Department of Cardiology, The First Affiliated Hospital of Chongqing Medical University.
Department of Endocrinology, Diabetes Center of People's Liberation Army, Strategic Support Force Medical Center.
Int Heart J. 2021 Jul 30;62(4):742-751. doi: 10.1536/ihj.20-772. Epub 2021 Jul 6.
Previous studies have indicated that low-dose new generation of P2Y12 receptor antagonists may be more suitable compared with clopidogrel at a standard dose for the dual antiplatelet therapy (DAPT) for East Asian patients receiving percutaneous coronary intervention (PCI). However, there remains no consensus in clinical practice. Thus, in this study, we aimed to determine the efficacy and safety of low-dose P2Y12 receptor antagonists, compared to clopidogrel at a standard dose, in DAPT in East Asian patients after PCI. We systematically searched literatures for randomized controlled trials (RCT) comparing low-dose P2Y12 receptor antagonists with standard-dose clopidogrel for the treatment of East Asian patients undergoing PCI. The endpoints of efficacy include major adverse cardiac events (MACEs), all-cause mortality, and the number of target vessel revascularization. The indicators of safety include major and minor bleeding events. Heterogeneity was evaluated by I statistic test. Begg's and Egger's tests were used to evaluate publication bias. In total, 2,747 subjects from 8 RCT studies were included. Low-dose new P2Y12 receptor antagonists, that is, ticagrelor or prasugrel, showed significantly lower incidence of MACEs, as compared with standard-dose clopidogrel, in the East Asian patients who are in DAPT after undergoing PCI. Further, no difference was noted for the risk of major and minor bleeding events. In East Asian patients undergoing PCI and receiving DAPT, the use of low-dose P2Y12 receptor antagonists, ticagrelor or prasugrel, has been determined to be superior than clopidogrel at standard dose; this has been evidenced by a lower incidence of MACEs without increasing the risk of bleeding.
先前的研究表明,与标准剂量氯吡格雷相比,低剂量新一代 P2Y12 受体拮抗剂可能更适合东亚经皮冠状动脉介入治疗(PCI)患者的双联抗血小板治疗(DAPT)。然而,在临床实践中仍未达成共识。因此,本研究旨在确定低剂量 P2Y12 受体拮抗剂与标准剂量氯吡格雷在东亚 PCI 后患者 DAPT 中的疗效和安全性。我们系统地检索了比较低剂量 P2Y12 受体拮抗剂与标准剂量氯吡格雷治疗接受 PCI 的东亚患者的随机对照试验(RCT)文献。疗效终点包括主要不良心脏事件(MACEs)、全因死亡率和靶血管血运重建的数量。安全性指标包括主要和次要出血事件。采用 I 统计量检验评估异质性。采用 Begg 和 Egger 检验评估发表偏倚。共纳入 8 项 RCT 研究的 2747 例受试者。与标准剂量氯吡格雷相比,低剂量新型 P2Y12 受体拮抗剂,即替格瑞洛或普拉格雷,在东亚 PCI 后接受 DAPT 的患者中,MACEs 的发生率明显降低。此外,主要和次要出血事件的风险无差异。在接受 PCI 并接受 DAPT 的东亚患者中,使用低剂量 P2Y12 受体拮抗剂,即替格瑞洛或普拉格雷,优于标准剂量氯吡格雷;这表现为 MACEs 的发生率降低,而出血风险没有增加。