Why the study?
Does proton pump inhibitor monotherapy increase the risk of adverse cardiovascular events in adults independent of clopidogrel?
Does proton pump inhibitor monotherapy increase the risk of adverse cardiovascular events in adults independent of clopidogrel?
There is no clear evidence from randomized controlled trials that PPI monotherapy increases cardiovascular risk independent of clopidogrel, despite an association seen in observational studies.
Observational associations should not alter PPI prescribing; reinforces RCT evidence of no independent cardiovascular risk.
Summary Background Clopidogrel's anti‐platelet effects may be attenuated by a pharmacokinetic interaction with co‐prescribed proton pump inhibitors, which inhibit oxidative pathways that convert clopidogrel into its active metabolites. Despite this, the impact of PPI s on cardiovascular risk in the absence of clopidogrel is not well defined. Aim To report on a systematic review and meta‐analysis of the association between PPI s and cardiovascular risk, independent of clopidogrel. Methods The databases of MEDLINE , EMBASE , Cochrane Central Register of Controlled Trials, Scopus, Web of Science, and ClinicalTrials.gov were systematically searched in October 2017. The primary outcome was association between PPI monotherapy and any adverse cardiovascular event. The secondary outcome was association between proton pump inhibitor monotherapy and acute myocardial infarction. Studies were excluded if they reported or did not adjust for concomitant anti‐platelet therapy or involved participants aged less than 18 years. Results A total of 22 studies were included in the systematic review. Data from 16 studies were included in the meta‐analysis (involving 447 408 participants). Of these, eight were randomised controlled trials, seven were observational studies and one was a retrospective analysis of a randomised controlled trial. An increased risk of any adverse cardiovascular event with PPI monotherapy was observed using pooled data from observational studies (risk ratio 1.25, 95% CI 1.11‐1.42, I 2 81%, P < 0.001), but not from randomised controlled trials (risk ratio 0.89, 95% CI 0.34‐2.33, I 2 0%, P = 0.85). Conclusion There is no clear evidence of an association between PPI monotherapy and increased cardiovascular risk.
No takes yet. Share an insight, caveat, or question.
Batchelor et al. (2018) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: