Ferguson J J, Kereiakes D J, Adgey A A, Fox K A, Hillegass W B, Pfisterer M, Vassanelli C
Texas Heart Institute, Houston 77225-0345, USA.
Am Heart J. 1998 Apr;135(4):S77-89. doi: 10.1016/s0002-8703(98)70300-x.
The platelet membrane glycoprotein IIb/IIIa receptor inhibitor abciximab is used for the treatment of patients undergoing high-risk percutaneous coronary interventions and is used in approximately one third of coronary interventions in the United States and a growing number of procedures in Europe. Recent clinical trials have shown that this potent antiplatelet agent significantly reduces the incidence of death and nonfatal myocardial infarction and the need for revascularization. With expanding experience since the commercial release of abciximab in February 1995, several strategies to enhance the safety of abciximab have emerged. In particular, new data confirm that the risk of bleeding-identified as a concern in the original EPIC trial-can be substantially reduced through the use of low-dose adjunctive heparin, early sheath removal, and fastidious postprocedure vascular access site care. Other recommendations for enhancing the safety of potent antiplatelet agents in a variety of clinical situations are provided. The following article reflects insights regarding the safety of glycoprotein IIb/IIIa inhibitors expressed by a group of international experts convened in Davos, Switzerland, February 16, 1997 This report attempts to review clinical progress to date, formulate recommendations, and map out potentially fruitful lines of inquiry for future investigation.
血小板膜糖蛋白IIb/IIIa受体抑制剂阿昔单抗用于治疗接受高风险经皮冠状动脉介入治疗的患者,在美国约三分之一的冠状动脉介入治疗中使用,在欧洲使用的手术数量也在不断增加。最近的临床试验表明,这种强效抗血小板药物可显著降低死亡和非致命性心肌梗死的发生率以及血管再通的需求。自1995年2月阿昔单抗上市以来,随着经验的不断积累,出现了几种提高阿昔单抗安全性的策略。特别是,新数据证实,通过使用低剂量辅助肝素、早期拔除鞘管以及精心护理术后血管穿刺部位,可大幅降低在最初的EPIC试验中被视为问题的出血风险。本文还提供了在各种临床情况下提高强效抗血小板药物安全性的其他建议。以下文章反映了1997年2月16日在瑞士达沃斯召开的一组国际专家对糖蛋白IIb/IIIa抑制剂安全性的见解。本报告试图回顾迄今为止的临床进展,制定建议,并规划未来研究可能富有成果的探究方向。