Everolimus-Eluting versus Paclitaxel-Eluting Stents in Percutaneous Coronary Intervention: Meta-Analysis of Randomized Trials.

Thrombosis Pub Date : 2012-01-01 Epub Date: 2012-05-09 DOI:10.1155/2012/126369
Ashraf Alazzoni, Ayman Al-Saleh, Sanjit S Jolly
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引用次数: 27

Abstract

Background. Individual randomized trials have suggested that everolimus-eluting stents may have improved clinical outcomes compared to paclitaxel-eluting stents, but individual trials are underpowered to examine outcomes such as mortality and very late stent thrombosis. Methods. Medline, Cochrane, and conference proceedings were searched for randomized trials comparing everolimus versus paclitaxel-eluting stents for percutaneous coronary intervention. Results. 6792 patients were included from 4 randomized controlled trials. Stent thrombosis was reduced with everolimus stents versus paclitaxel stents (0.7% versus 2.3%; OR: 0.32; CI: 0.20-0.51; P < 0.00001). The reductions in stent thrombosis were observed in (i) early stent thrombosis (within 30 days) (0.2% versus 0.9%; OR: 0.24; P = 0.0005), (ii) late (day 31-365) (0.2% versus 0.6%; OR: 0.32; P = 0.01), and (iii) very late stent thrombosis (>365 days) (0.2% versus 0.8%; OR: 0.34; P = 0.009). The rates of cardiovascular mortality were 1.2% in everolimus group and 1.6% in paclitaxel group (OR: 0.85; P = 0.43). Patients receiving everolimus-eluting stents had significantly lower myocardial infarction events and target vessel revascularization as compared to paclitaxel-eluting stents. Interpretation. Everolimus compared to paclitaxel-eluting stents reduced the incidence of early, late, and very late stent thrombosis as well as target vessel revascularization.

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依维莫司洗脱支架与紫杉醇洗脱支架经皮冠状动脉介入治疗:随机试验的荟萃分析。
背景。个别随机试验表明,与紫杉醇洗脱支架相比,依维莫司洗脱支架可能具有更好的临床结果,但个别试验不足以检查诸如死亡率和非常晚期支架血栓形成等结果。方法。Medline、Cochrane和会议记录检索了比较依维莫司和紫杉醇洗脱支架用于经皮冠状动脉介入治疗的随机试验。结果:从4项随机对照试验中纳入6792例患者。依维莫司支架与紫杉醇支架相比,支架内血栓形成减少(0.7% vs 2.3%;OR: 0.32;置信区间:0.20—-0.51;P < 0.00001)。支架血栓发生率的降低体现在:(1)早期支架血栓形成(30天内)(0.2% vs 0.9%;OR: 0.24;P = 0.0005), (ii)晚(31-365天)(0.2% vs 0.6%;OR: 0.32;P = 0.01),以及(iii)极晚支架血栓形成(>365天)(0.2% vs 0.8%;OR: 0.34;P = 0.009)。依维莫司组心血管死亡率为1.2%,紫杉醇组为1.6% (OR: 0.85;P = 0.43)。与紫杉醇洗脱支架相比,接受依维莫司洗脱支架的患者心肌梗死事件和靶血管重建术显著降低。解释。与紫杉醇洗脱支架相比,依维莫司降低了早期、晚期和极晚期支架血栓的发生率以及靶血管重建术。
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