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比伐卢定在经皮冠状动脉介入治疗患者常规治疗中的安全性和有效性。

Safety and effectiveness of bivalirudin in routine care of patients undergoing percutaneous coronary intervention.

机构信息

Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02120, USA.

出版信息

Eur Heart J. 2010 Mar;31(5):561-72. doi: 10.1093/eurheartj/ehp437. Epub 2009 Nov 25.

Abstract

AIMS

To evaluate the effectiveness and safety of bivalirudin as used in routine care. Bivalirudin has been studied as an alternative to heparin plus glycoprotein IIb/IIIa inhibitor (GPI) during percutaneous coronary intervention (PCI). Trials have indicated that bivalirudin is non-inferior to heparin with respect to death and repeat revascularization and may decrease the risk of major bleeds. The use of bivalirudin in routine care has not been evaluated.

METHODS AND RESULTS

Using a representative database, we identified 127 185 individuals who underwent inpatient PCI between June 2003 and December 2006 and were administered either bivalirudin plus provisional GPI or the comparator, heparin plus GPI. We estimated relative risks of blood transfusion, repeated PCI, and in-hospital death. The adjusted hazard ratio (HR) for blood transfusion was 0.67 (0.61-0.73); instrumental variable analysis showed an HR of 0.72 (0.12-4.47). We observed a risk of in-hospital death of 0.80% in the bivalirudin group and 2.1% in the heparin group; the adjusted HR was 0.51 (0.44-0.60).

CONCLUSION

In our non-randomized study of routine care, we observed a reduction in blood transfusions and in short-term mortality for patients treated with bivalirudin compared with heparin plus GPI. The mortality benefit was more pronounced in our study than in randomized trials.

摘要

目的

评估常规治疗中使用比伐卢定的疗效和安全性。比伐卢定已被研究作为经皮冠状动脉介入治疗(PCI)中肝素加糖蛋白 IIb/IIIa 抑制剂(GPI)的替代药物。试验表明,比伐卢定在死亡和再次血运重建方面不劣于肝素,并且可能降低大出血风险。比伐卢定在常规治疗中的应用尚未得到评估。

方法和结果

使用代表性数据库,我们确定了 2003 年 6 月至 2006 年 12 月期间接受住院 PCI 治疗的 127185 名个体,他们接受了比伐卢定加临时 GPI 或对照药物肝素加 GPI 治疗。我们估计了输血、重复 PCI 和住院期间死亡的相对风险。输血的调整后危险比(HR)为 0.67(0.61-0.73);工具变量分析显示 HR 为 0.72(0.12-4.47)。我们观察到比伐卢定组住院期间死亡风险为 0.80%,肝素组为 2.1%;调整后的 HR 为 0.51(0.44-0.60)。

结论

在我们对常规治疗的非随机研究中,与肝素加 GPI 相比,接受比伐卢定治疗的患者输血减少,短期死亡率降低。与随机试验相比,我们的研究中死亡率的获益更为显著。

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