Does P2Y12 inhibitor monotherapy reduce bleeding or improve ischemic outcomes compared to dual antiplatelet therapy in patients after coronary revascularisation without an indication for oral anticoagulation?
P2Y12 inhibitor monotherapy after coronary revascularization provides similar ischemic protection but lower bleeding risk compared to DAPT.
OBJECTIVE: inhibitor monotherapy compared with dual antiplatelet therapy (DAPT) and whether these associations are modified by patients' characteristics. DESIGN: Individual patient level meta-analysis of randomised controlled trials. DATA SOURCES: Searches were conducted in Ovid Medline, Embase, and three websites (www.tctmd.com, www.escardio.org, www.acc.org/cardiosourceplus) from inception to 16 July 2020. The primary authors provided individual participant data. ELIGIBILITY CRITERIA: monotherapy and DAPT on centrally adjudicated endpoints after coronary revascularisation in patients without an indication for oral anticoagulation. MAIN OUTCOME MEASURES: The primary outcome was a composite of all cause death, myocardial infarction, and stroke, tested for non-inferiority against a margin of 1.15 for the hazard ratio. The key safety endpoint was Bleeding Academic Research Consortium (BARC) type 3 or type 5 bleeding. RESULTS: inhibitor rather than clopidogrel was part of the DAPT regimen. CONCLUSIONS: inhibitor monotherapy was associated with a similar risk of death, myocardial infarction, or stroke, with evidence that this association may be modified by sex, and a lower bleeding risk compared with DAPT. REGISTRATION: PROSPERO CRD42020176853.
Valgimigli et al. (Wed,) studied this question.
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