Evidence map›Paper›PMID 40719229›Full record

ArticlePharmacotherapy2025

Effect of P2Y12 Inhibitors on Major Adverse Cardiovascular Events After Coronary Artery Bypass Graft Surgery: A Population-Based Cohort Study.

Arden R Barry, Hamed Helisaz, Abdollah Safari, Peter S Loewen

Abstract read
In one paragraph

Article in Pharmacotherapy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Arden R BarryFaculty of Pharmaceutical Sciences, The University of British Columbia, Vancouver, British Columbia, Canada.ORCID 0000-0002-0287-898X
Hamed HelisazGranTAZ Consulting, Vancouver, British Columbia, Canada.ORCID 0000-0001-7739-1407
Abdollah SafariSchool of Mathematics, Statistics, and Computer Science, College of Science, University of Tehran, Tehran, Iran.ORCID 0000-0001-9715-3086
Peter S LoewenFaculty of Pharmaceutical Sciences, The University of British Columbia, Vancouver, British Columbia, Canada.ORCID 0000-0001-7160-6438

Funding

Faculty of Pharmaceutical Sciences, University of British Columbia
6 · The paper itself

Abstract

backgroundPatients who undergo coronary artery bypass graft (CABG) surgery remain at high risk for major adverse cardiovascular events (MACE) despite contemporary preventive pharmacotherapy. Although commonly used in practice, it is uncertain whether P2Y12 inhibitors reduce MACE in patients post-CABG surgery.

methodsThis retrospective, population-based cohort study evaluated the effect of exposure to P2Y12 inhibitors, versus no exposure, on MACE using linked administrative databases that included all cardiac revascularization procedures, hospitalizations, and prescriptions for the population of British Columbia, Canada. All adults who underwent CABG surgery from 2002 to 2020 were eligible. The primary outcome was time to MACE, defined as a composite of all-cause death, nonfatal myocardial infarction, and nonfatal ischemic stroke using Cox proportional hazards models with inverse probability treatment weighting.

resultsIncluded were 15,439 patients. Mean age was 66 years, and 83% were male. Fifty-seven percent had a previous myocardial infarction. Sixteen percent were prescribed a P2Y12 inhibitor (of which, 83% were prescribed clopidogrel) within 30 days of CABG surgery. Median exposure time was 23 months. After probability-weighting and adjustment for relevant covariates, exposure to P2Y12 inhibitors reduced the 1- and 5-year hazard of MACE (hazard ratio [HR] 0.39, 95% confidence interval [CI] 0.27-0.55 and HR 0.65, 95% CI 0.54-0.79, respectively). Exposure to P2Y12 inhibitors was also associated with a lower hazard of all-cause death, cardiovascular death, and an extended MACE outcome that included unstable angina and percutaneous coronary intervention. Adherence to P2Y12 inhibitor therapy, based on the proportion of days covered, did not affect these outcomes.

conclusionsIn this population-based cohort study, use of P2Y12 inhibitors reduced the hazard of MACE in patients post-CABG surgery at 1 and 5 years of follow-up. These results support the use of P2Y12 inhibitors (primarily clopidogrel), in addition to other standard cardiovascular preventive therapy, in patients who undergo CABG surgery.

Indexed as

Cardiovascular DiseasesCoronary Artery BypassPostoperative ComplicationsPurinergic P2Y Receptor AntagonistsAgedBritish ColumbiaClopidogrelCohort StudiesFemaleHumansMaleMiddle AgedMyocardial InfarctionRetrospective StudiesClopidogrelPurinergic P2Y Receptor Antagonistscoronary artery bypasscoronary artery diseasemedication adherenceplatelet aggregation inhibitorspurinergic P2Y receptor antagonists

Identifiers

PMID40719229
PMCPMC12424524

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.