Per-oral endoscopic myotomy is a safe and effective treatment for Zenker's diverticulum: a retrospective multicenter study.

Marc A Ward, Lucas Fair, Jennifer Misenhimer, Simón Esteva, Ian Greenberg, Gerald Ogola, Bola Aladegbami, Steven G Leeds, Prashant Kedia
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Abstract

Zenker per-oral endoscopic myotomy (ZPOEM) has become a promising technique for Zenker's diverticulum (ZD). The aim of this study was to add to the limited body of literature evaluating the safety and efficacy of ZPOEM. A prospectively maintained database was retrospectively reviewed to identify patients who underwent ZPOEM at two separate institutions between January 2020 and January 2022. Demographics, preoperative and postoperative clinical data, intraoperative data, adverse events, and length of stay were analyzed. A total of 40 patients (mean age 72.5 years, 62.5% male) were included. Average operative time was 54.7 minutes and average length of stay was 1.1 days. There were three adverse events, and only one was related to the technical aspects of the procedure. Patients showed improvement in the Functional Oral Intake Scale (FOIS) scores at 1 month (5 vs 7, p < 0.0001). The median FOIS scores remained 7 at both 6 and 12 months, although this improvement was not statistically significant at these time intervals (p = 0.46 and 0.37, respectively). Median dysphagia scores were decreased at 1 (2.5 vs 0, p < 0.0001), 6 (2.5 vs 0, p < 0.0001), and 12 months (2.5 vs 0, p = 0.016). The number of patients reporting ≥1 symptom was also decreased at 1 (40 vs 9, p < 0.0001) and 6 months (40 vs 1, p = 0.041). Although the number of patients reporting ≥1 symptom remained consistent at 12 months, this was not statistically significant (40 vs 1, p = 0.13). ZPOEM is a safe and highly effective treatment for the management of ZD. .

经口内窥镜肌切开术是治疗Zenker憩室安全有效的方法:一项回顾性多中心研究。
Zenker经口内窥镜肌切开术(ZPOEM)是治疗Zenker憩室(ZD)的一种很有前途的技术。本研究的目的是补充有限的文献来评估ZPOEM的安全性和有效性。回顾性审查前瞻性维护的数据库,以确定2020年1月至2022年1月期间在两个独立机构接受ZPOEM治疗的患者。分析了人口统计学、术前和术后临床资料、术中资料、不良事件和住院时间。共纳入40例患者,平均年龄72.5岁,男性62.5%。平均手术时间54.7分钟,平均住院时间1.1天。有三个不良事件,其中只有一个与手术的技术方面有关。患者在1个月时功能性口服摄入量表(FOIS)评分有所改善(5 vs 7, p
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