic, Azvudine has been used to treat patients with COVID-19. Therefore, the objective of this meta-analysis study was to compare Azvudine and Nirmatrelvir-Ritonavir in hospitalised patients. The global online databases were used to identify relevant studies published between January 2019 and October 2024. The quality of all articles was determined using the Newcastle-Ottawa Scale (NOS) checklist. In this study, heterogeneity assay was assessed using the Cochran's Q-test and the I2 index, and STATA software version.14 (StataCorp) was used for statistical analysis. Egger's test, Begg's test, and funnel plot were performed to estimate of the publication bias, and the impact of each study on the overall estimate was assessed using sensitivity analysis. In this study, 19 studies were included in this meta-analysis. The results of the meta-analysis showed that the relative risk of death in the Azvudine treatment group compared with the Nirmatrelvir-Ritonavir treatment group was 0.64 (95% CI: 0. 44, 0. 93). These results suggest that treatment with Azvudine may provide significant clinical benefit in patients hospitalised with COVID-19.},
}
MeSH Terms:
show MeSH Terms
hide MeSH Terms
Humans
*Ritonavir/therapeutic use
*COVID-19 Drug Treatment
SARS-CoV-2/drug effects
*Antiviral Agents/therapeutic use
Hospitalization
Drug Combinations
COVID-19/virology
Lactams
Leucine
Nitriles
Proline
RevDate: 2026-02-20
CmpDate: 2026-02-20
Post-MIS-C cardiovascular outcomes: a systematic review.
European journal of pediatrics, 185(3):.
Limited knowledge and variability in findings exist regarding the resolution of cardiovascular outcomes following Multisystem Inflammatory Syndrome in Children (MIS-C). We conducted a systematic review to estimate the frequency of cardiovascular outcomes following MIS-C. A systematic search was conducted in Pubmed/Medline, Scopus, Embase, SciELO, LILACS, Cochrane Library, Web of Science, and medRxiv were searched up to February 2024. We included studies reporting cardiovascular events that began in acute MIS-C and persisted after discharge. Screening and data extraction were performed by independent reviewers. We performed a random-effects meta-analysis and assessed the certainty of the evidence using the GRADE approach. Eighty-four studies (n = 4,778) were included; seven had a comparator group. The frequency of cardiovascular outcomes-including coronary abnormalities (Z-score ≥ 2), left ventricle ejection fraction < 55%, diastolic dysfunction, myocarditis, and pericardial effusion-decreased over time, with most resolving by 6 to 9 months. However, cardiac magnetic resonance imaging studies identified myocardial edema and/or fibrosis persisting up to 12 months, and two studies reported coronary abnormalities at 18- to 24-month follow-up. Evidence certainty was very low. Compared to children with COVID-19 or healthy controls, MIS-C showed more cardiovascular events and greater subclinical myocardial dysfunction, as assessed by strain analysis, during a 6-month follow-up. Compared with other etiologies of myocarditis, MIS-C myocarditis was associated with better cardiovascular outcomes but shorter exercise duration and lower aerobic capacity on stress testing. Conclusions: Cardiovascular outcomes following MIS-C improved over time, but certain subclinical cardiac abnormalities persisted up to 12 to 24 months. These findings may support long-term follow-up after MIS-C.Trial registration: Protocol registration number: PROSPERO, CRD42022336784.
Additional Links: PMID-41721085
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@article {pmid41721085,
year = {2026},
author = {Alvarado-Gamarra, G and Alcala-Marcos, K and Celis, CR and Balmaceda-Nieto, P and Cieza, L and Morán-Mariños, C and Grados-Espinoza, P and Alva-Díaz, C and Ecker, L and Ochoa, TJ and Franchi, LM and Howard, LM and Grijalva, CG and Lanata, CF},
title = {Post-MIS-C cardiovascular outcomes: a systematic review.},
journal = {European journal of pediatrics},
volume = {185},
number = {3},
pages = {},
pmid = {41721085},
issn = {1432-1076},
support = {D43TW012468/TW/FIC NIH HHS/United States ; },
mesh = {Humans ; Child ; *COVID-19/complications ; *Systemic Inflammatory Response Syndrome/complications ; *Cardiovascular Diseases/etiology/epidemiology ; SARS-CoV-2 ; },
abstract = {Limited knowledge and variability in findings exist regarding the resolution of cardiovascular outcomes following Multisystem Inflammatory Syndrome in Children (MIS-C). We conducted a systematic review to estimate the frequency of cardiovascular outcomes following MIS-C. A systematic search was conducted in Pubmed/Medline, Scopus, Embase, SciELO, LILACS, Cochrane Library, Web of Science, and medRxiv were searched up to February 2024. We included studies reporting cardiovascular events that began in acute MIS-C and persisted after discharge. Screening and data extraction were performed by independent reviewers. We performed a random-effects meta-analysis and assessed the certainty of the evidence using the GRADE approach. Eighty-four studies (n = 4,778) were included; seven had a comparator group. The frequency of cardiovascular outcomes-including coronary abnormalities (Z-score ≥ 2), left ventricle ejection fraction < 55%, diastolic dysfunction, myocarditis, and pericardial effusion-decreased over time, with most resolving by 6 to 9 months. However, cardiac magnetic resonance imaging studies identified myocardial edema and/or fibrosis persisting up to 12 months, and two studies reported coronary abnormalities at 18- to 24-month follow-up. Evidence certainty was very low. Compared to children with COVID-19 or healthy controls, MIS-C showed more cardiovascular events and greater subclinical myocardial dysfunction, as assessed by strain analysis, during a 6-month follow-up. Compared with other etiologies of myocarditis, MIS-C myocarditis was associated with better cardiovascular outcomes but shorter exercise duration and lower aerobic capacity on stress testing. Conclusions: Cardiovascular outcomes following MIS-C improved over time, but certain subclinical cardiac abnormalities persisted up to 12 to 24 months. These findings may support long-term follow-up after MIS-C.Trial registration: Protocol registration number: PROSPERO, CRD42022336784.},
}
MeSH Terms:
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Humans
Child
*COVID-19/complications
*Systemic Inflammatory Response Syndrome/complications
*Cardiovascular Diseases/etiology/epidemiology
SARS-CoV-2
RevDate: 2026-02-20
Active surveillance methods to identify adverse events of special interest (AESIs) following vaccination against pandemic diseases: A scoping review.
Vaccine, 77:128341 pii:S0264-410X(26)00149-0 [Epub ahead of print].
INTRODUCTION: Active post-vaccination surveillance is vital for ensuring vaccine safety, particularly in monitoring Adverse Events of Special Interest (AESIs). This scoping review synthesises evidence on methodologies employed in active surveillance studies, with a focus on influenza and COVID-19 vaccines.
METHODS: Literature was identified via PubMed, Embase, Web of Science, Scopus, Google Scholar, and manual searches, using key terms including influenza, COVID-19, vaccine, and AESI. Two authors independently screened studies and extracted data on study characteristics, methods, and outcomes. Findings were synthesised narratively and presented in tables and figures, following the PRISMA-ScR guideline.
RESULTS: Of 427 included studies, most were published after 2020 (74.0%) and focused on COVID-19 vaccines (69.3%), particularly mRNA platforms (51.3%). The majority were conducted in North America and Europe, with 85.5% from high-income countries; multinational studies accounted for 6.6%, and single-centre studies with national or subnational coverage for 63.0%. Cohort designs predominated (40.5%), mostly retrospective (74.2%), utilising registries (24.0%) and electronic health records (22.4%), including artificial intelligence for signal detection and prediction (2.7%). Nearly half (49.6%) linked multiple data sources, though outcome verification was reported in fewer than half (45.9%). Incidence rates (16.5%) and risk/hazard ratios (14.8%) were the most reported measures. Neurological (21.8%) and cardiac (21.3%) AESIs, particularly Guillain-Barré Syndrome and myocarditis, were most frequently investigated.
CONCLUSION: Active surveillance for vaccine safety has increased but remains concentrated in high-income countries. Methodological approaches to detection, verification, and validation vary widely. Introducing active surveillance methodologies in low- and middle-income countries is crucial to achieving more equitable global monitoring of vaccine safety.
Additional Links: PMID-41719864
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@article {pmid41719864,
year = {2026},
author = {Chandra, LA and Nugroho, DB and Thobari, JA and Dimaguila, GL and Buttery, J},
title = {Active surveillance methods to identify adverse events of special interest (AESIs) following vaccination against pandemic diseases: A scoping review.},
journal = {Vaccine},
volume = {77},
number = {},
pages = {128341},
doi = {10.1016/j.vaccine.2026.128341},
pmid = {41719864},
issn = {1873-2518},
abstract = {INTRODUCTION: Active post-vaccination surveillance is vital for ensuring vaccine safety, particularly in monitoring Adverse Events of Special Interest (AESIs). This scoping review synthesises evidence on methodologies employed in active surveillance studies, with a focus on influenza and COVID-19 vaccines.
METHODS: Literature was identified via PubMed, Embase, Web of Science, Scopus, Google Scholar, and manual searches, using key terms including influenza, COVID-19, vaccine, and AESI. Two authors independently screened studies and extracted data on study characteristics, methods, and outcomes. Findings were synthesised narratively and presented in tables and figures, following the PRISMA-ScR guideline.
RESULTS: Of 427 included studies, most were published after 2020 (74.0%) and focused on COVID-19 vaccines (69.3%), particularly mRNA platforms (51.3%). The majority were conducted in North America and Europe, with 85.5% from high-income countries; multinational studies accounted for 6.6%, and single-centre studies with national or subnational coverage for 63.0%. Cohort designs predominated (40.5%), mostly retrospective (74.2%), utilising registries (24.0%) and electronic health records (22.4%), including artificial intelligence for signal detection and prediction (2.7%). Nearly half (49.6%) linked multiple data sources, though outcome verification was reported in fewer than half (45.9%). Incidence rates (16.5%) and risk/hazard ratios (14.8%) were the most reported measures. Neurological (21.8%) and cardiac (21.3%) AESIs, particularly Guillain-Barré Syndrome and myocarditis, were most frequently investigated.
CONCLUSION: Active surveillance for vaccine safety has increased but remains concentrated in high-income countries. Methodological approaches to detection, verification, and validation vary widely. Introducing active surveillance methodologies in low- and middle-income countries is crucial to achieving more equitable global monitoring of vaccine safety.},
}
RevDate: 2026-02-20
CmpDate: 2026-02-20
A scoping review of vaccine certificate implementation in Canada and OECD countries during the COVID-19 pandemic: Outcomes and lessons learned.
Human vaccines & immunotherapeutics, 22(1):2622178.
Vaccine certificates were introduced during the COVID-19 pandemic to document vaccination status, promote uptake and enable safer reopening of society. While these policies supported public health efforts, their implementation raised operational, ethical and legal concerns, sparking debate about their future use in health emergencies. We conducted a scoping review to synthesize the implementation processes, challenges and outcomes of vaccine certificate systems in Canada and other OECD countries. An academic search was conducted in August 2024, across Ovid MEDLINE, Embase and Scopus using controlled vocabulary and key words for sources published from 2020 onward. Grey literature was searched using Google and targeted government and organizational websites. Data were synthesized descriptively and analyzed deductively based on three pre-identified themes - public health, technological, and ethical-legal considerations - derived from the UK Royal Society's framework on COVID-19 vaccine certificate design. The search captured 128 sources (72 academic and 56 gray literature), covering all OECD countries except Chile, Colombia, Costa Rica, Mexico and Norway. Identified subthemes included: (1) purpose and trade-offs; (2) public health, socio-economic and health system impacts, (3) technological infrastructure and data security; (4) equity and accessibility; (5) privacy and surveillance; and (6) public acceptance and trust. Vaccine certificates aimed to support public health goals but posed challenges in digital implementation, particularly in creating secure and interoperable systems and raised concerns around equity, discrimination and privacy. Vaccine certificates show promise for future public health use. However, their success will depend on addressing ethical concerns, ensuring interoperability and strengthening digital infrastructure, regulations and public trust.
Additional Links: PMID-41719449
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@article {pmid41719449,
year = {2026},
author = {Nilormi, A and Bensimon, CM and Thomas, M and Wiles, S and Wilson, K},
title = {A scoping review of vaccine certificate implementation in Canada and OECD countries during the COVID-19 pandemic: Outcomes and lessons learned.},
journal = {Human vaccines & immunotherapeutics},
volume = {22},
number = {1},
pages = {2622178},
doi = {10.1080/21645515.2026.2622178},
pmid = {41719449},
issn = {2164-554X},
mesh = {Humans ; Canada/epidemiology ; *COVID-19/prevention & control/epidemiology ; *COVID-19 Vaccines/administration & dosage ; Organisation for Economic Co-Operation and Development ; SARS-CoV-2/immunology ; *Vaccination/legislation & jurisprudence ; Public Health ; Pandemics/prevention & control ; },
abstract = {Vaccine certificates were introduced during the COVID-19 pandemic to document vaccination status, promote uptake and enable safer reopening of society. While these policies supported public health efforts, their implementation raised operational, ethical and legal concerns, sparking debate about their future use in health emergencies. We conducted a scoping review to synthesize the implementation processes, challenges and outcomes of vaccine certificate systems in Canada and other OECD countries. An academic search was conducted in August 2024, across Ovid MEDLINE, Embase and Scopus using controlled vocabulary and key words for sources published from 2020 onward. Grey literature was searched using Google and targeted government and organizational websites. Data were synthesized descriptively and analyzed deductively based on three pre-identified themes - public health, technological, and ethical-legal considerations - derived from the UK Royal Society's framework on COVID-19 vaccine certificate design. The search captured 128 sources (72 academic and 56 gray literature), covering all OECD countries except Chile, Colombia, Costa Rica, Mexico and Norway. Identified subthemes included: (1) purpose and trade-offs; (2) public health, socio-economic and health system impacts, (3) technological infrastructure and data security; (4) equity and accessibility; (5) privacy and surveillance; and (6) public acceptance and trust. Vaccine certificates aimed to support public health goals but posed challenges in digital implementation, particularly in creating secure and interoperable systems and raised concerns around equity, discrimination and privacy. Vaccine certificates show promise for future public health use. However, their success will depend on addressing ethical concerns, ensuring interoperability and strengthening digital infrastructure, regulations and public trust.},
}
MeSH Terms:
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hide MeSH Terms
Humans
Canada/epidemiology
*COVID-19/prevention & control/epidemiology
*COVID-19 Vaccines/administration & dosage
Organisation for Economic Co-Operation and Development
SARS-CoV-2/immunology
*Vaccination/legislation & jurisprudence
Public Health
Pandemics/prevention & control
RevDate: 2026-02-20
Designing Hybrid Work Organization in the Post-Pandemic Era: A Systematic Literature Review.
Work (Reading, Mass.) [Epub ahead of print].
BackgroundIn the post-COVID-19 context, hybrid work (HW) expanded rapidly, often without systematic organizational design or alignment to task demands, generating conceptual ambiguities and limited guidance for configuring HW as an organizational system.ObjectiveTo update the conceptualization of HW and identify elements for designing hybrid work organization (HWO) from a task-based perspective.MethodsA systematic literature review was conducted from June to August 2025 following PRISMA guidelines. Peer-reviewed English-language articles (2020-2025) were retrieved from Scopus, and grey literature (2022-2025) was incorporated through complementary searches and snowballing. Research quality was appraised using MMAT and AACODS tools. Of 363 records screened, 110 full texts were assessed, and 25 met inclusion criteria.ResultsHW emerges as a sociotechnical phenomenon embedded in the digital transformation of work. A multidimensional lens - spatial, temporal, digital/virtual, and social - applied to task categories (individual, collaborative, coordination) identified key designable elements for HWO. Findings indicate that HW extends beyond fixed remote-on-site ratios, emphasizing intentional alternation, task-fit configurations, and dynamic adjustments as work evolves.ConclusionsHWO is context-specific and adaptive, shaped by task requirements rather than predefined schedules or locations. No single model prevails; instead, tailored configurations reflect the variability of real work. Advancing HW as a sociotechnical system requires rethinking organizational culture and management logic, shifting from presence and control-oriented paradigms toward flexible, task-driven, and performance-focused approaches. Progress depends on treating organizational design as a participatory process that aligns arrangements with demands.
Additional Links: PMID-41719175
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@article {pmid41719175,
year = {2026},
author = {Martins Bruno, AC and José de Castro Moura Duarte, F},
title = {Designing Hybrid Work Organization in the Post-Pandemic Era: A Systematic Literature Review.},
journal = {Work (Reading, Mass.)},
volume = {},
number = {},
pages = {10519815261423140},
doi = {10.1177/10519815261423140},
pmid = {41719175},
issn = {1875-9270},
abstract = {BackgroundIn the post-COVID-19 context, hybrid work (HW) expanded rapidly, often without systematic organizational design or alignment to task demands, generating conceptual ambiguities and limited guidance for configuring HW as an organizational system.ObjectiveTo update the conceptualization of HW and identify elements for designing hybrid work organization (HWO) from a task-based perspective.MethodsA systematic literature review was conducted from June to August 2025 following PRISMA guidelines. Peer-reviewed English-language articles (2020-2025) were retrieved from Scopus, and grey literature (2022-2025) was incorporated through complementary searches and snowballing. Research quality was appraised using MMAT and AACODS tools. Of 363 records screened, 110 full texts were assessed, and 25 met inclusion criteria.ResultsHW emerges as a sociotechnical phenomenon embedded in the digital transformation of work. A multidimensional lens - spatial, temporal, digital/virtual, and social - applied to task categories (individual, collaborative, coordination) identified key designable elements for HWO. Findings indicate that HW extends beyond fixed remote-on-site ratios, emphasizing intentional alternation, task-fit configurations, and dynamic adjustments as work evolves.ConclusionsHWO is context-specific and adaptive, shaped by task requirements rather than predefined schedules or locations. No single model prevails; instead, tailored configurations reflect the variability of real work. Advancing HW as a sociotechnical system requires rethinking organizational culture and management logic, shifting from presence and control-oriented paradigms toward flexible, task-driven, and performance-focused approaches. Progress depends on treating organizational design as a participatory process that aligns arrangements with demands.},
}
RevDate: 2026-02-20
CmpDate: 2026-02-20
Golgi Fragmentation as a Potential Link Between SARS-CoV-2 Infection and Alzheimer's Disease: Mechanisms and Implications for Neurodegeneration in Long COVID.
Sub-cellular biochemistry, 111:463-482.
The COVID-19 pandemic has impacted millions of people worldwide, and recent studies have shown that SARS-CoV-2 infection can lead to an Alzheimer's-like neuropathological and biomarker phenotype, as well as clinical symptoms of "brain fog". This raises an intriguing question: "How and where might the molecular pathways underlying SARS-CoV-2 infection and Alzheimer's disease (AD) converge?" One common feature of both SARS-CoV-2 infection and AD is the alteration of the endomembrane system, particularly the fragmentation of the Golgi apparatus. In this review article, we summarize the existing literature on SARS-CoV-2 infection biology and speculate about the potential mechanisms linking Golgi defects, SARS-CoV-2 infection, and neurodegeneration.
Additional Links: PMID-41718988
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@article {pmid41718988,
year = {2026},
author = {Wang, Y and Gandy, S},
title = {Golgi Fragmentation as a Potential Link Between SARS-CoV-2 Infection and Alzheimer's Disease: Mechanisms and Implications for Neurodegeneration in Long COVID.},
journal = {Sub-cellular biochemistry},
volume = {111},
number = {},
pages = {463-482},
pmid = {41718988},
issn = {0306-0225},
mesh = {Humans ; *Alzheimer Disease/pathology/metabolism/virology ; *COVID-19/pathology/complications/metabolism/virology ; *Golgi Apparatus/pathology/metabolism/virology ; *SARS-CoV-2/metabolism ; Animals ; },
abstract = {The COVID-19 pandemic has impacted millions of people worldwide, and recent studies have shown that SARS-CoV-2 infection can lead to an Alzheimer's-like neuropathological and biomarker phenotype, as well as clinical symptoms of "brain fog". This raises an intriguing question: "How and where might the molecular pathways underlying SARS-CoV-2 infection and Alzheimer's disease (AD) converge?" One common feature of both SARS-CoV-2 infection and AD is the alteration of the endomembrane system, particularly the fragmentation of the Golgi apparatus. In this review article, we summarize the existing literature on SARS-CoV-2 infection biology and speculate about the potential mechanisms linking Golgi defects, SARS-CoV-2 infection, and neurodegeneration.},
}
MeSH Terms:
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Humans
*Alzheimer Disease/pathology/metabolism/virology
*COVID-19/pathology/complications/metabolism/virology
*Golgi Apparatus/pathology/metabolism/virology
*SARS-CoV-2/metabolism
Animals
RevDate: 2026-02-20
Mosques as Community Resilience Centers During Disasters: A Systematic Review of COVID-19 Interventions.
Journal of community health [Epub ahead of print].
Additional Links: PMID-41718962
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@article {pmid41718962,
year = {2026},
author = {Sheikhi, RA and Heidari, M and Kahrizsangi, MB},
title = {Mosques as Community Resilience Centers During Disasters: A Systematic Review of COVID-19 Interventions.},
journal = {Journal of community health},
volume = {},
number = {},
pages = {},
pmid = {41718962},
issn = {1573-3610},
support = {6867//Sahrekord University of Medical Sciences/ ; },
}
RevDate: 2026-02-22
CmpDate: 2026-02-20
Proteomic Insights into Venous Thromboembolism.
Medical sciences (Basel, Switzerland), 14(1):.
Venous thromboembolism (VTE), including pulmonary embolism (PE) and deep vein thrombosis (DVT), remains a major cause of morbidity and mortality worldwide, with significant clinical challenges in diagnosis and risk stratification. Traditional diagnostic tools, including clinical prediction scores, D-dimer testing, and imaging, are limited by suboptimal specificity or sensitivity. In this context, proteomics-based approaches have emerged as powerful tools to elucidate the molecular mechanisms of VTE and to identify novel diagnostic and prognostic biomarkers. This review synthesizes recent advances in proteomic research relevant to VTE. We searched four databases (PubMed, ScienceDirect, Springer Nature, and Wiley) using the keywords "acute pulmonary embolism", "acute venous thromboembolism", and "proteomics". Thirty proteomic studies investigating VTE were examined. Across these studies, proteomic profiling consistently revealed alterations in pathways related to coagulation, inflammation, platelet activation, endothelial dysfunction, and fibrin clot structure. Multiple protein classes, including acute-phase reactants, complement components, coagulation factors, and platelet-derived proteins, have demonstrated potential value in improving diagnostic accuracy and refining prognostic stratification. Proteomic analyses have also revealed distinct molecular signatures between isolated PE and isolated DVT, supporting the concept of biologically heterogeneous VTE phenotypes. Furthermore, emerging evidence from COVID-19-associated thrombosis, cancer-associated VTE, and non-invasive sources such as exhaled breath condensate underscores the expanding clinical relevance of proteomic approaches. Although technical limitations and heterogeneity across studies remain challenges, the integration of proteomic data with clinical and genetic information holds promise for advancing precision medicine in VTE.
Additional Links: PMID-41718141
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@article {pmid41718141,
year = {2026},
author = {Manole, OM and Petre, BA and Onofrei, V},
title = {Proteomic Insights into Venous Thromboembolism.},
journal = {Medical sciences (Basel, Switzerland)},
volume = {14},
number = {1},
pages = {},
pmid = {41718141},
issn = {2076-3271},
mesh = {Humans ; *Venous Thromboembolism/metabolism/diagnosis ; *Proteomics/methods ; Biomarkers/metabolism/blood ; Pulmonary Embolism/diagnosis/metabolism ; Venous Thrombosis/diagnosis/metabolism ; COVID-19/complications ; },
abstract = {Venous thromboembolism (VTE), including pulmonary embolism (PE) and deep vein thrombosis (DVT), remains a major cause of morbidity and mortality worldwide, with significant clinical challenges in diagnosis and risk stratification. Traditional diagnostic tools, including clinical prediction scores, D-dimer testing, and imaging, are limited by suboptimal specificity or sensitivity. In this context, proteomics-based approaches have emerged as powerful tools to elucidate the molecular mechanisms of VTE and to identify novel diagnostic and prognostic biomarkers. This review synthesizes recent advances in proteomic research relevant to VTE. We searched four databases (PubMed, ScienceDirect, Springer Nature, and Wiley) using the keywords "acute pulmonary embolism", "acute venous thromboembolism", and "proteomics". Thirty proteomic studies investigating VTE were examined. Across these studies, proteomic profiling consistently revealed alterations in pathways related to coagulation, inflammation, platelet activation, endothelial dysfunction, and fibrin clot structure. Multiple protein classes, including acute-phase reactants, complement components, coagulation factors, and platelet-derived proteins, have demonstrated potential value in improving diagnostic accuracy and refining prognostic stratification. Proteomic analyses have also revealed distinct molecular signatures between isolated PE and isolated DVT, supporting the concept of biologically heterogeneous VTE phenotypes. Furthermore, emerging evidence from COVID-19-associated thrombosis, cancer-associated VTE, and non-invasive sources such as exhaled breath condensate underscores the expanding clinical relevance of proteomic approaches. Although technical limitations and heterogeneity across studies remain challenges, the integration of proteomic data with clinical and genetic information holds promise for advancing precision medicine in VTE.},
}
MeSH Terms:
show MeSH Terms
hide MeSH Terms
Humans
*Venous Thromboembolism/metabolism/diagnosis
*Proteomics/methods
Biomarkers/metabolism/blood
Pulmonary Embolism/diagnosis/metabolism
Venous Thrombosis/diagnosis/metabolism
COVID-19/complications
RevDate: 2026-02-23
CmpDate: 2026-02-23
Climatic factors drive global viral respiratory infections with regional heterogeneity: A systematic review and meta-analysis.
Environment international, 208:110120.
BACKGROUND: Climate change is altering global respiratory virus transmission, yet pathogen-specific climate sensitivities remain unclear across diverse geographical settings.
METHODS: We searched six databases (inception-10 May 2024) for studies quantifying associations between climate factors and virus respiratory infections (VRIs). Random-effects models pooled relative risks (RRs) per unit increase in temperature, relative humidity, precipitation, and wind speed, with climate sensitivity assessed by Köppen-Geiger zones.
RESULTS: From 108 studies comprising 9.22 million VRI cases, three climate patterns emerged. First, temperature was the dominant driver: each 1°C increase reduced respiratory syncytial virus (RSV; RR 0.13, 95% CI 0.08-0.22), influenza virus (IV; RR 0.37, 95% CI 0.23-0.58), human metapneumovirus (HMPV; RR 0.48, 95% CI 0.32-0.73), SARS-CoV-2 (RR 0.52, 95% CI 0.35-0.78), and human coronavirus (HCoV; RR 0.21, 95% CI 0.07-0.61) risks, but increased parainfluenza virus (PIV; RR 2.35, 95% CI 1.46-3.77) and human bocavirus (HBoV; RR 1.86, 95% CI 1.04-3.32) risks. Second, other climate factors showed selective effects: higher humidity decreased IVB risk (RR 0.61, 95% CI 0.40-0.94) but increased enterovirus risk (RR 2.21, 95% CI 1.08-4.51); precipitation decreased IV risk (RR 0.67, 95% CI 0.51-0.89) but increased PIV risk (RR 1.91, 95% CI 1.21-2.99); wind speed amplified IV (RR 1.51, 95% CI 1.01-2.27) and HCoV transmission (RR 5.36, 95% CI 3.43-8.38). Third, climate-zone analyses revealed substantial heterogeneity: in temperate regions, low temperature and humidity increased the risk of most infections (except PIV and HBoV); risks of SARS-CoV-2 and SARS-CoV risks decreased in temperate but increased in continental regions; RSV and HMPV showed greater sensitivity in tropical regions; while in arid regions, MERS-CoV risk increased with temperature but decreased with humidity and wind speed.
