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糖蛋白IIb/IIIa抑制剂临床试验结果概述。

An overview of the results of clinical trials with glycoprotein IIb/IIIa inhibitors.

作者信息

Adgey A A

机构信息

Royal Victoria Hospital, Belfast, Northern Ireland.

出版信息

Am Heart J. 1998 Apr;135(4):S43-55. doi: 10.1016/s0002-8703(98)70297-2.

Abstract

The era of platelet glycoprotein (GP) IIb/IIIa receptor inhibition in cardiology was inaugurated in 1994 with the publication of the Evaluation of 7E3 for the Prevention of Ischemic Complications (EPIC) trial results. EPIC demonstrated that the GP IIb/IIIa blocker abciximab, administered as a bolus and 12-hour infusion, afforded protection against ischemic complications in high-risk patients undergoing angioplasty and atherectomy, including those with unstable angina or evolving myocardial infarction (MI). A significant reduction in the incidence of death, acute MI, or revascularization was apparent at 30 days and also sustained at 6-month and 3-year follow-up. The subsequent Evaluation in PTCA to Improve Long-Term Outcome with Abciximab GP IIb/IIIa Blockade (EPILOG) study extended these findings to the full spectrum of coronary intervention patients, confirming that abciximab provided similar benefits in low-risk patients as well. The EPILOG trial also proved that any excess bleeding risk associated with potent antiplatelet therapy could be brought down to placebo levels through the use of a low-dose, weight-adjusted heparin regimen, early vascular sheath removal, and elimination of routine postprocedural heparinization. The potential for an advantage of GP IIb/IIIa blockade in patients with refractory unstable angina/non-Q-wave MI was demonstrated in the c7E3 Fab Antiplatelet Therapy in Unstable Refractory Angina (CAPTURE) trial, which showed that a 24-hour preprocedural abciximab infusion effectively stabilized these patients, thereby enhancing the safety of intervention and reducing the 30-day incidence of ischemic events. A similar pattern of benefit has emerged from clinical trials of such other GP IIb/IIIa inhibitors as eptifibatide, lamifiban, and tirofiban. Trials are currently underway to clarify the benefits of GP IIb/IIIa blockers in patients undergoing stenting and as an adjunct to thrombolytic therapy or primary angioplasty in patients with acute MI (ST-segment elevation).

摘要

1994年,随着《7E3预防缺血性并发症的评估》(EPIC)试验结果的发表,心脏病学领域血小板糖蛋白(GP)IIb/IIIa受体抑制时代拉开了帷幕。EPIC试验表明,作为推注和12小时输注给药的GP IIb/IIIa阻滞剂阿昔单抗,可为接受血管成形术和旋切术的高危患者(包括不稳定型心绞痛或进展性心肌梗死患者)预防缺血性并发症。在30天时,死亡、急性心肌梗死或血运重建的发生率显著降低,并且在6个月和3年随访时仍持续降低。随后的《阿昔单抗GP IIb/IIIa阻断在PTCA中改善长期预后的评估》(EPILOG)研究将这些发现扩展至所有冠状动脉介入治疗患者,证实阿昔单抗在低危患者中也有类似益处。EPILOG试验还证明,通过使用低剂量、根据体重调整的肝素方案、早期拔除血管鞘以及取消术后常规肝素化,与强效抗血小板治疗相关的任何额外出血风险都可降至安慰剂水平。在《不稳定难治性心绞痛的c7E3 Fab抗血小板治疗》(CAPTURE)试验中证实了GP IIb/IIIa阻断在难治性不稳定型心绞痛/非Q波心肌梗死患者中的潜在优势,该试验表明术前24小时输注阿昔单抗可有效稳定这些患者,从而提高干预的安全性并降低30天缺血事件的发生率。其他GP IIb/IIIa抑制剂(如依替巴肽、拉米非班和替罗非班)的临床试验也出现了类似的获益模式。目前正在进行试验,以阐明GP IIb/IIIa阻滞剂在接受支架置入术的患者中的益处,以及作为急性心肌梗死(ST段抬高)患者溶栓治疗或直接血管成形术辅助治疗的益处。

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