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EUS-guided choledochoduodenostomy for malignant distal biliary obstruction after failed ERCP: a retrospective nationwide analysis

医学 支架 不利影响 回顾性队列研究 临床终点 胆管 外科 内镜治疗 胆总管 临床试验 内窥镜检查 内科学
作者
Alessandro Fugazza,Carlo Fabbri,R. Di Mitri,Maria Chiara Petrone,Matteo Colombo,Luigi Cugia,Arnaldo Amato,Edoardo Forti,Cecilia Binda,Marcello Maida,Emanuele Sinagra,Alessandro Repici,Ilaria Tarantino,Andrea Anderloni,Giulio Donato,Germana de Nucci,Mauro Manno,V. Pollino,Raffaele Macchiarelli,Nicola Leone,Roberta Badas,M Lovera,Elia Armellini,A. Redaelli,Benedetto Mangiavillano,Mario Luciano Brancaccio,Fabia Attili,Thomas Trian,Giovanni Aragona,Kareem Khalaf,Elisabetta Conte
出处
期刊:Gastrointestinal Endoscopy [Elsevier]
卷期号:95 (5): 896-904.e1 被引量:13
标识
DOI:10.1016/j.gie.2021.12.032
摘要

EUS-guided choledochoduodenostomy (EUS-CDS) with a lumen-apposing metal stent (LAMS) has been proposed as an alternative procedure in patients with distal malignant biliary obstruction (DMBO) and failed ERCP.This multicenter, retrospective analysis included all cases of EUS-CDS with LAMS performed in patients with DMBO and failed ERCP in 23 Italian centers from January 2016 to July 2020. Primary endpoints were technical and clinical success. Secondary endpoints were the assessment of the adverse event (AE) rate and variables associated with technical success.Two hundred fifty-six patients (44.9% women) with a mean age of 73.9 ± 12.6 years were included in the study. The most common etiology of DMBO was pancreatic adenocarcinoma (75%), followed by ampullary cancer (8.6%) and cholangiocarcinoma (6.6%). The common bile duct median diameter was 17.3 ± 3.9 mm. Technical and clinical success were achieved in 239 of 256 (93.3%), and 230 of 239 (96.2%) patients, respectively. The mean follow-up was 151 ± 162 days. Twenty-seven AEs occurred in 25 of 239 patients (10.5%) (3 mild, 21 moderate, and 3 severe). No fatal AEs occurred. Reinterventions to manage AEs with endoscopic or radiologic procedures occurred in 22 patients (9.2%).The results of our study show that EUS-CDS with LAMSs in patients with DMBO and failed ERCP represent a viable alternative in terms of effectiveness and safety with acceptable AE rates. (Clinical trial registration number: NCT03903523.).
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