CONCLUSION: This analysis identified climate-sensitive VRIs with temperature as key predictor, pathogen-specific sensitivities, and distinct regional patterns, informing targeted climate-based intervention strategies.
Additional Links: PMID-41690197
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@article {pmid41690197,
year = {2026},
author = {Shang, X and Zheng, J and Liu, X and Guo, K and Zhang, N and He, R and Gan, Y and Zhang, WH and Jia, P and Yang, L and Zhu, B},
title = {Climatic factors drive global viral respiratory infections with regional heterogeneity: A systematic review and meta-analysis.},
journal = {Environment international},
volume = {208},
number = {},
pages = {110120},
doi = {10.1016/j.envint.2026.110120},
pmid = {41690197},
issn = {1873-6750},
mesh = {Humans ; *Respiratory Tract Infections/epidemiology/virology ; *Climate Change ; *Climate ; *Virus Diseases/epidemiology ; Temperature ; SARS-CoV-2 ; },
abstract = {BACKGROUND: Climate change is altering global respiratory virus transmission, yet pathogen-specific climate sensitivities remain unclear across diverse geographical settings.
METHODS: We searched six databases (inception-10 May 2024) for studies quantifying associations between climate factors and virus respiratory infections (VRIs). Random-effects models pooled relative risks (RRs) per unit increase in temperature, relative humidity, precipitation, and wind speed, with climate sensitivity assessed by Köppen-Geiger zones.
RESULTS: From 108 studies comprising 9.22 million VRI cases, three climate patterns emerged. First, temperature was the dominant driver: each 1°C increase reduced respiratory syncytial virus (RSV; RR 0.13, 95% CI 0.08-0.22), influenza virus (IV; RR 0.37, 95% CI 0.23-0.58), human metapneumovirus (HMPV; RR 0.48, 95% CI 0.32-0.73), SARS-CoV-2 (RR 0.52, 95% CI 0.35-0.78), and human coronavirus (HCoV; RR 0.21, 95% CI 0.07-0.61) risks, but increased parainfluenza virus (PIV; RR 2.35, 95% CI 1.46-3.77) and human bocavirus (HBoV; RR 1.86, 95% CI 1.04-3.32) risks. Second, other climate factors showed selective effects: higher humidity decreased IVB risk (RR 0.61, 95% CI 0.40-0.94) but increased enterovirus risk (RR 2.21, 95% CI 1.08-4.51); precipitation decreased IV risk (RR 0.67, 95% CI 0.51-0.89) but increased PIV risk (RR 1.91, 95% CI 1.21-2.99); wind speed amplified IV (RR 1.51, 95% CI 1.01-2.27) and HCoV transmission (RR 5.36, 95% CI 3.43-8.38). Third, climate-zone analyses revealed substantial heterogeneity: in temperate regions, low temperature and humidity increased the risk of most infections (except PIV and HBoV); risks of SARS-CoV-2 and SARS-CoV risks decreased in temperate but increased in continental regions; RSV and HMPV showed greater sensitivity in tropical regions; while in arid regions, MERS-CoV risk increased with temperature but decreased with humidity and wind speed.
CONCLUSION: This analysis identified climate-sensitive VRIs with temperature as key predictor, pathogen-specific sensitivities, and distinct regional patterns, informing targeted climate-based intervention strategies.},
}
MeSH Terms:
show MeSH Terms
hide MeSH Terms
Humans
*Respiratory Tract Infections/epidemiology/virology
*Climate Change
*Climate
*Virus Diseases/epidemiology
Temperature
SARS-CoV-2
RevDate: 2026-02-23
CmpDate: 2026-02-23
The escalating threat of multidrug-resistant organisms: COVID-19 impact, global burden, and the Taiwanese experience.
Expert review of anti-infective therapy, 24(1):63-73.
INTRODUCTION: The COVID-19 pandemic has intensified global health challenges, including a silent but escalating crisis: multidrug-resistant organisms (MDROs). As healthcare systems strained under viral outbreaks, infection control and antimicrobial stewardship efforts suffered, accelerating the spread of antimicrobial resistance (AMR).
AREAS COVERED: This review examines the indirect effects of the COVID-19 pandemic on AMR, emphasizing changes in antibiotic utilization, healthcare-associated infections, and resistance trends. Global and regional epidemiological data are presented, with a special focus on Taiwan's evolving MDROs landscape, clinical burden, and strategic responses.
EXPERT OPINION: COVID-19 has both exposed and intensified vulnerabilities in AMR control. While the pandemic fostered certain infection control practices, it also disrupted antimicrobial oversight, leading to surges in MDROs prevalence. Taiwan's experience underscores the value of coordinated guidelines, real-time diagnostics, and artificial intelligence-driven stewardship. Rebuilding and future-proofing AMR responses requires integrated global policies, sustained surveillance, and innovation in diagnostics and therapeutics. Unless comprehensive action is taken, MDROs may emerge as the defining post-pandemic threat to modern medicine.
Additional Links: PMID-41579048
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@article {pmid41579048,
year = {2026},
author = {Chao, CM and Liu, JW and Tang, HJ and Lai, CC},
title = {The escalating threat of multidrug-resistant organisms: COVID-19 impact, global burden, and the Taiwanese experience.},
journal = {Expert review of anti-infective therapy},
volume = {24},
number = {1},
pages = {63-73},
doi = {10.1080/14787210.2026.2623135},
pmid = {41579048},
issn = {1744-8336},
mesh = {Humans ; Taiwan/epidemiology ; *COVID-19/epidemiology ; *Drug Resistance, Multiple, Bacterial ; Antimicrobial Stewardship ; *Anti-Bacterial Agents/therapeutic use/administration & dosage/pharmacology ; Global Health ; *Cross Infection/epidemiology/drug therapy/microbiology ; SARS-CoV-2 ; },
abstract = {INTRODUCTION: The COVID-19 pandemic has intensified global health challenges, including a silent but escalating crisis: multidrug-resistant organisms (MDROs). As healthcare systems strained under viral outbreaks, infection control and antimicrobial stewardship efforts suffered, accelerating the spread of antimicrobial resistance (AMR).
AREAS COVERED: This review examines the indirect effects of the COVID-19 pandemic on AMR, emphasizing changes in antibiotic utilization, healthcare-associated infections, and resistance trends. Global and regional epidemiological data are presented, with a special focus on Taiwan's evolving MDROs landscape, clinical burden, and strategic responses.
EXPERT OPINION: COVID-19 has both exposed and intensified vulnerabilities in AMR control. While the pandemic fostered certain infection control practices, it also disrupted antimicrobial oversight, leading to surges in MDROs prevalence. Taiwan's experience underscores the value of coordinated guidelines, real-time diagnostics, and artificial intelligence-driven stewardship. Rebuilding and future-proofing AMR responses requires integrated global policies, sustained surveillance, and innovation in diagnostics and therapeutics. Unless comprehensive action is taken, MDROs may emerge as the defining post-pandemic threat to modern medicine.},
}
MeSH Terms:
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Humans
Taiwan/epidemiology
*COVID-19/epidemiology
*Drug Resistance, Multiple, Bacterial
Antimicrobial Stewardship
*Anti-Bacterial Agents/therapeutic use/administration & dosage/pharmacology
Global Health
*Cross Infection/epidemiology/drug therapy/microbiology
SARS-CoV-2
RevDate: 2026-02-23
CmpDate: 2023-06-15
Indian consensus statements on irritable bowel syndrome in adults: A guideline by the Indian Neurogastroenterology and Motility Association and jointly supported by the Indian Society of Gastroenterology.
Indian journal of gastroenterology : official journal of the Indian Society of Gastroenterology, 42(2):249-273.
The Indian Neurogastroenterology and Motility Association (INMA), earlier named the Indian Motility and Functional Diseases Association developed this evidence-based practice guidelines for the management of irritable bowel syndrome (IBS). A modified Delphi process was used to develop this consensus containing 28 statements, which were concerning diagnostic criteria, epidemiology, etiopathogenesis and comorbidities, investigations, lifestyle modifications and treatments. Owing to the Coronavirus disease-19 (COVID-19) pandemic, lockdowns and mobility restrictions, web-based meetings and electronic voting were the major tools used to develop this consensus. A statement was regarded as accepted when the sum of "completely accepted" and "accepted with minor reservation" voted responses were 80% or higher. Finally, the consensus was achieved on all 28 statements. The consensus team members are of the view that this work may find use in teaching, patient care, and research on IBS in India and other nations.
Additional Links: PMID-36961659
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@article {pmid36961659,
year = {2023},
author = {Ghoshal, UC and Sachdeva, S and Pratap, N and Karyampudi, A and Mustafa, U and Abraham, P and Bhatt, CB and Chakravartty, K and Chaudhuri, S and Goyal, O and Makharia, GK and Panigrahi, MK and Parida, PK and Patwari, S and Sainani, R and Sadasivan, S and Srinivas, M and Upadhyay, R and Venkataraman, J},
title = {Indian consensus statements on irritable bowel syndrome in adults: A guideline by the Indian Neurogastroenterology and Motility Association and jointly supported by the Indian Society of Gastroenterology.},
journal = {Indian journal of gastroenterology : official journal of the Indian Society of Gastroenterology},
volume = {42},
number = {2},
pages = {249-273},
pmid = {36961659},
issn = {0975-0711},
mesh = {Adult ; Humans ; Communicable Disease Control ; Comorbidity ; *COVID-19/epidemiology/complications ; *Gastroenterology ; *Irritable Bowel Syndrome/diagnosis/epidemiology/etiology ; },
abstract = {The Indian Neurogastroenterology and Motility Association (INMA), earlier named the Indian Motility and Functional Diseases Association developed this evidence-based practice guidelines for the management of irritable bowel syndrome (IBS). A modified Delphi process was used to develop this consensus containing 28 statements, which were concerning diagnostic criteria, epidemiology, etiopathogenesis and comorbidities, investigations, lifestyle modifications and treatments. Owing to the Coronavirus disease-19 (COVID-19) pandemic, lockdowns and mobility restrictions, web-based meetings and electronic voting were the major tools used to develop this consensus. A statement was regarded as accepted when the sum of "completely accepted" and "accepted with minor reservation" voted responses were 80% or higher. Finally, the consensus was achieved on all 28 statements. The consensus team members are of the view that this work may find use in teaching, patient care, and research on IBS in India and other nations.},
}
MeSH Terms:
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Adult
Humans
Communicable Disease Control
Comorbidity
*COVID-19/epidemiology/complications
*Gastroenterology
*Irritable Bowel Syndrome/diagnosis/epidemiology/etiology
RevDate: 2026-02-23
CmpDate: 2020-04-10
[Health protection guideline of conference designated hotel during COVID-19 outbreak].
Zhonghua yu fang yi xue za zhi [Chinese journal of preventive medicine], 54(4):342-344.
This guideline stipulates the management requirements, personal protection and comprehensive security of conference designated hotels. It is applicable to the unified standard prevention and control of conference designated hotels during COVID-19 outbreak.
Additional Links: PMID-32268635
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PubMed:
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@article {pmid32268635,
year = {2020},
author = {, },
title = {[Health protection guideline of conference designated hotel during COVID-19 outbreak].},
journal = {Zhonghua yu fang yi xue za zhi [Chinese journal of preventive medicine]},
volume = {54},
number = {4},
pages = {342-344},
doi = {10.3760/cma.j.cn112150-20200217-00127},
pmid = {32268635},
issn = {0253-9624},
mesh = {Humans ; Betacoronavirus ; China ; *Communicable Disease Control/methods ; Congresses as Topic ; *Coronavirus Infections/prevention & control ; COVID-19 ; Disease Outbreaks ; *Pandemics/prevention & control ; *Pneumonia, Viral/prevention & control ; *Private Facilities ; *Public Health/methods ; SARS-CoV-2 ; },
abstract = {This guideline stipulates the management requirements, personal protection and comprehensive security of conference designated hotels. It is applicable to the unified standard prevention and control of conference designated hotels during COVID-19 outbreak.},
}
MeSH Terms:
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Humans
Betacoronavirus
China
*Communicable Disease Control/methods
Congresses as Topic
*Coronavirus Infections/prevention & control
COVID-19
Disease Outbreaks
*Pandemics/prevention & control
*Pneumonia, Viral/prevention & control
*Private Facilities
*Public Health/methods
SARS-CoV-2
RevDate: 2026-02-22
CmpDate: 2026-02-20
Cardiovascular Complications of Seasonal Influenza in the Pre- and Post-COVID-19 Era: Epidemiology, Mechanisms, and Clinical Implications.
Medical sciences (Basel, Switzerland), 14(1):.
Influenza has long been a well-documented contributor to cardiovascular morbidity and mortality, particularly among high-risk groups. COVID-19 has notably altered the seasonality and natural history of pandemic influenza, with broad implications for related cardiac complications. This review examines the interaction between influenza and cardiovascular illness, especially myocardial infarction, congestive heart failure, stroke, and other acute cardiac events. We review the impact of the COVID-19 pandemic on influenza transmission dynamics, public health policy, and the evolving burden of cardiovascular complications. New evidence indicates that both diseases exacerbate endothelial dysfunction, systemic inflammation, and prothrombotic states, thereby increasing cardiovascular risk. A comparative analysis of pre- and post-COVID-19 influenza-related cardiac complications clarifies evolving trends and guides future preventive strategies. In light of the recent resurgence of influenza following the relaxation of COVID-19 mitigation measures, maximizing vaccine coverage and collaborating to manage viral infections in patients with cardiovascular disease are critical. This review focuses on key research needs to understand long-term cardiac consequences and the urgent requirement for targeted public health strategies to counter viral-mediated cardiovascular threats. In the post-COVID era, integrating influenza and COVID-19 vaccination strategies into cardiovascular risk management may represent a critical opportunity to reduce virus-triggered cardiovascular morbidity and mortality.
Additional Links: PMID-41718104
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@article {pmid41718104,
year = {2026},
author = {Nebuwa, CN and Orjichukwu, CK and Orjichukwu, RO and Akpunonu, PK and Ugwu, PC and Nnabuife, SG},
title = {Cardiovascular Complications of Seasonal Influenza in the Pre- and Post-COVID-19 Era: Epidemiology, Mechanisms, and Clinical Implications.},
journal = {Medical sciences (Basel, Switzerland)},
volume = {14},
number = {1},
pages = {},
pmid = {41718104},
issn = {2076-3271},
mesh = {Humans ; *COVID-19/epidemiology/complications ; *Influenza, Human/complications/epidemiology ; *Cardiovascular Diseases/epidemiology/etiology ; Seasons ; SARS-CoV-2 ; Pandemics ; },
abstract = {Influenza has long been a well-documented contributor to cardiovascular morbidity and mortality, particularly among high-risk groups. COVID-19 has notably altered the seasonality and natural history of pandemic influenza, with broad implications for related cardiac complications. This review examines the interaction between influenza and cardiovascular illness, especially myocardial infarction, congestive heart failure, stroke, and other acute cardiac events. We review the impact of the COVID-19 pandemic on influenza transmission dynamics, public health policy, and the evolving burden of cardiovascular complications. New evidence indicates that both diseases exacerbate endothelial dysfunction, systemic inflammation, and prothrombotic states, thereby increasing cardiovascular risk. A comparative analysis of pre- and post-COVID-19 influenza-related cardiac complications clarifies evolving trends and guides future preventive strategies. In light of the recent resurgence of influenza following the relaxation of COVID-19 mitigation measures, maximizing vaccine coverage and collaborating to manage viral infections in patients with cardiovascular disease are critical. This review focuses on key research needs to understand long-term cardiac consequences and the urgent requirement for targeted public health strategies to counter viral-mediated cardiovascular threats. In the post-COVID era, integrating influenza and COVID-19 vaccination strategies into cardiovascular risk management may represent a critical opportunity to reduce virus-triggered cardiovascular morbidity and mortality.},
}
MeSH Terms:
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Humans
*COVID-19/epidemiology/complications
*Influenza, Human/complications/epidemiology
*Cardiovascular Diseases/epidemiology/etiology
Seasons
SARS-CoV-2
Pandemics
RevDate: 2026-02-22
CmpDate: 2026-02-20
The Role of L-Arginine and Liposomal Vitamin C Supplementation as an Adjunct in Seasonal Respiratory Viral Infection Recovery.
Advances in respiratory medicine, 94(1):.
Respiratory seasonal viral infections remain one of the most important issues in community medicine. The heterogeneity of etiological agents and the characteristics of the hosts airway antiviral defenses account for the complex management of these infections. The clinical consequence of this picture is that, despite the widespread use of vaccination as the primary prevention strategy, the rates of acute respiratory complications remain still high. In addition, they determine post-infectious fatigue and organ dysfunction. Inflammation and oxidative stress are the principal pathogenic mechanisms responsible for clinical complications during respiratory seasonal viral infections. Nowadays, a growing body of evidence indicates that adjunctive nutritional support can contribute to relieve the symptoms during the acute and subacute phases of respiratory viral infections. We assess the data in the literature regarding the combination of L-Arginine and Liposomal Vitamin C as adjuvant treatment for respiratory seasonal viral infections. The database of the National Library of Medicine (PubMed) was searched using the keywords "L-Arginine, Vitamin C, dietary supplements, seasonal respiratory viral infections". The treatment of symptoms during acute and post-acute respiratory viral infections requires an integrated approach that includes vitamins and nutritional supplementation. The combination of L-Arginine and Liposomal Vitamin C seems to represent a nutritional support able to mitigate symptoms occurring during the acute or post-acute phase of infection.
Additional Links: PMID-41718064
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@article {pmid41718064,
year = {2026},
author = {Trimarco, V and Gallo, P and Ghazihosseini, S and Izzo, A and Rozza, PI and Spinelli, A and Cristiano, S and De Rosa, C and Rozza, F and Morisco, C},
title = {The Role of L-Arginine and Liposomal Vitamin C Supplementation as an Adjunct in Seasonal Respiratory Viral Infection Recovery.},
journal = {Advances in respiratory medicine},
volume = {94},
number = {1},
pages = {},
pmid = {41718064},
issn = {2543-6031},
mesh = {Humans ; *Arginine/therapeutic use/administration & dosage ; *Ascorbic Acid/administration & dosage/therapeutic use ; *Dietary Supplements ; *Respiratory Tract Infections/drug therapy/virology ; Liposomes ; *Vitamins/administration & dosage/therapeutic use ; Seasons ; *Virus Diseases/drug therapy ; },
abstract = {Respiratory seasonal viral infections remain one of the most important issues in community medicine. The heterogeneity of etiological agents and the characteristics of the hosts airway antiviral defenses account for the complex management of these infections. The clinical consequence of this picture is that, despite the widespread use of vaccination as the primary prevention strategy, the rates of acute respiratory complications remain still high. In addition, they determine post-infectious fatigue and organ dysfunction. Inflammation and oxidative stress are the principal pathogenic mechanisms responsible for clinical complications during respiratory seasonal viral infections. Nowadays, a growing body of evidence indicates that adjunctive nutritional support can contribute to relieve the symptoms during the acute and subacute phases of respiratory viral infections. We assess the data in the literature regarding the combination of L-Arginine and Liposomal Vitamin C as adjuvant treatment for respiratory seasonal viral infections. The database of the National Library of Medicine (PubMed) was searched using the keywords "L-Arginine, Vitamin C, dietary supplements, seasonal respiratory viral infections". The treatment of symptoms during acute and post-acute respiratory viral infections requires an integrated approach that includes vitamins and nutritional supplementation. The combination of L-Arginine and Liposomal Vitamin C seems to represent a nutritional support able to mitigate symptoms occurring during the acute or post-acute phase of infection.},
}
MeSH Terms:
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Humans
*Arginine/therapeutic use/administration & dosage
*Ascorbic Acid/administration & dosage/therapeutic use
*Dietary Supplements
*Respiratory Tract Infections/drug therapy/virology
Liposomes
*Vitamins/administration & dosage/therapeutic use
Seasons
*Virus Diseases/drug therapy
RevDate: 2026-02-22
Impact of nirmatrelvir/ritonavir on the risk of long COVID in outpatients: a systematic review and meta-analysis.
Expert review of anti-infective therapy [Epub ahead of print].
BACKGROUND: This study systematically synthesized existing evidence to evaluate whether outpatient treatment with nirmatrelvir/ritonavir during the acute phase reduces the incidence of long COVID.
METHODS: We conducted a systematic search of Europe PMC, Medline, Scopus, and the Cochrane Library from inception to 15 September 2025. Eligible studies compared COVID-19 outpatients prescribed nirmatrelvir/ritonavir during the acute phase with those who did not receive the drug. Pooled odds ratios (ORs) with 95% confidence intervals (CIs) were calculated using a random-effects model.
RESULTS: Nineteen studies met inclusion criteria. Overall, nirmatrelvir/ritonavir use during acute infection was associated with a significant reduction in the likelihood of developing post-COVID-19 condition (OR 0.85; 95% CI: 0.80-0.91; p < 0.00001; I[2] = 99%). Protective effects were consistently observed across multiple clinical domains, including cardiovascular (arrhythmia, ischemic disease, heart failure), pulmonary (dyspnea, COPD), thromboembolic (DVT, PE), neurological (stroke, cognitive impairment, headache), psychiatric (depression), gastrointestinal, metabolic (new-onset diabetes), renal (AKI), and general symptoms (malaise and fatigue). Conversely, no significant differences were noted for cough, asthma, dysautonomia, anxiety, PTSD, sleep disturbances, musculoskeletal pain, or olfactory/gustatory dysfunction.
CONCLUSIONS: Early outpatient treatment with nirmatrelvir/ritonavir may mitigate the risk of developing several domains of long COVID, though its benefits are not uniform across all symptom categories.
Additional Links: PMID-41717886
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PubMed:
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@article {pmid41717886,
year = {2026},
author = {Cucunawangsih, C and Ansori, ANM and Vatvani, AD and Hariyanto, TI},
title = {Impact of nirmatrelvir/ritonavir on the risk of long COVID in outpatients: a systematic review and meta-analysis.},
journal = {Expert review of anti-infective therapy},
volume = {},
number = {},
pages = {1-14},
doi = {10.1080/14787210.2026.2636175},
pmid = {41717886},
issn = {1744-8336},
abstract = {BACKGROUND: This study systematically synthesized existing evidence to evaluate whether outpatient treatment with nirmatrelvir/ritonavir during the acute phase reduces the incidence of long COVID.
METHODS: We conducted a systematic search of Europe PMC, Medline, Scopus, and the Cochrane Library from inception to 15 September 2025. Eligible studies compared COVID-19 outpatients prescribed nirmatrelvir/ritonavir during the acute phase with those who did not receive the drug. Pooled odds ratios (ORs) with 95% confidence intervals (CIs) were calculated using a random-effects model.
RESULTS: Nineteen studies met inclusion criteria. Overall, nirmatrelvir/ritonavir use during acute infection was associated with a significant reduction in the likelihood of developing post-COVID-19 condition (OR 0.85; 95% CI: 0.80-0.91; p < 0.00001; I[2] = 99%). Protective effects were consistently observed across multiple clinical domains, including cardiovascular (arrhythmia, ischemic disease, heart failure), pulmonary (dyspnea, COPD), thromboembolic (DVT, PE), neurological (stroke, cognitive impairment, headache), psychiatric (depression), gastrointestinal, metabolic (new-onset diabetes), renal (AKI), and general symptoms (malaise and fatigue). Conversely, no significant differences were noted for cough, asthma, dysautonomia, anxiety, PTSD, sleep disturbances, musculoskeletal pain, or olfactory/gustatory dysfunction.
CONCLUSIONS: Early outpatient treatment with nirmatrelvir/ritonavir may mitigate the risk of developing several domains of long COVID, though its benefits are not uniform across all symptom categories.},
}
RevDate: 2026-02-20
CmpDate: 2026-02-20
Oral and maxillofacial manifestations of COVID-19.
GMS hygiene and infection control, 21:Doc05.
An overview of oral and maxillofacial manifestations associated with COVID-19 is provided. The symptoms range from white, red and mixed inflamed mucosal areas, necrosis, swelling, ulcers, vesicle, bulla, pustule, pigmentation, depapillated and fissured tongue and bleeding in the ulcers. Pre-COVID symptoms included complete loss of taste, along with reduced sense of taste and alterations in the taste perception.
Additional Links: PMID-41716970
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@article {pmid41716970,
year = {2026},
author = {Palwankar, P and Palaniappan, J and Kuttappan, K and Pandey, R and Verma, S and Bhardwaj, A and Shunmugavelu, K},
title = {Oral and maxillofacial manifestations of COVID-19.},
journal = {GMS hygiene and infection control},
volume = {21},
number = {},
pages = {Doc05},
pmid = {41716970},
issn = {2196-5226},
abstract = {An overview of oral and maxillofacial manifestations associated with COVID-19 is provided. The symptoms range from white, red and mixed inflamed mucosal areas, necrosis, swelling, ulcers, vesicle, bulla, pustule, pigmentation, depapillated and fissured tongue and bleeding in the ulcers. Pre-COVID symptoms included complete loss of taste, along with reduced sense of taste and alterations in the taste perception.},
}
RevDate: 2026-02-20
CmpDate: 2026-02-20
Performance and utility of contact tracing for COVID-19 in the WHO South-East Asia Region: implications for future pandemic preparedness.
The Lancet regional health. Southeast Asia, 45:100728.
UNLABELLED: Contact tracing was widely implemented during the COVID-19 pandemic, but its real-world performance and utility for decision-making remain poorly understood. A qualitative study was conducted to appraise the performance and utility of contact tracing for COVID-19 in the WHO South-East Asia Region, based on interviews with government and non-governmental organisation technical staff and decision makers in Indonesia, Nepal and Thailand. Our findings highlight the good performance of contact tracing when sufficiently resourced and when case load is low, but reveal declining utility as case incidence increases. This study presents key definitions and a pragmatic approach for appraising contact tracing performance and utility throughout a major health emergency response. Countries should prospectively define objectives for contact tracing, establish monitoring and evaluation frameworks, adjust their contact tracing approaches informed by risk assessments, and consider other available public health interventions when its performance and utility decline.
FUNDING: Governments of Germany and Australia.
