Extended Clopidogrel Monotherapy vs DAPT in Patients With Acute Coronary Syndromes at High Ischemic and Bleeding Risk

医学 氯吡格雷 经皮冠状动脉介入治疗 传统PCI 临床终点 内科学 P2Y12 阿司匹林 心肌梗塞 心脏病学 冲程(发动机) 急性冠脉综合征 随机对照试验 机械工程 工程类
作者
Yang Li,Jing Li,Bin Wang,Quanmin Jing,Yujie Zeng,Aijie Hou,Zhifang Wang,Aijun Liu,Jinliang Zhang,Yaojun Zhang,Ping Zhang,Daming Jiang,Bin Liu,Jiamao Fan,Jun Zhang,Li Li,Guohai Su,Ming Yang,Weihong Jiang,Peng Qu,Hesong Zeng,Li Lu,Miaohan Qiu,Leisheng Ru,Shao‐Liang Chen,Yujie Zhou,Shubin Qiao,Gregg W. Stone,Dominick J. Angiolillo,Yaling Han
出处
期刊:JAMA Cardiology [American Medical Association]
标识
DOI:10.1001/jamacardio.2024.0534
摘要

Purinergic receptor P2Y12 (P2Y12) inhibitor monotherapy after a certain period of dual antiplatelet therapy (DAPT) may be an attractive option of maintenance antiplatelet treatment for patients undergoing percutaneous coronary intervention (PCI) who are at both high bleeding and ischemic risk (birisk).To determine if extended P2Y12 inhibitor monotherapy with clopidogrel is superior to ongoing DAPT with aspirin and clopidogrel after 9 to 12 months of DAPT after PCI in birisk patients with acute coronary syndromes (ACS).This was a multicenter, double-blind, placebo-controlled, randomized clinical trial including birisk patients with ACS who had completed 9 to 12 months of DAPT after drug-eluting stent implantation and were free from adverse events for at least 6 months at 101 China centers between February 2018 and December 2020. Study data were analyzed from April 2023 to May 2023.Patients were randomized either to clopidogrel plus placebo or clopidogrel plus aspirin for an additional 9 months.The primary end point was Bleeding Academic Research Consortium (BARC) types 2, 3, or 5 bleeding 9 months after randomization. The key secondary end point was major adverse cardiac and cerebral events (MACCE; the composite of all-cause death, myocardial infarction, stroke or clinically driven revascularization). The primary end point was tested for superiority, and the MACCE end point was tested for sequential noninferiority and superiority.A total of 7758 patients (mean [SD] age, 64.8 [9.0] years; 4575 male [59.0%]) were included in this study. The primary end point of BARC types 2, 3, or 5 bleeding occurred in 95 of 3873 patients (2.5%) assigned to clopidogrel plus placebo and 127 of 3885 patients (3.3%) assigned to clopidogrel plus aspirin (hazard ratio [HR], 0.75; 95% CI, 0.57-0.97; difference, -0.8%; 95% CI, -1.6% to -0.1%; P = .03). The incidence of MACCE was 2.6% (101 of 3873 patients) in the clopidogrel plus placebo group and 3.5% (136 of 3885 patients) in the clopidogrel plus aspirin group (HR, 0.74; 95% CI, 0.57-0.96; difference, -0.9%; 95% CI, -1.7% to -0.1%; P < .001 for noninferiority; P = .02 for superiority).Among birisk patients with ACS who completed 9 to 12 months of DAPT after drug-eluting stent implantation and were free from adverse events for at least 6 months before randomization, an extended 9-month clopidogrel monotherapy regimen was superior to continuing DAPT with clopidogrel in reducing clinically relevant bleeding without increasing ischemic events.ClinicalTrials.gov Identifier: NCT03431142.
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