Short Versus One-Year Dual Antiplatelet Therapy After Percutaneous Coronary Intervention: an Updated Meta-Analysis.

IF 2.3 3区 医学 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS
Meghna Joseph, Mrinal Murali Krishna, Chidubem Ezenna, Vinicius Pereira, Mahmoud Ismayl, Michael G Nanna, Sripal Bangalore, Andrew M Goldsweig
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引用次数: 0

Abstract

The present guidelines recommend dual antiplatelet therapy (DAPT) for 6 to 12 months after percutaneous coronary intervention (PCI), with recent trials assessing the safety and efficacy of shortening DAPT duration to ≤3 months. A systematic search of PubMed, Scopus, and Cochrane Central databases identified studies comparing short DAPT, followed by P2Y12i monotherapy (78% ticagrelor) versus standard 12-month DAPT in patients who underwent PCI with a drug-eluting stent. A total of 9 randomized controlled trials, including 42,770 patients (short DAPT n = 21,370, 49.96%), of whom 28,307 (66.18%) presented with acute coronary syndrome (ACS). Short DAPT significantly reduced net adverse clinical events (NACEs) (risk ratio [RR] 0.78, 95% confidence interval [CI] 0.67 to 0.91, p = 0.001, I2 = 62%), major bleeding (RR 0.54, 95% CI 0.39 to 0.73, p <0.001, I2 = 63%), and any bleeding (RR 0.55, 95% CI 0.43 to 0.72, p <0.001, I2 = 77%) at 12 months compared with 1-year DAPT. No significant differences were observed in major adverse cardiovascular/cerebrovascular events, myocardial infarction, stroke, stent thrombosis, mortality, or revascularization. Ticagrelor monotherapy after short DAPT further reduced major adverse cardiovascular/cerebrovascular events (RR 0.85, 95% CI 0.73 to 0.99, p = 0.040, I² = 22%), NACE (RR 0.74, 95% CI 0.61 to 0.89, p = 0.001, I² = 68%), and major bleeding (RR 0.56, 95% CI 0.40 to 0.78, p <0.001, I² = 71%) compared with 1-year DAPT; however, the test for subgroup interaction (Pinteraction >0.05) for clopidogrel subgroup was not significant. P2Y12i monotherapy reduced the risk of NACEs (RR 0.77, 95%CI 0.66 to 0.90, p = 0.001, I2 = 52%, Pinteraction = 0.58) and major bleeding (RR 0.44, 95%CI 0.35 to 0.55, p <0.001, I2 = 0%, Pinteraction <0.01) in the ACS cohort but not in the chronic coronary syndrome cohort. In conclusion, short DAPT for ≤3 months followed by P2Y12i monotherapy (particularly, ticagrelor) was associated with decreased NACEs and bleeding without differences in other outcomes and should be considered a favorable option in patients with either ACS or chronic coronary syndrome after PCI with a drug-eluting stent.

经皮冠状动脉介入术后短期与 1 年双联抗血小板疗法:最新系统回顾和元分析。
目前的指南建议经皮冠状动脉介入治疗(PCI)后进行 6 至 12 个月的双联抗血小板疗法(DAPT),最近的试验评估了将 DAPT 持续时间缩短至 ≤3 个月的安全性和有效性。通过对 PubMed、Scopus 和 Cochrane Central 数据库进行系统性检索,发现了一些研究对使用药物洗脱支架(DES)接受 PCI 治疗的患者进行短 DAPT 后 P2Y12i 单药治疗(78% 为替卡格雷)与标准 12 个月 DAPT 进行了比较。共纳入了九项随机对照试验,包括 42,770 名患者(短期 DAPT n=21,370 人,占 49.96%),其中 28,307 人(66.18%)患有急性冠状动脉综合征(ACS)。与为期1年的DAPT相比,短DAPT可在12个月内明显降低NACE(RR 0.78;95%CI 0.67-0.91;P=0.001;I2=62%)、大出血(RR 0.54;95%CI 0.39-0.73;P2=63%)以及任何出血(RR 0.55;95%CI 0.43-0.72;P2=77%)。在MACCE、心肌梗死、中风、支架血栓形成、死亡率或血管重建方面未观察到明显差异。氯吡格雷亚组在短期 DAPT 后接受替卡格雷单药治疗可进一步降低 MACCE(RR 0.85,95% CI 0.73-0.99,p=0.040;I²=22%)、NACE(RR 0.74,95% CI 0.61-0.89,p=0.001;I²=68%)和大出血(RR 0.56,95% CI 0.40-0.78,pinteraction>0.05),但差异不显著。P2Y12i 单药治疗降低了 NACE(RR 0.77;95%CI 0.66-0.90;P=0.001;I2=52%,Pinteraction=0.58)和大出血(RR 0.44;95%CI 0.35-0.55;P2=0%,Pinteraction=0.58)的风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
American Journal of Cardiology
American Journal of Cardiology 医学-心血管系统
CiteScore
4.00
自引率
3.60%
发文量
698
审稿时长
33 days
期刊介绍: Published 24 times a year, The American Journal of Cardiology® is an independent journal designed for cardiovascular disease specialists and internists with a subspecialty in cardiology throughout the world. AJC is an independent, scientific, peer-reviewed journal of original articles that focus on the practical, clinical approach to the diagnosis and treatment of cardiovascular disease. AJC has one of the fastest acceptance to publication times in Cardiology. Features report on systemic hypertension, methodology, drugs, pacing, arrhythmia, preventive cardiology, congestive heart failure, valvular heart disease, congenital heart disease, and cardiomyopathy. Also included are editorials, readers'' comments, and symposia.
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