Additional Links: PMID-41716714
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Citation:
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@article {pmid41716714,
year = {2026},
author = {Bannister-Tyrrell, M and Teague, K and Strachan, DL and Barrett, A and Marthias, T and Strachan, CE and Doungngern, P and Thakur, N and Kamal, M and Brindle, H and Jinnai, Y and Kato, M and Vogt, F},
title = {Performance and utility of contact tracing for COVID-19 in the WHO South-East Asia Region: implications for future pandemic preparedness.},
journal = {The Lancet regional health. Southeast Asia},
volume = {45},
number = {},
pages = {100728},
pmid = {41716714},
issn = {2772-3682},
abstract = {UNLABELLED: Contact tracing was widely implemented during the COVID-19 pandemic, but its real-world performance and utility for decision-making remain poorly understood. A qualitative study was conducted to appraise the performance and utility of contact tracing for COVID-19 in the WHO South-East Asia Region, based on interviews with government and non-governmental organisation technical staff and decision makers in Indonesia, Nepal and Thailand. Our findings highlight the good performance of contact tracing when sufficiently resourced and when case load is low, but reveal declining utility as case incidence increases. This study presents key definitions and a pragmatic approach for appraising contact tracing performance and utility throughout a major health emergency response. Countries should prospectively define objectives for contact tracing, establish monitoring and evaluation frameworks, adjust their contact tracing approaches informed by risk assessments, and consider other available public health interventions when its performance and utility decline.
FUNDING: Governments of Germany and Australia.},
}
RevDate: 2026-02-20
CmpDate: 2026-02-20
Lymphocyte Suppression and Exhaustion, Conventional, and Accelerated.
APMIS : acta pathologica, microbiologica, et immunologica Scandinavica, 134(2):e70175.
The essential mammalian immune system lymphocytes include T cells, B cells, and natural killer cells. Any impairments of their functionalities can have severe consequences, since these lymphocytes each contribute as an interactive team in responding to pathogen infections or cancers. Such impairments include lymphocyte exhaustion, such as T cell, B cell, or natural killer cell exhaustion, or lymphocyte suppression impairing one or more of these cells. Lymphocyte exhaustion can have any intensity from mild to severe, having a severity scale worsened by various exposures and time periods of constant antigenic activation. Lymphocyte exhaustion can potentially have a conventional timing pathway or a hypothesized accelerated (pipelined) timing pathway. Lymphocyte suppressions initiated from pathogen infections are also possible, and this can also impair multiple types of lymphocytes. Finally, accelerated T cell exhaustion is possible, and this can explain several puzzling characteristics of virulent viral pandemics, especially in individuals having pathogen or cancer comorbidities. For instance, accelerated T cell exhaustion can explain a substantial percentage of the SARS-CoV-2 pandemic fatalities and also explain the relatively small, but significant, numbers of hyperinflammatory diseases or autoimmune diseases which were initiated in small percentages of individuals by SARS-CoV-2 infections.
Additional Links: PMID-41716011
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PubMed:
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@article {pmid41716011,
year = {2026},
author = {Roe, K},
title = {Lymphocyte Suppression and Exhaustion, Conventional, and Accelerated.},
journal = {APMIS : acta pathologica, microbiologica, et immunologica Scandinavica},
volume = {134},
number = {2},
pages = {e70175},
doi = {10.1111/apm.70175},
pmid = {41716011},
issn = {1600-0463},
mesh = {Humans ; *COVID-19/immunology ; SARS-CoV-2/immunology ; T-Lymphocytes/immunology ; Killer Cells, Natural/immunology ; Animals ; Neoplasms/immunology ; B-Lymphocytes/immunology ; *Lymphocytes/immunology ; Pandemics ; },
abstract = {The essential mammalian immune system lymphocytes include T cells, B cells, and natural killer cells. Any impairments of their functionalities can have severe consequences, since these lymphocytes each contribute as an interactive team in responding to pathogen infections or cancers. Such impairments include lymphocyte exhaustion, such as T cell, B cell, or natural killer cell exhaustion, or lymphocyte suppression impairing one or more of these cells. Lymphocyte exhaustion can have any intensity from mild to severe, having a severity scale worsened by various exposures and time periods of constant antigenic activation. Lymphocyte exhaustion can potentially have a conventional timing pathway or a hypothesized accelerated (pipelined) timing pathway. Lymphocyte suppressions initiated from pathogen infections are also possible, and this can also impair multiple types of lymphocytes. Finally, accelerated T cell exhaustion is possible, and this can explain several puzzling characteristics of virulent viral pandemics, especially in individuals having pathogen or cancer comorbidities. For instance, accelerated T cell exhaustion can explain a substantial percentage of the SARS-CoV-2 pandemic fatalities and also explain the relatively small, but significant, numbers of hyperinflammatory diseases or autoimmune diseases which were initiated in small percentages of individuals by SARS-CoV-2 infections.},
}
MeSH Terms:
show MeSH Terms
hide MeSH Terms
Humans
*COVID-19/immunology
SARS-CoV-2/immunology
T-Lymphocytes/immunology
Killer Cells, Natural/immunology
Animals
Neoplasms/immunology
B-Lymphocytes/immunology
*Lymphocytes/immunology
Pandemics
RevDate: 2026-02-20
CmpDate: 2026-02-20
Implementation and Impact of Tele-Intensive Care Unit (Tele-ICU) Models on Critical Care Outcomes: A Systematic Review.
Nursing in critical care, 31(2):e70401.
BACKGROUND: Tele-Intensive Care Unit (Tele-ICU) models have expanded rapidly in response to global critical care workforce shortages, rising patient acuity and the demands of the COVID-19 pandemic. Contemporary evidence shows substantial variation in Tele-ICU configurations and outcomes, underscoring the need for an updated synthesis that evaluates clinical, staff-related and system-level effects across diverse settings.
AIM: To examine the implementation and impact of Tele-ICU models on critical care outcomes and to compare results across hub-and-spoke, hybrid, consultative and tele-recovery configurations.
STUDY DESIGN: A systematic review was conducted and reported according to PRISMA 2020 and Joanna Briggs Institute guidelines. PubMed, CINAHL, Scopus, Web of Science and Google Scholar were searched for peer-reviewed studies published between January 2020 and October 2025. Owing to heterogeneity in Tele-ICU models, outcomes and effect measures, a narrative synthesis was performed.
RESULTS: Sixteen studies published between 2020 and 2025 were included, comprising quantitative, qualitative and mixed-methods designs conducted across high-, middle- and low-resource healthcare settings. Overall, Tele-ICU implementation was associated with reductions in ICU and hospital mortality, improved adherence to evidence-based clinical protocols, enhanced interprofessional communication and reduced clinician documentation burden. Hub-and-spoke and hybrid Tele-ICU models demonstrated the most consistent clinical and workforce benefits, whereas consultative and low-cost models primarily improved access to specialist care in resource-limited contexts. Across studies, nursing roles expanded to include digital patient surveillance, tele-round coordination, protocol facilitation and virtual family communication. Evidence regarding long-term sustainability and cost-effectiveness was limited and inconsistently reported.
CONCLUSIONS: Tele-ICU models enhance clinical performance, support nursing practice and improve system-level responsiveness across diverse contexts. While benefits are consistent, outcomes vary by model design, local infrastructure and implementation readiness. Longitudinal and economic evaluations are needed to inform sustainable, scalable Tele-ICU strategies.
Tele-ICU models support bedside nurses by improving access to specialist input, strengthening adherence to evidence-based care and enhancing patient safety. Evidence shows that Tele-ICU reduces workload, improves communication and enables nurses to coordinate digital monitoring and family updates, contributing to more consistent and equitable critical care delivery, particularly in high-acuity and resource-limited settings.
Additional Links: PMID-41715908
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@article {pmid41715908,
year = {2026},
author = {Qtait, M and Farajalla, F and Alqaissi, N and Jaradat, Y},
title = {Implementation and Impact of Tele-Intensive Care Unit (Tele-ICU) Models on Critical Care Outcomes: A Systematic Review.},
journal = {Nursing in critical care},
volume = {31},
number = {2},
pages = {e70401},
doi = {10.1111/nicc.70401},
pmid = {41715908},
issn = {1478-5153},
mesh = {Humans ; *Telemedicine/organization & administration ; *Intensive Care Units/organization & administration ; *COVID-19/epidemiology ; *Critical Care/organization & administration ; *Critical Care Outcomes ; SARS-CoV-2 ; Critical Care Nursing ; },
abstract = {BACKGROUND: Tele-Intensive Care Unit (Tele-ICU) models have expanded rapidly in response to global critical care workforce shortages, rising patient acuity and the demands of the COVID-19 pandemic. Contemporary evidence shows substantial variation in Tele-ICU configurations and outcomes, underscoring the need for an updated synthesis that evaluates clinical, staff-related and system-level effects across diverse settings.
AIM: To examine the implementation and impact of Tele-ICU models on critical care outcomes and to compare results across hub-and-spoke, hybrid, consultative and tele-recovery configurations.
STUDY DESIGN: A systematic review was conducted and reported according to PRISMA 2020 and Joanna Briggs Institute guidelines. PubMed, CINAHL, Scopus, Web of Science and Google Scholar were searched for peer-reviewed studies published between January 2020 and October 2025. Owing to heterogeneity in Tele-ICU models, outcomes and effect measures, a narrative synthesis was performed.
RESULTS: Sixteen studies published between 2020 and 2025 were included, comprising quantitative, qualitative and mixed-methods designs conducted across high-, middle- and low-resource healthcare settings. Overall, Tele-ICU implementation was associated with reductions in ICU and hospital mortality, improved adherence to evidence-based clinical protocols, enhanced interprofessional communication and reduced clinician documentation burden. Hub-and-spoke and hybrid Tele-ICU models demonstrated the most consistent clinical and workforce benefits, whereas consultative and low-cost models primarily improved access to specialist care in resource-limited contexts. Across studies, nursing roles expanded to include digital patient surveillance, tele-round coordination, protocol facilitation and virtual family communication. Evidence regarding long-term sustainability and cost-effectiveness was limited and inconsistently reported.
CONCLUSIONS: Tele-ICU models enhance clinical performance, support nursing practice and improve system-level responsiveness across diverse contexts. While benefits are consistent, outcomes vary by model design, local infrastructure and implementation readiness. Longitudinal and economic evaluations are needed to inform sustainable, scalable Tele-ICU strategies.
Tele-ICU models support bedside nurses by improving access to specialist input, strengthening adherence to evidence-based care and enhancing patient safety. Evidence shows that Tele-ICU reduces workload, improves communication and enables nurses to coordinate digital monitoring and family updates, contributing to more consistent and equitable critical care delivery, particularly in high-acuity and resource-limited settings.},
}
MeSH Terms:
show MeSH Terms
hide MeSH Terms
Humans
*Telemedicine/organization & administration
*Intensive Care Units/organization & administration
*COVID-19/epidemiology
*Critical Care/organization & administration
*Critical Care Outcomes
SARS-CoV-2
Critical Care Nursing
RevDate: 2026-02-21
Telerehabilitation in the management of urinary incontinence in women: a narrative review.
BMC women's health, 26(1):.
Urinary incontinence (UI) is a prevalent condition affecting millions worldwide, particularly women, with significant impacts on physical, psychological, and socioeconomic aspects of life (Haylen et al., Neurourol Urodyn 29:4–20, 2010; Aoki et al., Nat Rev Dis Primers 3:1–20, 2017). Conventional management includes behavioral therapy, pelvic floor muscle training (PFMT), and pharmacological interventions, but barriers such as social stigma, access to specialists, and poor treatment adherence persist (Nitti Rev Urol 3, 2001; Sinclair et al., Obstet Gynaecol 13:143-8, 2011; Minassian et al., 111:324-31, 2008; Milsom et al., Eur Urol 65:79-95, 2014). Telerehabilitation—defined as the delivery of rehabilitation services via electronic information and communication technologies (e.g., video conferencing and phone calls for improved access; mobile apps, websites, and virtual reality (VR) for enhanced engagement and self-management)—offers a potentially promising alternative to overcome these obstacles (Buckingham et al., JMIRx Med 3:e30516, 2022). This narrative review synthesizes evidence from studies conducted between January 2000 and November 6, 2025 on telerehabilitation’s role in UI management in women, focusing on stress UI, PFMT efficacy, and comparative outcomes with in-person therapy. It addresses gaps in prior systematic reviews by focusing on patient-centered designs and cultural adaptations. Key findings from 25 included studies indicate that telerehabilitation is feasible, effective in reducing UI symptoms, improving quality of life (QoL), and enhancing adherence, particularly through mobile apps and group-based interventions (Asklund et al., Neurourol Urodyn 36:1369-76, 2017; Sjostrom et al., BJU Int 112:362-72, 2013; Hoffman et al., Gynecol Scand 96:1180-7, 2017). However, limitations include heterogeneity in interventions, small sample sizes in many studies, lack of long-term data, absence of male participants, limited validation in rural or cognitively impaired populations, and insufficient cultural adaptations for diverse groups. Recommendations include developing tailored telerehabilitation programs incorporating biofeedback and interdisciplinary approaches to address UI holistically. This review highlights telerehabilitation’s potential as a scalable, cost-effective intervention, particularly post-COVID-19, and calls for further research in diverse female populations.
Additional Links: PMID-41612314
PubMed:
Citation:
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@article {pmid41612314,
year = {2026},
author = {Roshdi, G and Motealleh, A},
title = {Telerehabilitation in the management of urinary incontinence in women: a narrative review.},
journal = {BMC women's health},
volume = {26},
number = {1},
pages = {},
pmid = {41612314},
issn = {1472-6874},
abstract = {Urinary incontinence (UI) is a prevalent condition affecting millions worldwide, particularly women, with significant impacts on physical, psychological, and socioeconomic aspects of life (Haylen et al., Neurourol Urodyn 29:4–20, 2010; Aoki et al., Nat Rev Dis Primers 3:1–20, 2017). Conventional management includes behavioral therapy, pelvic floor muscle training (PFMT), and pharmacological interventions, but barriers such as social stigma, access to specialists, and poor treatment adherence persist (Nitti Rev Urol 3, 2001; Sinclair et al., Obstet Gynaecol 13:143-8, 2011; Minassian et al., 111:324-31, 2008; Milsom et al., Eur Urol 65:79-95, 2014). Telerehabilitation—defined as the delivery of rehabilitation services via electronic information and communication technologies (e.g., video conferencing and phone calls for improved access; mobile apps, websites, and virtual reality (VR) for enhanced engagement and self-management)—offers a potentially promising alternative to overcome these obstacles (Buckingham et al., JMIRx Med 3:e30516, 2022). This narrative review synthesizes evidence from studies conducted between January 2000 and November 6, 2025 on telerehabilitation’s role in UI management in women, focusing on stress UI, PFMT efficacy, and comparative outcomes with in-person therapy. It addresses gaps in prior systematic reviews by focusing on patient-centered designs and cultural adaptations. Key findings from 25 included studies indicate that telerehabilitation is feasible, effective in reducing UI symptoms, improving quality of life (QoL), and enhancing adherence, particularly through mobile apps and group-based interventions (Asklund et al., Neurourol Urodyn 36:1369-76, 2017; Sjostrom et al., BJU Int 112:362-72, 2013; Hoffman et al., Gynecol Scand 96:1180-7, 2017). However, limitations include heterogeneity in interventions, small sample sizes in many studies, lack of long-term data, absence of male participants, limited validation in rural or cognitively impaired populations, and insufficient cultural adaptations for diverse groups. Recommendations include developing tailored telerehabilitation programs incorporating biofeedback and interdisciplinary approaches to address UI holistically. This review highlights telerehabilitation’s potential as a scalable, cost-effective intervention, particularly post-COVID-19, and calls for further research in diverse female populations.},
}
RevDate: 2026-02-21
CmpDate: 2026-02-21
Associations Between the US Department of Agriculture COVID-19 Pandemic Waivers and Summer Meal Programs Access and Participation: A Systematic Review.
Journal of the Academy of Nutrition and Dietetics, 126(3):156249.
BACKGROUND: The US Department of Agriculture (USDA) Summer Meal Programs (SMPs) are funded to ensure children from low-income households continue to have access to food over the summer months when most schools are closed for instruction. However, these programs are underutilized compared with school meal programs, in part due to barriers to accessing SMPs. During the COVID-19 pandemic, USDA waived several restrictions related to area eligibility and meal distribution.
OBJECTIVES: To systematically review the evidence of the association between USDA pandemic waivers and SMPs access (ie, scope and coverage) and participation.
METHODS: Three electronic databases were searched (PubMed, Education Resources Information Center, and Thomson Reuters Web of Science) to identify peer-reviewed and government studies that examined associations between USDA pandemic waivers and changes in the number of SMP sponsors, sites, participants, and/or meals served. Inclusion criteria included studies conducted in the United States and published in English between August 2021 and June 2024. Qualitative studies, studies conducted only during the school year, or studies that did not examine the association between the waivers and relevant outcomes were excluded. Risk of bias was assessed using an adapted version of the Newcastle-Ottawa Scale. Articles were narratively synthesized.
RESULTS: Twelve articles met the inclusion criteria. The majority found increases in the number of SMP sites that were sponsored by public schools after the pandemic waivers. However, some studies found decreases specifically among nonpublic school-sponsored sites. The majority also found increases in the number of children and/or meals served, even in the presence of fewer sites.
CONCLUSIONS: Evidence suggests that the pandemic waivers were associated with improvements in scope, coverage, and participation in SMPs. Continued support of state agencies to administer SMPs using flexible and innovative strategies should be considered.
Additional Links: PMID-41349892
Publisher:
PubMed:
Citation:
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@article {pmid41349892,
year = {2026},
author = {Cohen, JFW and Bennett, BL and Calvert, HG and Schwartz, MB and Turner, L and Toossi, S},
title = {Associations Between the US Department of Agriculture COVID-19 Pandemic Waivers and Summer Meal Programs Access and Participation: A Systematic Review.},
journal = {Journal of the Academy of Nutrition and Dietetics},
volume = {126},
number = {3},
pages = {156249},
doi = {10.1016/j.jand.2025.156249},
pmid = {41349892},
issn = {2212-2672},
mesh = {Humans ; *COVID-19/epidemiology ; *United States Department of Agriculture ; United States ; *Food Services/statistics & numerical data ; Child ; *Food Assistance/statistics & numerical data ; Schools ; SARS-CoV-2 ; *Meals ; Pandemics ; Poverty ; Seasons ; },
abstract = {BACKGROUND: The US Department of Agriculture (USDA) Summer Meal Programs (SMPs) are funded to ensure children from low-income households continue to have access to food over the summer months when most schools are closed for instruction. However, these programs are underutilized compared with school meal programs, in part due to barriers to accessing SMPs. During the COVID-19 pandemic, USDA waived several restrictions related to area eligibility and meal distribution.
OBJECTIVES: To systematically review the evidence of the association between USDA pandemic waivers and SMPs access (ie, scope and coverage) and participation.
METHODS: Three electronic databases were searched (PubMed, Education Resources Information Center, and Thomson Reuters Web of Science) to identify peer-reviewed and government studies that examined associations between USDA pandemic waivers and changes in the number of SMP sponsors, sites, participants, and/or meals served. Inclusion criteria included studies conducted in the United States and published in English between August 2021 and June 2024. Qualitative studies, studies conducted only during the school year, or studies that did not examine the association between the waivers and relevant outcomes were excluded. Risk of bias was assessed using an adapted version of the Newcastle-Ottawa Scale. Articles were narratively synthesized.
RESULTS: Twelve articles met the inclusion criteria. The majority found increases in the number of SMP sites that were sponsored by public schools after the pandemic waivers. However, some studies found decreases specifically among nonpublic school-sponsored sites. The majority also found increases in the number of children and/or meals served, even in the presence of fewer sites.
CONCLUSIONS: Evidence suggests that the pandemic waivers were associated with improvements in scope, coverage, and participation in SMPs. Continued support of state agencies to administer SMPs using flexible and innovative strategies should be considered.},
}
MeSH Terms:
show MeSH Terms
hide MeSH Terms
Humans
*COVID-19/epidemiology
*United States Department of Agriculture
United States
*Food Services/statistics & numerical data
Child
*Food Assistance/statistics & numerical data
Schools
SARS-CoV-2
*Meals
Pandemics
Poverty
Seasons
RevDate: 2026-02-19
CmpDate: 2026-02-19
Life-Threatening SARS-CoV-2-Associated Encephalopathy and Multiorgan Failure in Children, Asia and Oceania, 2022-2024.
Emerging infectious diseases, 32(2):169-179.
SARS-CoV-2 infections in children occasionally manifest with severe neurologic signs. We report a case series of life-threatening encephalopathy associated with SARS-CoV-2 in 25 children in Australia, Japan, Singapore, and Taiwan during February 2022-January 2024. All children had severe encephalopathy develop, characterized by rapidly progressive cerebral edema, conditions known as acute shock with encephalopathy and multiorgan failure or acute fulminant cerebral edema. Among the 25 patients, 22 (88%) eventually died; 11 (44%) children died within 24 hours of hospitalization. In addition, 18 (72%) had illness manifest with shock, and 14 (56%) had multiorgan failure develop within 6 hours of neurologic onset. Serum concentrations of cytokines/chemokines including interleukin 6 and tumor necrosis factor-α were significantly higher within 24 hours of onset than for controls. SARS-CoV-2-associated encephalopathy cases such as those described here represent an emerging neurologic crisis with high mortality rate resulting from rapidly progressive brain edema and multiorgan failure.
Additional Links: PMID-41714597
Publisher:
PubMed:
Citation:
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@article {pmid41714597,
year = {2026},
author = {Kasai, M and Sakuma, H and Suzuki, M and Nishiyama, M and Kawata, N and Lin, JJ and Lin, KL and Han, V and Mohammad, SS and Dale, RC and Thomas, T and Muramatsu, K and Mitani, O and Kobayashi, Y and Ishida, K and Abe, Y and Kuki, I and Takanashi, JI},
title = {Life-Threatening SARS-CoV-2-Associated Encephalopathy and Multiorgan Failure in Children, Asia and Oceania, 2022-2024.},
journal = {Emerging infectious diseases},
volume = {32},
number = {2},
pages = {169-179},
doi = {10.3201/eid3202.250549},
pmid = {41714597},
issn = {1080-6059},
mesh = {Humans ; *COVID-19/complications/epidemiology ; *Multiple Organ Failure/virology/epidemiology/etiology/mortality ; SARS-CoV-2 ; Male ; Female ; Child ; Child, Preschool ; *Brain Diseases/virology/epidemiology ; Infant ; Brain Edema/virology/etiology ; Adolescent ; Pandemics ; Asia/epidemiology ; Japan/epidemiology ; Australia/epidemiology ; Singapore/epidemiology ; Taiwan/epidemiology ; },
abstract = {SARS-CoV-2 infections in children occasionally manifest with severe neurologic signs. We report a case series of life-threatening encephalopathy associated with SARS-CoV-2 in 25 children in Australia, Japan, Singapore, and Taiwan during February 2022-January 2024. All children had severe encephalopathy develop, characterized by rapidly progressive cerebral edema, conditions known as acute shock with encephalopathy and multiorgan failure or acute fulminant cerebral edema. Among the 25 patients, 22 (88%) eventually died; 11 (44%) children died within 24 hours of hospitalization. In addition, 18 (72%) had illness manifest with shock, and 14 (56%) had multiorgan failure develop within 6 hours of neurologic onset. Serum concentrations of cytokines/chemokines including interleukin 6 and tumor necrosis factor-α were significantly higher within 24 hours of onset than for controls. SARS-CoV-2-associated encephalopathy cases such as those described here represent an emerging neurologic crisis with high mortality rate resulting from rapidly progressive brain edema and multiorgan failure.},
}
MeSH Terms:
show MeSH Terms
hide MeSH Terms
Humans
*COVID-19/complications/epidemiology
*Multiple Organ Failure/virology/epidemiology/etiology/mortality
SARS-CoV-2
Male
Female
Child
Child, Preschool
*Brain Diseases/virology/epidemiology
Infant
Brain Edema/virology/etiology
Adolescent
Pandemics
Asia/epidemiology
Japan/epidemiology
Australia/epidemiology
Singapore/epidemiology
Taiwan/epidemiology
RevDate: 2026-02-20
CmpDate: 2026-02-20
Respiratory virus immune response in the aged host.
Immunity & ageing : I & A, 23(1):10.
Viruses are a major cause of acute respiratory illness in older adults and pose a substantial burden as the elderly population continues to grow. In the current COVID-19 global health crisis, achieving a better understanding of the aging immune system proves to be an imperative step in preventing and treating respiratory viral infections in older patients. Furthermore, many common respiratory viruses infecting older adults, including human metapneumovirus and parainfluenza virus, do not have licensed vaccines, thereby increasing the risk of severe infection in the aged host. Moreover, given the slowed immune response of older adults, vaccine efficacy for respiratory viruses such as influenza in older adults is minimal, indicating the need to develop more potent vaccines. A better understanding of the aging immune system would allow vaccines to target immunological deficits in the aged host. Three aspects of the aging immune system affect the response to respiratory viruses and vaccines: [1] innate immunity [2], the “inflammaging” hypothesis, and [3] the adaptive immune response. Several innate immune cells (neutrophils, macrophages, dendritic cells, and natural killer cells) as well as adaptive immune cells (T and B lymphocytes) exhibit significant functional impairment in older adults. The inflammaging hypothesis bridges the innate and adaptive arms of the immune system. This review aims to consolidate current knowledge and fill gaps in our understanding of the aged immune response to respiratory viruses.
Additional Links: PMID-41668138
PubMed:
Citation:
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@article {pmid41668138,
year = {2026},
author = {Parks, OB and Kalavacharla, A and Williams, JV},
title = {Respiratory virus immune response in the aged host.},
journal = {Immunity & ageing : I & A},
volume = {23},
number = {1},
pages = {10},
pmid = {41668138},
issn = {1742-4933},
support = {HL159915/HL/NHLBI NIH HHS/United States ; AI085062//National Institute of Allergy and Infectious Diseases/ ; HL159915/HL/NHLBI NIH HHS/United States ; },
abstract = {Viruses are a major cause of acute respiratory illness in older adults and pose a substantial burden as the elderly population continues to grow. In the current COVID-19 global health crisis, achieving a better understanding of the aging immune system proves to be an imperative step in preventing and treating respiratory viral infections in older patients. Furthermore, many common respiratory viruses infecting older adults, including human metapneumovirus and parainfluenza virus, do not have licensed vaccines, thereby increasing the risk of severe infection in the aged host. Moreover, given the slowed immune response of older adults, vaccine efficacy for respiratory viruses such as influenza in older adults is minimal, indicating the need to develop more potent vaccines. A better understanding of the aging immune system would allow vaccines to target immunological deficits in the aged host. Three aspects of the aging immune system affect the response to respiratory viruses and vaccines: [1] innate immunity [2], the “inflammaging” hypothesis, and [3] the adaptive immune response. Several innate immune cells (neutrophils, macrophages, dendritic cells, and natural killer cells) as well as adaptive immune cells (T and B lymphocytes) exhibit significant functional impairment in older adults. The inflammaging hypothesis bridges the innate and adaptive arms of the immune system. This review aims to consolidate current knowledge and fill gaps in our understanding of the aged immune response to respiratory viruses.},
}
RevDate: 2026-02-21
CmpDate: 2026-02-21
Taurine intake ameliorates lactic acidosis and hyperferritinemia occurring after mRNA SARS-CoV-2 vaccination in a patient with β-thalassemia trait: a case report and review of literature.
