Department of Medicine, University of Florida, Gainesville, FL, USA.
J Am Coll Cardiol. 2011 Mar 8;57(10):1190-9. doi: 10.1016/j.jacc.2010.10.030.
The purpose of this study was to investigate the efficacy and safety of glycoprotein IIb/IIIa inhibitors (GPIs) during elective percutaneous coronary intervention (PCI).
Studies have documented that GPIs are useful during PCI; however, much of this research was conducted before the routine use of coronary stents and thienopyridines.
We searched the MEDLINE, Cochrane clinical trials, and ClinicalTrials.gov databases from inception for studies that randomly assigned patients undergoing elective PCI to a GPI versus control. Trials were included if stents and thienopyridines were used routinely and clinical outcomes were reported. Outcomes were assessed within 30 days. A DerSimonian-Laird model was used to construct random effects summary risk ratios (RRs) and 95% confidence intervals (CIs).
Our search yielded 22 studies with 10,123 patients. The incidence of nonfatal myocardial infarction was 5.1% with GPI versus 8.3% with control (RR: 0.66, 95% CI: 0.55 to 0.79, p < 0.0001). Major bleeding was 1.2% versus 0.9% (RR: 1.37, 95% CI: 0.83 to 2.25, p = 0.22), minor bleeding was 3.0% versus 1.7% (RR: 1.70, 95% CI: 1.28 to 2.26, p < 0.0001), and mortality was 0.3% versus 0.5% (RR: 0.70, 95% CI: 0.36 to 1.33, p = 0.27), respectively.
In the current era of elective PCI performed with stents and thienopyridines, GPIs provide clinical benefit. These agents reduce nonfatal myocardial infarction without a notable increase in major bleeding; however, they increase the risk of minor bleeding. All-cause mortality is not reduced.
本研究旨在探讨糖蛋白 IIb/IIIa 抑制剂(GPI)在择期经皮冠状动脉介入治疗(PCI)中的疗效和安全性。
研究表明 GPI 在 PCI 中具有一定作用;然而,这些研究大多是在冠状动脉支架和噻吩吡啶常规应用之前进行的。
我们从 MEDLINE、Cochrane 临床试验和 ClinicalTrials.gov 数据库中检索了自成立以来将择期行 PCI 的患者随机分配至 GPI 组或对照组的研究。如果支架和噻吩吡啶常规使用且报告了临床结局,则纳入试验。结局在 30 天内评估。采用 DerSimonian-Laird 模型构建随机效应汇总风险比(RR)和 95%置信区间(CI)。
我们的检索结果包括 22 项研究,共纳入 10123 例患者。GPI 组和对照组的非致死性心肌梗死发生率分别为 5.1%和 8.3%(RR:0.66,95%CI:0.55 至 0.79,p<0.0001)。大出血发生率分别为 1.2%和 0.9%(RR:1.37,95%CI:0.83 至 2.25,p=0.22),小出血发生率分别为 3.0%和 1.7%(RR:1.70,95%CI:1.28 至 2.26,p<0.0001),死亡率分别为 0.3%和 0.5%(RR:0.70,95%CI:0.36 至 1.33,p=0.27)。
在当前应用支架和噻吩吡啶进行择期 PCI 的时代,GPI 具有临床获益。这些药物可降低非致死性心肌梗死的发生风险,而不显著增加大出血的风险;然而,它们增加了小出血的风险。全因死亡率并未降低。