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首页> 外文期刊>International Journal of Cardiology >Intracoronary abciximab reduces death and major adverse cardiovascular events in acute coronary syndromes: A meta-analysis of clinical trials
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Intracoronary abciximab reduces death and major adverse cardiovascular events in acute coronary syndromes: A meta-analysis of clinical trials

机译:冠脉内阿昔单抗减少急性冠脉综合征的死亡和重大不良心血管事件:临床试验的荟萃分析

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Background: Successful reperfusion of epicardial coronary arteries does not necessarily result in actual myocardial perfusion. Local intracoronary (IC) delivery of GP IIb/IIIa inhibitors (GPI) has been proposed to achieve further clinical efficacy when compared to standard intravenous (IV) administration. However clinical trials have shown conflicting results. The aim of the present study was to compare IC with IV abciximab administration on mortality and MACEs in patients with ACS undergoing PCI. Methods: We performed a meta-analysis of all available clinical trials comparing intracoronary versus intravenous abciximab administration. Results: At short-term analysis, incidence of MACEs was significantly lower in the IC group than in the IV group (OR=0.56; 95% CI 0.35-0.89; p=0.015). Interestingly, subgroup analysis showed that most benefit was coming from those studies with a main baseline LVEFb50% (OR=0.33 95% CI 0.18-0.59). Similarly, long-termincidence ofMACEswas significantly lower in the IC group than in the IV group (OR=0.47; 95% CI 0.31-0.71; p<0.001), with most benefit coming from those studies enrolling patients with a main baseline EFb50% (OR=0.38 95% CI 0.23-0.63 p<0.001). In addition, long-term incidence of death was also lower in the IC group than in the IV group (OR=0.42; 95% CI 0.20-0.86; p=0.009). Conclusions: Our meta-analysis provides evidence of a net clinical benefit for intracoronary versus intravenous abciximab administration, with the highest benefit observed in high-risk ACS patients, such as those with reduced baseline LVEF.
机译:背景:成功的心外膜冠状动脉再灌注不一定会导致实际的心肌灌注。与标准静脉内(IV)给药相比,GP IIb / IIIa抑制剂(GPI)的局部冠状动脉内(IC)递送已被提出以实现进一步的临床疗效。然而,临床试验显示出矛盾的结果。本研究的目的是比较IC与IV abciximab给药对接受PCI的ACS患者的死亡率和MACE的影响。方法:我们对所有可用的临床试验进行了荟萃分析,比较了冠脉内和静脉内阿昔单抗的给药。结果:在短期分析中,IC组的MACE发生率显着低于IV组(OR = 0.56; 95%CI 0.35-0.89; p = 0.015)。有趣的是,亚组分析显示,最大收益来自那些主要基线LVEFb50%(OR = 0.33 95%CI 0.18-0.59)的研究。同样,IC组的MACE长期发生率显着低于IV组(OR = 0.47; 95%CI 0.31-0.71; p <0.001),其中最大的受益来自那些纳入主要基线EFb50%的患者的研究( OR = 0.38 95%CI 0.23-0.63 p <0.001)。此外,IC组的长期死亡发生率也低于IV组(OR = 0.42; 95%CI 0.20-0.86; p = 0.009)。结论:我们的荟萃分析提供了冠状动脉内和静脉内阿昔单抗给药的净临床获益的证据,在高风险ACS患者(例如基线LVEF降低的患者)中观察到了最高的获益。

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