Mid-Western Vascular Unit, Limerick, Ireland.
Int J Surg. 2012;10(3):124-8. doi: 10.1016/j.ijsu.2012.02.008. Epub 2012 Feb 17.
Restenosis is a fundamental weakness of percutaneous femoropopliteal angioplasty (PTA). The potential of endovascular brachytherapy (EVBT) to reduce restenosis has been evaluated in randomized clinical trials, but no pooled analysis has been undertaken.
A systematic review was undertaken to identify randomized controlled trials in which PTA alone was compared to PTA plus EVBT. The Pubmed and Medline databases, American Heart Association OASIS database and conference proceedings from the Peripheral Vascular Surgery Society and Vascular Society of Great Britain and Ireland were searched. Eligible studies were randomised controlled trials comparing PTA to PTA plus EVBT in human subjects with at least one clinical outcome reported (restenosis, complications, patency). Study quality was assessed by the Jadad score. Random-effects modeling was used to generate pooled effect size estimates.
Six trials (687 patients) were identified. EVBT reduced 12-month restenosis rates (pooled odds ratio 0.50; 95% CI 0.301-0.836; p=0.008). The benefit disappeared by 24 months. The short-term risk of new lesions elsewhere in the treated artery was significantly increased by EVBT (pooled odds ratio 8.65; 95% CI 2.176-34.391; p=0.002).
While limited by the small sample sizes in the included trials, this analysis suggests that the early benefit of EVBT is counter-balanced by the increased risk of new lesions and the lack of medium- to long-term reductions in restenosis risk. Based upon the best available evidence, EVBT cannot be recommended for routine clinical use.
再狭窄是经皮股腘动脉成形术(PTA)的一个基本缺陷。腔内近距离放射治疗(EVBT)降低再狭窄的潜力已经在随机临床试验中得到了评估,但尚未进行汇总分析。
系统检索了单独 PTA 与 PTA 加 EVBT 比较的随机对照试验,检索了 Pubmed 和 Medline 数据库、美国心脏协会 OASIS 数据库以及外周血管外科学会和大不列颠及爱尔兰血管学会的会议记录。合格的研究是将 PTA 与 PTA 加 EVBT 比较的随机对照试验,至少报告了一项临床结局(再狭窄、并发症、通畅率)。通过 Jadad 评分评估研究质量。使用随机效应模型生成汇总效应大小估计值。
确定了 6 项试验(687 例患者)。EVBT 降低了 12 个月的再狭窄率(汇总比值比 0.50;95%CI 0.301-0.836;p=0.008)。该获益在 24 个月时消失。EVBT 显著增加了治疗动脉中其他部位新病变的短期风险(汇总比值比 8.65;95%CI 2.176-34.391;p=0.002)。
尽管纳入试验的样本量较小,但本分析表明,EVBT 的早期获益被新病变风险增加所抵消,且从中期到长期来看,再狭窄风险并未降低。根据现有最佳证据,不能推荐 EVBT 常规临床使用。