Tantry Udaya S, Bliden Kevin P, Chaudhary Rahul, Novakovic Marko, Rout Amit, Gurbel Paul A
Sinai Center for Thrombosis Research, Sinai Hospital of Baltimore, LifeBridge Health, Baltimore, MD 21215, USA.
Division of Hospital Internal Medicine, Department of Internal Medicine, Mayo Clinic, Rochester, MN 55905, USA.
Future Cardiol. 2020 Sep;16(5):373-384. doi: 10.2217/fca-2019-0090. Epub 2020 Apr 20.
Vorapaxar specifically and effectively inhibits protease activated receptor-1 and may reduce thrombin-mediated ischemic events without interfering primary hemostasis. In the TRA-2P-TIMI 50 trial, vorapaxar reduced the risk of primary ischemic outcome but with increased bleeding risk. In the analysis, in patients with a history of myocardial infarction, peripheral artery disease, the net clinical outcome favored vorapaxar therapy with 10% reduction in cardiovascular death, myocardial infarction, stroke, urgent coronary revascularization and moderate or severe bleeding. Based on these favorable results, vorapaxar was approved for the reduction of thrombotic cardiovascular events in patients with prior myocardial infarction or with peripheral artery disease on top of standard antiplatelet therapy. A careful patient selection is needed to balance efficacy versus safety.
沃拉帕沙能特异性且有效地抑制蛋白酶激活受体-1,并且在不干扰原发性止血的情况下,可能降低凝血酶介导的缺血事件。在TRA-2P-TIMI 50试验中,沃拉帕沙降低了原发性缺血结局的风险,但出血风险增加。在分析中,对于有心肌梗死病史、外周动脉疾病的患者,总体临床结局有利于沃拉帕沙治疗,心血管死亡、心肌梗死、中风、紧急冠状动脉血运重建以及中度或重度出血风险降低了10%。基于这些有利结果,沃拉帕沙被批准用于在标准抗血小板治疗基础上,降低既往有心肌梗死或外周动脉疾病患者的血栓性心血管事件风险。需要谨慎选择患者以平衡疗效与安全性。