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急性 ST 段抬高型心肌梗死患者抗血小板治疗选择的循证评价。

An evidence-based review of current anti-platelet options for STEMI patients.

机构信息

Pitié-Salpêtrière University Hospital, France.

出版信息

Int J Cardiol. 2013 Jun 20;166(2):294-303. doi: 10.1016/j.ijcard.2012.04.160. Epub 2012 Jun 17.

DOI:10.1016/j.ijcard.2012.04.160
PMID:22709725
Abstract

Drug-eluting stents are the default treatment for acute coronary syndromes, unless concerns or contraindications preclude dual antiplatelet therapy (DAPT). Platelet microemboli and mediators from activated platelets can undermine the restoration of perfusion. Therefore, ST-segment elevation MI (STEMI) patients should receive antiplatelet treatments regardless of reperfusion strategy. This review offers an evidence-based comparison of the P2Y12 antagonists that have been evaluated in STEMI. While several studies support clopidogrel in STEMI, the benefits emerge several hours after administration and vary considerably reflecting genetic, cellular and clinical inter-individual differences. Although higher clopidogrel loading doses may improve outcomes, ticagrelor and prasugrel are more potent, produce less inter-individual variability, and show a faster onset of action. Ticagrelor and prasugrel improve outcomes compared to clopidogrel, with manageable bleeding risks, although further studies with a longer follow up are needed. Studies directly comparing ticagrelor and prasugrel are now needed. In the meantime, most current guidelines focus on clopidogrel and, therefore, need revision. While several polymorphisms influence platelet activity, CYP2C19 variants are the most consistently linked to clopidogrel responsiveness. Consensus groups should consider the studies needed to allow routine pharmacogenomic testing. The evidence-based use of P2Y12 antagonists in DAPT should further reduce the morbidity and mortality associated with STEMI.

摘要

药物洗脱支架是急性冠状动脉综合征的默认治疗方法,除非存在双重抗血小板治疗(DAPT)的相关顾虑或禁忌证。激活血小板产生的血小板微栓子和介质可能会破坏灌注的恢复。因此,无论再灌注策略如何,ST 段抬高型心肌梗死(STEMI)患者均应接受抗血小板治疗。本综述提供了在 STEMI 中评估的 P2Y12 拮抗剂的循证比较。虽然有几项研究支持氯吡格雷用于 STEMI,但获益在给药数小时后才显现,且因遗传、细胞和临床个体差异而差异很大。虽然较高的氯吡格雷负荷剂量可能改善结局,但替格瑞洛和普拉格雷作用更强、个体间变异性更小,且起效更快。与氯吡格雷相比,替格瑞洛和普拉格雷可改善结局,且出血风险可管理,但仍需要进行随访时间更长的进一步研究。目前需要开展直接比较替格瑞洛和普拉格雷的研究。同时,大多数现行指南主要关注氯吡格雷,因此需要进行修订。虽然多种多态性会影响血小板活性,但 CYP2C19 变异与氯吡格雷反应性的相关性最一致。共识小组应考虑开展必要的研究,以实现常规药物基因组检测。DAPT 中 P2Y12 拮抗剂的循证应用应进一步降低 STEMI 相关的发病率和死亡率。

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