Clinical outcomes of pre-attached reinforced stapler reloads in bariatric surgery: A prospective case series

医学 外科 不利影响 袖状胃切除术 临床终点 入射(几何) 前瞻性队列研究 胃分流术 减肥 随机对照试验 内科学 肥胖 物理 光学
作者
Ahmed Ahmed,Salvador Morales-Conde,M Legrand,Simon W. Nienhuijs,Jacqués Himpens,Long R. Jiao,Olivier Facy
出处
期刊:International Journal of Surgery Open [Wolters Kluwer]
卷期号:32: 100337-100337
标识
DOI:10.1016/j.ijso.2021.100337
摘要

ABSTRACT Background: Staple line reinforcement during surgery may decrease morbidity or reduce the risk of staple line leaks and bleeding. There is debate regarding the benefit, safety, and best form of reinforcement. This case series characterizes the safety of a stapler with a pre-attached buttress in bariatric surgeries. Methods: This prospective, multicenter, post-market study examined the use of stapler reloads with built in reinforcement material. The primary endpoint is the incidence of reported device-related adverse events up to 30 days after laparoscopic Roux-en-Y gastric bypass (RYGB) and laparoscopic sleeve gastrectomy (SG) surgeries. Specific outcomes included bleeding (≥50 mL), leaks, and 30-day readmissions. Outcomes: A total of 51 patients (19 RYGB, 32 SG) were assessed after exclusion criteria were applied. Intraoperatively, no leaks or bleeding related to the staple line occurred. Four patients (8% overall, 3 RYGB, 1 SG) experienced bleeding unrelated to the staple line and staple line intervention, in these cases, was not required. Four subjects (8%, all SG) required readmission and each were attributed as unrelated to the investigational device. No unanticipated device-related events were observed. Two adverse events (bleeding) occurred post-operatively that were attributed as possibly related to the device; both were endoscopically managed. Conclusions: This study demonstrates that there were no serious safety concerns from the AEs observed related to reinforced reload use during or in the 30-day course after 51 common bariatric procedures in a multicenter setting. Trial registration: The study was registered with clinicaltrials.gov (NCT02500537). Thoracic subjects from this study are described in a separate manuscript. Highlights

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