Effect of low‐dose aspirin on health outcomes: An umbrella review of systematic reviews and meta‐analyses

Nicola Veronese, Jacopo Demurtas, Trevor Thompson, Marco Solmi, Gabriella Pesolillo, Stefano Celotto, Tommaso Barnini, Brendon Stubbs, Stefania Maggi, Alberto Pilotto, Graziano Onder, Evropi Theodoratou, Alberto Vaona, Joseph Firth, Lee Smith, Ai Koyanagi, John P.a. Ioannidis, Ioanna Tzoulaki

Research output: Contribution to journalArticlepeer-review


Methods Aspirin is associated with several health outcomes, but the overall benefit/risk balance related to aspirin use is unclear. We searched three major databases up to 15 August 2019 for meta‐analyses of observational studies and randomized controlled trials (RCTs) including low‐dose aspirin compared to placebo or other treatments. Based on random‐effects summary effect sizes, 95% prediction intervals, heterogeneity, small‐study effects and excess significance, significant meta‐analyses of observational studies were classified from convincing (class I) to weak (class IV). For meta‐analyses of RCTs, outcomes with random effects P ‐value < .005 and a moderate/high GRADE assessment, were classified as strong evidence. From 6802 hits, 67 meta‐analyses (156 outcomes) were eligible. Results Observational data showed highly suggestive evidence for aspirin use and increased risk of upper gastrointestinal bleeding (RR = 2.28, 95% CI: 1.97–2.64). In RCTs of low‐dose aspirin, we observed strong evidence for lower risk of CVD in people without CVD (RR = 0.83; 95% CI: 0.79–0.87) and in general population (RR = 0.83; 95% CI: 0.79–0.89), higher risk of major gastrointestinal (RR = 1.47; 95% CI: 1.26–1.72) and intracranial bleeding (RR = 1.34; 95% CI: 1.18–1.53), and of major bleedings in people without CVD (RR = 1.62; 95% CI: 1.26–2.08). Conclusion Compared to other active medications, low‐dose aspirin had strong evidence for lower risk of bleeding, but also lower comparative efficacy. Low‐dose aspirin significantly lowers CVD risk and increases risk of bleeding. Evidence for multiple other health outcomes is limited.
Original languageEnglish
JournalBritish Journal of Clinical Pharmacology
Publication statusPublished - 2 Jun 2020


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