首页> 外文期刊>The American heart journal >The efficacy and safety of clopidogrel in vascular surgery patients with immediate postoperative asymptomatic troponin T release for the prevention of late cardiac events: Rationale and design of the Dutch Echocardiographic Cardiac Risk Evaluation Applying Stress Echo-VII (DECREASE-VII) trial.
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The efficacy and safety of clopidogrel in vascular surgery patients with immediate postoperative asymptomatic troponin T release for the prevention of late cardiac events: Rationale and design of the Dutch Echocardiographic Cardiac Risk Evaluation Applying Stress Echo-VII (DECREASE-VII) trial.

机译:氯吡格雷在术后立即无症状肌钙蛋白T释放以预防晚期心脏事件的血管外科手术患者中的功效和安全性:采用压力Echo-VII(DECREASE-VII)试验的荷兰超声心动图心脏风险评估的原理和设计。

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BACKGROUND: Major vascular surgery patients are at high risk for developing asymptomatic perioperative myocardial ischemia reflected by a postoperative troponin release without the presence of chest pain or electrocardiographic abnormalities. Long-term prognosis is severely compromised and characterized by an increased risk of long-term mortality and cardiovascular events. Current guidelines on perioperative care recommend single antiplatelet therapy with aspirin as prophylaxis for cardiovascular events. However, as perioperative surgical stress results in a prolonged hypercoagulable state, the postoperative addition of clopidogrel to aspirin within 7 days after perioperative asymptomatic cardiac ischemia could provide improved effective prevention for cardiovascular events. STUDY DESIGN: DECREASE-VII is a phase III, randomized, double-blind, placebo-controlled, multicenter clinical trial designed to evaluate the efficacy and safety of early postoperative dual antiplatelet therapy (aspirin and clopidogrel) for the prevention of cardiovascular events after major vascular surgery. Eligible patients undergoing a major vascular surgery (abdominal aorta or lower extremity vascular surgery) who developed perioperative asymptomatic troponin release are randomized 1:1 to clopidogrel or placebo (300-mg loading dose, followed by 75 mg daily) in addition to standard medical treatment with aspirin. The primary efficacy end point is the composite of cardiovascular death, stroke, or severe ischemia of the coronary or peripheral arterial circulation leading to an intervention. The evaluation of long-term safety includes bleeding defined by TIMI criteria. Recruitment began early 2010. The trial will continue until 750 patients are included and followed for at least 12 months. SUMMARY: DECREASE-VII is evaluating whether early postoperative dual antiplatelet therapy for patients developing asymptomatic cardiac ischemia after vascular surgery reduces cardiovascular events with a favorable safety profile.
机译:背景:大型血管外科手术患者发生肌钙蛋白释放后无胸痛或心电图异常,反映出无症状围手术期心肌缺血的高风险。长期预后严重受到损害,其特点是长期死亡和心血管事件的风险增加。当前围手术期护理指南建议使用抗阿司匹林的单一抗血小板疗法预防心血管事件。然而,由于围手术期的外科手术应激导致长时间的高凝状态,因此在围手术期无症状心脏缺血后7天内向阿司匹林中添加氯吡格雷可改善心血管事件的预防效果。研究设计:DECREASE-VII是一项III期,随机,双盲,安慰剂对照的多中心临床试验,旨在评估术后早期双重抗血小板治疗(阿司匹林和氯吡格雷)在预防重大心血管事件后的有效性和安全性。血管外科。符合条件的,进行围手术期无症状肌钙蛋白释放的大血管手术(腹主动脉或下肢血管手术)的患者,除标准药物治疗外,按1:1比例随机分配至氯吡格雷或安慰剂(300毫克负荷剂量,然后每天75毫克)与阿司匹林。主要功效终点是心血管死亡,中风或导致干预的冠状动脉或外周动脉循环严重缺血的综合症状。长期安全性评估包括TIMI标准定义的出血。招募始于2010年初。试验将持续进行,直到包括750名患者,并随访至少12个月。摘要:DECREASE-VII正在评估在血管外科手术后发生无症状性心脏缺血的患者中,术后早期双重抗血小板治疗是否可以降低心血管事件并具有良好的安全性。

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