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No association of low‐dose aspirin with severe COVID‐19 in France: A cohort of 31.1 million people without cardiovascular disease
BACKGROUND: Aspirin at low doses has been reported to be a potential drug candidate to treat or prevent severe coronavirus disease 2019 (COVID‐19). OBJECTIVES: We aimed to explore whether low‐dose aspirin used for primary cardiovascular prevention was associated with a lower risk of severe COVID‐19....
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9204394/ https://www.ncbi.nlm.nih.gov/pubmed/35755854 http://dx.doi.org/10.1002/rth2.12743 |
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author | Botton, Jérémie Semenzato, Laura Dupouy, Julie Dray‐Spira, Rosemary Weill, Alain Saint‐Lary, Olivier Zureik, Mahmoud |
author_facet | Botton, Jérémie Semenzato, Laura Dupouy, Julie Dray‐Spira, Rosemary Weill, Alain Saint‐Lary, Olivier Zureik, Mahmoud |
author_sort | Botton, Jérémie |
collection | PubMed |
description | BACKGROUND: Aspirin at low doses has been reported to be a potential drug candidate to treat or prevent severe coronavirus disease 2019 (COVID‐19). OBJECTIVES: We aimed to explore whether low‐dose aspirin used for primary cardiovascular prevention was associated with a lower risk of severe COVID‐19. METHOD: A large cohort of patients without known cardiovascular comorbidities was constructed from the entire French population registered in national health care databases. In total, 31.1 million patients aged ≥40 years, including 1.5 million reimbursed for low‐dose aspirin at least at three time points during the 6 months before the epidemic, were followed until hospitalization with a COVID‐19 diagnosis or intubation/death for hospitalized patients. RESULTS: Cox models adjusted for age and sex showed a positive association between low‐dose aspirin and the risk of hospitalization (hazard ratio [HR], 1.33; 95% confidence interval (CI), 1.29‐1.37]) or death/intubation (HR, 1.40 [95% CI, 1.33‐1.47]). In fully adjusted models, associations were close to null (HR, 1.03 [95% CI, 1.00‐1.06] and 1.04 [95% CI, 0.98‐1.10], respectively). CONCLUSION: There was no evidence for an effect of low‐dose aspirin for primary cardiovascular prevention in reducing severe COVID‐19. |
format | Online Article Text |
id | pubmed-9204394 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92043942022-06-24 No association of low‐dose aspirin with severe COVID‐19 in France: A cohort of 31.1 million people without cardiovascular disease Botton, Jérémie Semenzato, Laura Dupouy, Julie Dray‐Spira, Rosemary Weill, Alain Saint‐Lary, Olivier Zureik, Mahmoud Res Pract Thromb Haemost Brief Reports BACKGROUND: Aspirin at low doses has been reported to be a potential drug candidate to treat or prevent severe coronavirus disease 2019 (COVID‐19). OBJECTIVES: We aimed to explore whether low‐dose aspirin used for primary cardiovascular prevention was associated with a lower risk of severe COVID‐19. METHOD: A large cohort of patients without known cardiovascular comorbidities was constructed from the entire French population registered in national health care databases. In total, 31.1 million patients aged ≥40 years, including 1.5 million reimbursed for low‐dose aspirin at least at three time points during the 6 months before the epidemic, were followed until hospitalization with a COVID‐19 diagnosis or intubation/death for hospitalized patients. RESULTS: Cox models adjusted for age and sex showed a positive association between low‐dose aspirin and the risk of hospitalization (hazard ratio [HR], 1.33; 95% confidence interval (CI), 1.29‐1.37]) or death/intubation (HR, 1.40 [95% CI, 1.33‐1.47]). In fully adjusted models, associations were close to null (HR, 1.03 [95% CI, 1.00‐1.06] and 1.04 [95% CI, 0.98‐1.10], respectively). CONCLUSION: There was no evidence for an effect of low‐dose aspirin for primary cardiovascular prevention in reducing severe COVID‐19. John Wiley and Sons Inc. 2022-06-17 /pmc/articles/PMC9204394/ /pubmed/35755854 http://dx.doi.org/10.1002/rth2.12743 Text en © 2022 The Authors. Research and Practice in Thrombosis and Haemostasis published by Wiley Periodicals LLC on behalf of International Society on Thrombosis and Haemostasis (ISTH). https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Brief Reports Botton, Jérémie Semenzato, Laura Dupouy, Julie Dray‐Spira, Rosemary Weill, Alain Saint‐Lary, Olivier Zureik, Mahmoud No association of low‐dose aspirin with severe COVID‐19 in France: A cohort of 31.1 million people without cardiovascular disease |
title | No association of low‐dose aspirin with severe COVID‐19 in France: A cohort of 31.1 million people without cardiovascular disease |
title_full | No association of low‐dose aspirin with severe COVID‐19 in France: A cohort of 31.1 million people without cardiovascular disease |
title_fullStr | No association of low‐dose aspirin with severe COVID‐19 in France: A cohort of 31.1 million people without cardiovascular disease |
title_full_unstemmed | No association of low‐dose aspirin with severe COVID‐19 in France: A cohort of 31.1 million people without cardiovascular disease |
title_short | No association of low‐dose aspirin with severe COVID‐19 in France: A cohort of 31.1 million people without cardiovascular disease |
title_sort | no association of low‐dose aspirin with severe covid‐19 in france: a cohort of 31.1 million people without cardiovascular disease |
topic | Brief Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9204394/ https://www.ncbi.nlm.nih.gov/pubmed/35755854 http://dx.doi.org/10.1002/rth2.12743 |
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