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用于降低急性冠脉综合征患者支架血栓形成的普拉格雷和替格瑞洛的药物治疗考虑。

Pharmacotherapeutic considerations for the use of prasugrel and ticagrelor to reduce stent thrombosis in patients with acute coronary syndrome.

机构信息

1Department of Clinical Medicine, Cardiovascular Sciences and Immunology, Federico II University, Naples, Italy.

出版信息

Angiology. 2014 Feb;65(2):130-6. doi: 10.1177/0003319712467530. Epub 2012 Dec 4.

Abstract

Despite the improvement in stent technology, stent thrombosis (ST), a potentially catastrophic event, still occurs. Among several risk factors for ST, high on-treatment platelet reactivity to clopidogrel has been demonstrated to play a role, occurring in about one-third of the patients. In order to overcome this limitation, prasugrel and ticagrelor, newer P2Y12 inhibitors, have been developed and approved for clinical use. Two large clinical trials, TRial to assess Improvement in Therapeutic Outcomes by optimizing platelet inhibitioN with prasugrel-thrombolysis in myocardial infarction (TRITON-TIMI) 38 and Study of Platelet Inhibition and Patient Outcomes (PLATO), evaluated these drugs in patients with acute coronary syndrome (ACS), showing a significant improvement in efficacy end points (including a prominent reduction in ST occurrence) compared to clopidogrel. In contrast, the TRILOGY ACS trial found no benefit with prasugrel compared to clopidogrel in patients with medically treated ACS. The aim of this review is to consider decision-making strategies between prasugrel and ticagrelor in daily clinical practice.

摘要

尽管支架技术有所改进,但支架血栓形成(ST)仍然是一种潜在的灾难性事件。在 ST 的几个危险因素中,氯吡格雷治疗后的血小板高反应性已被证明起作用,约三分之一的患者存在这种情况。为了克服这一局限性,新型 P2Y12 抑制剂普拉格雷和替格瑞洛已被开发并批准用于临床。两项大型临床试验——评估通过优化血小板抑制治疗改善治疗结局的噻吩并吡啶试验(TRITON-TIMI)38 研究和血小板抑制与患者结局研究(PLATO),评估了这些药物在急性冠脉综合征(ACS)患者中的疗效终点(包括 ST 发生率的显著降低),与氯吡格雷相比,疗效显著改善。相比之下,TRILOGY ACS 试验发现,在接受药物治疗的 ACS 患者中,与氯吡格雷相比,普拉格雷并无获益。本综述旨在考虑在日常临床实践中,在普拉格雷和替格瑞洛之间做出决策的策略。

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