Journal of medical case reports, 20(1):.
BACKGROUND: Taurine is a powerful antioxidant necessary for mitochondrial function. Lactic acidosis is a complication encountered in the condition mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS), which can be successfully treated with supplemental taurine. Furthermore, taurine regulates the production of iron-dependent proteins such as ferritin that can act as chelating agents to sequester labile iron.
CASE PRESENTATION: A 38-year-old Greek male with a β-zero thalassemia trait developed multiple severe symptoms soon after his first and only mRNA (Pfizer) SARS-CoV-2 vaccination that included hematological stress to be a candidate for blood transfusion. Amongst the hematological readings, the patient had lactate levels > 4 mmol/ml, indicating lactic acidosis, and ferritin levels > 820 ng/ml, representing hyperferritinemia. Moreover, the patient has organic acid and plasma metabolite levels in the urine that are indicative of mitochondrial dysfunction. Regular taurine intake (500 mg/day) for years helped the patient control lactate and ferritin levels and avoid more serious clinical decompensation.
CONCLUSION: Regular taurine intake helps to avoid lactic acidosis and reverse hyperferritinemia after mRNA SARS-CoV-2 vaccination in a patient with β-zero thalassemia trait with no obvious genetic trait linked to mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes. Taurine seemed to be protective for mitochondria.
Additional Links: PMID-41606631
PubMed:
Citation:
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@article {pmid41606631,
year = {2026},
author = {Kyriakopoulos, AM and McCullough, PA and Seneff, S},
title = {Taurine intake ameliorates lactic acidosis and hyperferritinemia occurring after mRNA SARS-CoV-2 vaccination in a patient with β-thalassemia trait: a case report and review of literature.},
journal = {Journal of medical case reports},
volume = {20},
number = {1},
pages = {},
pmid = {41606631},
issn = {1752-1947},
support = {6950759//Quanta Computer, Inc./ ; },
mesh = {Humans ; Male ; Adult ; *Acidosis, Lactic/drug therapy/etiology/prevention & control ; *Taurine/therapeutic use/administration & dosage ; *Hyperferritinemia/drug therapy/etiology ; *beta-Thalassemia/complications ; *COVID-19 Vaccines/adverse effects ; COVID-19/prevention & control ; SARS-CoV-2 ; Ferritins/blood ; },
abstract = {BACKGROUND: Taurine is a powerful antioxidant necessary for mitochondrial function. Lactic acidosis is a complication encountered in the condition mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS), which can be successfully treated with supplemental taurine. Furthermore, taurine regulates the production of iron-dependent proteins such as ferritin that can act as chelating agents to sequester labile iron.
CASE PRESENTATION: A 38-year-old Greek male with a β-zero thalassemia trait developed multiple severe symptoms soon after his first and only mRNA (Pfizer) SARS-CoV-2 vaccination that included hematological stress to be a candidate for blood transfusion. Amongst the hematological readings, the patient had lactate levels > 4 mmol/ml, indicating lactic acidosis, and ferritin levels > 820 ng/ml, representing hyperferritinemia. Moreover, the patient has organic acid and plasma metabolite levels in the urine that are indicative of mitochondrial dysfunction. Regular taurine intake (500 mg/day) for years helped the patient control lactate and ferritin levels and avoid more serious clinical decompensation.
CONCLUSION: Regular taurine intake helps to avoid lactic acidosis and reverse hyperferritinemia after mRNA SARS-CoV-2 vaccination in a patient with β-zero thalassemia trait with no obvious genetic trait linked to mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes. Taurine seemed to be protective for mitochondria.},
}
MeSH Terms:
show MeSH Terms
hide MeSH Terms
Humans
Male
Adult
*Acidosis, Lactic/drug therapy/etiology/prevention & control
*Taurine/therapeutic use/administration & dosage
*Hyperferritinemia/drug therapy/etiology
*beta-Thalassemia/complications
*COVID-19 Vaccines/adverse effects
COVID-19/prevention & control
SARS-CoV-2
Ferritins/blood
RevDate: 2026-02-19
From 2020 to 2025: Comprehensive review Decoding novel structural inhibitors for M[pro] of SARS-CoV-2.
Biochemical pharmacology pii:S0006-2952(26)00122-X [Epub ahead of print].
While the immediate global threat of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has subsided, the virus remains a persistent cause of regional outbreaks and public health concerns. The main protease (M[pro]), essential for viral polyprotein processing and replication, remains one of the most validated and strategically important antiviral targets. In this comprehensive review, we critically evaluate the landscape of M[pro] inhibitor development from 2020 to 2025, encompassing four key categories: peptidomimetic inhibitors, non-peptide small molecules, natural product-derived compounds, and proteolysis-targeting chimeras (PROTACs). By integrating mechanistic insights with structural and technological advancements, this work highlights emerging opportunities for the rational design of next-generation M[pro]-targeted antivirals capable of addressing both current and future coronavirus threats.
Additional Links: PMID-41713622
Publisher:
PubMed:
Citation:
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@article {pmid41713622,
year = {2026},
author = {Zhang, X and Xu, Y and Jiang, Y and Huang, J and Li, X},
title = {From 2020 to 2025: Comprehensive review Decoding novel structural inhibitors for M[pro] of SARS-CoV-2.},
journal = {Biochemical pharmacology},
volume = {},
number = {},
pages = {117791},
doi = {10.1016/j.bcp.2026.117791},
pmid = {41713622},
issn = {1873-2968},
abstract = {While the immediate global threat of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has subsided, the virus remains a persistent cause of regional outbreaks and public health concerns. The main protease (M[pro]), essential for viral polyprotein processing and replication, remains one of the most validated and strategically important antiviral targets. In this comprehensive review, we critically evaluate the landscape of M[pro] inhibitor development from 2020 to 2025, encompassing four key categories: peptidomimetic inhibitors, non-peptide small molecules, natural product-derived compounds, and proteolysis-targeting chimeras (PROTACs). By integrating mechanistic insights with structural and technological advancements, this work highlights emerging opportunities for the rational design of next-generation M[pro]-targeted antivirals capable of addressing both current and future coronavirus threats.},
}
RevDate: 2026-02-19
CmpDate: 2026-02-19
Securing Federated Learning With Blockchain in the Medical Field: Systematic Literature Review.
Journal of medical Internet research, 28:e79052.
BACKGROUND: The exponential growth of medical data and advancements in artificial intelligence (AI) have accelerated the development of data-driven health care. However, the secure and efficient sharing of sensitive medical data across institutions remains a major challenge due to privacy concerns, data silos, and regulatory restrictions. Traditional centralized systems are prone to data breaches and single points of failure, while existing privacy-preserving techniques face high computational and communication costs.
OBJECTIVE: This study aims to provide a comprehensive review of the recent advances in blockchain-based federated learning (BCFL) within the medical field. By exploring the synergistic integration of federated learning and blockchain, this review evaluates how BCFL enhances data security, supports privacy-preserving cross-institutional collaboration, and facilitates practical applications in health care, including medical data sharing, Internet of Medical Things, public health surveillance, and telemedicine.
METHODS: We conducted a systematic literature review using databases such as PubMed, IEEE Xplore, Web of Science, and Google Scholar. Boolean logic and domain-specific keywords were used to retrieve studies from 2018 to 2025. After automated deduplication and multistage manual screening, over 100 high-quality papers were included. These works cover BCFL's theoretical foundations, system architectures, application domains, limitations, and future directions.
RESULTS: BCFL frameworks combine the decentralized trust and auditability of blockchain with the privacy-preserving collaborative learning capabilities of federated learning. This integration mitigates risks such as model tampering, data leakage, and a lack of incentives in federated systems. Applications span across cross-institutional medical data sharing, Internet of Medical Things, epidemic forecasting, and telemedicine. Architectures including fully coupled, flexibly coupled, and loosely coupled models offer varying trade-offs between efficiency, scalability, and security.
CONCLUSIONS: BCFL represents a transformative paradigm for secure, collaborative, and privacy-preserving medical AI. By combining decentralized trust, incentive-driven participation, and privacy-enhancing machine learning, BCFL paves the way for next-generation smart health care systems. Despite current technical and practical challenges, BCFL demonstrates strong potential to support precision medicine, global health data collaboration, and large-scale AI deployment in health care.
Additional Links: PMID-41712960
PubMed:
Citation:
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@article {pmid41712960,
year = {2026},
author = {Wang, X and Xie, Y and Chen, X and Yang, J and Li, R and Gao, W and Yan, Z and Zhou, H and Ye, Z},
title = {Securing Federated Learning With Blockchain in the Medical Field: Systematic Literature Review.},
journal = {Journal of medical Internet research},
volume = {28},
number = {},
pages = {e79052},
pmid = {41712960},
issn = {1438-8871},
mesh = {*Blockchain ; *Computer Security ; Humans ; *Artificial Intelligence ; Telemedicine ; Information Dissemination ; Federated Learning ; },
abstract = {BACKGROUND: The exponential growth of medical data and advancements in artificial intelligence (AI) have accelerated the development of data-driven health care. However, the secure and efficient sharing of sensitive medical data across institutions remains a major challenge due to privacy concerns, data silos, and regulatory restrictions. Traditional centralized systems are prone to data breaches and single points of failure, while existing privacy-preserving techniques face high computational and communication costs.
OBJECTIVE: This study aims to provide a comprehensive review of the recent advances in blockchain-based federated learning (BCFL) within the medical field. By exploring the synergistic integration of federated learning and blockchain, this review evaluates how BCFL enhances data security, supports privacy-preserving cross-institutional collaboration, and facilitates practical applications in health care, including medical data sharing, Internet of Medical Things, public health surveillance, and telemedicine.
METHODS: We conducted a systematic literature review using databases such as PubMed, IEEE Xplore, Web of Science, and Google Scholar. Boolean logic and domain-specific keywords were used to retrieve studies from 2018 to 2025. After automated deduplication and multistage manual screening, over 100 high-quality papers were included. These works cover BCFL's theoretical foundations, system architectures, application domains, limitations, and future directions.
RESULTS: BCFL frameworks combine the decentralized trust and auditability of blockchain with the privacy-preserving collaborative learning capabilities of federated learning. This integration mitigates risks such as model tampering, data leakage, and a lack of incentives in federated systems. Applications span across cross-institutional medical data sharing, Internet of Medical Things, epidemic forecasting, and telemedicine. Architectures including fully coupled, flexibly coupled, and loosely coupled models offer varying trade-offs between efficiency, scalability, and security.
CONCLUSIONS: BCFL represents a transformative paradigm for secure, collaborative, and privacy-preserving medical AI. By combining decentralized trust, incentive-driven participation, and privacy-enhancing machine learning, BCFL paves the way for next-generation smart health care systems. Despite current technical and practical challenges, BCFL demonstrates strong potential to support precision medicine, global health data collaboration, and large-scale AI deployment in health care.},
}
MeSH Terms:
show MeSH Terms
hide MeSH Terms
*Blockchain
*Computer Security
Humans
*Artificial Intelligence
Telemedicine
Information Dissemination
Federated Learning
RevDate: 2026-02-19
CmpDate: 2026-02-19
Long COVID-associated neurological symptoms and brain fog: Understanding the mechanism of neuroinflammation, BBB disruption, diagnostics, and therapeutics.
Molecular biology reports, 53(1):401.
Long COVID affects at least 10% of those with severe disease, and many experience neurological symptoms and brain fog. More than 200 symptoms are reported, yet a detailed understanding remains limited. This article summarizes current knowledge of neurological symptoms, brain fog, molecular mechanisms, neuroinflammation, blood-brain barrier disruption, diagnostics, and available therapeutics. Our review highlights the lack of diagnostics and treatments for these patients. We catalog the ongoing clinical trials, identify the urgent need for further therapeutics, and stress that advances in understanding pathophysiology will drive new treatments. We urge prioritizing animal model studies and improving diagnostics to accelerate the discovery and delivery of effective treatments for long COVID neurological symptoms.
Additional Links: PMID-41712028
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@article {pmid41712028,
year = {2026},
author = {Chakraborty, C and Bhattacharya, M and Chatterjee, S and Lee, SS},
title = {Long COVID-associated neurological symptoms and brain fog: Understanding the mechanism of neuroinflammation, BBB disruption, diagnostics, and therapeutics.},
journal = {Molecular biology reports},
volume = {53},
number = {1},
pages = {401},
pmid = {41712028},
issn = {1573-4978},
mesh = {Humans ; *Blood-Brain Barrier/pathology/metabolism/virology ; *COVID-19/complications/diagnosis/therapy ; *Neuroinflammatory Diseases/diagnosis/therapy/virology ; SARS-CoV-2 ; Animals ; Brain/pathology/virology ; *Nervous System Diseases/diagnosis/therapy/etiology ; Post-Acute COVID-19 Syndrome ; },
abstract = {Long COVID affects at least 10% of those with severe disease, and many experience neurological symptoms and brain fog. More than 200 symptoms are reported, yet a detailed understanding remains limited. This article summarizes current knowledge of neurological symptoms, brain fog, molecular mechanisms, neuroinflammation, blood-brain barrier disruption, diagnostics, and available therapeutics. Our review highlights the lack of diagnostics and treatments for these patients. We catalog the ongoing clinical trials, identify the urgent need for further therapeutics, and stress that advances in understanding pathophysiology will drive new treatments. We urge prioritizing animal model studies and improving diagnostics to accelerate the discovery and delivery of effective treatments for long COVID neurological symptoms.},
}
MeSH Terms:
show MeSH Terms
hide MeSH Terms
Humans
*Blood-Brain Barrier/pathology/metabolism/virology
*COVID-19/complications/diagnosis/therapy
*Neuroinflammatory Diseases/diagnosis/therapy/virology
SARS-CoV-2
Animals
Brain/pathology/virology
*Nervous System Diseases/diagnosis/therapy/etiology
Post-Acute COVID-19 Syndrome
RevDate: 2026-02-19
CmpDate: 2026-02-19
Diagnostic Performance of Artificial Intelligence in Detecting COVID-19 Pneumonia on Chest Imaging.
Cureus, 18(1):e101775.
The COVID-19 pandemic highlighted the need for rapid, accurate, and accessible diagnostic tools. Chest imaging modalities, including chest radiography (CXR) and computed tomography (CT), provided valuable diagnostic information and prompted the development of artificial intelligence (AI) systems to support image interpretation and improve workflow efficiency. This literature review synthesizes current evidence on the diagnostic performance, limitations, and clinical implications of AI models in COVID-19 pneumonia detection through CXR and CT evaluation. A PubMed search was conducted through October 2025 to identify studies evaluating AI systems for the detection of COVID-19 pneumonia using CXR and CT. Studies reporting diagnostic performance metrics, including sensitivity, specificity, accuracy, or area under the curve (AUC), were included. Study quality and risk of bias were assessed using the Quality Assessment of Diagnostic Accuracy Studies-2 (QUADAS-2) tool. Eleven studies met the inclusion criteria. CXR-based AI systems demonstrated sensitivities from 80% to 98% and specificities from 82% to 96%, often comparable to radiologist performance. CT-based AI models achieved accuracies between 90% and 96%. AI models demonstrated strong internal diagnostic performance on CXR and CT but showed reduced accuracy with external validation, underscoring limitations related to generalizability and retrospective study designs. AI models demonstrate promising diagnostic performance for detecting COVID-19 pneumonia on chest imaging and may enhance radiologist efficiency. However, challenges related to generalizability, model adaptability, and clinician trust remain. Future research should prioritize external validation and transparent reporting to ensure the safe and effective integration of AI into clinical practice.
Additional Links: PMID-41710827
PubMed:
Citation:
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@article {pmid41710827,
year = {2026},
author = {Chapman, SR and Willner, L and Abouafech, A and Roberti, C and Willner, C},
title = {Diagnostic Performance of Artificial Intelligence in Detecting COVID-19 Pneumonia on Chest Imaging.},
journal = {Cureus},
volume = {18},
number = {1},
pages = {e101775},
pmid = {41710827},
issn = {2168-8184},
abstract = {The COVID-19 pandemic highlighted the need for rapid, accurate, and accessible diagnostic tools. Chest imaging modalities, including chest radiography (CXR) and computed tomography (CT), provided valuable diagnostic information and prompted the development of artificial intelligence (AI) systems to support image interpretation and improve workflow efficiency. This literature review synthesizes current evidence on the diagnostic performance, limitations, and clinical implications of AI models in COVID-19 pneumonia detection through CXR and CT evaluation. A PubMed search was conducted through October 2025 to identify studies evaluating AI systems for the detection of COVID-19 pneumonia using CXR and CT. Studies reporting diagnostic performance metrics, including sensitivity, specificity, accuracy, or area under the curve (AUC), were included. Study quality and risk of bias were assessed using the Quality Assessment of Diagnostic Accuracy Studies-2 (QUADAS-2) tool. Eleven studies met the inclusion criteria. CXR-based AI systems demonstrated sensitivities from 80% to 98% and specificities from 82% to 96%, often comparable to radiologist performance. CT-based AI models achieved accuracies between 90% and 96%. AI models demonstrated strong internal diagnostic performance on CXR and CT but showed reduced accuracy with external validation, underscoring limitations related to generalizability and retrospective study designs. AI models demonstrate promising diagnostic performance for detecting COVID-19 pneumonia on chest imaging and may enhance radiologist efficiency. However, challenges related to generalizability, model adaptability, and clinician trust remain. Future research should prioritize external validation and transparent reporting to ensure the safe and effective integration of AI into clinical practice.},
}
RevDate: 2026-02-19
CmpDate: 2026-02-19
Virtual hospitals in the Kingdom of Saudi Arabia: A scoping review.
Saudi journal of anaesthesia, 20(1):188-196.
Virtual health hospitals have been on the rise significantly since COVID-19 globally. The Kingdom of Saudi Arabia has established several initiatives as part of Vision 2030, where Tele/Virtual Health is key part of this vision. The purpose of this review is to evaluate and establish the expected challenges and the potential value in virtual hospitals in Saudi Arabia. It also aims to identify and analyze gaps in existing knowledge to ideally aid the planning and commissioning of future research on this subject. Results of this review highlight several themes from the literature evolved as follow: 1) need for improvement in Saudi healthcare, 2) emergence of virtual healthcare due to COVID-19, 3) Virtual healthcare has many pros and cons to consider, and, 4) Virtual healthcare has many challenges.
Additional Links: PMID-41710641
PubMed:
Citation:
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@article {pmid41710641,
year = {2026},
author = {Alabdulhadi, O and Almashari, Y and Alharbi, M},
title = {Virtual hospitals in the Kingdom of Saudi Arabia: A scoping review.},
journal = {Saudi journal of anaesthesia},
volume = {20},
number = {1},
pages = {188-196},
pmid = {41710641},
issn = {1658-354X},
abstract = {Virtual health hospitals have been on the rise significantly since COVID-19 globally. The Kingdom of Saudi Arabia has established several initiatives as part of Vision 2030, where Tele/Virtual Health is key part of this vision. The purpose of this review is to evaluate and establish the expected challenges and the potential value in virtual hospitals in Saudi Arabia. It also aims to identify and analyze gaps in existing knowledge to ideally aid the planning and commissioning of future research on this subject. Results of this review highlight several themes from the literature evolved as follow: 1) need for improvement in Saudi healthcare, 2) emergence of virtual healthcare due to COVID-19, 3) Virtual healthcare has many pros and cons to consider, and, 4) Virtual healthcare has many challenges.},
}
RevDate: 2026-02-19
CmpDate: 2026-02-19
The role of vaccination and infection prevention in reducing perioperative complications: A public health-anesthesia nexus.
Saudi journal of anaesthesia, 20(1):166-173.
The intersection of vaccination strategies, infection prevention protocols, and perioperative care represents a critical nexus in modern anesthetic practice and public health. This comprehensive review examines the evolving role of immunization and infection control measures in reducing perioperative complications, with particular emphasis on the Saudi Arabian healthcare context. The coronavirus disease 2019 pandemic has highlighted the importance of vaccination timing in relation to elective surgery, while established infection prevention practices continue to form the cornerstone of safe perioperative care. In Saudi Arabia, national initiatives have demonstrated significant improvements in healthcare-associated infection rates, with central line-associated bloodstream infections decreasing from 2.5 per 1000 catheter-days in 2021 to 1.28 per 1000 catheter-days by 2024. The implementation of evidence-based vaccination protocols and comprehensive infection prevention strategies has shown measurable benefits in reducing surgical site infections, respiratory complications, and overall perioperative morbidity. Anesthesiologists play a pivotal role in this public health framework, serving as key stakeholders in perioperative optimization through vaccination status assessment, infection control adherence, and risk stratification. The Saudi healthcare system's commitment to infection prevention excellence, aligned with Vision 2030 objectives, provides a unique model for integrating public health principles into anesthetic practice. Current evidence supports the strategic timing of vaccinations relative to elective procedures, with recommendations for postponing elective surgery 3-7 days after inactivated vaccines and 14-21 days following live vaccines. This review synthesizes current evidence, identifies best practices, and proposes future directions for optimizing the vaccination-infection prevention-anesthesia nexus to improve patient outcomes and advance public health goals within the Saudi healthcare landscape.
Additional Links: PMID-41710600
PubMed:
Citation:
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@article {pmid41710600,
year = {2026},
author = {Almohammadi, AA},
title = {The role of vaccination and infection prevention in reducing perioperative complications: A public health-anesthesia nexus.},
journal = {Saudi journal of anaesthesia},
volume = {20},
number = {1},
pages = {166-173},
pmid = {41710600},
issn = {1658-354X},
abstract = {The intersection of vaccination strategies, infection prevention protocols, and perioperative care represents a critical nexus in modern anesthetic practice and public health. This comprehensive review examines the evolving role of immunization and infection control measures in reducing perioperative complications, with particular emphasis on the Saudi Arabian healthcare context. The coronavirus disease 2019 pandemic has highlighted the importance of vaccination timing in relation to elective surgery, while established infection prevention practices continue to form the cornerstone of safe perioperative care. In Saudi Arabia, national initiatives have demonstrated significant improvements in healthcare-associated infection rates, with central line-associated bloodstream infections decreasing from 2.5 per 1000 catheter-days in 2021 to 1.28 per 1000 catheter-days by 2024. The implementation of evidence-based vaccination protocols and comprehensive infection prevention strategies has shown measurable benefits in reducing surgical site infections, respiratory complications, and overall perioperative morbidity. Anesthesiologists play a pivotal role in this public health framework, serving as key stakeholders in perioperative optimization through vaccination status assessment, infection control adherence, and risk stratification. The Saudi healthcare system's commitment to infection prevention excellence, aligned with Vision 2030 objectives, provides a unique model for integrating public health principles into anesthetic practice. Current evidence supports the strategic timing of vaccinations relative to elective procedures, with recommendations for postponing elective surgery 3-7 days after inactivated vaccines and 14-21 days following live vaccines. This review synthesizes current evidence, identifies best practices, and proposes future directions for optimizing the vaccination-infection prevention-anesthesia nexus to improve patient outcomes and advance public health goals within the Saudi healthcare landscape.},
}
RevDate: 2026-02-19
CmpDate: 2026-02-19
Pre-clinical evaluation of mRNA-lipid nanoparticles' potency and toxicity: current practices and future directions.
In vitro models, 4(3-4):177-194.
Over the last few years, the success of COVID-19 mRNA vaccines has resulted in the emergence of RNA lipid nanoparticles (LNPs) with promising prospects for the prevention and treatment of various diseases. The context of the SARS-CoV-2 pandemic has led to the rapid development of vaccines with abbreviated non-clinical programs. However, there are currently no official guidelines defining the required standards for global marketing of mRNA based therapeutic products. Nevertheless, to guarantee a well-controlled product, it is essential to characterize both the drug substance and the final product in terms of their structure, composition, formulation, physico-chemical features, potency, and safety. This lack of guidance has resulted in a wide variety of heterogeneous in vitro tests being used to assess the potency and cytotoxicity of RNA-LNP. This review discusses the commonly used in vitro assays, primarily 2D monolayer assays, employed to evaluate the biological properties of RNA-LNP. We then explore novel alternative methods to bridge the gap between in vitro and in vivo results. We summarize (i) co-culture models, (ii) multilayer 3D assays and (iii) in vivo replacement models, exploring their potential applications in assessing the potency and safety of RNA-LNPs. Finally, we discuss the use of in silico and machine learning as models for optimizing and predicting the biological behavior of RNA-LNPs.
Additional Links: PMID-41710557
PubMed:
Citation:
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@article {pmid41710557,
year = {2025},
author = {Muzard, C and Seguin, J and Bonnefoy, J and Salkini, N and Serra, V and Alhareth, K and Lemdani, K and Mignet, N},
title = {Pre-clinical evaluation of mRNA-lipid nanoparticles' potency and toxicity: current practices and future directions.},
journal = {In vitro models},
volume = {4},
number = {3-4},
pages = {177-194},
pmid = {41710557},
issn = {2731-3441},
abstract = {Over the last few years, the success of COVID-19 mRNA vaccines has resulted in the emergence of RNA lipid nanoparticles (LNPs) with promising prospects for the prevention and treatment of various diseases. The context of the SARS-CoV-2 pandemic has led to the rapid development of vaccines with abbreviated non-clinical programs. However, there are currently no official guidelines defining the required standards for global marketing of mRNA based therapeutic products. Nevertheless, to guarantee a well-controlled product, it is essential to characterize both the drug substance and the final product in terms of their structure, composition, formulation, physico-chemical features, potency, and safety. This lack of guidance has resulted in a wide variety of heterogeneous in vitro tests being used to assess the potency and cytotoxicity of RNA-LNP. This review discusses the commonly used in vitro assays, primarily 2D monolayer assays, employed to evaluate the biological properties of RNA-LNP. We then explore novel alternative methods to bridge the gap between in vitro and in vivo results. We summarize (i) co-culture models, (ii) multilayer 3D assays and (iii) in vivo replacement models, exploring their potential applications in assessing the potency and safety of RNA-LNPs. Finally, we discuss the use of in silico and machine learning as models for optimizing and predicting the biological behavior of RNA-LNPs.},
}
RevDate: 2026-02-19
CmpDate: 2026-02-19
A narrative review of heterogeneity in SARS-CoV-2 infection outcomes and vaccine efficacy: strategizing pandemic preparedness in Africa.
Frontiers in public health, 14:1761547.
