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Risks of infection, hospital and ICU admission, and death from COVID-19 in people with asthma: systematic review and meta-analyses
  1. Afolarin Otunla1,
  2. Karen Rees2,
  3. Paddy Dennison3,
  4. Richard Hobbs4,
  5. Jana Suklan5,
  6. Ella Schofield1,
  7. James Gunnell1,
  8. Alexandra Mighiu1,
  9. Jamie Hartmann-Boyce4
  1. 1 Medical Sciences Division, University of Oxford, Oxford, UK
  2. 2 Freelance systematic reviewer, Warwickshire, UK
  3. 3 University Hospital Southampton NHS Foundation Trust, Southampton, UK
  4. 4 Nuffield Department of Primary Care Health Sciences, University of Oxford, Oxford, UK
  5. 5 NIHR Newcastle In Vitro Diagnostics, Translational and Clinical Research Institute, Newcastle University, Newcastle Upon Tyne, UK
  1. Correspondence to Dr Jamie Hartmann-Boyce, Nuffield Department of Primary Care Health Sciences, Oxford University, Oxford OX2 6GG, UK; jamie.hartmann-boyce{at}phc.ox.ac.uk

Abstract

Objectives To determine if and to what degree asthma may predispose to worse COVID-19 outcomes in order to inform treatment and prevention decisions, including shielding and vaccine prioritisation.

Design Systematic review and meta-analysis.

Setting Electronic databases were searched (October 2020) for clinical studies reporting at least one of the following stratified by asthma status: risk of infection with SARS-CoV-2; hospitalisation, intensive care unit (ICU) admission or mortality with COVID-19.

Participants Adults and children who tested positive for or were suspected to have COVID-19.

Main outcome measures Main outcome measures were the following stratified by asthma status: risk of infection with SARS-CoV-2; hospitalisation, ICU admission or mortality with COVID-19. We pooled odds ratios (ORs) and presented these with 95% confidence intervals (CI). Certainty was assessed using GRADE (Grading of Recommendations, Assessment, Development and Evaluations).

Results 30 (n=112 420) studies were included (12 judged high quality, 15 medium, 3 low). Few provided indication of asthma severity. Point estimates indicated reduced risks in people with asthma for all outcomes, but in all cases the evidence was judged to be of very low certainty and 95% CIs all included no difference and the possibility of increased risk (death: OR 0.90, 95% CI 0.72 to 1.13, I2=58%; hospitalisation: OR 0.95, 95% CI 0.71 to 1.26; ICU admission: OR 0.96, 95% CI 0.75 to 1.24). Findings on hospitalisation are also limited by substantial unexplained statistical heterogeneity. Within people with asthma, allergic asthma was associated with less COVID-19 risk and concurrent chronic obstructive pulmonary disease was associated with increased risk. In some studies, corticosteroids were associated with increased risk, but this may reflect increased risk in people with more severe asthma.

Conclusions Though absence of evidence of a clear association between asthma and worse outcomes from COVID-19 should not be interpreted as evidence of absence, the data reviewed indicate that risks from COVID-19 in people with asthma, as a whole, may be less than originally anticipated.

  • asthma
  • COVID-19
  • infections
  • infectious disease medicine

Data availability statement

Data are available upon reasonable request. Data sharing not applicable as no datasets were generated and/or analysed for this study. All data are from publicly available documents, and references are provided should readers wish to look at original sources.

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Data availability statement

Data are available upon reasonable request. Data sharing not applicable as no datasets were generated and/or analysed for this study. All data are from publicly available documents, and references are provided should readers wish to look at original sources.

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Footnotes

  • Twitter @jana.suklan, @jhb19

  • Contributors JH-B conceived the original review. AO, JH-B, JS, ES, JG, AM and KR screened the studies and extracted the data. AO drafted the manuscript and performed the statistical analysis with guidance from JH-B. RH, PD, KR and JH-B provided expert opinion. All authors contributed to and approved the final manuscript. All authors had full access to all the data in the study. JH-B acts as guarantor for this work.

  • Funding Funding from the WHO supported screening, data extraction and quality assessment as part of an original rapid review.

  • Competing interests None declared.

  • Provenance and peer review Not commissioned; externally peer reviewed.

  • Supplemental material This content has been supplied by the author(s). It has not been vetted by BMJ Publishing Group Limited (BMJ) and may not have been peer-reviewed. Any opinions or recommendations discussed are solely those of the author(s) and are not endorsed by BMJ. BMJ disclaims all liability and responsibility arising from any reliance placed on the content. Where the content includes any translated material, BMJ does not warrant the accuracy and reliability of the translations (including but not limited to local regulations, clinical guidelines, terminology, drug names and drug dosages), and is not responsible for any error and/or omissions arising from translation and adaptation or otherwise.