首页> 外文OA文献 >Prasugrel compared with high loading- and maintenance-dose clopidogrel in patients with planned percutaneous coronary intervention: the Prasugrel in Comparison to Clopidogrel for Inhibition of Platelet Activation and Aggregation-Thrombolysis in Myocardial Infarction 44 trial
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Prasugrel compared with high loading- and maintenance-dose clopidogrel in patients with planned percutaneous coronary intervention: the Prasugrel in Comparison to Clopidogrel for Inhibition of Platelet Activation and Aggregation-Thrombolysis in Myocardial Infarction 44 trial

机译:普拉格雷与计划经皮冠状动脉介入治疗患者的高负荷和维持剂量氯吡格雷相比:普拉格雷与氯吡格雷相比,抑制血小板活化和凝血 - 心肌梗塞溶栓治疗44试验

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摘要

BACKGROUND: The increasing use of higher-than-approved doses of clopidogrel in clinical practice is based in part on the desire for greater levels of inhibition of platelet aggregation (IPA). Prasugrel is a new thienopyridine that is more potent than standard-dose clopidogrel in healthy subjects and patients with stable coronary artery disease. The relative antiplatelet effects of prasugrel versus high-dose clopidogrel in percutaneous coronary intervention patients are unknown.METHODS AND RESULTS: Prasugrel in Comparison to Clopidogrel for Inhibition of Platelet Activation and Aggregation-Thrombolysis in Myocardial Infarction 44 (PRINCIPLE-TIMI 44) was a randomized, double-blind, 2-phase crossover study of prasugrel compared with high-dose clopidogrel in patients undergoing cardiac catheterization for planned percutaneous coronary intervention. The primary end point of the loading-dose phase (prasugrel 60 mg versus clopidogrel 600 mg) was IPA with 20 mumol/L ADP at 6 hours. Patients with percutaneous coronary intervention entered the maintenance-dose phase, a 28-day crossover comparison of prasugrel 10 mg/d versus clopidogrel 150 mg/d with a primary end point of IPA after 14 days of either drug. In this study, 201 subjects were randomized. IPA at 6 hours was significantly higher in subjects receiving prasugrel (mean+/-SD, 74.8+/-13.0%) compared with clopidogrel (31.8+/-21.1%; Pandlt;0.0001). During the maintenance-dose phase, IPA with 20 mumol/L ADP was higher in subjects receiving prasugrel (61.3+/-17.8%) compared with clopidogrel (46.1+/-21.3%; Pandlt;0.0001). Results were consistent across all key secondary end points; significant differences emerged by 30 minutes and persisted across all time points.CONCLUSIONS: Among patients undergoing cardiac catheterization with planned percutaneous coronary intervention, loading with 60 mg prasugrel resulted in greater platelet inhibition than a 600-mg clopidogrel loading dose. Maintenance therapy with prasugrel 10 mg/d resulted in a greater antiplatelet effect than 150 mg/d clopidogrel.
机译:背景:在临床实践中越来越多地使用高于批准剂量的氯吡格雷部分是基于对更高水平抑制血小板聚集(IPA)的需求。普拉格雷(Prasugrel)是一种新的噻吩并吡啶,在健康受试者和患有稳定冠状动脉疾病的患者中,比标准剂量氯吡格雷更有效。方法和结果:普拉格雷与大剂量氯吡格雷在经皮冠状动脉介入治疗患者中的相对抗血小板作用尚不清楚。 ,普拉格雷与大剂量氯吡格雷在计划进行经皮冠状动脉介入治疗的心脏导管插入患者中进行的一项双盲,两阶段交叉研究。负荷剂量阶段的主要终点(普拉格雷60 mg对氯吡格雷600 mg)在6小时时为IPA,含20μmol/ L ADP。经皮冠状动脉介入治疗的患者进入维持剂量阶段,这两种药物的14天后,普拉格雷10 mg / d与氯吡格雷150 mg / d的主要终点为IPA,为期28天的比较。在这项研究中,将201名受试者随机分组。与氯吡格雷(31.8 +/- 21.1%; Pandlt; 0.0001)相比,接受普拉格雷的受试者在6小时时的IPA显着更高(平均+/- SD,74.8 +/- 13.0%)。在维持剂量阶段,接受普拉格雷(61.3 +/- 17.8%)的受试者的IPA和20μmol/ L ADP高于氯吡格雷(46.1 +/- 21.3%; Pandlt; 0.0001)。所有主要次要终点的结果均一致;结论:30分钟时出现显着差异,并且在所有时间点均持续存在。结论:在计划进行经皮冠状动脉介入治疗的情况下进行心脏导管插入的患者中,与600毫克氯吡格雷负荷剂量相比,60毫克普拉格雷对血小板的抑制作用更大。普拉格雷10 mg / d维持治疗比氯吡格雷150 mg / d产生更大的抗血小板作用。

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