Kleiman N S, Lincoff A M, Ohman E M, Harrington R A
Baylor College of Medicine and the Methodist Hospital, Houston, Tex, USA.
Am Heart J. 1998 Oct;136(4 Pt 2 Su):S32-42. doi: 10.1053/hj.1998.v136.93434.
The pathophysiologic basis for potent platelet inhibition in the acute coronary syndromes has been established. In the setting of PTCA for unstable angina and non-Q-wave myocardial infarction, there are clear data for a benefit of GP IIb/IIIa inhibition, whereas for primary PTCA in evolving myocardial infarction, preliminary data are very encouraging and a large-scale clinical trial is nearly completed. Glycoprotein IIb/IIIa inhibition as an adjunct to medical therapy for unstable angina is also the subject of encouraging preliminary data, and 3 large-scale clinical trials have just been completed. Preliminary data have also been accrued for GP IIb/IIIa inhibition as conjunctive therapy with thrombolytic agents, and large clinical trials are now commencing.
急性冠状动脉综合征中强效血小板抑制的病理生理基础已经确立。在不稳定型心绞痛和非Q波心肌梗死的经皮冠状动脉腔内血管成形术(PTCA)情况下,有明确数据表明糖蛋白(GP)IIb/IIIa抑制具有益处;而在进展性心肌梗死的直接PTCA中,初步数据非常令人鼓舞,一项大规模临床试验即将完成。糖蛋白IIb/IIIa抑制作为不稳定型心绞痛药物治疗的辅助手段,也有令人鼓舞的初步数据,并且刚刚完成了3项大规模临床试验。关于糖蛋白IIb/IIIa抑制作为溶栓剂联合治疗的初步数据也已积累,大型临床试验现已开始。