Disease epidemiology during the COVID-19 pandemic differed greatly across the globe. In contrast to early pandemic predictions, Africa recorded the fewest SARS-CoV-2 related hospitalizations and deaths. Hypotheses proposed to explain this paradox include underreporting, age demographics, climate, national mitigation strategies, lifestyle factors, pre-existing cross-reactive protection, and host genetic determinants. This traditional, narrative review evaluates these hypotheses investigated in the published literature, and highlights knowledge gaps which limit our understanding and obscure validation of potential explanations. It also discusses how responses to vaccines, the primary intervention sought to control infectious disease outbreaks, may vary both within the African population and across other continents. Potential explanations in the literature include pre-existing immunity, poor nutrition, immune modulating co-infections, comorbidities, microbiome composition, genetic polymorphisms, and demographic factors. Previous studies have shown that pre-existing (infection-derived) immunity or cross-reactive immune responses can augment vaccine-elicited positive responses and can protect against reinfection in a way similar to immunization. Conversely, there are also studies showing that prior immunity interferes with the efficacy of new vaccines through mechanisms like original antigenic sin and immune imprinting. Thus, there is need for more immunology studies to understand the relative contribution of pre-existing cross-reactive immune responses to the epidemiology of new pathogens. These studies are particularly essential to understand the differences between pandemic preparedness and population vulnerability, as well as to inform vaccine development and vaccine effectiveness monitoring studies. SARS-CoV-2 serves as an important case study to understand heterogeneity between and within populations in immune responses to both the pathogen and to vaccination. This understanding is crucial in informing vaccine research and development aimed at supporting the 100-day mission for when the next pandemic threat emerges.
Additional Links: PMID-41710320
PubMed:
Citation:
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@article {pmid41710320,
year = {2026},
author = {Kerai, T and Woolhouse, M and Nyazema, NZ and Mutapi, F},
title = {A narrative review of heterogeneity in SARS-CoV-2 infection outcomes and vaccine efficacy: strategizing pandemic preparedness in Africa.},
journal = {Frontiers in public health},
volume = {14},
number = {},
pages = {1761547},
pmid = {41710320},
issn = {2296-2565},
mesh = {Humans ; *COVID-19/epidemiology/prevention & control/immunology ; Africa/epidemiology ; *Vaccine Efficacy ; SARS-CoV-2 ; *COVID-19 Vaccines/immunology ; *Pandemics/prevention & control ; Pandemic Preparedness ; },
abstract = {Disease epidemiology during the COVID-19 pandemic differed greatly across the globe. In contrast to early pandemic predictions, Africa recorded the fewest SARS-CoV-2 related hospitalizations and deaths. Hypotheses proposed to explain this paradox include underreporting, age demographics, climate, national mitigation strategies, lifestyle factors, pre-existing cross-reactive protection, and host genetic determinants. This traditional, narrative review evaluates these hypotheses investigated in the published literature, and highlights knowledge gaps which limit our understanding and obscure validation of potential explanations. It also discusses how responses to vaccines, the primary intervention sought to control infectious disease outbreaks, may vary both within the African population and across other continents. Potential explanations in the literature include pre-existing immunity, poor nutrition, immune modulating co-infections, comorbidities, microbiome composition, genetic polymorphisms, and demographic factors. Previous studies have shown that pre-existing (infection-derived) immunity or cross-reactive immune responses can augment vaccine-elicited positive responses and can protect against reinfection in a way similar to immunization. Conversely, there are also studies showing that prior immunity interferes with the efficacy of new vaccines through mechanisms like original antigenic sin and immune imprinting. Thus, there is need for more immunology studies to understand the relative contribution of pre-existing cross-reactive immune responses to the epidemiology of new pathogens. These studies are particularly essential to understand the differences between pandemic preparedness and population vulnerability, as well as to inform vaccine development and vaccine effectiveness monitoring studies. SARS-CoV-2 serves as an important case study to understand heterogeneity between and within populations in immune responses to both the pathogen and to vaccination. This understanding is crucial in informing vaccine research and development aimed at supporting the 100-day mission for when the next pandemic threat emerges.},
}
MeSH Terms:
show MeSH Terms
hide MeSH Terms
Humans
*COVID-19/epidemiology/prevention & control/immunology
Africa/epidemiology
*Vaccine Efficacy
SARS-CoV-2
*COVID-19 Vaccines/immunology
*Pandemics/prevention & control
Pandemic Preparedness
RevDate: 2026-02-19
CmpDate: 2026-02-19
Effectiveness of stigma reduction interventions and outbreak response adaptations in infectious disease outbreaks: a systematic review.
Frontiers in public health, 14:1755092.
INTRODUCTION: Stigma is a common and recurring feature of infectious disease outbreaks where it may have detrimental effects on individual wellbeing and undermine outbreak response. This systematic review explores stigma reduction interventions in infectious disease outbreaks.
METHODS: Eligible studies were searched for in Medline, Embase, PsycINFO, and Global Health databases and through reference screening. Risk of bias was assessed using study design-specific tools and the results of included studies underwent narrative synthesis.
RESULTS: Eleven studies conducted across coronavirus disease 2019 (COVID-19), Ebola disease, mpox, severe acute respiratory syndrome (SARS), and a hypothetical infectious-disease scenario, met the inclusion criteria. Five studies reported reductions in stigma, four reported mixed or null results, and two reported increases in stigma. The most promising strategies for outbreak-related stigma reduction were embedding anti-stigma messaging within health communication, providing psychosocial support, and fostering genuinely participatory community involvement.
DISCUSSION: Evidence on how to effectively reduce stigma during outbreaks remains limited. Strengthening the theoretical foundations, measurement tools, and evaluation designs of stigma-reduction interventions will be essential to inform evidence-based outbreak preparedness and response policies. This would help decision-makers ensure that risk communication, community engagement, and service delivery minimise stigma and improve uptake of testing, care, and preventive measures.
Additional Links: PMID-41710305
PubMed:
Citation:
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@article {pmid41710305,
year = {2026},
author = {Paterson, A and Spies, R and Zauchenberger, CZ and Cheyne, A and Olliaro, PL and Rojek, A},
title = {Effectiveness of stigma reduction interventions and outbreak response adaptations in infectious disease outbreaks: a systematic review.},
journal = {Frontiers in public health},
volume = {14},
number = {},
pages = {1755092},
pmid = {41710305},
issn = {2296-2565},
mesh = {Humans ; *Social Stigma ; *Disease Outbreaks/prevention & control ; COVID-19/psychology/epidemiology ; Hemorrhagic Fever, Ebola/psychology/epidemiology ; Severe Acute Respiratory Syndrome/psychology/epidemiology ; *Communicable Diseases/psychology/epidemiology ; },
abstract = {INTRODUCTION: Stigma is a common and recurring feature of infectious disease outbreaks where it may have detrimental effects on individual wellbeing and undermine outbreak response. This systematic review explores stigma reduction interventions in infectious disease outbreaks.
METHODS: Eligible studies were searched for in Medline, Embase, PsycINFO, and Global Health databases and through reference screening. Risk of bias was assessed using study design-specific tools and the results of included studies underwent narrative synthesis.
RESULTS: Eleven studies conducted across coronavirus disease 2019 (COVID-19), Ebola disease, mpox, severe acute respiratory syndrome (SARS), and a hypothetical infectious-disease scenario, met the inclusion criteria. Five studies reported reductions in stigma, four reported mixed or null results, and two reported increases in stigma. The most promising strategies for outbreak-related stigma reduction were embedding anti-stigma messaging within health communication, providing psychosocial support, and fostering genuinely participatory community involvement.
DISCUSSION: Evidence on how to effectively reduce stigma during outbreaks remains limited. Strengthening the theoretical foundations, measurement tools, and evaluation designs of stigma-reduction interventions will be essential to inform evidence-based outbreak preparedness and response policies. This would help decision-makers ensure that risk communication, community engagement, and service delivery minimise stigma and improve uptake of testing, care, and preventive measures.},
}
MeSH Terms:
show MeSH Terms
hide MeSH Terms
Humans
*Social Stigma
*Disease Outbreaks/prevention & control
COVID-19/psychology/epidemiology
Hemorrhagic Fever, Ebola/psychology/epidemiology
Severe Acute Respiratory Syndrome/psychology/epidemiology
*Communicable Diseases/psychology/epidemiology
RevDate: 2026-02-19
CmpDate: 2026-02-19
The populism-euroscepticism nexus in a contested Europe: The EUPopLink COST Action.
Open research Europe, 6:27.
The EUPopLink COST Action (CA23102) addresses the complex and changing relationship between populism and Euroscepticism in contemporary Europe. While often viewed as "two sides of the same coin," the nexus between these two phenomena is contingent and strategic rather than deterministic. Not all populists are Eurosceptic, and Euroscepticism is not always populist in nature. This publication synthesizes current scholarly debates, highlighting how the European Union (EU) is frequently framed as the populist "other", i.e., a remote, technocratic elite standing in opposition to the "pure people". The nature of this opposition varies significantly across the ideological spectrum, e.g. right-wing populism targets the EU primarily through a "traditionalist-authoritarian-nationalist" (TAN) lens, viewing it as a threat to national sovereignty and cultural identity, while left-wing populism critiques the EU based on socio-economic cleavages, challenging neoliberal governance and austerity while often advocating for a more democratic "Social Europe". The analysis further explores how the polycrisis era-marked by financial instability, the COVID-19 pandemic, and geopolitical conflict-has led to a sophisticated two-level strategy among populist actors. This involves increased institutional pragmatism coupled with radicalized, opportunistic communication, particularly on social media. Finally, the publication outlines the EUPopLink mandate, which seeks to standardize conceptual frameworks and generate an unprecedented body of comparative data through forthcoming country reports. By linking the supply and demand sides of electoral competition, the project aims to provide policymakers and scholars with the tools necessary to mitigate the negative consequences of these disruptive political forces.
Additional Links: PMID-41710161
PubMed:
Citation:
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@article {pmid41710161,
year = {2026},
author = {Andreadis, I and Vasilopoulou, S},
title = {The populism-euroscepticism nexus in a contested Europe: The EUPopLink COST Action.},
journal = {Open research Europe},
volume = {6},
number = {},
pages = {27},
pmid = {41710161},
issn = {2732-5121},
abstract = {The EUPopLink COST Action (CA23102) addresses the complex and changing relationship between populism and Euroscepticism in contemporary Europe. While often viewed as "two sides of the same coin," the nexus between these two phenomena is contingent and strategic rather than deterministic. Not all populists are Eurosceptic, and Euroscepticism is not always populist in nature. This publication synthesizes current scholarly debates, highlighting how the European Union (EU) is frequently framed as the populist "other", i.e., a remote, technocratic elite standing in opposition to the "pure people". The nature of this opposition varies significantly across the ideological spectrum, e.g. right-wing populism targets the EU primarily through a "traditionalist-authoritarian-nationalist" (TAN) lens, viewing it as a threat to national sovereignty and cultural identity, while left-wing populism critiques the EU based on socio-economic cleavages, challenging neoliberal governance and austerity while often advocating for a more democratic "Social Europe". The analysis further explores how the polycrisis era-marked by financial instability, the COVID-19 pandemic, and geopolitical conflict-has led to a sophisticated two-level strategy among populist actors. This involves increased institutional pragmatism coupled with radicalized, opportunistic communication, particularly on social media. Finally, the publication outlines the EUPopLink mandate, which seeks to standardize conceptual frameworks and generate an unprecedented body of comparative data through forthcoming country reports. By linking the supply and demand sides of electoral competition, the project aims to provide policymakers and scholars with the tools necessary to mitigate the negative consequences of these disruptive political forces.},
}
RevDate: 2026-02-19
CmpDate: 2026-02-19
Lessons from a Low-Resource Country: A Narrative Review of Virtual Learning Adoption and Challenges in Medical Education in Iran During COVID-19.
Advances in medical education and practice, 17:561822.
OBJECTIVE: The global COVID-19 pandemic has had a profound impact on the education system. Education shifted to virtual methods, while there was not enough time to plan and choose a proper educational platform. In this study, we present an up-to-date review of the most commonly used virtual education platforms in Iran during the COVID-19 pandemic.
METHODS: This narrative review systematically searched Persian and English articles (2020-2024) in Medline, EMBASE, Scopus, Web of Science, ERIC, SID, CIVILICA, and PubMed using keywords: "COVID-19", "virtual learning", "online learning", "distance learning", "post-COVID infection", "real and virtual simulation", and "educational platforms".
RESULTS: Virtual classes have become increasingly popular during the pandemic. Adobe Connect, Sky Room, Skype, Big Blue Button, Google Meet, Gharar, Zoom, and Navaid System were the most commonly used platforms during the COVID pandemic in Iran. The most frequently utilized systems included Shad (predominant in general education and training) and Navid (leading in medical sciences). Shad had excelled in scalability and institutional integration but faced connectivity issues in rural areas. Despite its technical strengths, Navid was criticized because of insufficient interactivity and misalignment with learner needs in medical English.
DISCUSSION: During COVID-19, online medical education in Iran relied mainly on domestic platforms, which have some limitations. To ensure future equity and competency, a shift toward hybrid models incorporating offline-capable Learning Management Systems (LMS), simulation, and digital literacy training is essential.
Additional Links: PMID-41709949
PubMed:
Citation:
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@article {pmid41709949,
year = {2026},
author = {Vatankhah, H and Vatanparast, M and Royani, Z and Mansouri, G},
title = {Lessons from a Low-Resource Country: A Narrative Review of Virtual Learning Adoption and Challenges in Medical Education in Iran During COVID-19.},
journal = {Advances in medical education and practice},
volume = {17},
number = {},
pages = {561822},
pmid = {41709949},
issn = {1179-7258},
abstract = {OBJECTIVE: The global COVID-19 pandemic has had a profound impact on the education system. Education shifted to virtual methods, while there was not enough time to plan and choose a proper educational platform. In this study, we present an up-to-date review of the most commonly used virtual education platforms in Iran during the COVID-19 pandemic.
METHODS: This narrative review systematically searched Persian and English articles (2020-2024) in Medline, EMBASE, Scopus, Web of Science, ERIC, SID, CIVILICA, and PubMed using keywords: "COVID-19", "virtual learning", "online learning", "distance learning", "post-COVID infection", "real and virtual simulation", and "educational platforms".
RESULTS: Virtual classes have become increasingly popular during the pandemic. Adobe Connect, Sky Room, Skype, Big Blue Button, Google Meet, Gharar, Zoom, and Navaid System were the most commonly used platforms during the COVID pandemic in Iran. The most frequently utilized systems included Shad (predominant in general education and training) and Navid (leading in medical sciences). Shad had excelled in scalability and institutional integration but faced connectivity issues in rural areas. Despite its technical strengths, Navid was criticized because of insufficient interactivity and misalignment with learner needs in medical English.
DISCUSSION: During COVID-19, online medical education in Iran relied mainly on domestic platforms, which have some limitations. To ensure future equity and competency, a shift toward hybrid models incorporating offline-capable Learning Management Systems (LMS), simulation, and digital literacy training is essential.},
}
RevDate: 2026-02-19
CmpDate: 2026-02-19
Layout Types and Efficiency Improvement Strategies for Open Points of Dispensing in Vaccine and Antibiotic Distribution: A Scoping Review.
Prehospital and disaster medicine, 41(1):e1 pii:S1049023X26108838.
INTRODUCTION: Regarding pandemics or bioterrorism incidents, prompt and secure distribution of vaccines and prophylactic antibiotics is crucial. Open Points of Dispensing (PODs) are established to serve the public, and their effectiveness depends on the internal spatial layout and operational workflow design. However, studies on systematic classifications of open POD configurations and comprehensive syntheses of strategies for enhancing operational efficiency are lacking.
STUDY OBJECTIVE: This scoping review aimed to classify open POD layout types used for vaccine and antibiotic distribution and to consolidate strategies that improve efficiency across various workflow stations.
METHODS: A scoping review was conducted following the PRISMA-ScR guidelines. A comprehensive literature search was conducted across PubMed, Embase, and Web of Science databases, spanning from January 2001 through July 2025. The search strategy involved incorporating keyword combinations related to "points of dispensing," "mass vaccination," "mass prophylaxis," and specific pathogens such as anthrax, influenza, and COVID-19. Extracted data included the POD layout typologies, process designs, and efficiency metrics. The findings were synthesized using a narrative approach.
RESULTS: Nineteen studies met the inclusion criteria and were analyzed. Vaccine PODs were classified into four primary layouts, namely station-based sequential-flow, cell-based, fixed-seat service, and pop-up PODs. Antibiotic PODs were categorized into two types, namely sequential processing and selective-expedited processing. Each layout exhibited unique operational characteristics, including sequential versus integrated clinical stations (for vaccine PODs) and standard versus expedited dispensing lines (for antibiotic PODs). Efficiency enhancement strategies across workflow stations included task integration, use of digital tools, simplification of documentation, optimization of medication preparation, and staffing adjustments guided by simulation modeling.
CONCLUSION: This review provides a systematic classification of open POD layouts and summarizes the strategies for improving efficiency across workflow stations. The derived insights offer practical guidance for planning and operating PODs in future public health emergency responses.
Additional Links: PMID-41709444
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PubMed:
Citation:
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@article {pmid41709444,
year = {2026},
author = {Park, JJ and Na, SH and Park, H and Lee, J and Seo, Y},
title = {Layout Types and Efficiency Improvement Strategies for Open Points of Dispensing in Vaccine and Antibiotic Distribution: A Scoping Review.},
journal = {Prehospital and disaster medicine},
volume = {41},
number = {1},
pages = {e1},
doi = {10.1017/S1049023X26108838},
pmid = {41709444},
issn = {1945-1938},
mesh = {Humans ; *Anti-Bacterial Agents/supply & distribution ; *Vaccines/supply & distribution ; COVID-19/prevention & control ; *Efficiency, Organizational ; SARS-CoV-2 ; },
abstract = {INTRODUCTION: Regarding pandemics or bioterrorism incidents, prompt and secure distribution of vaccines and prophylactic antibiotics is crucial. Open Points of Dispensing (PODs) are established to serve the public, and their effectiveness depends on the internal spatial layout and operational workflow design. However, studies on systematic classifications of open POD configurations and comprehensive syntheses of strategies for enhancing operational efficiency are lacking.
STUDY OBJECTIVE: This scoping review aimed to classify open POD layout types used for vaccine and antibiotic distribution and to consolidate strategies that improve efficiency across various workflow stations.
METHODS: A scoping review was conducted following the PRISMA-ScR guidelines. A comprehensive literature search was conducted across PubMed, Embase, and Web of Science databases, spanning from January 2001 through July 2025. The search strategy involved incorporating keyword combinations related to "points of dispensing," "mass vaccination," "mass prophylaxis," and specific pathogens such as anthrax, influenza, and COVID-19. Extracted data included the POD layout typologies, process designs, and efficiency metrics. The findings were synthesized using a narrative approach.
RESULTS: Nineteen studies met the inclusion criteria and were analyzed. Vaccine PODs were classified into four primary layouts, namely station-based sequential-flow, cell-based, fixed-seat service, and pop-up PODs. Antibiotic PODs were categorized into two types, namely sequential processing and selective-expedited processing. Each layout exhibited unique operational characteristics, including sequential versus integrated clinical stations (for vaccine PODs) and standard versus expedited dispensing lines (for antibiotic PODs). Efficiency enhancement strategies across workflow stations included task integration, use of digital tools, simplification of documentation, optimization of medication preparation, and staffing adjustments guided by simulation modeling.
CONCLUSION: This review provides a systematic classification of open POD layouts and summarizes the strategies for improving efficiency across workflow stations. The derived insights offer practical guidance for planning and operating PODs in future public health emergency responses.},
}
MeSH Terms:
show MeSH Terms
hide MeSH Terms
Humans
*Anti-Bacterial Agents/supply & distribution
*Vaccines/supply & distribution
COVID-19/prevention & control
*Efficiency, Organizational
SARS-CoV-2
RevDate: 2026-02-18
CmpDate: 2026-02-18
Pulmonary diffusing capacity for nitric oxide in disease: a scoping review.
European respiratory review : an official journal of the European Respiratory Society, 35(179):.
OBJECTIVE: This scoping review aims to map the available studies on single-breath pulmonary diffusing capacity for nitric oxide (D LNO) in various clinical diseases and identify gaps for future research.
METHODS: We followed the JBI methodology for scoping reviews. A systematic literature search was conducted in Embase, MEDLINE (EBSCOhost), PubMed, Scopus, Web of Science and the Cochrane Library to identify studies on D LNO from 1983 to 2025. Two reviewers screened abstracts using Rayyan software and extracted data using standardised templates implemented into REDCap (Research Electronic Data Capture).
RESULTS: We identified 1638 studies, of which 69 met the eligibility criteria. These studies represented respiratory (n=22), immunological/genetic/systemic (n=14), post-COVID-19 sequelae (n=13), cardiovascular (n=9), metabolic/endocrine/renal (n=6), environmental-related (n=3) and other (n=2) conditions. There was substantial heterogeneity in disease categories, sample sizes and reporting methods. Nearly half of the studies (49.3%) used convenience sampling, where participant selection processes are often poorly described; 62.3% included <50 participants. Only 18.8% reported a sample size calculation, and 10.1% registered or published a study protocol. Disparate findings within disease categories were often difficult to interpret; and small sample sizes limited generalisability. In some specific conditions, D LNO showed sensitivity in detecting interstitial and fibrotic changes compared to conventional single-breath pulmonary diffusing capacity for carbon monoxide (D LCO) while simultaneous D LNO-D LCO measurements permitted the detection of pulmonary vascular-haematological perturbations.
CONCLUSION: Single-breath D LNO-D LCO may provide additional pathophysiological insight by assessing the relative contributions from membrane and blood resistance of diffusion. Larger studies are required to clarify its interpretation across disease states.
Additional Links: PMID-41708119
PubMed:
Citation:
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@article {pmid41708119,
year = {2026},
author = {Radtke, T and Pham-Ngoc, H and Hua-Huy, T and Hsia, CCW and Dressel, H and Dinh-Xuan, AT},
title = {Pulmonary diffusing capacity for nitric oxide in disease: a scoping review.},
journal = {European respiratory review : an official journal of the European Respiratory Society},
volume = {35},
number = {179},
pages = {},
pmid = {41708119},
issn = {1600-0617},
mesh = {Humans ; *Pulmonary Diffusing Capacity ; *Nitric Oxide/metabolism ; *Lung/physiopathology/metabolism ; *COVID-19/physiopathology ; Predictive Value of Tests ; },
abstract = {OBJECTIVE: This scoping review aims to map the available studies on single-breath pulmonary diffusing capacity for nitric oxide (D LNO) in various clinical diseases and identify gaps for future research.
METHODS: We followed the JBI methodology for scoping reviews. A systematic literature search was conducted in Embase, MEDLINE (EBSCOhost), PubMed, Scopus, Web of Science and the Cochrane Library to identify studies on D LNO from 1983 to 2025. Two reviewers screened abstracts using Rayyan software and extracted data using standardised templates implemented into REDCap (Research Electronic Data Capture).
RESULTS: We identified 1638 studies, of which 69 met the eligibility criteria. These studies represented respiratory (n=22), immunological/genetic/systemic (n=14), post-COVID-19 sequelae (n=13), cardiovascular (n=9), metabolic/endocrine/renal (n=6), environmental-related (n=3) and other (n=2) conditions. There was substantial heterogeneity in disease categories, sample sizes and reporting methods. Nearly half of the studies (49.3%) used convenience sampling, where participant selection processes are often poorly described; 62.3% included <50 participants. Only 18.8% reported a sample size calculation, and 10.1% registered or published a study protocol. Disparate findings within disease categories were often difficult to interpret; and small sample sizes limited generalisability. In some specific conditions, D LNO showed sensitivity in detecting interstitial and fibrotic changes compared to conventional single-breath pulmonary diffusing capacity for carbon monoxide (D LCO) while simultaneous D LNO-D LCO measurements permitted the detection of pulmonary vascular-haematological perturbations.
CONCLUSION: Single-breath D LNO-D LCO may provide additional pathophysiological insight by assessing the relative contributions from membrane and blood resistance of diffusion. Larger studies are required to clarify its interpretation across disease states.},
}
MeSH Terms:
show MeSH Terms
hide MeSH Terms
Humans
*Pulmonary Diffusing Capacity
*Nitric Oxide/metabolism
*Lung/physiopathology/metabolism
*COVID-19/physiopathology
Predictive Value of Tests
RevDate: 2026-02-18
Chronic fatigue syndrome: From etiology and mechanism to diagnosis and treatment.
Journal of psychiatric research, 196:171-184 pii:S0022-3956(26)00110-X [Epub ahead of print].
Myalgic encephalomyelitis (ME), commonly known as chronic fatigue syndrome (CFS), is a long-lasting neurological disease. The cause of ME remains uncertain, characterized by unrelenting or recurring fatigue not alleviated by rest. In recent times, CFS incidence has been on the rise annually, showing a tendency towards younger sufferers. Especially post-COVID-19, its prevalence has surged, posing a significant threat to 21st-century health. CFS symptoms are intricate and diverse. Patients typically endure extreme fatigue lasting over six months, accompanied by physical and neuropsychiatric symptoms like sore throat, muscle/joint pain, anxiety, and distress. These severely disrupt daily life and work, heightening illness risks and financial strain. With the unknown etiology, current treatments have limited success and may induce psychological issues such as anxiety and depression. This paper delivers an extensive and thorough overview of the latest developments in the studies concerning the pathogenesis, diagnostic standards, and therapeutic approaches for chronic fatigue syndrome. Integrating and assessing the existing knowledge body related to this field systematically, we aim to facilitate continuous research and gain a deeper understanding of this complex medical problem whose mechanism remains largely unknown. Moreover, valuable insights and practical recommendations for future related treatments and research are also provided.
Additional Links: PMID-41707618
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PubMed:
Citation:
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@article {pmid41707618,
year = {2026},
author = {Xu, Q and Zhao, M and Wang, Q and He, Y and Ye, G and Yang, J and Huang, W and Ren, J},
title = {Chronic fatigue syndrome: From etiology and mechanism to diagnosis and treatment.},
journal = {Journal of psychiatric research},
volume = {196},
number = {},
pages = {171-184},
doi = {10.1016/j.jpsychires.2026.02.026},
pmid = {41707618},
issn = {1879-1379},
abstract = {Myalgic encephalomyelitis (ME), commonly known as chronic fatigue syndrome (CFS), is a long-lasting neurological disease. The cause of ME remains uncertain, characterized by unrelenting or recurring fatigue not alleviated by rest. In recent times, CFS incidence has been on the rise annually, showing a tendency towards younger sufferers. Especially post-COVID-19, its prevalence has surged, posing a significant threat to 21st-century health. CFS symptoms are intricate and diverse. Patients typically endure extreme fatigue lasting over six months, accompanied by physical and neuropsychiatric symptoms like sore throat, muscle/joint pain, anxiety, and distress. These severely disrupt daily life and work, heightening illness risks and financial strain. With the unknown etiology, current treatments have limited success and may induce psychological issues such as anxiety and depression. This paper delivers an extensive and thorough overview of the latest developments in the studies concerning the pathogenesis, diagnostic standards, and therapeutic approaches for chronic fatigue syndrome. Integrating and assessing the existing knowledge body related to this field systematically, we aim to facilitate continuous research and gain a deeper understanding of this complex medical problem whose mechanism remains largely unknown. Moreover, valuable insights and practical recommendations for future related treatments and research are also provided.},
}
RevDate: 2026-02-20
CmpDate: 2026-02-20
mRNA-Based Cancer Vaccines: A Review of the Current Scenario and Future Prospects.
Protein and peptide letters, 32(11):776-790.
