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NSAIDs and COVID-19: A Systematic Review and Meta-analysis
BACKGROUND: Nonsteroidal anti-inflammatory drugs (NSAIDs) have been discouraged for the treatment of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infections, fearing that they could increase the risk of infection or the severity of SARS-CoV-2. METHODS: Original studies providing info...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8327046/ https://www.ncbi.nlm.nih.gov/pubmed/34339037 http://dx.doi.org/10.1007/s40264-021-01089-5 |
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author | Moore, Nicholas Bosco-Levy, Pauline Thurin, Nicolas Blin, Patrick Droz-Perroteau, Cécile |
author_facet | Moore, Nicholas Bosco-Levy, Pauline Thurin, Nicolas Blin, Patrick Droz-Perroteau, Cécile |
author_sort | Moore, Nicholas |
collection | PubMed |
description | BACKGROUND: Nonsteroidal anti-inflammatory drugs (NSAIDs) have been discouraged for the treatment of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infections, fearing that they could increase the risk of infection or the severity of SARS-CoV-2. METHODS: Original studies providing information on exposure to NSAIDs and coronavirus disease 2019 (COVID-19) outcomes were retrieved and were included in a descriptive analysis and a meta-analysis with Cochrane Revue Manager (REVMAN 5.4), using inverse variance odds ratio (OR) with random- or fixed-effects models. RESULTS: Of 92,853 papers mentioning COVID-19, 266 mentioned NSAIDs and 61 mentioned ibuprofen; 19 papers had analysable data. Three papers described NSAID exposure and the risk of SARS-CoV-2 positivity, five papers described the risk of hospital admission in positive patients, 10 papers described death, and six papers described severe composite outcomes. Five papers studied exposure to ibuprofen and death. Using random-effects models, there was no excess risk of SARS-CoV-2 positivity (OR 0.86, 95% confidence interval [CI] 0.71–1.05). In SARS-CoV-2-positive patients, exposure to NSAIDs was not associated with excess risk of hospital admission (OR 0.90, 95% CI 0.80–1.17), death (OR 0.88, 95% CI 0.80–0.98), or severe outcomes (OR 1.14, 95% CI 0.90–1.44). With ibuprofen, there was no increased risk of death (OR 0.94, 95% CI 0.78–1.13). Using a fixed-effect model did not modify the results, nor did the sensitivity analyses. CONCLUSION: The theoretical risks of NSAIDs or ibuprofen in SARS-CoV-2 infection are not confirmed by observational data. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s40264-021-01089-5. |
format | Online Article Text |
id | pubmed-8327046 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-83270462021-08-02 NSAIDs and COVID-19: A Systematic Review and Meta-analysis Moore, Nicholas Bosco-Levy, Pauline Thurin, Nicolas Blin, Patrick Droz-Perroteau, Cécile Drug Saf Systematic Review BACKGROUND: Nonsteroidal anti-inflammatory drugs (NSAIDs) have been discouraged for the treatment of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infections, fearing that they could increase the risk of infection or the severity of SARS-CoV-2. METHODS: Original studies providing information on exposure to NSAIDs and coronavirus disease 2019 (COVID-19) outcomes were retrieved and were included in a descriptive analysis and a meta-analysis with Cochrane Revue Manager (REVMAN 5.4), using inverse variance odds ratio (OR) with random- or fixed-effects models. RESULTS: Of 92,853 papers mentioning COVID-19, 266 mentioned NSAIDs and 61 mentioned ibuprofen; 19 papers had analysable data. Three papers described NSAID exposure and the risk of SARS-CoV-2 positivity, five papers described the risk of hospital admission in positive patients, 10 papers described death, and six papers described severe composite outcomes. Five papers studied exposure to ibuprofen and death. Using random-effects models, there was no excess risk of SARS-CoV-2 positivity (OR 0.86, 95% confidence interval [CI] 0.71–1.05). In SARS-CoV-2-positive patients, exposure to NSAIDs was not associated with excess risk of hospital admission (OR 0.90, 95% CI 0.80–1.17), death (OR 0.88, 95% CI 0.80–0.98), or severe outcomes (OR 1.14, 95% CI 0.90–1.44). With ibuprofen, there was no increased risk of death (OR 0.94, 95% CI 0.78–1.13). Using a fixed-effect model did not modify the results, nor did the sensitivity analyses. CONCLUSION: The theoretical risks of NSAIDs or ibuprofen in SARS-CoV-2 infection are not confirmed by observational data. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s40264-021-01089-5. Springer International Publishing 2021-08-02 2021 /pmc/articles/PMC8327046/ /pubmed/34339037 http://dx.doi.org/10.1007/s40264-021-01089-5 Text en © The Author(s), under exclusive licence to Springer Nature Switzerland AG 2021 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Systematic Review Moore, Nicholas Bosco-Levy, Pauline Thurin, Nicolas Blin, Patrick Droz-Perroteau, Cécile NSAIDs and COVID-19: A Systematic Review and Meta-analysis |
title | NSAIDs and COVID-19: A Systematic Review and Meta-analysis |
title_full | NSAIDs and COVID-19: A Systematic Review and Meta-analysis |
title_fullStr | NSAIDs and COVID-19: A Systematic Review and Meta-analysis |
title_full_unstemmed | NSAIDs and COVID-19: A Systematic Review and Meta-analysis |
title_short | NSAIDs and COVID-19: A Systematic Review and Meta-analysis |
title_sort | nsaids and covid-19: a systematic review and meta-analysis |
topic | Systematic Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8327046/ https://www.ncbi.nlm.nih.gov/pubmed/34339037 http://dx.doi.org/10.1007/s40264-021-01089-5 |
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