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首页> 外文期刊>American journal of therapeutics >Efficacy and Safety of Prasugrel Compared With Clopidogrel for Patients With Acute Coronary Syndrome Undergoing Percutaneous Coronary Intervention
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Efficacy and Safety of Prasugrel Compared With Clopidogrel for Patients With Acute Coronary Syndrome Undergoing Percutaneous Coronary Intervention

机译:普拉布雷的疗效和安全性与氯吡格雷对急性冠状动脉综合征进行经皮冠状动脉介入的患者相比

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Dual antiplatelet therapy comprising aspirin and a P2Y12 inhibitor (clopidogrel, prasugrel, or ticagrelor) is essential to prevent thrombotic complications after percutaneous coronary intervention (PCI). The comparative efficacy between clopidogrel at a higher loading dose (600 mg) and prasugrel is uncertain. The aim of this study was to compare efficacy and safety of clopidogrel (higher loading dose) with prasugrel (loading dose of 60 mg) along with their respective maintenance doses in patients with acute coronary syndrome (ACS) undergoing PCI at 1 year. This is a retrospective, observational, pilot study. Patients with ACS who underwent PCI and received clopidogrel 600 mg or prasugrel 60 mg loading dose followed by maintenance doses of 75 mg and 10 mg, respectively, daily between July 1, 2009 and June 30, 2011 were enrolled. For patients who have died during the study period, investigators attempted to identify the cause of deaths through medical records or death certificates. Two hundred twenty-one patients were enrolled in the study. Primary efficacy end point, composite of death from cardiovascular causes, nonfatal myocardial infarction, or nonfatal stroke occurring through 1 year were not significantly different between the 2 treatment groups. Bleeding events were also not significant between the clopidogrel (N = 136) and prasugrel (N = 85) groups: 9.6% versus 8.2%, P = 0.85. Prasugrel is at least as effective and safe as clopidogrel in patients with ACS undergoing early invasive management.
机译:包含阿司匹林和P2Y12抑制剂(Clopidogrel,Prasugrel或TiCagreloLor)的双抗血小板治疗对于预防经皮冠状动脉干预(PCI)后的血栓形成并发症是必不可少的。氯吡格雷在更高负荷剂量(600mg)和普拉布雷之间的比较疗效是不确定的。本研究的目的是将氯吡格雷(较高负荷剂量)与普拉什雷(负载剂量为60mg)的疗效和安全性以及其在1年急性冠状动脉综合征(ACS)患者中的各自的维持剂量。这是回顾性,观测,试点研究。接受PCI和接受氯吡格雷600毫克或普拉苏格雷60mg负载剂量的ACS患者,然后分别为每日75毫克和10毫克的维持剂量,2011年7月1日至6月30日之间进行了入学。对于在研究期间死亡的患者,调查人员试图通过医疗记录或死亡证明识别死亡原因。在研究中注册了两百二十一名患者。初级疗效终点,通过1年发生的心血管原因,非致癌心肌梗死或非致卒中的死亡复合在2个治疗组之间没有显着差异。氯吡格雷(n = 136)和普拉布雷(n = 85)组之间的出血事件也不重要:9.6%对8.2%,p = 0.85。 Prasugrel至少与ACS正在进行早期侵入性管理的患者中的氯吡格雷有效和安全。

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