Messenger RNA (mRNA) has gained increasing attention as a valuable tool to cure various human diseases, particularly malignant tumors. Such growing interest has been triggered largely by the phenomenal clinical success of mRNA vaccines developed using lipid nanoparticle (LNP) technology against COVID-19. mRNA may be used to produce cancer immunotherapies in numerous different ways, including cancer vaccines to induce or enhance immunity to tumor-specific antigens (TSAs) or tumor-associated antigens (TAAs). mRNA can also be used to adoptively transfer T-cells for the expression of antigen receptors, such as chimeric antigen receptors (CARs), therapeutic antibodies, and immunomodulatory proteins to re-engineer the tumor microenvironment. However, the therapeutic potential of mRNA-based cancer immunotherapy is not fully utilized due to a few limitations, such as mRNA instability, production of immunogenicity, and a lack of efficient in-vivo delivery methods. This review provides an overview of the current advancements and future directions of mRNA-based cancer therapies, including various delivery routes and therapeutic platforms. It addresses the mechanistic basis of mRNA cancer vaccines, non-replicating and self-amplifying mRNA, as well as their clinical development, personalized vaccines, and applications of mRNA for encoding antigen receptors, antibodies, and immunomodulatory proteins. Moreover, the review addresses nanoparticle-based platforms, such as lipid nanoparticles (LNPs), polymeric nanoparticles, and peptide-based nanoparticles, all used to improve the therapeutic effectiveness of mRNA-based drugs by improving their targeted delivery to tissues. This review aims to provide insights into the use of state-of-the-art mRNA-based cancer immunotherapy.
Additional Links: PMID-41540524
Publisher:
PubMed:
Citation:
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@article {pmid41540524,
year = {2025},
author = {Bhattacharya, S and Easmin, N and Panja, A and Nayak, A and Sur, D},
title = {mRNA-Based Cancer Vaccines: A Review of the Current Scenario and Future Prospects.},
journal = {Protein and peptide letters},
volume = {32},
number = {11},
pages = {776-790},
doi = {10.2174/0109298665402963251022054441},
pmid = {41540524},
issn = {1875-5305},
mesh = {Humans ; *Cancer Vaccines/immunology/therapeutic use/genetics ; *Neoplasms/therapy/immunology ; *RNA, Messenger/immunology/genetics/therapeutic use ; Nanoparticles/chemistry ; Immunotherapy/methods ; Animals ; mRNA Vaccines ; COVID-19/immunology ; Antigens, Neoplasm/immunology/genetics ; },
abstract = {Messenger RNA (mRNA) has gained increasing attention as a valuable tool to cure various human diseases, particularly malignant tumors. Such growing interest has been triggered largely by the phenomenal clinical success of mRNA vaccines developed using lipid nanoparticle (LNP) technology against COVID-19. mRNA may be used to produce cancer immunotherapies in numerous different ways, including cancer vaccines to induce or enhance immunity to tumor-specific antigens (TSAs) or tumor-associated antigens (TAAs). mRNA can also be used to adoptively transfer T-cells for the expression of antigen receptors, such as chimeric antigen receptors (CARs), therapeutic antibodies, and immunomodulatory proteins to re-engineer the tumor microenvironment. However, the therapeutic potential of mRNA-based cancer immunotherapy is not fully utilized due to a few limitations, such as mRNA instability, production of immunogenicity, and a lack of efficient in-vivo delivery methods. This review provides an overview of the current advancements and future directions of mRNA-based cancer therapies, including various delivery routes and therapeutic platforms. It addresses the mechanistic basis of mRNA cancer vaccines, non-replicating and self-amplifying mRNA, as well as their clinical development, personalized vaccines, and applications of mRNA for encoding antigen receptors, antibodies, and immunomodulatory proteins. Moreover, the review addresses nanoparticle-based platforms, such as lipid nanoparticles (LNPs), polymeric nanoparticles, and peptide-based nanoparticles, all used to improve the therapeutic effectiveness of mRNA-based drugs by improving their targeted delivery to tissues. This review aims to provide insights into the use of state-of-the-art mRNA-based cancer immunotherapy.},
}
MeSH Terms:
show MeSH Terms
hide MeSH Terms
Humans
*Cancer Vaccines/immunology/therapeutic use/genetics
*Neoplasms/therapy/immunology
*RNA, Messenger/immunology/genetics/therapeutic use
Nanoparticles/chemistry
Immunotherapy/methods
Animals
mRNA Vaccines
COVID-19/immunology
Antigens, Neoplasm/immunology/genetics
RevDate: 2026-02-21
CmpDate: 2026-02-21
Long COVID: a review of mechanisms and treatment modalities.
Inflammopharmacology, 34(2):1111-1121.
Long COVID is defined by the World Health Organisation (WHO) as a condition arising within 3 months of an acute COVID infection with symptoms lasting for a minimum of 2 weeks. However, this syndrome is poorly understood and has been recorded to include many systemic manifestations, including neurological, respiratory, cardiovascular, gastrointestinal, dermatological, psychosocial, and metabolic systems. Constitutional symptoms also include fatigue, insomnia, body weight changes, poor attention span, hair loss, sexual dysfunction, myalgia, and joint pain, with fatigue being the most common. Given the various proposed mechanisms published in the literature, the postulated mechanisms and pathways are discussed in this paper to contribute to the understanding of defining this syndrome. In this review article, the authors first explored how endothelial damage from COVID infection can lead to a hypercoagulable state. In addition, the effects of an insufficient initial immune response can lead to viral persistence alongside a potentially prolonged hyperactive immune response that includes a cytokine storm and mast cell activation syndrome. Furthermore, the viral persistence can be exacerbated by antibody-dependent enhancement or complicated by molecular mimicry. Current pharmacological therapies are explored and evaluated to investigate their efficacy in addressing this complex and chronic presentation. This review article has been written after an extensive literature review to increase the understanding and awareness regarding Long COVID, as a sincere effort to direct further research for an effective diagnosis and management.
Additional Links: PMID-41428252
PubMed:
Citation:
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@article {pmid41428252,
year = {2026},
author = {Yet, M and Teo, HS and Kwa, H and Yeo, J and Wang, SSY},
title = {Long COVID: a review of mechanisms and treatment modalities.},
journal = {Inflammopharmacology},
volume = {34},
number = {2},
pages = {1111-1121},
pmid = {41428252},
issn = {1568-5608},
mesh = {Humans ; *COVID-19/therapy/complications/immunology/physiopathology ; Post-Acute COVID-19 Syndrome ; SARS-CoV-2 ; COVID-19 Drug Treatment ; },
abstract = {Long COVID is defined by the World Health Organisation (WHO) as a condition arising within 3 months of an acute COVID infection with symptoms lasting for a minimum of 2 weeks. However, this syndrome is poorly understood and has been recorded to include many systemic manifestations, including neurological, respiratory, cardiovascular, gastrointestinal, dermatological, psychosocial, and metabolic systems. Constitutional symptoms also include fatigue, insomnia, body weight changes, poor attention span, hair loss, sexual dysfunction, myalgia, and joint pain, with fatigue being the most common. Given the various proposed mechanisms published in the literature, the postulated mechanisms and pathways are discussed in this paper to contribute to the understanding of defining this syndrome. In this review article, the authors first explored how endothelial damage from COVID infection can lead to a hypercoagulable state. In addition, the effects of an insufficient initial immune response can lead to viral persistence alongside a potentially prolonged hyperactive immune response that includes a cytokine storm and mast cell activation syndrome. Furthermore, the viral persistence can be exacerbated by antibody-dependent enhancement or complicated by molecular mimicry. Current pharmacological therapies are explored and evaluated to investigate their efficacy in addressing this complex and chronic presentation. This review article has been written after an extensive literature review to increase the understanding and awareness regarding Long COVID, as a sincere effort to direct further research for an effective diagnosis and management.},
}
MeSH Terms:
show MeSH Terms
hide MeSH Terms
Humans
*COVID-19/therapy/complications/immunology/physiopathology
Post-Acute COVID-19 Syndrome
SARS-CoV-2
COVID-19 Drug Treatment
RevDate: 2026-02-18
Political trust and health compliance during a health crisis: A systematic literature review from the COVID-19 pandemic.
Social science & medicine (1982), 395:119093 pii:S0277-9536(26)00169-3 [Epub ahead of print].
Political trust is considered crucial for enhancing civic compliance with government policies and instructions, particularly during a health crisis. However, evidence from the COVID-19 pandemic, a major global health crisis, suggest a more nuanced relationship. Aiming to explore and clarify the nature of and the conditions for the political trust and civic compliance relationship in the context of a health crisis in the general population, at the overall societal-level, this study systematically reviews relevant literature from the COVID-19 pandemic, across 62 countries. Our findings indicate that the positive relationship between political trust and compliance is not self-evident, as 42% of the reviewed studies (63 of 151) report non-significant, mixed or negative results. Moreover, conceptual and methodological features seem to affect the likelihood of this association, such as the object of trust and compliance behavior, the behavior's execution timeframe and its legal status, and the manner in which political trust and compliance are measured. Potential consequences are discussed.
Additional Links: PMID-41707545
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PubMed:
Citation:
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@article {pmid41707545,
year = {2026},
author = {Goren, T and Vashdi, DR and Beeri, I},
title = {Political trust and health compliance during a health crisis: A systematic literature review from the COVID-19 pandemic.},
journal = {Social science & medicine (1982)},
volume = {395},
number = {},
pages = {119093},
doi = {10.1016/j.socscimed.2026.119093},
pmid = {41707545},
issn = {1873-5347},
abstract = {Political trust is considered crucial for enhancing civic compliance with government policies and instructions, particularly during a health crisis. However, evidence from the COVID-19 pandemic, a major global health crisis, suggest a more nuanced relationship. Aiming to explore and clarify the nature of and the conditions for the political trust and civic compliance relationship in the context of a health crisis in the general population, at the overall societal-level, this study systematically reviews relevant literature from the COVID-19 pandemic, across 62 countries. Our findings indicate that the positive relationship between political trust and compliance is not self-evident, as 42% of the reviewed studies (63 of 151) report non-significant, mixed or negative results. Moreover, conceptual and methodological features seem to affect the likelihood of this association, such as the object of trust and compliance behavior, the behavior's execution timeframe and its legal status, and the manner in which political trust and compliance are measured. Potential consequences are discussed.},
}
RevDate: 2026-02-18
CmpDate: 2026-02-18
Belongingness and loneliness in higher education: a meta-analysis of pre- and post-pandemic trends.
Frontiers in psychology, 16:1625957.
INTRODUCTION: This meta-analysis seeks to explore how the complex relationship between loneliness and belongingness in higher education students can be explained by a set of pre- and post-COVID-19 pandemic dynamics.
METHODS: A meta-analysis including 56 studies and involving a total of 30,062 participants was conducted, and the review explores direct relations and moderation through age, education, and country.
RESULTS: Results indicate a moderate-to-strong negative relationship between loneliness and belongingness (r = -0.48, 95% CI [-0.529, -0.422]), such that a consistent association was found across situations such that increases in one's level of loneliness is associated with decreases in one's level of belongingness. Nevertheless, there was no small-degree of inter-study heterogeneity (Q = 1058.86, p < 0.0001, I[2] = 94.33%), which is a potential reason for the differences in the study populations and methods, employing a random-effects model to account for these discrepancies. After further scrutiny of the results, location, and year of study, and country did not moderate the effect size, which in turn reflects the stability of the association across context and time. In the subgroup analysis the effect size of the relationship between the level of the Information Technology (IT) usage and the externalisation was lower in the time of the pandemic than in the time preceding the pandemic. The effect size of the pre-pandemic group is -0.515 (95% CI: -0.589 to -0.441, p < 0.001 < 0.001) and the effect size of pandemic group is slightly smaller with -0.427 (95% CI: -0.502 to -0.352, p < 0.001 < 0.001). This means that although the level of loneliness have normalised, there have been a subtonic influence on perceived belonging of the novelty stressor caused by breakdowns in social connection from pandemic-level influences. In addition, no significant publication bias was observed.
DISCUSSION: Overall, these findings confirm the strong negative association between loneliness and sense of belonging and emphasise the important role in providing community support for students, especially during social disruptions.
Additional Links: PMID-41705169
PubMed:
Citation:
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@article {pmid41705169,
year = {2025},
author = {Dost, G},
title = {Belongingness and loneliness in higher education: a meta-analysis of pre- and post-pandemic trends.},
journal = {Frontiers in psychology},
volume = {16},
number = {},
pages = {1625957},
pmid = {41705169},
issn = {1664-1078},
abstract = {INTRODUCTION: This meta-analysis seeks to explore how the complex relationship between loneliness and belongingness in higher education students can be explained by a set of pre- and post-COVID-19 pandemic dynamics.
METHODS: A meta-analysis including 56 studies and involving a total of 30,062 participants was conducted, and the review explores direct relations and moderation through age, education, and country.
RESULTS: Results indicate a moderate-to-strong negative relationship between loneliness and belongingness (r = -0.48, 95% CI [-0.529, -0.422]), such that a consistent association was found across situations such that increases in one's level of loneliness is associated with decreases in one's level of belongingness. Nevertheless, there was no small-degree of inter-study heterogeneity (Q = 1058.86, p < 0.0001, I[2] = 94.33%), which is a potential reason for the differences in the study populations and methods, employing a random-effects model to account for these discrepancies. After further scrutiny of the results, location, and year of study, and country did not moderate the effect size, which in turn reflects the stability of the association across context and time. In the subgroup analysis the effect size of the relationship between the level of the Information Technology (IT) usage and the externalisation was lower in the time of the pandemic than in the time preceding the pandemic. The effect size of the pre-pandemic group is -0.515 (95% CI: -0.589 to -0.441, p < 0.001 < 0.001) and the effect size of pandemic group is slightly smaller with -0.427 (95% CI: -0.502 to -0.352, p < 0.001 < 0.001). This means that although the level of loneliness have normalised, there have been a subtonic influence on perceived belonging of the novelty stressor caused by breakdowns in social connection from pandemic-level influences. In addition, no significant publication bias was observed.
DISCUSSION: Overall, these findings confirm the strong negative association between loneliness and sense of belonging and emphasise the important role in providing community support for students, especially during social disruptions.},
}
RevDate: 2026-02-18
Food Insecurity in Families With Children or Young People With Autism: A Systematic Review and Meta-Analysis.
Nutrition bulletin [Epub ahead of print].
Food insecurity is frequently reported among families of children with autism spectrum conditions (ASC), yet there is limited evidence synthesising its prevalence and impact. This systematic review aimed to examine and meta-analyse the existing literature on food insecurity in families of children and young people with ASC. A comprehensive search across nine databases identified 39 papers, of which 11 met the inclusion criteria. Studies were included if they involved autistic children or young people under the age of 25 (and/or their family members) and focused on food insecurity. Eligible studies were critically appraised, and data were synthesised using both narrative and meta-analytic approaches. Meta-analyses of nine studies estimated a pooled prevalence of food insecurity at 29% (SE: 5%; 95% CI: 17%-40%; z = 5.35, p < 0.001), which increased to 31% following adjustment for publication bias. The review also found that food insecurity worsened during the COVID-19 pandemic, contributing to increased caregiver stress and disruptions in eating behaviours. This review demonstrates the high prevalence of food insecurity among families of children with ASC and the complex interplay of social, economic and behavioural challenges they face. Addressing food insecurity in autistic households requires policy responses that extend beyond financial aid to consider the sensory, behavioural and nutritional needs specific to ASC. Future research should adopt standardised measures and prioritise the development and evaluation of inclusive, tailored food support systems that reflect the lived experiences of neurodiverse families.
Additional Links: PMID-41703981
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PubMed:
Citation:
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@article {pmid41703981,
year = {2026},
author = {Tuschick, E and Smith, J and Harrison, B and Youngman, M and Giles, EL},
title = {Food Insecurity in Families With Children or Young People With Autism: A Systematic Review and Meta-Analysis.},
journal = {Nutrition bulletin},
volume = {},
number = {},
pages = {},
doi = {10.1111/nbu.70047},
pmid = {41703981},
issn = {1467-3010},
abstract = {Food insecurity is frequently reported among families of children with autism spectrum conditions (ASC), yet there is limited evidence synthesising its prevalence and impact. This systematic review aimed to examine and meta-analyse the existing literature on food insecurity in families of children and young people with ASC. A comprehensive search across nine databases identified 39 papers, of which 11 met the inclusion criteria. Studies were included if they involved autistic children or young people under the age of 25 (and/or their family members) and focused on food insecurity. Eligible studies were critically appraised, and data were synthesised using both narrative and meta-analytic approaches. Meta-analyses of nine studies estimated a pooled prevalence of food insecurity at 29% (SE: 5%; 95% CI: 17%-40%; z = 5.35, p < 0.001), which increased to 31% following adjustment for publication bias. The review also found that food insecurity worsened during the COVID-19 pandemic, contributing to increased caregiver stress and disruptions in eating behaviours. This review demonstrates the high prevalence of food insecurity among families of children with ASC and the complex interplay of social, economic and behavioural challenges they face. Addressing food insecurity in autistic households requires policy responses that extend beyond financial aid to consider the sensory, behavioural and nutritional needs specific to ASC. Future research should adopt standardised measures and prioritise the development and evaluation of inclusive, tailored food support systems that reflect the lived experiences of neurodiverse families.},
}
RevDate: 2026-02-17
CmpDate: 2026-02-17
Global trends of pandemic-prone and epidemic-prone disease outbreaks in 2024.
BMJ global health, 11(2): pii:bmjgh-2025-020708.
During 2024, the number of pandemic-prone and epidemic-prone disease outbreaks worldwide was estimated at 301. The data highlight a shift in disease outbreak patterns, with a decline in the number of countries reporting public health events of concern linked to COVID-19 and a rise in those reporting outbreaks of viral diseases transmitted by vectors.About 90% of the outbreaks in 2024 were associated with COVID-19, dengue, yellow fever, Oropouche virus disease and influenza (linked to identified zoonotic or pandemic influenza virus). Although disease outbreaks can affect any country anywhere, they tend to disproportionately occur in countries facing many other socio-economic development, climatic and humanitarian challenges. In this regard, sub-Saharan Africa and the subregion of Latin America and the Caribbean-home to just 23.3% of the world's population-reported the highest number of disease outbreaks in 2024 with about 57% of the total. Particularly, the sub-Saharan Africa region has been the site of nearly 32% of recorded outbreaks since 1996. Future research should include efforts to improve the quality and availability of disease outbreaks data-particularly in the most exposed or vulnerable regions-and to promote the scientific use of such information for foresight purposes and for forecasting future health events of concern to support anticipatory action.
Additional Links: PMID-41702637
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PubMed:
Citation:
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@article {pmid41702637,
year = {2026},
author = {Torres Munguía, JA and Martínez-Zarzoso, I},
title = {Global trends of pandemic-prone and epidemic-prone disease outbreaks in 2024.},
journal = {BMJ global health},
volume = {11},
number = {2},
pages = {},
doi = {10.1136/bmjgh-2025-020708},
pmid = {41702637},
issn = {2059-7908},
mesh = {Humans ; *Global Health/statistics & numerical data ; *Disease Outbreaks/statistics & numerical data ; *COVID-19/epidemiology ; *Pandemics/statistics & numerical data ; SARS-CoV-2 ; },
abstract = {During 2024, the number of pandemic-prone and epidemic-prone disease outbreaks worldwide was estimated at 301. The data highlight a shift in disease outbreak patterns, with a decline in the number of countries reporting public health events of concern linked to COVID-19 and a rise in those reporting outbreaks of viral diseases transmitted by vectors.About 90% of the outbreaks in 2024 were associated with COVID-19, dengue, yellow fever, Oropouche virus disease and influenza (linked to identified zoonotic or pandemic influenza virus). Although disease outbreaks can affect any country anywhere, they tend to disproportionately occur in countries facing many other socio-economic development, climatic and humanitarian challenges. In this regard, sub-Saharan Africa and the subregion of Latin America and the Caribbean-home to just 23.3% of the world's population-reported the highest number of disease outbreaks in 2024 with about 57% of the total. Particularly, the sub-Saharan Africa region has been the site of nearly 32% of recorded outbreaks since 1996. Future research should include efforts to improve the quality and availability of disease outbreaks data-particularly in the most exposed or vulnerable regions-and to promote the scientific use of such information for foresight purposes and for forecasting future health events of concern to support anticipatory action.},
}
MeSH Terms:
show MeSH Terms
hide MeSH Terms
Humans
*Global Health/statistics & numerical data
*Disease Outbreaks/statistics & numerical data
*COVID-19/epidemiology
*Pandemics/statistics & numerical data
SARS-CoV-2
RevDate: 2026-02-17
CmpDate: 2026-02-17
Von Willebrand Factor at the Crossroads of Hemostasis and Inflammation.
Hamostaseologie, 46(1):34-43.
Von Willebrand factor (VWF) is a large multimeric glycoprotein critical for hemostasis, mediating platelet adhesion to injured vessels and stabilizing circulating factor VIII. However, accumulating evidence reveals a complex, context-dependent role for VWF in inflammation and innate immunity that extends well beyond coagulation. VWF acts not only as a biomarker of endothelial activation but also as an active participant in immune responses. VWF directly interacts with major immune cell types-including macrophages, polymorphonuclear leukocytes (neutrophils), and dendritic cells-through both its endothelial-anchored and plasma forms. VWF facilitates leukocyte recruitment and transmigration across the vessel wall, while its interactions also promote macrophage and neutrophil activation as well as NET formation. VWF's immunomodulatory functions are further highlighted by its binding to extracellular DNA, smooth muscle cells, complement components (C1q and C3), and bacterial pathogens under flow conditions. Furthermore, VWF indirectly influences inflammation via its crucial role in Weibel-Palade body formation, a process that co-packages vital inflammatory mediators like P-selectin and angiopoietin-2. Markedly elevated VWF levels are consistently observed across acute and chronic inflammatory conditions such as sepsis, COVID-19, and autoimmune disorders, confirming its relevance as both a diagnostic marker and a therapeutic target. A comprehensive understanding of VWF's diverse functions in vascular inflammation is crucial for developing targeted therapeutics-including nanobodies, ADAMTS13 variants, and VWF interaction inhibitors-capable of modulating pathological thrombo-inflammation while preserving physiological hemostasis.
Additional Links: PMID-41702386
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PubMed:
Citation:
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@article {pmid41702386,
year = {2026},
author = {Yadegari, H},
title = {Von Willebrand Factor at the Crossroads of Hemostasis and Inflammation.},
journal = {Hamostaseologie},
volume = {46},
number = {1},
pages = {34-43},
doi = {10.1055/a-2755-5477},
pmid = {41702386},
issn = {2567-5761},
mesh = {Humans ; *von Willebrand Factor/immunology/physiology/metabolism ; *Hemostasis/immunology ; *Inflammation/immunology ; COVID-19/immunology/blood ; Immunity, Innate ; SARS-CoV-2 ; },
abstract = {Von Willebrand factor (VWF) is a large multimeric glycoprotein critical for hemostasis, mediating platelet adhesion to injured vessels and stabilizing circulating factor VIII. However, accumulating evidence reveals a complex, context-dependent role for VWF in inflammation and innate immunity that extends well beyond coagulation. VWF acts not only as a biomarker of endothelial activation but also as an active participant in immune responses. VWF directly interacts with major immune cell types-including macrophages, polymorphonuclear leukocytes (neutrophils), and dendritic cells-through both its endothelial-anchored and plasma forms. VWF facilitates leukocyte recruitment and transmigration across the vessel wall, while its interactions also promote macrophage and neutrophil activation as well as NET formation. VWF's immunomodulatory functions are further highlighted by its binding to extracellular DNA, smooth muscle cells, complement components (C1q and C3), and bacterial pathogens under flow conditions. Furthermore, VWF indirectly influences inflammation via its crucial role in Weibel-Palade body formation, a process that co-packages vital inflammatory mediators like P-selectin and angiopoietin-2. Markedly elevated VWF levels are consistently observed across acute and chronic inflammatory conditions such as sepsis, COVID-19, and autoimmune disorders, confirming its relevance as both a diagnostic marker and a therapeutic target. A comprehensive understanding of VWF's diverse functions in vascular inflammation is crucial for developing targeted therapeutics-including nanobodies, ADAMTS13 variants, and VWF interaction inhibitors-capable of modulating pathological thrombo-inflammation while preserving physiological hemostasis.},
}
MeSH Terms:
show MeSH Terms
hide MeSH Terms
Humans
*von Willebrand Factor/immunology/physiology/metabolism
*Hemostasis/immunology
*Inflammation/immunology
COVID-19/immunology/blood
Immunity, Innate
SARS-CoV-2
RevDate: 2026-02-17
Human genetics of susceptibility to live-attenuated viral vaccines.
Current opinion in virology, 75:101512 pii:S1879-6257(26)00004-0 [Epub ahead of print].
Alongside the development of antibiotics, vaccination is the medical innovation with arguably the greatest impact on human health. Testament to its success is the eradication of infectious diseases, such as smallpox, that devastated human populations for almost 4000 years. Live-attenuated vaccines (LAV), which retain the capacity for infection and replication, were the first to be developed and remain highly efficacious, underpinning successful human vaccination campaigns (e.g. polio virus, measles virus, yellow fever virus). The cost of this success is the capacity of LAVs to cause disease in a small proportion of recipients, typically owing to overt or previously unappreciated immunodeficiency. From the careful investigation of such rare events, major clinical and scientific lessons about human antiviral immunity have been drawn. Here, we review features of pathogenic LAV dissemination, which continue to inform our understanding of critical steps in the immune control of LAVs. We discuss recent data on specific variants identified in geographically isolated populations and reflect on more common phenocopies of these monogenic defects, with potential implications for vaccine practice and policy. Collectively, these insights may inform approaches to the growing population of individuals rendered more vulnerable to LAVs by aging, multimorbidity or medical intervention. They also serve to highlight the clinical need for therapeutic strategies to combat pathogenic LAV dissemination.
Additional Links: PMID-41702338
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PubMed:
Citation:
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@article {pmid41702338,
year = {2026},
author = {Hazenberg, P and Duncan, CJ},
title = {Human genetics of susceptibility to live-attenuated viral vaccines.},
journal = {Current opinion in virology},
volume = {75},
number = {},
pages = {101512},
doi = {10.1016/j.coviro.2026.101512},
pmid = {41702338},
issn = {1879-6265},
abstract = {Alongside the development of antibiotics, vaccination is the medical innovation with arguably the greatest impact on human health. Testament to its success is the eradication of infectious diseases, such as smallpox, that devastated human populations for almost 4000 years. Live-attenuated vaccines (LAV), which retain the capacity for infection and replication, were the first to be developed and remain highly efficacious, underpinning successful human vaccination campaigns (e.g. polio virus, measles virus, yellow fever virus). The cost of this success is the capacity of LAVs to cause disease in a small proportion of recipients, typically owing to overt or previously unappreciated immunodeficiency. From the careful investigation of such rare events, major clinical and scientific lessons about human antiviral immunity have been drawn. Here, we review features of pathogenic LAV dissemination, which continue to inform our understanding of critical steps in the immune control of LAVs. We discuss recent data on specific variants identified in geographically isolated populations and reflect on more common phenocopies of these monogenic defects, with potential implications for vaccine practice and policy. Collectively, these insights may inform approaches to the growing population of individuals rendered more vulnerable to LAVs by aging, multimorbidity or medical intervention. They also serve to highlight the clinical need for therapeutic strategies to combat pathogenic LAV dissemination.},
}
RevDate: 2026-02-17
Impact of the COVID-19 pandemic on cancer screening in Europe: A systematic review of disruptions, barriers, and policy responses.
