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比较接受有创策略的患者中比伐卢定与肝素加糖蛋白 IIb/IIIa 抑制剂的疗效:随机临床试验的荟萃分析。

Comparison of bivalirudin versus heparin plus glycoprotein IIb/IIIa inhibitors in patients undergoing an invasive strategy: a meta-analysis of randomized clinical trials.

机构信息

David Geffen School of Medicine at University of California, Los Angeles (Division of Cardiology), Los Angeles, CA, United States.

出版信息

Int J Cardiol. 2011 Nov 3;152(3):369-74. doi: 10.1016/j.ijcard.2010.08.007. Epub 2010 Sep 16.

Abstract

OBJECTIVE

This meta-analysis was performed to assess the efficacy and safety of bivalirudin compared with unfractionated heparin or enoxaparin plus glycoprotein (GP) IIb/IIIa inhibitors in patients undergoing percutaneous coronary intervention (PCI).

BACKGROUND

Pharmacotherapy for patients undergoing PCI includes bivalirudin, heparin, and GP IIb/IIIa inhibitors. We sought to compare ischemic and bleeding outcomes with bivalirudin versus heparin plus GP IIb/IIIa inhibitors in patients undergoing PCI.

METHODS

A literature search was conducted to identify fully published randomized trials that compared bivalirudin with heparin plus GP IIb/IIIa inhibitors in patients undergoing PCI.

RESULTS

A total of 19,772 patients in 5 clinical trials were included in the analysis (9785 patients received bivalirudin and 9987 patients received heparin plus GP IIb/IIIa inhibitors during PCI). Anticoagulation with bivalirudin, as compared with heparin plus glycoprotein IIb/IIIa inhibitors, results in no difference in major adverse cardiovascular events (odds ratio [OR] 1.07, 95% confidence interval [CI] 0.96 to 1.19), death (OR 0.93, 95% CI 0.72 to 1.21), or urgent revascularization (OR 1.06, 95% CI 0.86 to 1.30). There is a trend towards a higher risk of myocardial infarction (OR 1.12, 95% CI 0.99 to 1.28) but a significantly lower risk of TIMI major bleeding with bivalirudin (OR 0.55, 95% CI 0.44 to 0.69).

CONCLUSION

In patients who undergo PCI, anticoagulation with bivalirudin as compared with unfractionated heparin or enoxaparin plus GP IIb/IIIa inhibitors results in similar ischemic adverse events but a reduction in major bleeding.

摘要

目的

本荟萃分析旨在评估与未分级肝素或依诺肝素加糖蛋白(GP)IIb/IIIa 抑制剂相比,比伐卢定在接受经皮冠状动脉介入治疗(PCI)的患者中的疗效和安全性。

背景

接受 PCI 的患者的药物治疗包括比伐卢定、肝素和 GP IIb/IIIa 抑制剂。我们旨在比较比伐卢定与肝素加 GP IIb/IIIa 抑制剂在接受 PCI 的患者中的缺血和出血结局。

方法

进行了文献检索,以确定比较比伐卢定与肝素加 GP IIb/IIIa 抑制剂在接受 PCI 的患者中的完全发表的随机试验。

结果

共有 5 项临床试验中的 19772 名患者纳入分析(9785 名患者接受比伐卢定治疗,9987 名患者在 PCI 期间接受肝素加 GP IIb/IIIa 抑制剂治疗)。与肝素加糖蛋白 IIb/IIIa 抑制剂相比,比伐卢定抗凝治疗在主要不良心血管事件(比值比 [OR] 1.07,95%置信区间 [CI] 0.96 至 1.19)、死亡(OR 0.93,95% CI 0.72 至 1.21)或紧急血运重建(OR 1.06,95% CI 0.86 至 1.30)方面无差异。心肌梗死的风险呈上升趋势(OR 1.12,95% CI 0.99 至 1.28),但比伐卢定 TIMI 主要出血的风险显著降低(OR 0.55,95% CI 0.44 至 0.69)。

结论

在接受 PCI 的患者中,与未分级肝素或依诺肝素加 GP IIb/IIIa 抑制剂相比,比伐卢定抗凝治疗可导致相似的缺血不良事件,但大出血减少。

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