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Treatment strategies for coronary in-stent restenosis: systematic review and hierarchical Bayesian network meta-analysis of 24 randomised trials and 4880 patients

机译:冠状动脉支架内再狭窄的治疗策略:24项随机试验和4880例患者的系统评价和分级贝叶斯网络荟萃分析

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摘要

>Study question What is the most safe and effective interventional treatment for coronary in-stent restenosis?>Methods In a hierarchical Bayesian network meta-analysis, PubMed, Embase, Scopus, Cochrane Library, Web of Science, ScienceDirect, and major scientific websites were screened up to 10 August 2015. Randomised controlled trials of patients with any type of coronary in-stent restenosis (either of bare metal stents or drug eluting stents; and either first or recurrent instances) were included. Trials including multiple treatments at the same time in the same group or comparing variants of the same intervention were excluded. Primary endpoints were target lesion revascularisation and late lumen loss, both at six to 12 months. The main analysis was complemented by network subanalyses, standard pairwise comparisons, and subgroup and sensitivity analyses.>Study answer and limitations Twenty four trials (4880 patients), including seven interventional treatments, were identified. Compared with plain balloons, bare metal stents, brachytherapy, rotational atherectomy, and cutting balloons, drug coated balloons and drug eluting stents were associated with a reduced risk of target lesion revascularisation and major adverse cardiac events, and with reduced late lumen loss. Treatment ranking indicated that drug eluting stents had the highest probability (61.4%) of being the most effective for target lesion vascularisation; drug coated balloons were similarly indicated as the most effective treatment for late lumen loss (probability 70.3%). The comparative efficacy of drug coated balloons and drug eluting stents was similar for target lesion revascularisation (summary odds ratio 1.10, 95% credible interval 0.59 to 2.01) and late lumen loss reduction (mean difference in minimum lumen diameter 0.04 mm, 95% credible interval −0.20 to 0.10). Risks of death, myocardial infarction, and stent thrombosis were comparable across all treatments, but these analyses were limited by a low number of events. Trials had heterogeneity regarding investigation periods, baseline characteristics, and endpoint reporting, with a lack of information at long term follow-up. Direct and indirect evidence was also inconsistent for the comparison between drug eluting stents and drug coated balloons. >What this study adds Compared with other currently available interventional treatments for coronary in-stent restenosis, drug coated balloons and drug eluting stents are associated with superior clinical and angiographic outcomes, with a similar comparative efficacy. >Funding, competing interests, data sharing This study received no external funding. The authors declare no competing interests. No additional data available.
机译:>研究问题什么是最有效的冠状动脉支架内再狭窄介入治疗?>方法在分级贝叶斯网络荟萃分析中,PubMed,Embase,Scopus,Cochrane库,Web of Science,ScienceDirect和主要科学网站的筛选截止至2015年8月10日。对任何类型的冠状动脉支架内再狭窄(裸金属支架或药物洗脱支架;以及初次或复发病例)的患者进行随机对照试验)。不包括在同一组中同时进行多种治疗或比较同一干预措施的变体的试验。主要终点是靶病变血运重建和晚期管腔丢失,均在6至12个月时出现。主要分析得到网络亚分析,标准成对比较以及亚组和敏感性分析的补充。>研究答案和局限性确定了二十四项试验(4880例患者),包括七种介入治疗方法。与普通球囊相比,裸露金属支架,近距离放射治疗,旋磨术和切开球囊,药物涂层球囊和药物洗脱支架与靶病变血运重建和严重不良心脏事件的风险降低以及晚期管腔丢失减少有关。治疗排名表明,药物洗脱支架对靶病变血管形成最有效的可能性最高(61.4%)。同样地,药物涂层球囊被认为是晚期管腔丢失的最有效治疗方法(概率为70.3%)。对于目标病变血运重建(总比值比为1.10,95%可信区间为0.59至2.01)和晚期管腔损失减少(最小管腔直径的均值差为0.04 mm,95%可信区间),药物涂层球囊和药物洗脱支架的比较功效相似。 -0.20至0.10)。在所有治疗中,死亡,心肌梗塞和支架血栓形成的风险均相当,但这些分析受到事件少的限制。试验在调查期,基线特征和终点报告方面存在异质性,长期随访缺乏信息。对于药物洗脱支架和药物涂层球囊之间的比较,直接和间接证据也不一致。 >这项研究的补充与目前其他可用于冠状动脉支架内再狭窄的介入治疗相比,药物涂层球囊和药物洗脱支架具有更好的临床和血管造影结果,具有相似的比较疗效。 >资金,利益冲突,数据共享。该研究未获得外部资金。作者宣称没有利益冲突。没有其他可用数据。

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