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器械辅助小肠镜检查:我们是否准备好摒弃螺旋式小肠镜了?

Device-assisted enteroscopy: Are we ready to dismiss the spiral?

作者信息

Mussetto Alessandro, Merola Elettra, Casadei Cesare, Salvi Daniele, Fornaroli Fabiola, Cocca Silvia, Trebbi Margherita, Gabbrielli Armando, Spada Cristiano, Michielan Andrea

机构信息

Department of Gastroenterology, S Maria della Croci Hosp, Ravenna 48121, Italy.

Department of Gastroenterology Unit, G.B. Grassi Hospital (ASL Roma 3), Roma 00122, Italy.

出版信息

World J Gastroenterol. 2024 Jul 14;30(26):3185-3192. doi: 10.3748/wjg.v30.i26.3185.

Abstract

Motorized spiral enteroscopy (MSE) is the latest advance in device-assisted enteroscopy. Adverse events related to MSE were discussed in a recent large systematic review and meta-analysis and were directly compared with those of balloon enteroscopy in a case-matched study and a randomized controlled trial. Following the real-life application of MSE, an unexpected safety issue emerged regarding esophageal injury and the technique has been withdrawn from the global market, despite encouraging results in terms of diagnostic and therapeutic yield. We conducted an Italian multicenter real-life prospective study, which was prematurely terminated after the withdrawal of MSE from the market. The primary goals were the evaluation of MSE performance (both diagnostic and therapeutic) and its safety in routine endoscopic practice, particularly in the early phase of introduction in the endoscopic unit. A subanalysis, which involved patients who underwent MSE after unsuccessful balloon enteroscopy, demonstrated, for the first time, the promising performance of MSE as a rescue procedure. Given its remarkable performance in clinical practice and its potential role as a backup technique following a previously failed enteroscopy, it may be more appropriate to refine and enhance MSE in the future rather than completely abandoning it.

摘要

电动螺旋式小肠镜检查(MSE)是设备辅助小肠镜检查的最新进展。近期一项大型系统评价和荟萃分析讨论了与MSE相关的不良事件,并在一项病例匹配研究和一项随机对照试验中将其与气囊小肠镜检查的不良事件进行了直接比较。在MSE实际应用后,出现了一个关于食管损伤的意外安全问题,尽管在诊断和治疗效果方面取得了令人鼓舞的结果,但该技术已从全球市场撤出。我们进行了一项意大利多中心真实世界前瞻性研究,该研究在MSE退出市场后提前终止。主要目标是评估MSE在常规内镜实践中的性能(包括诊断和治疗)及其安全性,特别是在内镜科室引入的早期阶段。一项亚分析纳入了气囊小肠镜检查失败后接受MSE检查的患者,首次证明了MSE作为一种补救措施的良好性能。鉴于其在临床实践中的卓越表现以及作为先前小肠镜检查失败后的备用技术的潜在作用,未来对MSE进行改进和完善可能比完全放弃它更为合适。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3855/11287405/caec1cd25d48/WJG-30-3185-g001.jpg

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