首页> 外文期刊>JAMA: the Journal of the American Medical Association >Standard- vs high-dose clopidogrel based on platelet function testing after percutaneous coronary intervention: the GRAVITAS randomized trial.
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Standard- vs high-dose clopidogrel based on platelet function testing after percutaneous coronary intervention: the GRAVITAS randomized trial.

机译:基于经皮冠状动脉介入后血小板函数检测的标准化高剂量氯吡格雷:Gravitas随机试验。

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CONTEXT: High platelet reactivity while receiving clopidogrel has been linked to cardiovascular events after percutaneous coronary intervention (PCI), but a treatment strategy for this issue is not well defined. OBJECTIVE: To evaluate the effect of high-dose compared with standard-dose clopidogrel in patients with high on-treatment platelet reactivity after PCI. DESIGN, SETTING, AND PATIENTS: Randomized, double-blind, active-control trial (Gauging Responsiveness with A VerifyNow assay-Impact on Thrombosis And Safety [GRAVITAS]) of 2214 patients with high on-treatment reactivity 12 to 24 hours after PCI with drug-eluting stents at 83 centers in North America between July 2008 and April 2010. INTERVENTIONS: High-dose clopidogrel (600-mg initial dose, 150 mg daily thereafter) or standard-dose clopidogrel (no additional loading dose, 75 mg daily) for 6 months. MAIN OUTCOME MEASURES: The primary end point was the 6-month incidence of death from cardiovascular causes, nonfatal myocardial infarction, or stent thrombosis. The key safety end point was severe or moderate bleeding according to the Global Utilization of Streptokinase and t-PA for Occluded Coronary Arteries (GUSTO) definition. A key pharmacodynamic end point was the rate of persistently high on-treatment reactivity at 30 days. RESULTS: At 6 months, the primary end point had occurred in 25 of 1109 patients (2.3%) receiving high-dose clopidogrel compared with 25 of 1105 patients (2.3%) receiving standard-dose clopidogrel (hazard ratio [HR], 1.01; 95% confidence interval [CI], 0.58-1.76; P = .97). Severe or moderate bleeding was not increased with the high-dose regimen (15 [1.4%] vs 25 [2.3%], HR, 0.59; 95% CI, 0.31-1.11; P = .10). Compared with standard-dose clopidogrel, high-dose clopidogrel provided a 22% (95% CI, 18%-26%) absolute reduction in the rate of high on-treatment reactivity at 30 days (62%; 95% CI, 59%-65% vs 40%; 95% CI, 37%-43%; P < .001). CONCLUSIONS: Among patients with high on-treatment reactivity after PCI with drug-eluting stents, the use of high-dose clopidogrel compared with standard-dose clopidogrel did not reduce the incidence of death from cardiovascular causes, nonfatal myocardial infarction, or stent thrombosis. TRIAL REGISTRATION: clinicaltrials.gov Identifier: NCT00645918.
机译:背景信息:在经皮冠状动脉干预(PCI)后,接受氯吡格雷的高血小板反应性与心血管事件有关,但该问题的治疗策略并不明确。目的:评价高剂量与PCI高治疗血小板反应性患者的标准剂量氯吡格雷相比。设计,设定和患者:随机,双盲,主动控制试验(用VerifyNow测定的血栓和安全性对血栓形成和安全性的响应性 - 血栓形成和安全性[Gravitas])在PCI后12至24小时的2214名患者2008年7月和2010年4月的北美83个中心的药物洗脱支架。干预:高剂量氯吡格雷(600mg初始剂量,每日150毫克)或标准剂量氯吡格雷(每天没有额外的负载剂量,每日75毫克) 6个月。主要观察措施:主要终点是心血管原因,非缺乏心肌梗死或支架血栓形成的6个月死亡率。关键安全终点根据链孢菌酶和T-PA用于闭塞冠状动脉(GUSTO)定义的全球使用严重或中等出血。关键药效学结束点是30天持续高处理的持续性反应性的速率。结果:6个月,1109名患者(2.3%)的主要终点接受高剂量氯吡格雷,与1105名患者(2.3%)接受标准剂量氯吡格雷(危险比[HR],1.01; 95%置信区间[CI],0.58-1.76; p = .97)。使用高剂量方案(15 [1.4%],HR,0.59; 95%CI,0.31-1.11; P = .10),严重或中度出血不会增加(15 [1.4%],HR,0.59; p = .10)。与标准剂量氯吡格雷相比,高剂量氯吡格雷提供22%(95%CI,18%-26%)的绝对降低在30天的高处理反应性的速率下降(62%; 95%CI,59% -65%vs 40%; 95%CI,37%-43%; P <.001)。结论:在PCI与药物洗脱支架高剂量后的患者患者中,与标准剂量氯吡格雷相比,使用高剂量氯吡格雷并未降低心血管原因,非缺乏心肌梗死或支架血栓形成死亡的发生率。试验注册:ClinicalTrials.gov标识符:NCT00645918。

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