Gibson C Michael, Ten Yuli, Murphy Sabina A, Ciaglo Lauren N, Southard Matthew C, Lincoff A Michael, Waksman Ron
Cardiovascular Division, Beth Israel Deaconess Medical Center, Boston, Massachusetts, USA.
Am J Cardiol. 2007 Jun 15;99(12):1687-90. doi: 10.1016/j.amjcard.2007.01.053. Epub 2007 Apr 26.
The REPLACE-2 trial of patients who underwent urgent or elective percutaneous coronary intervention (PCI) demonstrated a significantly lower bleeding risk with bivalirudin plus provisional glycoprotein IIb/IIIa inhibitor compared with unfractionated heparin with planned glycoprotein IIb/IIIa inhibitor. The goal of this analysis was to evaluate whether a hazard existed when unfractionated heparin or low-molecular-weight heparin was administered before study medication in the REPLACE-2 trial. The REPLACE-2 trial randomized 6,010 patients undergoing PCI to receive bivalirudin plus provisional glycoprotein IIb/IIIa inhibitor or unfractionated heparin plus planned glycoprotein IIb/IIIa inhibitor. The present study compared bleeding among patients treated with or without antithrombin therapy in the 48 hours before study treatment. Among patients treated with bivalirudin, there was no difference in protocol-defined major or minor bleeding, bleeding according to Thrombolysis In Myocardial Infarction criteria, or noncoronary artery bypass graft blood transfusions between the patients treated with versus without antithrombin therapy (p=NS). However, in patients treated with unfractionated heparin plus planned glycoprotein IIb/IIIa inhibitor, there was a significant increase in the composite of protocol-defined major or minor bleeding and in noncoronary artery bypass graft blood transfusions (p<0.05 for 3-way comparison vs no unfractionated heparin and for 2-way comparisons of no unfractionated heparin vs unfractionated heparin or low-molecular-weight heparin). In conclusion, in patients treated with bivalirudin, pretreatment with antithrombin therapy was not associated with increased bleeding. In contrast, among patients randomized to receive unfractionated heparin and planned glycoprotein IIb/IIIa, pretreatment with antithrombin therapy was associated with increased protocol-defined composite major or minor bleeding and increased need for transfusion.
在接受紧急或择期经皮冠状动脉介入治疗(PCI)的患者中进行的REPLACE-2试验表明,与使用普通肝素加计划性糖蛋白IIb/IIIa抑制剂相比,比伐卢定加临时糖蛋白IIb/IIIa抑制剂的出血风险显著降低。本分析的目的是评估在REPLACE-2试验中,在研究用药前给予普通肝素或低分子量肝素是否存在风险。REPLACE-2试验将6010例接受PCI的患者随机分为两组,分别接受比伐卢定加临时糖蛋白IIb/IIIa抑制剂或普通肝素加计划性糖蛋白IIb/IIIa抑制剂。本研究比较了在研究治疗前48小时接受或未接受抗凝血酶治疗的患者的出血情况。在接受比伐卢定治疗的患者中,接受与未接受抗凝血酶治疗的患者在方案定义的严重或轻微出血、根据心肌梗死溶栓标准的出血或非冠状动脉搭桥输血方面没有差异(p=无显著性差异)。然而,在接受普通肝素加计划性糖蛋白IIb/IIIa抑制剂治疗的患者中,方案定义的严重或轻微出血与非冠状动脉搭桥输血的综合情况显著增加(与未使用普通肝素相比,三方比较p<0.05;与未使用普通肝素相比,普通肝素与低分子量肝素的两方比较p<0.05)。总之,在接受比伐卢定治疗的患者中,抗凝血酶治疗预处理与出血增加无关。相比之下,在随机接受普通肝素和计划性糖蛋白IIb/IIIa的患者中,抗凝血酶治疗预处理与方案定义的综合严重或轻微出血增加以及输血需求增加有关。