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糖蛋白IIb/IIIa抑制剂联合纤溶治疗在急性心肌梗死中的应用。

Use of glycoprotein IIb/IIIa inhibition plus fibrinolysis in acute myocardial infarction.

作者信息

Hudson M P, Greenbaum A B, Harrington R A, Ohman E M

机构信息

Duke University Medical Center, Duke Clinical Research Institute, Durham, North Carolina 27715, USA.

出版信息

J Thromb Thrombolysis. 1999 Jun;7(3):241-5. doi: 10.1023/a:1008974909124.

Abstract

Pharmacological reperfusion therapy for acute myocardial infarction with intravenous fibrinolytic agents improves survival yet fails to achieve early and complete coronary blood flow in nearly half of treated patients. In principle, glycoprotein (GP) IIb/IIIa inhibitors, potent antiplatelet agents, might improve the efficacy and clinical outcomes associated with fibrinolysis. Preclinical research suggests more rapid and effective reperfusion with combined platelet GP IIb/IIIa inhibition and fibrinolysis. Early clinical studies confirm improved early patency and more rapid electrocardiographic resolution, but increased bleeding complications, with the addition of GP IIb/IIIa antagonists to conventional fibrinolysis. Future studies may combine reduced-dose fibrinolytic therapy with GP IIb/IIIa inhibition to optimize efficacy and safety.

摘要

使用静脉内纤维蛋白溶解剂对急性心肌梗死进行的药物再灌注治疗可提高生存率,但在近一半的治疗患者中未能实现早期和完全的冠状动脉血流。原则上,糖蛋白(GP)IIb/IIIa抑制剂这种强效抗血小板药物可能会提高与纤维蛋白溶解相关的疗效和临床结果。临床前研究表明,联合抑制血小板GP IIb/IIIa和纤维蛋白溶解可实现更快速有效的再灌注。早期临床研究证实,在传统纤维蛋白溶解治疗中添加GP IIb/IIIa拮抗剂可改善早期血管通畅并加快心电图恢复,但会增加出血并发症。未来的研究可能会将小剂量纤维蛋白溶解疗法与GP IIb/IIIa抑制相结合,以优化疗效和安全性。

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