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      Asthma and risk of infection, hospitalization, ICU admission and mortality from COVID-19: Systematic review and meta-analysis

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          Abstract

          Objective

          As COVID-19 spreads across the world, there are concerns that people with asthma are at a higher risk of acquiring the disease, or of poorer outcomes. This systematic review aimed to summarize evidence on the risk of infection, severe illness and death from COVID-19 in people with asthma.

          Data sources and study selection

          A comprehensive search of electronic databases including preprint repositories and WHO COVID-19 database was conducted (until 26 May 2020). Studies reporting COVID-19 in people with asthma were included. For binary outcomes, we performed Sidik-Jonkman random effects meta-analysis. We explored quantitative heterogeneity by subgroup analyses, meta regression and evaluating the I 2 statistic.

          Results

          Fifty-seven studies with an overall sample size of 587 280 were included. The prevalence of asthma among those infected with COVID-19 was 7.46% (95% CI = 6.25–8.67). Non-severe asthma was more common than severe asthma (9.61% vs. 4.13%). Pooled analysis showed a 14% risk ratio reduction in acquiring COVID-19 (95% CI = 0.80–0.94; p < 0.0001) and 13% reduction in hospitalization with COVID-19 (95% CI = 0.77–0.99, p = 0.03) for people with asthma compared with those without. There was no significant difference in the combined risk of requiring admission to ICU and/or receiving mechanical ventilation for people with asthma (RR = 0.87 95% CI = 0.94–1.37; p = 0.19) and risk of death from COVID-19 (RR = 0.87; 95% CI = 0.68–1.10; p = 0.25).

          Conclusion

          The findings from this study suggest that the prevalence of people with asthma among COVID-19 patients is similar to the global prevalence of asthma. The overall findings suggest that people with asthma have a lower risk than those without asthma for acquiring COVID-19 and have similar clinical outcomes.

          Glossary
          Abbreviations:

          ACE-2:

          angiotensin-converting-enzyme-2;

          CDC:

          United States Center for Disease Control and Prevention;

          COPD:

          chronic obstructive pulmonary disease;

          COVID-19:

          coronavirus disease 2019;

          ICU:

          intensive care unit;

          ICS:

          inhaled corticosteroids;

          MERS:

          Middle East Respiratory Syndrome;

          RRR:

          relative risk reduction;

          SARS-CoV-1:

          severe acute respiratory syndrome coronavirus 1;

          SARS-CoV-2:

          severe acute respiratory syndrome coronavirus 2

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          Most cited references83

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          Characteristics of and Important Lessons From the Coronavirus Disease 2019 (COVID-19) Outbreak in China: Summary of a Report of 72 314 Cases From the Chinese Center for Disease Control and Prevention

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            Dexamethasone in Hospitalized Patients with Covid-19 — Preliminary Report

            Abstract Background Coronavirus disease 2019 (Covid-19) is associated with diffuse lung damage. Glucocorticoids may modulate inflammation-mediated lung injury and thereby reduce progression to respiratory failure and death. Methods In this controlled, open-label trial comparing a range of possible treatments in patients who were hospitalized with Covid-19, we randomly assigned patients to receive oral or intravenous dexamethasone (at a dose of 6 mg once daily) for up to 10 days or to receive usual care alone. The primary outcome was 28-day mortality. Here, we report the preliminary results of this comparison. Results A total of 2104 patients were assigned to receive dexamethasone and 4321 to receive usual care. Overall, 482 patients (22.9%) in the dexamethasone group and 1110 patients (25.7%) in the usual care group died within 28 days after randomization (age-adjusted rate ratio, 0.83; 95% confidence interval [CI], 0.75 to 0.93; P<0.001). The proportional and absolute between-group differences in mortality varied considerably according to the level of respiratory support that the patients were receiving at the time of randomization. In the dexamethasone group, the incidence of death was lower than that in the usual care group among patients receiving invasive mechanical ventilation (29.3% vs. 41.4%; rate ratio, 0.64; 95% CI, 0.51 to 0.81) and among those receiving oxygen without invasive mechanical ventilation (23.3% vs. 26.2%; rate ratio, 0.82; 95% CI, 0.72 to 0.94) but not among those who were receiving no respiratory support at randomization (17.8% vs. 14.0%; rate ratio, 1.19; 95% CI, 0.91 to 1.55). Conclusions In patients hospitalized with Covid-19, the use of dexamethasone resulted in lower 28-day mortality among those who were receiving either invasive mechanical ventilation or oxygen alone at randomization but not among those receiving no respiratory support. (Funded by the Medical Research Council and National Institute for Health Research and others; RECOVERY ClinicalTrials.gov number, NCT04381936; ISRCTN number, 50189673.)
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              Presenting Characteristics, Comorbidities, and Outcomes Among 5700 Patients Hospitalized With COVID-19 in the New York City Area

              There is limited information describing the presenting characteristics and outcomes of US patients requiring hospitalization for coronavirus disease 2019 (COVID-19).
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                Author and article information

                Journal
                J Asthma
                J Asthma
                The Journal of Asthma
                Taylor & Francis
                0277-0903
                1532-4303
                1 April 2021
                2021
                : 1-14
                Affiliations
                [a ]Respiratory Division, The George Institute for Global Health , Newtown, New South Wales, Australia
                [b ]School of Medical Sciences, Faculty of Medicine, The University of New South Wales , Kensington, New South Wales, Australia
                [c ]Mental Health Division, The George Institute for Global Health, Newtown , New South Wales, Australia
                [d ]Statistics Division, The George Institute for Global Health, Newtown , New South Wales, Australia
                [e ]Concord Clinical School, Medical Education Centre, Concord Repatriation General Hospital , Kensington, Concord, New South Wales, Australia
                Author notes
                CONTACT Christine Jenkins christine.jenkins@ 123456sydney.edu.au The George Institute for Global Health , PO Box M201, Missenden Road, Sydney2050, Australia.
                Author information
                https://orcid.org/0000-0003-2257-4374
                Article
                1888116
                10.1080/02770903.2021.1888116
                8022341
                33556287
                af16caac-fe1a-453b-ac8e-de2eae82cc98
                © 2021 Taylor & Francis Group, LLC

                This article is made available via the PMC Open Access Subset for unrestricted re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the COVID-19 pandemic or until permissions are revoked in writing. Upon expiration of these permissions, PMC is granted a perpetual license to make this article available via PMC and Europe PMC, consistent with existing copyright protections.

                History
                Page count
                Figures: 5, Tables: 1, Pages: 14, Words: 8759
                Categories
                Research-Article

                Immunology
                severe acute respiratory syndrome coronavirus 2,novel coronavirus 2019,coronavirus,ventilator support,critical care medicine,meta-analysis,respiratory infections

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