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Stroke risk and NSAIDs: a systematic review of observational studies

Authors


  • On behalf of the Investigators of The Safety of Nonsteroidal Anti-inflammatory Drugs (SOS) project http://www.sos-nsaids-project.org/

  • NRG and CVL abstracted and compiled the data, BC performed the analyses, and CVL drafted the manuscript. CVL, NRG, BC, JC, AP, LS, MS, and SPG facilitated the interpretation of the findings. CVL, NRG, JC, AP, LS, MS, and SPG oversaw the design of the study and helped to draft the manuscript. All coauthors participated in the writing of the manuscript and approved the version submitted for publication.

C. Varas-Lorenzo, RTI Health Solutions, Travesera de Gracia 56, Atico 1º, 08006, Barcelona 02451, Spain. E-mail: cvaras@rti.org

ABSTRACT

Aims

To perform a quantitative systematic review of observational studies on the risk of stroke associated with the use of individual NSAIDs.

Methods and results

Searches were conducted using the Medline database within PubMed (1990–2008). Observational cohort or case–control studies were eligible if reported on the risk of cardiovascular events associated with individual NSAIDs versus the nonuse of NSAIDs. We found 3193 articles, in which 75 were eligible for review and abstraction. Of the 75 articles, 6 reported relative risk (RR) of stroke. Data were abstracted into a database using a standardized entry form. Two authors assessed study quality, and discrepancies were resolved by consensus.

The pooled RR of all subtypes of incident stroke was increased with the current use of rofecoxib (RR = 1.64, 95% CI = 1.15–2.33) and diclofenac (RR = 1.27, 95% CI = 1.08–1.48). The pooled estimates for naproxen, ibuprofen, and celecoxib were close to unity. The risk of ischemic stroke was also increased with rofecoxib (RR = 1.82, 95% CI = 1.09–3.04) and diclofenac (RR = 1.20, 95% CI = 0.99–1.45). Data were inadequate to estimate the pooled RR by dose and duration, for other individual NSAIDs or nonischemic stroke subtypes.

Conclusion

This meta-analysis supports an increased risk of ischemic stroke with the current use of rofecoxib and diclofenac. Additional studies are required to evaluate most individual NSAIDS, the effect of dose and duration, and the subtypes of stroke. Copyright © 2011 John Wiley & Sons, Ltd.

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