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Approaching an age of reason with antiplatelet therapy.

机译:抗血小板治疗已接近合理年龄。

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The antiplatelet drug prasugrel is one of a new generation of thienopyridines, drugs that inhibit the platelet P2Y12 receptor. With its increased active metabolite formation, prasugrel provides more rapid and consistent platelet inhibition than does clopidogrel.12The recently published TRITON-TIMI 38 trial was the first large-scale study to assess prasugrel in patients with acute coronary syndromes undergoing percutaneous coronary intervention. The trial established that the number of ischaemic events could be reduced by increasing the potency of platelet-inhibition. However, this was at the cost of an increased risk of major bleeding, especially in certain vulnerable subgroups.3 An important and prespecified subgroup analysis of TRITON-TIMI 38, focusing on patients who received coronary stents, is reported in today's Lancet.4 The so-called subgroup actually comprises 94% of the main study population, with outcomes similar to those in the main TRITON-TIMI 38 trial-an identical 0-81 hazard ratio for prasugrel versus clopidogrel for the primary ischaemic endpoint of cardiovascular death, non-fatal myocardial infarction, and stroke.
机译:抗血小板药物普拉格雷(Prasugrel)是新一代的噻吩并吡啶类药物,一种抑制血小板P2Y12受体的药物。由于普拉格雷的活性代谢物形成增加,因此与氯吡格雷相比,血小板抑制作用更快,更一致。12最近发表的TRITON-TIMI 38试验是第一项评估经皮冠状动脉介入治疗的急性冠脉综合征患者普拉格雷的大规模研究。该试验确定,可以通过增加血小板抑制的效力来减少缺血事件的数量。但是,这是以增加大出血的风险为代价的,尤其是在某些脆弱的亚组中。3如今的《柳叶刀》报道了TRITON-TIMI 38的一项重要且预先设定的亚组分析,重点是接受冠状动脉支架的患者。4所谓的亚组实际上占主要研究人群的94%,其结果与TRITON-TIMI 38主要试验中的结果相似-对于心血管死亡的主要缺血性终点,普拉格雷与氯吡格雷的危险比相同,为0-81,非致命的心肌梗塞和中风。

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  • 来源
    《The Lancet》 |2008年第9621期|共2页
  • 作者

    Ajani AE; Lefkovits J;

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