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Long time clinical outcomes of limus-eluting stent versus paclitaxel-eluting stent in patients undergoing percutaneous coronary artery intervention: A meta-analysis of randomized controlled clinical trials

机译:经皮冠状动脉介入治疗患者中limus洗脱支架与紫杉醇洗脱支架的长期临床疗效:随机对照临床试验的荟萃分析

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Background: The meta-analysis was aimed to compare the long time (> 2 year) clinical outcomes of limus-based stents (LBS) and paclitaxel-eluting stents (PES). LBS and PES are two kinds of most common coronary artery stents in clinics.Methods: Electronic data bases of PubMed, Cochrane, and EMBASE were searched. We included randomized controlled clinical trials (RCT) comparing LBS and PES with long time clinical outcomes. Methodological quality of eligible trials was assessed using “risk of bias” tool. The efficacy endpoints included target lesion revascularization (TLR), target vessel revascularization (TVR), and stent thrombosis (ST), and the safety endpoints included all cause death, cardiac death, and myocardial infarction (MI). Odds ratios (OR) and 95% confidence intervals (95% CI) were calculated for each endpoint.Results: A total of 23 RCTs and 19,319 participants were included and analyzed in this meta-analysis. All trials were of an acceptable quality. At 2 years, LBS showed reduced risk of revascularization and ST (TLR: OR = 0.59, 95% CI 0.44–0.78; TVR: OR = 0.63, 95% CI 0.55–0.71; ST: OR = 0.55, 95% CI 0.41–0.73) and a lower rate of MI (OR = 0.67, 95% CI 0.57–0.79). Subgroup analysis showed that both everolimus-eluting stents and sirolimus-eluting stents had better clinical outcomes compared with PES. The comparisons of 3, 4 and 5 year follow-up results revealed that the clinical outcomes of PES were non-inferior to those of LBS but LBS was associated with reduced risk of MI and ST at 3 years.Conclusions: LBS is associated with better clinical outcomes at 2 years. Both LBS and PES showed similar efficacy and safety at long time period.
机译:背景:荟萃分析旨在比较基于利姆斯的支架(LBS)和紫杉醇洗脱支架(PES)的长期(> 2年)临床结局。 LBS和PES是临床上最常见的两种冠状动脉支架。方法:搜索PubMed,Cochrane和EMBASE的电子数据库。我们纳入了将LBS和PES与长期临床结果进行比较的随机对照临床试验(RCT)。使用“偏倚风险”工具评估合格试验的方法学质量。疗效终点包括目标病变血运重建(TLR),目标血管血运重建(TVR)和支架血栓形成(ST),安全终点包括所有原因死亡,心源性死亡和心肌梗塞(MI)。计算每个终点的赔率(OR)和95%置信区间(95%CI)。结果:本荟萃分析共纳入了23个RCT和19,319名参与者。所有试验的质量均可接受。在2年时,LBS显示血运重建和ST风险降低(TLR:OR = 0.59,95%CI 0.44–0.78; TVR:OR = 0.63,95%CI 0.55–0.71; ST:OR = 0.55,95%CI 0.41– 0.73)和较低的心梗率(OR = 0.67,95%CI 0.57–0.79)。亚组分析显示,与PES相比,依维莫司洗脱支架和西罗莫司洗脱支架均具有更好的临床疗效。对3年,4年和5年随访结果的比较显示,PES的临床结局不逊于LBS,但LBS与3年MI和ST风险降低相关。 2年时的临床结果。 LBS和PES长期显示出相似的功效和安全性。

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