Zeymer Uwe, Gitt Anselm, Zahn Ralf, Jünger Claus, Bauer Timm, Heer Tobias, Koeth Oliver, Senges Jochen
Herzzentrum Ludwigshafen, Medizinische Klinik B, Ludwigshafen, Germany.
EuroIntervention. 2009 Jan;4(4):524-8. doi: 10.4244/eijv4i4a88.
We sought to determine the efficacy of enoxaparin in unselected patients with STEMI treated with primary percutaneous coronary intervention in clinical practice.
In a retrospective analysis of the prospective MITRA-plus registry we compared the outcomes of patients with primary PCI and either enoxaparin or unfractionated heparin. A total of 2,655 patients with STEMI < 12 hours were included in this analysis, 374 (14%) were treated with enoxaparin and 2,281 (86%) with unfractionated heparin. In the univariate analysis enoxaparin reduced mortality (1.6% versus 6.0%, < 0.001), fewer non-fatal reinfarctions (1.9% versus 3.8%, p = 0.05) and no significant difference in major bleeding (5.6% versus 7.2%, p = 0.2) was observed. In the multivariable propensity score analysis enoxaparin was associated with a reduction in the combined endpoint of death and non-fatal reinfarction (odds ratio 0.42; 95% CI 0.2-0.8). This advantage was observed both in subgroups without (odds ratio 0.33 95% CI 0.1-0.8) and with GP IIb/IIIa inhibitors (odds ratio 0.44, 95% CI 0.2-1.0).
Our data suggest that in unselected patients with STEMI treated with primary PCI enoxaparin compared to unfractionated heparin reduces the combined endpoint of in-hospital death and reinfarction and does not increase severe bleeding complications.
我们试图确定在临床实践中,接受直接经皮冠状动脉介入治疗的非选择性ST段抬高型心肌梗死(STEMI)患者使用依诺肝素的疗效。
在对前瞻性MITRA-plus注册研究进行的回顾性分析中,我们比较了接受直接经皮冠状动脉介入治疗且使用依诺肝素或普通肝素的患者的结局。本分析共纳入2655例发病时间小于12小时的STEMI患者,其中374例(14%)接受依诺肝素治疗,2281例(86%)接受普通肝素治疗。单因素分析显示,依诺肝素降低了死亡率(1.6%对6.0%,P<0.001),非致命性再梗死发生率更低(1.9%对3.8%,P=0.05),且主要出血方面无显著差异(5.6%对7.2%,P=0.2)。在多变量倾向评分分析中,依诺肝素与死亡和非致命性再梗死的联合终点降低相关(比值比0.42;95%可信区间0.2-0.8)。在未使用(比值比0.33,95%可信区间0.1-0.8)和使用糖蛋白IIb/IIIa抑制剂(比值比0.44,95%可信区间0.2-1.0)的亚组中均观察到这一优势。
我们的数据表明,在接受直接经皮冠状动脉介入治疗的非选择性STEMI患者中,与普通肝素相比,依诺肝素可降低住院死亡和再梗死的联合终点,且不会增加严重出血并发症。