Cannon C P
Cardiovascular Division, Brigham and Women's Hospital, Boston, MA 02115, USA.
Clin Cardiol. 1999 Aug;22(8 Suppl):IV37-43. doi: 10.1002/clc.4960221607.
Although thrombolytic therapy has been a major advance in the treatment of acute ST-segment elevation myocardial infarction (MI), new thrombolytic agents have been unable to improve early reperfusion. Because aspirin has been shown to be a very effective adjunctive agent in patients with acute MI, it has been hypothesized that the use of platelet glycoprotein (GP) IIb/IIIa receptor inhibitors combined with thrombolytic agents would lead to more effective platelet inhibition and improved angiographic and clinical efficacy. Emerging experimental and clinical data, including the Thrombolysis in Myocardial Infarction (TIMI)-14 trial, suggest that combining GP IIb/IIIa receptor inhibition with reduced-dose thrombolytic therapy improves early infarct-related artery patency without increasing bleeding risk. Thus, given the strong clinical and physiologic rationale, clinical investigation in patients with acute ST-segment elevation MI is currently focused on combining GP IIb/IIIa receptor inhibitors with reduced-dose fibrinolytic agents in acute MI.
尽管溶栓治疗是急性ST段抬高型心肌梗死(MI)治疗的一项重大进展,但新型溶栓药物未能改善早期再灌注。由于阿司匹林已被证明是急性MI患者非常有效的辅助药物,因此有人推测,将血小板糖蛋白(GP)IIb/IIIa受体抑制剂与溶栓药物联合使用会导致更有效的血小板抑制,并改善血管造影和临床疗效。包括心肌梗死溶栓(TIMI)-14试验在内的新出现的实验和临床数据表明,将GP IIb/IIIa受体抑制与小剂量溶栓治疗相结合可改善早期梗死相关动脉通畅情况,而不增加出血风险。因此,鉴于强有力的临床和生理学依据,目前针对急性ST段抬高型MI患者的临床研究集中于在急性MI中将GP IIb/IIIa受体抑制剂与小剂量纤溶药物联合使用。