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新型口服P2Y12受体抑制剂在接受PCI的ST段抬高型心肌梗死患者中的疗效与安全性:一项系统评价和Meta分析

Efficacy and Safety of Novel Oral P2Y12 Receptor Inhibitors in Patients With ST-Segment Elevation Myocardial Infarction Undergoing PCI: A Systematic Review and Meta-Analysis.

作者信息

Sun Jianjun, Xiang Qian, Li Chao, Wang Zining, Hu Kun, Xie Qiufen, Cui Yimin

机构信息

*Department of Pharmacy, Peking University First Hospital, Beijing, China; and †Department of Pharmacy, Affiliated Hospital of Inner Mongolia Medical University, Hohhot, China.

出版信息

J Cardiovasc Pharmacol. 2017 Apr;69(4):215-227. doi: 10.1097/FJC.0000000000000459.

Abstract

The efficacy and safety of novel oral P2Y12 receptor inhibitors (prasugrel and ticagrelor) are subjects of contention in patients with ST-segment elevation myocardial infarction (STEMI) undergoing PCI, and the optimal duration of therapy remains uncertain. We searched PubMed, Embase, Cochrane Library, CNKI, VIP, and WanFang Data to identify randomized controlled trials comparing novel oral P2Y12 receptor inhibitors with clopidogrel in patients with STEMI undergoing PCI until February 2016. The primary efficacy and safety endpoint were all-cause mortality and major/minor bleeding. Twelve studies were included. Novel oral P2Y12 inhibitors significantly reduced the incidence of all-cause death (relative risk: 0.65, 95% confidence interval, 0.53-0.78), major adverse cardiac events [0.68 (0.56-0.83)], and stent thrombosis [0.56 (0.43-0.75)] without significant difference in bleeding (P = 0.11) compared with clopidogrel. Identical results were observed in the longer dual antiplatelet therapy (DAPT) and shorter-DAPT subgroups, albeit Chinese patients with ticagrelor treatment had a slight increase in bleeding (P = 0.08). Furthermore, the pooled relative risk ratio for each endpoint showed no significant difference between the longer-DAPT and shorter-DAPT subgroups. In conclusion, prasugrel and ticagrelor decreased the risk of all-cause death, major adverse cardiac events, and stent thrombosis without causing more bleeding events compared with clopidogrel in patients with STEMI undergoing PCI.

摘要

新型口服P2Y12受体抑制剂(普拉格雷和替格瑞洛)在接受经皮冠状动脉介入治疗(PCI)的ST段抬高型心肌梗死(STEMI)患者中的疗效和安全性存在争议,最佳治疗持续时间仍不确定。我们检索了PubMed、Embase、Cochrane图书馆、中国知网、维普资讯和万方数据,以确定截至2016年2月比较新型口服P2Y12受体抑制剂与氯吡格雷在接受PCI的STEMI患者中的随机对照试验。主要疗效和安全性终点为全因死亡率和主要/次要出血。纳入了12项研究。与氯吡格雷相比,新型口服P2Y12抑制剂显著降低了全因死亡发生率(相对风险:0.65,95%置信区间,0.53 - 0.78)、主要不良心脏事件[0.68(0.56 - 0.83)]和支架血栓形成[0.56(0.43 - 0.75)],出血方面无显著差异(P = 0.11)。在较长双联抗血小板治疗(DAPT)和较短DAPT亚组中观察到相同结果,尽管接受替格瑞洛治疗的中国患者出血略有增加(P = 0.08)。此外,各终点的合并相对风险比在较长DAPT和较短DAPT亚组之间无显著差异。总之,与氯吡格雷相比,普拉格雷和替格瑞洛降低了接受PCI的STEMI患者的全因死亡风险、主要不良心脏事件和支架血栓形成风险,且未导致更多出血事件。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a79/5578732/bb065db3fe81/jcvp-69-215-g001.jpg

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