Harrington R A
Duke Clinical Research Institute, Durham, North Carolina 27705, USA.
Am J Cardiol. 1997 Aug 18;80(4A):34B-38B. doi: 10.1016/s0002-9149(97)00575-4.
The acute ischemic coronary syndromes of unstable angina and non-Q-wave myocardial infarction are most commonly caused by intracoronary thrombosis at the site of ruptured atherosclerotic plaque. The main goals of therapy are the relief of ischemia and prevention of life-threatening thrombotic events. Current antithrombotic management includes heparin and aspirin, but recent insights into the pathophysiology of these syndromes have revealed that more effective management may be achieved by direct inhibition of the final common pathway to platelet aggregation--the platelet glycoprotein (GP) IIb-IIIa receptor. Earlier studies of the reversible peptide inhibitor of the GP IIb-IIIa receptor, eptifibatide (INTEGRILIN), in patients with unstable angina have demonstrated its potential in reducing acute ischemic events. The Platelet Glycoprotein IIb-IIIa in Unstable Angina: Receptor Suppression Using Integrilin Therapy (PURSUIT) trial, the largest clinical trial of any GP IIb-IIIa receptor inhibitor to date, is a recently completed phase III evaluation of eptifibatide as primary management for patients with acute coronary syndromes presenting without persistent ST-segment elevation.
不稳定型心绞痛和非Q波心肌梗死等急性缺血性冠状动脉综合征最常见的病因是动脉粥样硬化斑块破裂部位的冠状动脉内血栓形成。治疗的主要目标是缓解缺血并预防危及生命的血栓事件。目前的抗栓治疗包括肝素和阿司匹林,但最近对这些综合征病理生理学的深入了解表明,通过直接抑制血小板聚集的最终共同途径——血小板糖蛋白(GP)IIb-IIIa受体,可能实现更有效的治疗。早期对GP IIb-IIIa受体的可逆性肽抑制剂依替巴肽(INTEGRILIN)在不稳定型心绞痛患者中的研究已证明其在减少急性缺血事件方面的潜力。“不稳定型心绞痛中血小板糖蛋白IIb-IIIa:使用依替巴肽治疗的受体抑制”(PURSUIT)试验是迄今为止任何GP IIb-IIIa受体抑制剂最大规模的临床试验,是一项最近完成的III期评估,将依替巴肽作为无持续性ST段抬高的急性冠状动脉综合征患者的主要治疗方法。