首页> 美国卫生研究院文献>Vascular Health and Risk Management >Outcome of the HORIZONS-AMI trial: bivalirudin enhances long-term survival in patients with ST-elevation myocardial infarction undergoing angioplasty
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Outcome of the HORIZONS-AMI trial: bivalirudin enhances long-term survival in patients with ST-elevation myocardial infarction undergoing angioplasty

机译:HORIZONS-AMI试验的结果:比伐卢定可提高ST抬高型心肌梗死血管成形术患者的长期生存率

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摘要

Cardiovascular disease is the leading cause of death in the US. For patients with ST-elevation myocardial infarction (STEMI), urgent reperfusion of the culprit arterial occlusion, often achieved via primary percutaneous coronary intervention (PCI), reduces post-MI mortality and other major adverse cardiovascular events (MACE). Adjunctive antithrombotic and antiplatelet therapies are used during PCI to reduce MACE rates. Currently, a variety of antithrombotic options are available for peri-procedural use. The most commonly used agents include unfractionated heparin or low molecular weight heparin ± glycoprotein IIb/IIIa inhibitors (GPI). These agents reduce the rates of peri-procedural ischemic and thrombotic events, though these benefits come at the cost of an increase in bleeding complications. Bivalirudin is a direct thrombin inhibitor with a short half-life and linear pharmacokinetics, which results in predictable serum concentrations and anticoagulant effect. Bivalirudin has emerged as an efficacious and safe alternative to heparin plus GP IIb/IIIa inhibitors in both stable coronary artery disease and acute coronary syndrome patients. In the HORIZONS-AMI trial, monotherapy with bivalirudin was compared with the combination of heparin and a GPI in a large population of patients with STEMI who underwent primary PCI. Bivalirudin treatment was associated with improved event-free survival at 30 days and reduced rates of major bleeding. Based on the results of the trial, the American College of Cardiology/American Heart Association and European Society of Cardiology guidelines have incorporated recommendations for bivalirudin use in the setting of STEMI. Recently, 3-year follow-up data from the HORIZONS-AMI cohort were published, demonstrating sustained benefits in patients treated with bivalirudin, including reduced rates of mortality, cardiovascular mortality, reinfarction, and major bleeding events. These results further support the use of bivalirudin in the setting of primary PCI for STEMI given that its benefits are maintained through long-term follow-up.
机译:在美国,心血管疾病是主要的死亡原因。对于ST抬高型心肌梗死(STEMI)的患者,通常通过原发性经皮冠状动脉介入治疗(PCI)进行的急诊再灌注罪犯动脉闭塞可降低MI后死亡率和其他主要不良心血管事件(MACE)。 PCI期间使用辅助抗血栓和抗血小板疗法以降低MACE率。目前,围手术期使用了多种抗血栓药物。最常用的药物包括普通肝素或低分子量肝素±糖蛋白IIb / IIIa抑制剂(GPI)。这些药物降低了围手术期缺血和血栓形成事件的发生率,尽管这些益处是以增加出血并发症为代价的。比伐卢定是一种直接的凝血酶抑制剂,具有短的半衰期和线性的药代动力学,可导致可预测的血清浓度和抗凝作用。在稳定的冠状动脉疾病和急性冠脉综合征患者中,比伐卢定已成为肝素加GP IIb / IIIa抑制剂的一种有效且安全的替代品。在HORIZONS-AMI试验中,将比伐卢定单药治疗与肝素和GPI联合治疗在接受原发性PCI的大量STEMI患者中进行了比较。比伐卢定治疗与改善30天无事件生存率和减少大出血率有关。根据试验结果,美国心脏病学会/美国心脏协会和欧洲心脏病学会指南已将比伐卢定用于STEMI的建议纳入其中。最近,发表了HORIZONS-AMI队列的3年随访数据,证明了比伐卢定治疗患者的持续获益,包括降低的死亡率,心血管疾病的死亡率,再梗塞和重大出血事件。这些结果进一步支持了比伐卢定在STEMI的主要PCI中的应用,因为它的益处可以通过长期随访来维持。

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