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内镜下双侧支架内支架与支架间支架置入术治疗晚期恶性肝门部梗阻:Meta 分析和系统评价。

Endoscopic Bilateral Stent-in-Stent Versus Stent-by-Stent Deployment in Advanced Malignant Hilar Obstruction: A Meta-Analysis and Systematic Review.

机构信息

Department of Preventive Medicine, Korea University College of Medicine, Seoul, Korea.

Department of Urology, Soonchunhyang University Seoul Hospital, SoonChunHyang University School of Medicine, Seoul, Korea.

出版信息

Dig Dis Sci. 2022 Feb;67(2):716-728. doi: 10.1007/s10620-021-06885-8. Epub 2021 Feb 24.

Abstract

BACKGROUND AND AIM

There is no clear data to compare the effectiveness and safety of bilateral stent-in-stent (SIS) or stent-by-stent (SBS) deployment for advanced malignant hilar obstruction (MHO). This meta-analysis was done to investigate clinical outcomes of these deployment methods.

METHODS

We did a literature search to identify studies that reported the clinical outcomes of bilateral metal stents in patients with advanced MHO. Weighed pooled rates (WPR) along with 95% confidence interval (95% CI) were calculated in order to compare outcomes including technical and clinical success, adverse events, and stent occlusion between the two groups. We conducted a meta-analysis using a random-effects model.

RESULTS

Five comparative studies with 250 patients, and 20 single-arm studies for the SIS or SBS method were eligible for the meta-analysis and systematic review. The bilateral SIS deployment had a significantly higher technical success rate than did SBS deployment (OR 6.43; 95% CI 1.08-38.09). There was no difference in the clinical success (OR 1.23; 95% CI 0.45-3.38), overall adverse events rates (OR 0.42; 95% CI 0.15-1.18), or overall occlusion rate (OR 1.55; 95% CI 0.89-2.70). As a single-armed group, WPR of technical success of the SIS and SBS groups was 96.4% and 89.6%, respectively. Clinical success was 97.5% and 98.3%. Overall, adverse events were 35.9% and 22.6%. Occlusion rates were 27.7% and 37.7%.

CONCLUSIONS

Although there was a lack of quality data and heterogeneity, bilateral SIS deployment had a higher technical feasibility than did the SBS method in patients with advanced MHO, without differences in terms of clinical success, adverse events, or occlusion rates.

摘要

背景与目的

对于晚期恶性肝门部梗阻(MHO),目前尚无明确的数据比较双支架内支架(SIS)或支架对支架(SBS)植入的有效性和安全性。本荟萃分析旨在探讨这些植入方法的临床结果。

方法

我们进行了文献检索,以确定报道晚期 MHO 患者双侧金属支架临床结果的研究。计算了加权汇总率(WPR)及其 95%置信区间(95%CI),以比较两组之间的技术和临床成功率、不良事件和支架闭塞等结果。我们使用随机效应模型进行了荟萃分析。

结果

纳入了 5 项比较研究,共 250 例患者,以及 20 项 SIS 或 SBS 方法的单臂研究,符合荟萃分析和系统评价的条件。双侧 SIS 植入的技术成功率明显高于 SBS 植入(OR 6.43;95%CI 1.08-38.09)。临床成功率(OR 1.23;95%CI 0.45-3.38)、总不良事件发生率(OR 0.42;95%CI 0.15-1.18)或总闭塞率(OR 1.55;95%CI 0.89-2.70)均无差异。作为单臂组,SIS 和 SBS 组的技术成功率 WPR 分别为 96.4%和 89.6%。临床成功率分别为 97.5%和 98.3%。总不良事件发生率分别为 35.9%和 22.6%。闭塞率分别为 27.7%和 37.7%。

结论

尽管缺乏高质量数据和异质性,但对于晚期 MHO 患者,双侧 SIS 植入的技术可行性高于 SBS 方法,在临床成功率、不良事件或闭塞率方面无差异。

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