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比较直接经皮冠状动脉介入治疗中应用阿昔单抗与小分子糖蛋白Ⅱb/Ⅲa 抑制剂的疗效:当代随机对照试验的荟萃分析。

A comparison of abciximab and small-molecule glycoprotein IIb/IIIa inhibitors in patients undergoing primary percutaneous coronary intervention: a meta-analysis of contemporary randomized controlled trials.

机构信息

Division of Cardiovascular Medicine, Department of Internal Medicine, University of Michigan Medical School, Ann Arbor, MI 48109-5853, USA.

出版信息

Circ Cardiovasc Interv. 2009 Jun;2(3):230-6. doi: 10.1161/CIRCINTERVENTIONS.108.847996. Epub 2009 Apr 21.

Abstract

BACKGROUND

Current guidelines recommend abciximab as the preferred agent for patients undergoing primary percutaneous coronary intervention, yet small-molecule glycoprotein IIb/IIIa inhibitors are more commonly used in clinical practice. The objective of our meta-analysis was to evaluate for differences in clinical outcome between small-molecule glycoprotein IIb/IIIa inhibitors and abciximab in patients with ST-segment elevation myocardial infarction undergoing primary percutaneous coronary intervention.

METHODS AND RESULTS

Five randomized trials (n=2138 patients) comparing tirofiban or eptifibatide with abciximab as an adjunctive therapy to primary percutaneous coronary intervention were included in this meta-analysis. Summary odds ratios (ORs) for 30-day death, reinfarction, and major bleeding were calculated using random- and fixed-effect models. There were no differences in 30-day mortality (1.9% for small molecule versus 2.3% for abciximab; OR, 0.84; 95% CI, 0.46 to 1.55; P=0.58), reinfarction (1.3% versus 1.2%; OR, 1.22; 95% CI, 0.51 to 2.91; P=0.69), or major bleeding (1.7% versus 1.3%; OR, 1.21; 95% CI, 0.58 to 2.49; P=0.61) between the 2 adjunctive strategies. Similarly, there was no significant difference in the incidence of death (3.9% versus 5%; OR, 0.77; 95% CI, 0.41 to 1.46; P=0.43) or reinfarction on follow-up at 8 months between small-molecule glycoprotein IIb/IIIa inhibitors and abciximab.

CONCLUSIONS

In patients undergoing primary percutaneous coronary intervention for ST-segment elevation myocardial infarction, no difference in outcome could be identified in patients treated with small-molecule glycoprotein IIb/IIIa inhibitor or abciximab.

摘要

背景

目前的指南建议将阿昔单抗作为行直接经皮冠状动脉介入治疗(PCI)的患者的首选药物,但在临床实践中小分子糖蛋白 IIb/IIIa 抑制剂更为常用。我们的荟萃分析旨在评估小分子糖蛋白 IIb/IIIa 抑制剂与阿昔单抗在接受直接 PCI 的 ST 段抬高型心肌梗死患者中的临床结局差异。

方法和结果

本荟萃分析纳入了 5 项比较替罗非班或依替巴肽与阿昔单抗作为直接 PCI 辅助治疗的随机试验(n=2138 例患者)。使用随机和固定效应模型计算 30 天死亡、再梗死和主要出血的汇总优势比(OR)。30 天死亡率(小分子组为 1.9%,阿昔单抗组为 2.3%;OR,0.84;95%CI,0.46 至 1.55;P=0.58)、再梗死率(1.3%与 1.2%;OR,1.22;95%CI,0.51 至 2.91;P=0.69)或主要出血率(1.7%与 1.3%;OR,1.21;95%CI,0.58 至 2.49;P=0.61)在这两种辅助策略之间没有差异。同样,在小分子糖蛋白 IIb/IIIa 抑制剂和阿昔单抗治疗的患者中,在 8 个月的随访时,死亡(3.9%与 5%;OR,0.77;95%CI,0.41 至 1.46;P=0.43)或再梗死的发生率也没有显著差异。

结论

在接受直接 PCI 治疗的 ST 段抬高型心肌梗死患者中,小分子糖蛋白 IIb/IIIa 抑制剂或阿昔单抗治疗的患者的结局没有差异。

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