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10.1016/j.eclinm.2020.100652

http://scihub22266oqcxt.onion/10.1016/j.eclinm.2020.100652
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33283178!7701906!33283178
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suck abstract from ncbi

pmid33283178      EClinicalMedicine 2020 ; 29 (?): 100652
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  • The "sex gap" in COVID-19 trials: a scoping review #MMPMID33283178
  • Schiffer VMMM; Janssen EBNJ; van Bussel BCT; Jorissen LLM; Tas J; Sels JEM; Bergmans DCJJ; Dinh THT; van Kuijk SMJ; Hana A; Mehagnoul-Schipper J; Scheeren CIE; Mesotten D; Stessel B; Marx G; Hof AWJVT; Spaanderman MEA; van Mook WNKA; van der Horst ICC; Ghossein-Doha C
  • EClinicalMedicine 2020[Dec]; 29 (?): 100652 PMID33283178show ga
  • BACKGROUND: Many studies investigate the role of pharmacological treatments on disease course in Corona Virus Disease 2019 (COVID-19). Sex disparities in genetics, immunological responses, and hormonal mechanisms may underlie the substantially higher fatality rates reported in male COVID-19 patients. To optimise care for COVID-19 patients, prophylactic and therapeutic studies should include sex-specific design and analyses. Therefore, in this scoping review, we investigated whether studies on pharmacological treatment in COVID-19 were performed based on a priori sex-specific design or post-hoc sex-specific analyses. METHODS: We systematically searched PubMed, EMBASE, UpToDate, clinical trial.org, and MedRxiv for studies on pharmacological treatment for COVID-19 until June 6th, 2020. We included case series, randomized controlled trials, and observational studies in humans (>/=18 years) investigating antiviral, antimalarial, and immune system modulating drugs. Data were collected on 1) the proportion of included females, 2) whether sex stratification was performed (a priori by design or post-hoc), and 3) whether effect modification by sex was investigated. FINDINGS: 30 studies were eligible for inclusion, investigating remdesivir (n = 2), lopinavir/ritonavir (n = 5), favipiravir (n = 1), umifenovir (n = 1), hydroxychloroquine/chloroquine (n = 8), convalescent plasma (n = 6), interleukin-6 (IL-6) pathway inhibitors (n = 5), interleukin-1 (IL-1) pathway inhibitors (n = 1) and corticosteroids (n = 3). Only one study stratified its data based on sex in a post-hoc analysis, whereas none did a priori by design. None of the studies investigated effect modification by sex. A quarter of the studies included twice as many males as females. INTERPRETATION: Analyses assessing potential interference of sex with (side-)effects of pharmacological therapy for COVID-19 are rarely reported. Considering sex differences in case-fatality rates and genetic, immunological, and hormonal mechanisms, studies should include sex-specific analyses in their design to optimise COVID-19 care. FUNDING: None.
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