Cancer treatment and research communications, 47:101115 pii:S2468-2942(26)00024-9 [Epub ahead of print].
BACKGROUND: Cancer screening is a cornerstone of cancer control, but the COVID-19 pandemic caused unprecedented disruption to preventive healthcare worldwide. In Europe, national screening programmes were severely affected, with consequences extending beyond screening to diagnosis, treatment, and equity. While several country-specific studies exist, cross-regional syntheses remain scarce. Understanding the scale, determinants, and outcomes of these disruptions is crucial to building resilient, equiTable screening systems.
AIM/OBJECTIVE: This systematic review synthesises evidence on the impact of the COVID-19 pandemic on cancer screening across Europe, examining differences by cancer type, screening modality, and national context. It also explores downstream effects, barriers, enablers, and policy responses to guide future preparedness.
METHODS: Following PRISMA guidelines, six databases and grey literature sources were searched for studies published between December 2019 and January 2025. Eligible studies included quantitative and qualitative analyses of screening activity during the pandemic. Data were extracted on study characteristics, outcomes, and contextual factors. Given the heterogeneity of measures, findings were summarised using descriptive statistics and thematic synthesis.
RESULT: Forty-five studies from 18 European countries revealed a 30-60 % reduction in screening participation at peak disruption, varying by cancer type and country. Consequences included delayed diagnoses, stage migration, increased projected mortality, and widening inequalities. Major barriers included service suspension, staff redeployment, and fear of infection. Enablers comprised adaptive communication, safety protocols, and digital innovations.
CONCLUSION: COVID-19 caused substantial and uneven disruption to European cancer screening. Protecting continuity, institutionalising innovations, and addressing inequities are critical to enhancing resilience for future health crises.
Additional Links: PMID-41702131
Publisher:
PubMed:
Citation:
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@article {pmid41702131,
year = {2026},
author = {Wang, Z and Ren, B and Rawaf, S and Tabche, C},
title = {Impact of the COVID-19 pandemic on cancer screening in Europe: A systematic review of disruptions, barriers, and policy responses.},
journal = {Cancer treatment and research communications},
volume = {47},
number = {},
pages = {101115},
doi = {10.1016/j.ctarc.2026.101115},
pmid = {41702131},
issn = {2468-2942},
abstract = {BACKGROUND: Cancer screening is a cornerstone of cancer control, but the COVID-19 pandemic caused unprecedented disruption to preventive healthcare worldwide. In Europe, national screening programmes were severely affected, with consequences extending beyond screening to diagnosis, treatment, and equity. While several country-specific studies exist, cross-regional syntheses remain scarce. Understanding the scale, determinants, and outcomes of these disruptions is crucial to building resilient, equiTable screening systems.
AIM/OBJECTIVE: This systematic review synthesises evidence on the impact of the COVID-19 pandemic on cancer screening across Europe, examining differences by cancer type, screening modality, and national context. It also explores downstream effects, barriers, enablers, and policy responses to guide future preparedness.
METHODS: Following PRISMA guidelines, six databases and grey literature sources were searched for studies published between December 2019 and January 2025. Eligible studies included quantitative and qualitative analyses of screening activity during the pandemic. Data were extracted on study characteristics, outcomes, and contextual factors. Given the heterogeneity of measures, findings were summarised using descriptive statistics and thematic synthesis.
RESULT: Forty-five studies from 18 European countries revealed a 30-60 % reduction in screening participation at peak disruption, varying by cancer type and country. Consequences included delayed diagnoses, stage migration, increased projected mortality, and widening inequalities. Major barriers included service suspension, staff redeployment, and fear of infection. Enablers comprised adaptive communication, safety protocols, and digital innovations.
CONCLUSION: COVID-19 caused substantial and uneven disruption to European cancer screening. Protecting continuity, institutionalising innovations, and addressing inequities are critical to enhancing resilience for future health crises.},
}
RevDate: 2026-02-17
Staying Functional Through Connection and Adaptation: When Islets Inspire Islet Biologists.
Diabetes pii:164451 [Epub ahead of print].
In response to the lockdowns and travel bans during the coronavirus disease 2019 pandemic, Peter C. Butler at the University of California, Los Angeles (UCLA), started a virtual islet biology seminar series. After the authors of this article joined him as co-organizers, this initiative became the Islet Research Seminar Series (IRSS). Like islets of Langerhans adapt to their changing environment, the islet biology community quickly embraced this new format. The IRSS evolved into a lasting scientific forum that convenes weekly and is attended by islet biologists from the U.S., Canada, Europe, and Israel. The series covers a range of topics in islet biology, with presentations from scientists representing all career stages. It has proven particularly valuable for trainees and early-stage investigators in exposing them to a variety of topics in islet biology without travel required and facilitating more spontaneous interactions with senior scientists than at in-person meetings. While the online format is not meant to replace live scientific conferences, we believe that the IRSS plays a unique role in keeping the islet biology community connected and abreast of the most recent scientific discoveries in our field. The success of this platform stands as a testament to the scientific community to adapt and thrive through challenges. This article is dedicated to Peter C. Butler, UCLA, who initiated the IRSS.
Additional Links: PMID-41700931
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PubMed:
Citation:
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@article {pmid41700931,
year = {2026},
author = {Dhawan, S and Hughes, J and Matveyenko, AV and Poitout, V},
title = {Staying Functional Through Connection and Adaptation: When Islets Inspire Islet Biologists.},
journal = {Diabetes},
volume = {},
number = {},
pages = {},
doi = {10.2337/dbi25-0036},
pmid = {41700931},
issn = {1939-327X},
support = {//J.W. Kieckhefer Foundation/ ; R01DK098468/DK/NIDDK NIH HHS/United States ; R01DK132597/DK/NIDDK NIH HHS/United States ; R01DK138974/DK/NIDDK NIH HHS/United States ; R01DK140088/DK/NIDDK NIH HHS/United States ; R01DK140365/DK/NIDDK NIH HHS/United States ; RGPIN-2022-03732//Natural Sciences and Engineering Research Council of Canada/ ; //Diabetes Canada/ ; PJT-469193//Institute of Nutrition, Metabolism and Diabetes/ ; },
abstract = {In response to the lockdowns and travel bans during the coronavirus disease 2019 pandemic, Peter C. Butler at the University of California, Los Angeles (UCLA), started a virtual islet biology seminar series. After the authors of this article joined him as co-organizers, this initiative became the Islet Research Seminar Series (IRSS). Like islets of Langerhans adapt to their changing environment, the islet biology community quickly embraced this new format. The IRSS evolved into a lasting scientific forum that convenes weekly and is attended by islet biologists from the U.S., Canada, Europe, and Israel. The series covers a range of topics in islet biology, with presentations from scientists representing all career stages. It has proven particularly valuable for trainees and early-stage investigators in exposing them to a variety of topics in islet biology without travel required and facilitating more spontaneous interactions with senior scientists than at in-person meetings. While the online format is not meant to replace live scientific conferences, we believe that the IRSS plays a unique role in keeping the islet biology community connected and abreast of the most recent scientific discoveries in our field. The success of this platform stands as a testament to the scientific community to adapt and thrive through challenges. This article is dedicated to Peter C. Butler, UCLA, who initiated the IRSS.},
}
RevDate: 2026-02-19
CmpDate: 2026-02-17
How Can Pharmacology Help Us Overcome the Challenges of Drug Repositioning as Antivirals to Treat Emerging Pathogens? The Example of Covid-19.
Clinical and translational science, 19(2):e70505.
The Covid-19 pandemic highlighted the urgent need for effective therapies against emerging pathogens. Drug repurposing, defined as the use of existing medications for new therapeutic purposes, was extensively pursued for SARS-CoV-2 but has not yielded successful treatments. This narrative review critically examines the pharmacological and methodological factors that contributed to these unsuccessful outcomes, paying particular attention to tests of azithromycin and hydroxychloroquine. There are many reasons the promise of repurposed drugs was not realized. Many repurposed compounds displayed promising in vitro antiviral activity that did not translate into clinical efficacy. Major pharmacokinetic (PK) limitations, for example, poor oral bioavailability, low concentrations in pulmonary tissue, and extensive plasma protein binding, prevented these drugs from reaching therapeutic levels in humans. Preclinical research often relied on non-human cell lines and animal models that inadequately reflected human physiology, leading to misleading experimental outcomes. Clinical trials were often undermined by methodological limitations, including endpoints with uncertain clinical significance, suboptimal comparators, and insufficient attention paid to key PK and pharmacodynamic (PD) parameters such as half maximal effective concentration (EC50) values. This narrative review emphasizes the importance of integrating comprehensive PK/PD assessments, relevant experimental models, and rigorous trial design to strengthen drug development during future health crises. The relative success of antivirals including molnupiravir, nirmatrelvir, and remdesivir, which were either novel or previously unapproved compounds, suggests the value of designing and developing targeted antivirals. We must coordinate global research, develop pharmacologically sound strategies, and use evidence-based decision-making to effectively prepare for future pandemics and quickly produce effective treatments.
Additional Links: PMID-41699407
PubMed:
Citation:
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@article {pmid41699407,
year = {2026},
author = {Ben Ghezala, I and Peiffer-Smadja, N and Solas, C and Nougairède, A and Touret, F and Bardou, M},
title = {How Can Pharmacology Help Us Overcome the Challenges of Drug Repositioning as Antivirals to Treat Emerging Pathogens? The Example of Covid-19.},
journal = {Clinical and translational science},
volume = {19},
number = {2},
pages = {e70505},
pmid = {41699407},
issn = {1752-8062},
mesh = {Humans ; *Drug Repositioning/methods ; *Antiviral Agents/therapeutic use/pharmacology/pharmacokinetics ; *COVID-19 Drug Treatment ; *SARS-CoV-2/drug effects ; Animals ; Hydroxychloroquine/therapeutic use/pharmacology/pharmacokinetics ; COVID-19/virology ; },
abstract = {The Covid-19 pandemic highlighted the urgent need for effective therapies against emerging pathogens. Drug repurposing, defined as the use of existing medications for new therapeutic purposes, was extensively pursued for SARS-CoV-2 but has not yielded successful treatments. This narrative review critically examines the pharmacological and methodological factors that contributed to these unsuccessful outcomes, paying particular attention to tests of azithromycin and hydroxychloroquine. There are many reasons the promise of repurposed drugs was not realized. Many repurposed compounds displayed promising in vitro antiviral activity that did not translate into clinical efficacy. Major pharmacokinetic (PK) limitations, for example, poor oral bioavailability, low concentrations in pulmonary tissue, and extensive plasma protein binding, prevented these drugs from reaching therapeutic levels in humans. Preclinical research often relied on non-human cell lines and animal models that inadequately reflected human physiology, leading to misleading experimental outcomes. Clinical trials were often undermined by methodological limitations, including endpoints with uncertain clinical significance, suboptimal comparators, and insufficient attention paid to key PK and pharmacodynamic (PD) parameters such as half maximal effective concentration (EC50) values. This narrative review emphasizes the importance of integrating comprehensive PK/PD assessments, relevant experimental models, and rigorous trial design to strengthen drug development during future health crises. The relative success of antivirals including molnupiravir, nirmatrelvir, and remdesivir, which were either novel or previously unapproved compounds, suggests the value of designing and developing targeted antivirals. We must coordinate global research, develop pharmacologically sound strategies, and use evidence-based decision-making to effectively prepare for future pandemics and quickly produce effective treatments.},
}
MeSH Terms:
show MeSH Terms
hide MeSH Terms
Humans
*Drug Repositioning/methods
*Antiviral Agents/therapeutic use/pharmacology/pharmacokinetics
*COVID-19 Drug Treatment
*SARS-CoV-2/drug effects
Animals
Hydroxychloroquine/therapeutic use/pharmacology/pharmacokinetics
COVID-19/virology
RevDate: 2026-02-19
CmpDate: 2026-02-16
Modulation of immune responses by opioids through toll-like and P2X receptor signaling in COVID-19.
Purinergic signalling, 22(2):22.
The pathogenesis of COVID-19 involves complex interactions between viral replication and host immune dysregulation, mediated by toll-like receptors (TLRs) and P2X receptors (P2XRs). These receptors detect pathogen- and damage-associated molecular patterns (PAMPs and DAMPs), triggering inflammatory cascades. Opioids, beyond their analgesic role, modulate innate and adaptive immune responses via opioid receptors and indirectly through TLR and P2X signaling. This narrative review integrates experimental, clinical, and bioinformatic evidence to explore the mechanistic crosstalk between opioid signaling, TLRs (notably TLR2, TLR4, TLR9), and P2XRs (notably P2X4 and P2X7) in COVID-19 immunopathology. Chronic opioid exposure may either enhance or suppress inflammation depending on dose, duration, and immune context. In COVID-19, the hyperactivation of TLR4, TLR7, and TLR9 drives cytokine storms, while the release of ATP from damaged cells activates P2X7, thereby amplifying the inflammatory response. ATP breakdown into adenosine further modulates immunity via A2A and A2B receptors. Targeting TLR4 and P2X7 offers a promising therapeutic strategy to mitigate hyperinflammation and improve outcomes in COVID-19 and related inflammatory diseases. In addition, we outline how the Contact System, the Kallikrein-Kinin System (KKS), the Renin-Angiotensin System (RAS), and the NLRP3 inflammasome provide the innate inflammatory backdrop through which opioids and P2 receptor signaling may shape immune dysregulation in COVID-19. Notably, direct clinical evidence for opioid-P2 receptor interactions in COVID-19 remains limited, highlighting the need for targeted translational studies.
Additional Links: PMID-41697483
PubMed:
Citation:
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@article {pmid41697483,
year = {2026},
author = {Sheikholeslami, MA and Parvardeh, S and Ghafghazi, S and Zarei, M},
title = {Modulation of immune responses by opioids through toll-like and P2X receptor signaling in COVID-19.},
journal = {Purinergic signalling},
volume = {22},
number = {2},
pages = {22},
pmid = {41697483},
issn = {1573-9546},
mesh = {Humans ; *COVID-19/immunology/metabolism ; *Toll-Like Receptors/immunology/metabolism ; *Signal Transduction/drug effects/immunology ; *Analgesics, Opioid/pharmacology ; *Receptors, Purinergic P2X/immunology/metabolism ; SARS-CoV-2 ; Immunity, Innate/drug effects ; Animals ; },
abstract = {The pathogenesis of COVID-19 involves complex interactions between viral replication and host immune dysregulation, mediated by toll-like receptors (TLRs) and P2X receptors (P2XRs). These receptors detect pathogen- and damage-associated molecular patterns (PAMPs and DAMPs), triggering inflammatory cascades. Opioids, beyond their analgesic role, modulate innate and adaptive immune responses via opioid receptors and indirectly through TLR and P2X signaling. This narrative review integrates experimental, clinical, and bioinformatic evidence to explore the mechanistic crosstalk between opioid signaling, TLRs (notably TLR2, TLR4, TLR9), and P2XRs (notably P2X4 and P2X7) in COVID-19 immunopathology. Chronic opioid exposure may either enhance or suppress inflammation depending on dose, duration, and immune context. In COVID-19, the hyperactivation of TLR4, TLR7, and TLR9 drives cytokine storms, while the release of ATP from damaged cells activates P2X7, thereby amplifying the inflammatory response. ATP breakdown into adenosine further modulates immunity via A2A and A2B receptors. Targeting TLR4 and P2X7 offers a promising therapeutic strategy to mitigate hyperinflammation and improve outcomes in COVID-19 and related inflammatory diseases. In addition, we outline how the Contact System, the Kallikrein-Kinin System (KKS), the Renin-Angiotensin System (RAS), and the NLRP3 inflammasome provide the innate inflammatory backdrop through which opioids and P2 receptor signaling may shape immune dysregulation in COVID-19. Notably, direct clinical evidence for opioid-P2 receptor interactions in COVID-19 remains limited, highlighting the need for targeted translational studies.},
}
MeSH Terms:
show MeSH Terms
hide MeSH Terms
Humans
*COVID-19/immunology/metabolism
*Toll-Like Receptors/immunology/metabolism
*Signal Transduction/drug effects/immunology
*Analgesics, Opioid/pharmacology
*Receptors, Purinergic P2X/immunology/metabolism
SARS-CoV-2
Immunity, Innate/drug effects
Animals
RevDate: 2026-02-19
CmpDate: 2026-02-16
Biomarkers of long COVID in children and young adults: a scoping review.
European journal of pediatrics, 185(3):132.
UNLABELLED: Following the SARS-CoV-2 pandemic, a significant percentage of people are now experiencing long-term symptoms, despite a continuing lack of concrete documentation of physiological and risk profiles that hinders diagnosis and treatment, particularly in pediatric contexts. This review aims to highlight the existing evidence for measurable physiological markers for post-acute sequelae of SARS-CoV-2 infection (long COVID) in children, adolescents, and young adults. Titles providing data related to measurable biomarkers distinguishing young long COVID patients from controls were compiled and analyzed. Results were displayed in table and diagram form for optimal qualitative evaluation of the relationship between markers and symptomatology within the context of each organ system. Only human studies published in English, Italian, Portuguese, German, and Spanish between the 5th of February 2025 and the 31st of December 2025 were considered, and no other time constraints were applied. Following search and criteria evaluation, nine studies were included, totaling 41 occurrences identified in diseased patients with statistically significant variation from healthy controls. Markers suggest the presence of organic manifestations based on published literature, although more data and future studies will be necessary to establish clear connections.
CONCLUSION: The data compiled for this review adds to the body of evidence indicating a physiological manifestation of long COVID and its consequences. Further investigation into potential risk factors, pre- and post-pubescent manifestations, and specific inflammatory and immune pathways will be necessary for a more concrete understanding of long COVID and its effects on children, adolescents, and young adults.
WHAT IS KNOWN: • Long COVID is estimated to affect a significant population of patients, despite the lack of concrete physiological diagnostic and prognostic measures. • Pediatric incidence of the disease is still largely debated, and published data are scarce.
WHAT IS NEW: • A total of 41 biomarker occurrences were identified by selected studies, which were consistent with expected physiology behind reported symptoms. • The body of data discussed suggests the presence of physiological phenomena behind the long-term symptoms experienced by pediatric long- COVID patients.
Additional Links: PMID-41697443
PubMed:
Citation:
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@article {pmid41697443,
year = {2026},
author = {Camara, B and Buonsenso, D},
title = {Biomarkers of long COVID in children and young adults: a scoping review.},
journal = {European journal of pediatrics},
volume = {185},
number = {3},
pages = {132},
pmid = {41697443},
issn = {1432-1076},
mesh = {Humans ; *COVID-19/complications/diagnosis ; Child ; *Biomarkers/blood ; Adolescent ; Young Adult ; Post-Acute COVID-19 Syndrome ; SARS-CoV-2 ; },
abstract = {UNLABELLED: Following the SARS-CoV-2 pandemic, a significant percentage of people are now experiencing long-term symptoms, despite a continuing lack of concrete documentation of physiological and risk profiles that hinders diagnosis and treatment, particularly in pediatric contexts. This review aims to highlight the existing evidence for measurable physiological markers for post-acute sequelae of SARS-CoV-2 infection (long COVID) in children, adolescents, and young adults. Titles providing data related to measurable biomarkers distinguishing young long COVID patients from controls were compiled and analyzed. Results were displayed in table and diagram form for optimal qualitative evaluation of the relationship between markers and symptomatology within the context of each organ system. Only human studies published in English, Italian, Portuguese, German, and Spanish between the 5th of February 2025 and the 31st of December 2025 were considered, and no other time constraints were applied. Following search and criteria evaluation, nine studies were included, totaling 41 occurrences identified in diseased patients with statistically significant variation from healthy controls. Markers suggest the presence of organic manifestations based on published literature, although more data and future studies will be necessary to establish clear connections.
CONCLUSION: The data compiled for this review adds to the body of evidence indicating a physiological manifestation of long COVID and its consequences. Further investigation into potential risk factors, pre- and post-pubescent manifestations, and specific inflammatory and immune pathways will be necessary for a more concrete understanding of long COVID and its effects on children, adolescents, and young adults.
WHAT IS KNOWN: • Long COVID is estimated to affect a significant population of patients, despite the lack of concrete physiological diagnostic and prognostic measures. • Pediatric incidence of the disease is still largely debated, and published data are scarce.
WHAT IS NEW: • A total of 41 biomarker occurrences were identified by selected studies, which were consistent with expected physiology behind reported symptoms. • The body of data discussed suggests the presence of physiological phenomena behind the long-term symptoms experienced by pediatric long- COVID patients.},
}
MeSH Terms:
show MeSH Terms
hide MeSH Terms
Humans
*COVID-19/complications/diagnosis
Child
*Biomarkers/blood
Adolescent
Young Adult
Post-Acute COVID-19 Syndrome
SARS-CoV-2
RevDate: 2026-02-16
CmpDate: 2026-02-16
[Consequences of congenital COVID-19 on the cognitive development of affected children].
Medicina, 86 Suppl 1:2-7.
Congenital COVID-19 refers to infection with the SARS-CoV-2 virus acquired in utero as a result of maternal infection during pregnancy. Although vertical transmission of the virus from mother to fetus appears to be relatively infrequent, growing clinical and epidemiological evidence indicates that prenatal exposure to SARSCoV-2, as well as to the maternal immune response it elicits, may have significant implications for early neurological development. Therefore, understanding the potential cognitive consequences of congenital COVID-19 is essential for the long-term monitoring of child health in affected individuals and for the implementation of early intervention strategies. This post-pandemic perspective on the consequences for neural development has been supported by observations showing that neonates exposed to congenital COVID-19 infection have a tenfold higher incidence of developmental delay compared with those not exposed to the virus. In this review, we examine the pathogenic mechanisms that may explain the increased incidence of neurodevelopmental alterations.
Additional Links: PMID-41696833
PubMed:
Citation:
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@article {pmid41696833,
year = {2026},
author = {Martinez-Morga, M and Garrigos, D and Martinez-Morga, S and Martinez, S},
title = {[Consequences of congenital COVID-19 on the cognitive development of affected children].},
journal = {Medicina},
volume = {86 Suppl 1},
number = {},
pages = {2-7},
pmid = {41696833},
issn = {1669-9106},
mesh = {Humans ; *COVID-19/congenital/complications/transmission ; Pregnancy ; *Pregnancy Complications, Infectious/virology ; Female ; Infectious Disease Transmission, Vertical ; Infant, Newborn ; Child ; *Prenatal Exposure Delayed Effects/virology ; *Neurodevelopmental Disorders/virology/etiology ; SARS-CoV-2 ; Child Development ; *Developmental Disabilities/virology/etiology ; },
abstract = {Congenital COVID-19 refers to infection with the SARS-CoV-2 virus acquired in utero as a result of maternal infection during pregnancy. Although vertical transmission of the virus from mother to fetus appears to be relatively infrequent, growing clinical and epidemiological evidence indicates that prenatal exposure to SARSCoV-2, as well as to the maternal immune response it elicits, may have significant implications for early neurological development. Therefore, understanding the potential cognitive consequences of congenital COVID-19 is essential for the long-term monitoring of child health in affected individuals and for the implementation of early intervention strategies. This post-pandemic perspective on the consequences for neural development has been supported by observations showing that neonates exposed to congenital COVID-19 infection have a tenfold higher incidence of developmental delay compared with those not exposed to the virus. In this review, we examine the pathogenic mechanisms that may explain the increased incidence of neurodevelopmental alterations.},
}
MeSH Terms:
show MeSH Terms
hide MeSH Terms
Humans
*COVID-19/congenital/complications/transmission
Pregnancy
*Pregnancy Complications, Infectious/virology
Female
Infectious Disease Transmission, Vertical
Infant, Newborn
Child
*Prenatal Exposure Delayed Effects/virology
*Neurodevelopmental Disorders/virology/etiology
SARS-CoV-2
Child Development
*Developmental Disabilities/virology/etiology
RevDate: 2026-02-18
CmpDate: 2026-02-16
Help, near and far: a systematic review of post-COVID digital mental health solutions for domestic violence victims.
Frontiers in public health, 13:1687396.
INTRODUCTION: Domestic violence (DV), as a global pandemic, poses a significant challenge within the field of public health, gravely impacting the mental and physical health of victims. Modern digital technologies have been proposed as promising interventions for DV-related mental health problems. We therefore evaluated their effectiveness.
OBJECTIVE: To systematically review digital interventions targeting the mental health of DV survivors and to summarize implications for health professionals and policy makers.
METHODS: We searched PubMed, EBSCO, and Web of Science (January 1, 2020-April 23, 2024) following PRISMA guidelines. Two reviewers independently screened records, applied predefined eligibility criteria, and extracted data. Owing to heterogeneity, we performed a narrative synthesis. Meanwhile, based on the results of the literature review, this paper proposes a series of policy recommendations from a post-COVID-19 era perspective, integrating societal context and relevant policies.
RESULTS: Nine studies met the inclusion criteria. Three reported no significant mental-health benefits, whereas the remainder showed improvements in outcomes such as depression, anxiety, PTSD symptoms, emotion regulation, perceived support, or safety preparedness using tools including mobile apps, web-based programs, virtual reality, chatbots, and video adjuncts.
CONCLUSION: Digital interventions show promise for improving mental-health outcomes among DV survivors, but their implementation requires attention to safety, engagement, cultural adaptation, and integration with offline services.
PROSPERO, https://www.crd.york.ac.uk/PROSPERO/view/CRD42023488560.
Additional Links: PMID-41696706
PubMed:
Citation:
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@article {pmid41696706,
year = {2025},
author = {Yu, P and Zhu, P and Kudiza, A and Kaburu, FM and Intizar, M and Tong, C and Zhang, R and Jiang, J and Yu, X and Kuang, Q and Chen, R and da Veiga, CP and Xiang, YT and Su, Z},
title = {Help, near and far: a systematic review of post-COVID digital mental health solutions for domestic violence victims.},
journal = {Frontiers in public health},
volume = {13},
number = {},
pages = {1687396},
pmid = {41696706},
issn = {2296-2565},
mesh = {Humans ; *COVID-19/psychology ; *Domestic Violence/psychology ; *Mental Health ; *Crime Victims/psychology ; *Digital Technology ; *Survivors/psychology ; },
abstract = {INTRODUCTION: Domestic violence (DV), as a global pandemic, poses a significant challenge within the field of public health, gravely impacting the mental and physical health of victims. Modern digital technologies have been proposed as promising interventions for DV-related mental health problems. We therefore evaluated their effectiveness.
OBJECTIVE: To systematically review digital interventions targeting the mental health of DV survivors and to summarize implications for health professionals and policy makers.
