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药物洗脱支架治疗下肢动脉血管再通:随机试验的更新荟萃分析。

Drug-eluting stents for revascularization of infrapopliteal arteries: updated meta-analysis of randomized trials.

机构信息

Deutsches Herzzentrum, Technische Universität, Munich, Germany.

Deutsches Herzzentrum, Technische Universität, Munich, Germany.

出版信息

JACC Cardiovasc Interv. 2013 Dec;6(12):1284-93. doi: 10.1016/j.jcin.2013.08.007.

Abstract

OBJECTIVES

This study sought to undertake an updated meta-analysis of randomized trials investigating the outcomes of percutaneous revascularization with primary drug-eluting stenting in patients with atherosclerotic disease of infrapopliteal arteries.

BACKGROUND

In atherosclerotic disease of infrapopliteal arteries, drug-eluting stents (DESs) improve patency rates compared with plain balloon angioplasty or bare-metal stents (BMSs). However, the clinical impact of DES placement in this vascular territory still remains uncertain.

METHODS

We searched MEDLINE, Embase, CENTRAL (Cochrane Central Register of Controlled Trials), scientific session abstracts, and relevant Websites. The keywords used were "below the knee," "infrapopliteal artery," "angioplasty," "drug-eluting stent(s)," "bare metal stent(s)," "trial," and "randomized trial." Inclusion criteria were randomized design, intention-to-treat analysis, and a minimum of 6-month follow-up. Exclusion criteria were vessels treated other than infrapopliteal arteries; devices used other than DESs, plain balloons, or BMSs; and duplicated data. The primary endpoint was target lesion revascularization; secondary endpoints were restenosis, amputation, death, and improvement in Rutherford class.

RESULTS

A total of 611 patients from 5 trials were randomly assigned to DESs (n = 294) versus control therapy (plain balloon angioplasty/BMS implantation, n = 307). Overall, the median lesion length was 26.8 mm (interquartile range [IQR]: 18.2 to 30.0 mm) with a reference vessel diameter of 2.86 mm (IQR: 2.68 to 3.00 mm). At a median follow-up of 12 months (IQR: 12 to 36 months), DESs reduced the risk of target lesion revascularization (odds ratio [OR]: 0.31; 95% confidence interval [CI]: 0.18 to 0.54; p < 0.001), restenosis (OR: 0.25; 95% CI: 0.15 to 0.43; p < 0.001), and amputation (OR: 0.50; 95% CI: 0.26 to 0.97); p = 0.04) without a significant difference in terms of death (OR: 0.81; 95% CI: 0.45 to 1.49; p = 0.50) and Rutherford class improvement (OR: 1.36; 95% CI: 0.91 to 2.04; p = 0.13) versus control therapy.

CONCLUSIONS

In focal disease of infrapopliteal arteries, DES therapy reduces the risk of reintervention and amputation compared with plain balloon angioplasty or BMS implantation without any impact on mortality and Rutherford class at 1-year follow-up.

摘要

目的

本研究旨在对经皮腔内血管成形术联合药物洗脱支架(DES)治疗粥样硬化性下肢动脉疾病的随机试验进行更新的荟萃分析。

背景

在下肢动脉粥样硬化疾病中,与单纯球囊血管成形术或裸金属支架(BMS)相比,DES 可提高通畅率。然而,DES 在这一血管部位的临床影响仍不确定。

方法

我们检索了 MEDLINE、Embase、CENTRAL(Cochrane 对照试验中心注册库)、科学会议摘要和相关网站。使用的关键词为“膝下”、“下肢动脉”、“血管成形术”、“药物洗脱支架”、“裸金属支架”、“试验”和“随机试验”。纳入标准为随机设计、意向治疗分析和至少 6 个月的随访。排除标准为治疗的血管不是下肢动脉;使用的器械不是 DES、普通球囊或 BMS;以及重复数据。主要终点为靶病变血运重建;次要终点为再狭窄、截肢、死亡和 Rutherford 分级改善。

结果

共有 5 项试验的 611 名患者被随机分配到 DES 组(n=294)和对照组(单纯球囊血管成形术/BMS 植入术,n=307)。总体而言,中位病变长度为 26.8mm(IQR:18.2-30.0mm),参考血管直径为 2.86mm(IQR:2.68-3.00mm)。中位随访时间为 12 个月(IQR:12-36 个月),DES 降低了靶病变血运重建的风险(比值比[OR]:0.31;95%置信区间[CI]:0.18-0.54;p<0.001)、再狭窄(OR:0.25;95%CI:0.15-0.43;p<0.001)和截肢(OR:0.50;95%CI:0.26-0.97;p=0.04),但在死亡(OR:0.81;95%CI:0.45-1.49;p=0.50)和 Rutherford 分级改善(OR:1.36;95%CI:0.91-2.04;p=0.13)方面与对照组无显著差异。

结论

在下肢动脉局灶性疾病中,与单纯球囊血管成形术或 BMS 植入术相比,DES 治疗可降低再介入和截肢的风险,而在 1 年随访时对死亡率和 Rutherford 分级无影响。

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