METHODS: We searched PubMed, EBSCO, and Web of Science (January 1, 2020-April 23, 2024) following PRISMA guidelines. Two reviewers independently screened records, applied predefined eligibility criteria, and extracted data. Owing to heterogeneity, we performed a narrative synthesis. Meanwhile, based on the results of the literature review, this paper proposes a series of policy recommendations from a post-COVID-19 era perspective, integrating societal context and relevant policies.
RESULTS: Nine studies met the inclusion criteria. Three reported no significant mental-health benefits, whereas the remainder showed improvements in outcomes such as depression, anxiety, PTSD symptoms, emotion regulation, perceived support, or safety preparedness using tools including mobile apps, web-based programs, virtual reality, chatbots, and video adjuncts.
CONCLUSION: Digital interventions show promise for improving mental-health outcomes among DV survivors, but their implementation requires attention to safety, engagement, cultural adaptation, and integration with offline services.
PROSPERO, https://www.crd.york.ac.uk/PROSPERO/view/CRD42023488560.},
}
MeSH Terms:
show MeSH Terms
hide MeSH Terms
Humans
*COVID-19/psychology
*Domestic Violence/psychology
*Mental Health
*Crime Victims/psychology
*Digital Technology
*Survivors/psychology
RevDate: 2026-02-19
CmpDate: 2026-02-19
Febrile seizure risk following monovalent COVID-19 mRNA vaccination in US children aged 2-5 years.
Vaccine, 75:128225.
OBJECTIVE: To evaluate febrile seizure risk following monovalent COVID-19 mRNA vaccination among children aged 2-5 years.
METHODS: The primary analysis evaluated children who had a febrile seizure outcome in the 0-1 days following COVID-19 vaccination. A self-controlled case series analysis was performed in three commercial insurance databases to compare the risk of seizure in the risk interval (0-1 days) to a control interval (8-63 days). The exposure of interest was receipt of dose 1 and/or dose 2 of monovalent COVID-19 mRNA vaccinations. The primary outcome was febrile seizure (0-1 day risk interval). A conditional Poisson regression model was used to compare outcome rates in risk and control intervals and estimate incidence rate ratios (IRR) and 95% confidence intervals (CIs). Meta-analyses were used to pool results across databases.
RESULTS: The primary meta-analysis found a statistically significant increased incidence of febrile seizure, in the 0-1 days following mRNA-1273 vaccination compared to the control interval (IRR: 2.52, 95% CI: 1.35 to 4.69, risk difference (RD)/100,000 doses = 3.22 (95% CI -0.31 to 6.75)). For the BNT162b2 vaccination, the IRR was elevated but not statistically significant (IRR: 1.41, 95% CI: 0.48 to 4.11, RD/100,000 doses = -0.25 (95% CI -2.75 to 2.24).
CONCLUSIONS: Among children aged 2-5 years, the analysis showed a small elevated incidence rate ratio of febrile seizures in the 0-1 days following the mRNA-1273 vaccination.
Additional Links: PMID-41643233
Publisher:
PubMed:
Citation:
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@article {pmid41643233,
year = {2026},
author = {Anderson, SA and Smith, ER and Wan, Z and Amend, KL and Secora, A and Djibo, DA and Kazemi, K and Song, J and Parlett, LE and Seeger, JD and Selvam, N and McMahill-Walraven, CN and Hu, M and Chillarige, Y and Forshee, RA},
title = {Febrile seizure risk following monovalent COVID-19 mRNA vaccination in US children aged 2-5 years.},
journal = {Vaccine},
volume = {75},
number = {},
pages = {128225},
doi = {10.1016/j.vaccine.2026.128225},
pmid = {41643233},
issn = {1873-2518},
mesh = {Humans ; *Seizures, Febrile/epidemiology/etiology ; Child, Preschool ; Male ; Female ; United States/epidemiology ; *COVID-19/prevention & control ; *Vaccination/adverse effects ; Incidence ; SARS-CoV-2/immunology ; BNT162 Vaccine/adverse effects ; 2019-nCoV Vaccine mRNA-1273/adverse effects ; *COVID-19 Vaccines/adverse effects/administration & dosage ; },
abstract = {OBJECTIVE: To evaluate febrile seizure risk following monovalent COVID-19 mRNA vaccination among children aged 2-5 years.
METHODS: The primary analysis evaluated children who had a febrile seizure outcome in the 0-1 days following COVID-19 vaccination. A self-controlled case series analysis was performed in three commercial insurance databases to compare the risk of seizure in the risk interval (0-1 days) to a control interval (8-63 days). The exposure of interest was receipt of dose 1 and/or dose 2 of monovalent COVID-19 mRNA vaccinations. The primary outcome was febrile seizure (0-1 day risk interval). A conditional Poisson regression model was used to compare outcome rates in risk and control intervals and estimate incidence rate ratios (IRR) and 95% confidence intervals (CIs). Meta-analyses were used to pool results across databases.
RESULTS: The primary meta-analysis found a statistically significant increased incidence of febrile seizure, in the 0-1 days following mRNA-1273 vaccination compared to the control interval (IRR: 2.52, 95% CI: 1.35 to 4.69, risk difference (RD)/100,000 doses = 3.22 (95% CI -0.31 to 6.75)). For the BNT162b2 vaccination, the IRR was elevated but not statistically significant (IRR: 1.41, 95% CI: 0.48 to 4.11, RD/100,000 doses = -0.25 (95% CI -2.75 to 2.24).
CONCLUSIONS: Among children aged 2-5 years, the analysis showed a small elevated incidence rate ratio of febrile seizures in the 0-1 days following the mRNA-1273 vaccination.},
}
MeSH Terms:
show MeSH Terms
hide MeSH Terms
Humans
*Seizures, Febrile/epidemiology/etiology
Child, Preschool
Male
Female
United States/epidemiology
*COVID-19/prevention & control
*Vaccination/adverse effects
Incidence
SARS-CoV-2/immunology
BNT162 Vaccine/adverse effects
2019-nCoV Vaccine mRNA-1273/adverse effects
*COVID-19 Vaccines/adverse effects/administration & dosage
RevDate: 2026-02-19
CmpDate: 2026-02-19
Transforming public mental health: a review on global trends, challenges, and pathways to change.
Health care analysis : HCA : journal of health philosophy and policy, 34(1):57-85.
This review synthesizes global trends, persistent challenges, and actionable pathways for overhauling public mental health systems, with a particular focus on low- and middle-income countries (LMICs). Thematic analysis of our review revealed that mental health disorders now affect nearly one in eight people worldwide, yet up to 75% of those in LMICs receive no treatment due to stigma, underfunding, workforce shortages, and fragmented systems, perpetuating a widening "treatment and care gap." Social inequities, harmful cultural norms, conflict, climate change, and gender disparities further amplify the risk and economic burden, projected to exceed US$6 trillion by 2030. Innovative financing approaches, including public-private partnerships and models from countries such as Norway and Australia, offer promising strategies for sustainable investments. The COVID-19 pandemic intensified mental health challenges but also raised global awareness, with leaders such as the United Nations Secretary-General and the United States Surgeon General foregrounding mental health crises in the public consciousness. Advocacy initiatives, including the FundaMentalSDG campaign, Lancet Commissions, Global Mental Health Action Network, and Global Mental Health Peer Network, have been pivotal in elevating mental health within the Sustainable Development Goals (SDGs) and linking it to social determinants. Emerging solutions include rights-based frameworks that emphasize participation and anti-discrimination, scaling up task-sharing and expanded roles for non-specialists through programs such as the World Health Organization's Mental Health Gap Action Programme, community-based interventions like Zimbabwe's Friendship Bench, and integration of mental health into primary care with dedicated counsellors, structured referral pathways, and digital innovations promising improved access and personalization. Sustained progress requires intersectoral collaboration across health, education, labor, and social sectors; embedding mental health into national health information systems; and investing in culturally adapted promotion and prevention interventions throughout the life course. Strengthening political commitment, global-local leadership, financing frameworks, and workforce capacity, particularly through continuous professional development and lived-experience participation, will accelerate progress toward the SDGs, underscoring the imperative for equitable financing and sustained political will globally.
Additional Links: PMID-41389117
PubMed:
Citation:
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@article {pmid41389117,
year = {2026},
author = {Okesanya, OJ and Oso, TA and Adebayo, UO and Obadofin, JA and Abdulghaniy, RO and Bamigbade, AA and Ogaya, JB and Ngwoke, I and Ahmed, MM and Aban, JL},
title = {Transforming public mental health: a review on global trends, challenges, and pathways to change.},
journal = {Health care analysis : HCA : journal of health philosophy and policy},
volume = {34},
number = {1},
pages = {57-85},
pmid = {41389117},
issn = {1573-3394},
mesh = {Humans ; COVID-19 ; *Global Health ; *Mental Disorders/therapy/epidemiology ; *Mental Health ; *Public Health/trends ; *Mental Health Services/organization & administration ; Developing Countries ; SARS-CoV-2 ; },
abstract = {This review synthesizes global trends, persistent challenges, and actionable pathways for overhauling public mental health systems, with a particular focus on low- and middle-income countries (LMICs). Thematic analysis of our review revealed that mental health disorders now affect nearly one in eight people worldwide, yet up to 75% of those in LMICs receive no treatment due to stigma, underfunding, workforce shortages, and fragmented systems, perpetuating a widening "treatment and care gap." Social inequities, harmful cultural norms, conflict, climate change, and gender disparities further amplify the risk and economic burden, projected to exceed US$6 trillion by 2030. Innovative financing approaches, including public-private partnerships and models from countries such as Norway and Australia, offer promising strategies for sustainable investments. The COVID-19 pandemic intensified mental health challenges but also raised global awareness, with leaders such as the United Nations Secretary-General and the United States Surgeon General foregrounding mental health crises in the public consciousness. Advocacy initiatives, including the FundaMentalSDG campaign, Lancet Commissions, Global Mental Health Action Network, and Global Mental Health Peer Network, have been pivotal in elevating mental health within the Sustainable Development Goals (SDGs) and linking it to social determinants. Emerging solutions include rights-based frameworks that emphasize participation and anti-discrimination, scaling up task-sharing and expanded roles for non-specialists through programs such as the World Health Organization's Mental Health Gap Action Programme, community-based interventions like Zimbabwe's Friendship Bench, and integration of mental health into primary care with dedicated counsellors, structured referral pathways, and digital innovations promising improved access and personalization. Sustained progress requires intersectoral collaboration across health, education, labor, and social sectors; embedding mental health into national health information systems; and investing in culturally adapted promotion and prevention interventions throughout the life course. Strengthening political commitment, global-local leadership, financing frameworks, and workforce capacity, particularly through continuous professional development and lived-experience participation, will accelerate progress toward the SDGs, underscoring the imperative for equitable financing and sustained political will globally.},
}
MeSH Terms:
show MeSH Terms
hide MeSH Terms
Humans
COVID-19
*Global Health
*Mental Disorders/therapy/epidemiology
*Mental Health
*Public Health/trends
*Mental Health Services/organization & administration
Developing Countries
SARS-CoV-2
RevDate: 2026-02-18
CmpDate: 2026-02-16
Infectious disease burden and surveillance challenges in Jordan and Palestine: a systematic review and meta-analysis.
Frontiers in digital health, 7:1713089.
BACKGROUND: Jordan and Palestine face public health challenges due to infectious diseases, with the added detrimental factors of long-term conflict, forced relocation, and lack of resources. Added to these are the increased rates of morbidity and mortality from having limited healthcare services available due to a lack of funding, poor disease surveillance systems, and entrenched systemic weaknesses. The purpose of this systematic review was to report the prevalence of infectious diseases in Jordan and Palestine in order to inform the development of targeted public health programs that use both standard and novel approaches to reduce the region's disease burden.
METHOD: As defined by the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines, the review included prospective, retrospective, cross-sectional, and case series studies published from January 2021 to February 2024. Non-English studies were excluded due to resource limitations, as were studies published before the COVID-19 pandemic (i.e., before January 2021) to focus on post-COVID-19-pandemic trends. We used diagnostic techniques (screening, laboratory, and confirmatory tests) to test for microorganisms in adults and children from at-risk populations in Jordan and Palestine. Test-negative controls were contrasted with patients who had positive test results. A manual reference screening process was added to a systematic search of PubMed and Scopus. Full-text, English-language publications published after January 2021 were eligible; protocols, reviews, case reports, and articles written in languages other than English were not. The Rayyan platform was used by two reviewers to independently screen studies. Infection type, causative microorganism, symptoms, mortality, risk factors, seasonal fluctuations, and study details (author, year, location, design, and participant characteristics) were among the extracted data. The Hoy 2012 Checklist was used to evaluate the risk of bias. Open Meta (Analyst) was used to analyze the 13 studies that satisfied the inclusion criteria. Study design, risk of bias, heterogeneity, publication bias, indirection, imprecision, effect size, and residual confounding were all considered when grading the quality of the evidence using the Grading of Recommendations, Assessment, Development, and Evaluation (GRADE) approach.
RESULTS: The results revealed that four studies addressed the prevalence of Brucella infection in Jordan and Palestine. The pooled estimate was 42.2% (95% CI: 18.8%-65.6%, I [2]: 99.7%, P: 0.001, n = 4 studies, 4,483 patients). In the studies that addressed diarrhea, in 31 of 159 (19.5%) cases, 20 were caused by Entamoeba (12.6%), 10 were caused by Blastocystis (6.3%), and 1 (0.6%) was caused by Cryptosporidium. As some cases had more than one parasite, the certainty of evidence (COE) was assessed as very low. The pooled estimate for viral causative agents of respiratory tract infections was 60% (95% CI: 11.8%-100%), while for bacterial causes, the pooled estimate was 24.4% (95% CI: 0%-68.3%). Respiratory syncytial virus (RSV) was the most common agent, with a pooled estimate of 57.9% (95% CI: 29.8%-85.9%), while influenza had a pooled estimate of 28.4% (95% CI: 5.3%-51.5%). Furthermore, two studies addressed the prevalence of meningitis in pediatric patients. In adult patients, of 192 patients known to have meningitis, a causative agent was identified in only 86 cases, with 83 (49%) classified as aseptic meningitis.
CONCLUSION: The review addressed the limitations of diagnostic capacity, reporting systems, and population-level data concerning high-burden and emerging pathogens within Jordan and Palestine. Specifically, the growth in the number of cases with respiratory tract infections, protozoal diarrheal diseases, and brucellosis indicates that improvements in surveillance systems and diagnostic processes need to be standardized and implemented throughout Jordan and Palestine to provide accurate and reliable diagnoses. In addition, improving the quality and quantity of the data and incorporating new technologies and other innovative approaches as a complement to existing public health indicators within Jordan and Palestine would be beneficial for better detecting these diseases at the earliest possible time and would provide the opportunity to establish evidence-based disease management strategies within the region.
Additional Links: PMID-41696692
PubMed:
Citation:
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@article {pmid41696692,
year = {2025},
author = {Badran, EF and Rayyan, A and Al Jaberi, M and Azzam, M and Ramadan, R and Khader, Y and Alqutob, R and Bakri, FG and Qasrawi, R and Yacoub, T and Sharaqa, A and Fraihat, N and Trigui, H and Sokhn, E and Tayyem, R and Musa, E and Kong, JD},
title = {Infectious disease burden and surveillance challenges in Jordan and Palestine: a systematic review and meta-analysis.},
journal = {Frontiers in digital health},
volume = {7},
number = {},
pages = {1713089},
pmid = {41696692},
issn = {2673-253X},
abstract = {BACKGROUND: Jordan and Palestine face public health challenges due to infectious diseases, with the added detrimental factors of long-term conflict, forced relocation, and lack of resources. Added to these are the increased rates of morbidity and mortality from having limited healthcare services available due to a lack of funding, poor disease surveillance systems, and entrenched systemic weaknesses. The purpose of this systematic review was to report the prevalence of infectious diseases in Jordan and Palestine in order to inform the development of targeted public health programs that use both standard and novel approaches to reduce the region's disease burden.
METHOD: As defined by the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines, the review included prospective, retrospective, cross-sectional, and case series studies published from January 2021 to February 2024. Non-English studies were excluded due to resource limitations, as were studies published before the COVID-19 pandemic (i.e., before January 2021) to focus on post-COVID-19-pandemic trends. We used diagnostic techniques (screening, laboratory, and confirmatory tests) to test for microorganisms in adults and children from at-risk populations in Jordan and Palestine. Test-negative controls were contrasted with patients who had positive test results. A manual reference screening process was added to a systematic search of PubMed and Scopus. Full-text, English-language publications published after January 2021 were eligible; protocols, reviews, case reports, and articles written in languages other than English were not. The Rayyan platform was used by two reviewers to independently screen studies. Infection type, causative microorganism, symptoms, mortality, risk factors, seasonal fluctuations, and study details (author, year, location, design, and participant characteristics) were among the extracted data. The Hoy 2012 Checklist was used to evaluate the risk of bias. Open Meta (Analyst) was used to analyze the 13 studies that satisfied the inclusion criteria. Study design, risk of bias, heterogeneity, publication bias, indirection, imprecision, effect size, and residual confounding were all considered when grading the quality of the evidence using the Grading of Recommendations, Assessment, Development, and Evaluation (GRADE) approach.
RESULTS: The results revealed that four studies addressed the prevalence of Brucella infection in Jordan and Palestine. The pooled estimate was 42.2% (95% CI: 18.8%-65.6%, I [2]: 99.7%, P: 0.001, n = 4 studies, 4,483 patients). In the studies that addressed diarrhea, in 31 of 159 (19.5%) cases, 20 were caused by Entamoeba (12.6%), 10 were caused by Blastocystis (6.3%), and 1 (0.6%) was caused by Cryptosporidium. As some cases had more than one parasite, the certainty of evidence (COE) was assessed as very low. The pooled estimate for viral causative agents of respiratory tract infections was 60% (95% CI: 11.8%-100%), while for bacterial causes, the pooled estimate was 24.4% (95% CI: 0%-68.3%). Respiratory syncytial virus (RSV) was the most common agent, with a pooled estimate of 57.9% (95% CI: 29.8%-85.9%), while influenza had a pooled estimate of 28.4% (95% CI: 5.3%-51.5%). Furthermore, two studies addressed the prevalence of meningitis in pediatric patients. In adult patients, of 192 patients known to have meningitis, a causative agent was identified in only 86 cases, with 83 (49%) classified as aseptic meningitis.
CONCLUSION: The review addressed the limitations of diagnostic capacity, reporting systems, and population-level data concerning high-burden and emerging pathogens within Jordan and Palestine. Specifically, the growth in the number of cases with respiratory tract infections, protozoal diarrheal diseases, and brucellosis indicates that improvements in surveillance systems and diagnostic processes need to be standardized and implemented throughout Jordan and Palestine to provide accurate and reliable diagnoses. In addition, improving the quality and quantity of the data and incorporating new technologies and other innovative approaches as a complement to existing public health indicators within Jordan and Palestine would be beneficial for better detecting these diseases at the earliest possible time and would provide the opportunity to establish evidence-based disease management strategies within the region.},
}
RevDate: 2026-02-18
CmpDate: 2026-02-16
Invasive pulmonary aspergillosis in the post-COVID-19 era: diagnosis, treatment, and what lies ahead.
Therapeutic advances in infectious disease, 13:20499361251406189.
Invasive pulmonary aspergillosis (IPA) is a severe opportunistic fungal infection that predominantly affects immunocompromised individuals, including those with hematologic malignancies, organ transplants, and, more recently, patients with post-COVID-19 immune dysregulation. Despite advancements in medical mycology, IPA continues to pose significant diagnostic and therapeutic challenges, contributing to high global morbidity and mortality. Diagnostic accuracy remains limited due to nonspecific clinical manifestations and the suboptimal performance of conventional tools such as bronchoalveolar lavage culture and galactomannan testing. However, recent innovations including polymerase chain reaction-based molecular assays, lateral flow devices, and immuno-positron emission tomography/magnetic resonance imaging offer improved sensitivity, specificity, and speed. Therapeutically, triazoles remain the cornerstone of IPA management, complemented by echinocandins and liposomal amphotericin B in refractory cases. The role of combination therapy and antifungal susceptibility testing is growing in response to rising azole resistance. Additionally, novel antifungal agents and immunotherapeutic approaches are currently under clinical investigation. Effective management of IPA requires a timely, multidisciplinary approach that combines advanced diagnostics with personalized antifungal strategies. Continued research is essential to standardize molecular techniques, refine immunotherapy, and expand access to next-generation antifungals to reduce the global burden of this life-threatening infection. This review aims to synthesize current evidence on the diagnosis and treatment of IPA, critically evaluate the strengths and limitations of existing diagnostic and therapeutic approaches, and explore emerging strategies to enhance clinical outcomes in the context of rising antifungal resistance.
Additional Links: PMID-41696621
PubMed:
Citation:
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@article {pmid41696621,
year = {2026},
author = {Nguyen Hai, C},
title = {Invasive pulmonary aspergillosis in the post-COVID-19 era: diagnosis, treatment, and what lies ahead.},
journal = {Therapeutic advances in infectious disease},
volume = {13},
number = {},
pages = {20499361251406189},
pmid = {41696621},
issn = {2049-9361},
abstract = {Invasive pulmonary aspergillosis (IPA) is a severe opportunistic fungal infection that predominantly affects immunocompromised individuals, including those with hematologic malignancies, organ transplants, and, more recently, patients with post-COVID-19 immune dysregulation. Despite advancements in medical mycology, IPA continues to pose significant diagnostic and therapeutic challenges, contributing to high global morbidity and mortality. Diagnostic accuracy remains limited due to nonspecific clinical manifestations and the suboptimal performance of conventional tools such as bronchoalveolar lavage culture and galactomannan testing. However, recent innovations including polymerase chain reaction-based molecular assays, lateral flow devices, and immuno-positron emission tomography/magnetic resonance imaging offer improved sensitivity, specificity, and speed. Therapeutically, triazoles remain the cornerstone of IPA management, complemented by echinocandins and liposomal amphotericin B in refractory cases. The role of combination therapy and antifungal susceptibility testing is growing in response to rising azole resistance. Additionally, novel antifungal agents and immunotherapeutic approaches are currently under clinical investigation. Effective management of IPA requires a timely, multidisciplinary approach that combines advanced diagnostics with personalized antifungal strategies. Continued research is essential to standardize molecular techniques, refine immunotherapy, and expand access to next-generation antifungals to reduce the global burden of this life-threatening infection. This review aims to synthesize current evidence on the diagnosis and treatment of IPA, critically evaluate the strengths and limitations of existing diagnostic and therapeutic approaches, and explore emerging strategies to enhance clinical outcomes in the context of rising antifungal resistance.},
}
RevDate: 2026-02-17
CmpDate: 2026-02-17
Early Outcomes of Cochlear Implantation for Pediatric COVID-19 Related Single Sided Deafness: Case Series and Literature Review.
The Annals of otology, rhinology, and laryngology, 135(3):212-216.
OBJECTIVE: Sudden sensorineural hearing loss (SSNHL) is a rare manifestation of COVID-19. Cochlear implantation (CI) has been reported for definitive management of COVID-19 related single sided deafness (SSD) in adults. We present the first cases of pediatric CI for presumed COVID-19 related SSD.
METHODS: Patients under 18 years were included who underwent CI following SSNHL after COVID-19 infection via retrospective review. Literature review was performed on PubMed for "cochlear implant" and "COVID" and "deafness or hearing loss."
RESULTS: A 13-year-old boy (patient A) and 6-year-old girl (patient B) met inclusion criteria; both patients underwent round window insertion of a perimodiolar electrode. For patient A, audiogram showed SNHL in the left ear; pre-operative word recognition score (WRS) and speech awareness threshold (SAT) were 20% at 100 dB HL and 90 dB HL, respectively. The patient underwent CI 9 months post-infection; SAT for patient A improved to 25 dB HL at 2.5 months after surgery. Patient B's pre-operative WRS and SAT in the affected ear were 0% at 100 dB HL and non-responsive, respectively. She underwent right CI 10 months post-infection; her SAT improved post-operatively to 20 dB HL at 2 post-operative months. Neither patient suffered from intra- or post-operative complication. Both patients and their caregivers reported subjective benefit from CI.
CONCLUSION: Single-sided deafness is a rare neurological complication from COVID-19. CI is a valuable tool for restoring hearing localization and awareness in this scenario. Early success with these cases demonstrates technical feasibility and benefit with this management of pediatric COVID-19 related SSD.
Additional Links: PMID-41235593
Publisher:
PubMed:
Citation:
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@article {pmid41235593,
year = {2026},
author = {Arya, P and Brooks, KA and Cross, A and Alfonso, KP and Govil, N},
title = {Early Outcomes of Cochlear Implantation for Pediatric COVID-19 Related Single Sided Deafness: Case Series and Literature Review.},
journal = {The Annals of otology, rhinology, and laryngology},
volume = {135},
number = {3},
pages = {212-216},
doi = {10.1177/00034894251386688},
pmid = {41235593},
issn = {1943-572X},
mesh = {Humans ; *COVID-19/complications ; Male ; *Cochlear Implantation/methods ; Child ; Adolescent ; Female ; SARS-CoV-2 ; *Hearing Loss, Sensorineural/surgery/etiology ; Treatment Outcome ; Retrospective Studies ; *Hearing Loss, Sudden/surgery/etiology ; *Hearing Loss, Unilateral/surgery/etiology ; },
abstract = {OBJECTIVE: Sudden sensorineural hearing loss (SSNHL) is a rare manifestation of COVID-19. Cochlear implantation (CI) has been reported for definitive management of COVID-19 related single sided deafness (SSD) in adults. We present the first cases of pediatric CI for presumed COVID-19 related SSD.
METHODS: Patients under 18 years were included who underwent CI following SSNHL after COVID-19 infection via retrospective review. Literature review was performed on PubMed for "cochlear implant" and "COVID" and "deafness or hearing loss."
RESULTS: A 13-year-old boy (patient A) and 6-year-old girl (patient B) met inclusion criteria; both patients underwent round window insertion of a perimodiolar electrode. For patient A, audiogram showed SNHL in the left ear; pre-operative word recognition score (WRS) and speech awareness threshold (SAT) were 20% at 100 dB HL and 90 dB HL, respectively. The patient underwent CI 9 months post-infection; SAT for patient A improved to 25 dB HL at 2.5 months after surgery. Patient B's pre-operative WRS and SAT in the affected ear were 0% at 100 dB HL and non-responsive, respectively. She underwent right CI 10 months post-infection; her SAT improved post-operatively to 20 dB HL at 2 post-operative months. Neither patient suffered from intra- or post-operative complication. Both patients and their caregivers reported subjective benefit from CI.
CONCLUSION: Single-sided deafness is a rare neurological complication from COVID-19. CI is a valuable tool for restoring hearing localization and awareness in this scenario. Early success with these cases demonstrates technical feasibility and benefit with this management of pediatric COVID-19 related SSD.},
}
MeSH Terms:
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Humans
*COVID-19/complications
Male
*Cochlear Implantation/methods
Child
Adolescent
Female
SARS-CoV-2
*Hearing Loss, Sensorineural/surgery/etiology
Treatment Outcome
Retrospective Studies
*Hearing Loss, Sudden/surgery/etiology
*Hearing Loss, Unilateral/surgery/etiology
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