SAME day amBulatory c (SAMBA): a multicenter, prospective, randomized clinical trial protocol

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
Catherine Arvieux, Fatah Tidadini, Sandrine Barbois, Eric Fontas, Michel Carles, Victor Gridel, Jean-Christophe Orban, Jean-Louis Quesada, Alison Foote, Coralie Cruzel, Sabine Anthony, Julie Bulsei, Céline Hivelin, Damien Massalou
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Abstract

A recent meta-analysis concluded that outpatient appendectomy appears feasible and safe, but there is a lack of high-quality evidence and a randomized trial is needed. The aim of this trial is to demonstrate that outpatient appendectomy is non-inferior to conventional inpatient appendectomy in terms of overall morbi-mortality on the 30th postoperative day (D30). SAMBA is a prospective, randomized, controlled, multicenter non-inferiority trial. We will include 1400 patients admitted to 15 French hospitals between January 2023 and June 2025. Inclusion criteria are patients aged between 15 and 74 years presenting acute uncomplicated appendicitis suitable to be operated by laparoscopy. Patients will be randomized to receive outpatient care (day-surgery) or conventional inpatient care with overnight hospitalization in the surgery department. The primary outcome is postoperative morbi-mortality at D30. Secondary outcomes include time from diagnosis to appendectomy, length of total hospital stay, re-hospitalization, interventional radiology, re-interventions until D30, conversion from outpatient to inpatient, and quality of life and patient satisfaction using validated questionnaires. The SAMBA trial tests the hypothesis that outpatient surgery (i.e., without an overnight hospital stay) of uncomplicated acute appendicitis is a feasible and reliable procedure in establishments with a technical platform able to support this management strategy. ClinicalTrials.gov NCT05691348. Registered on 20 January 2023.
SAMBA:多中心、前瞻性、随机临床试验方案
最近的一项荟萃分析认为,门诊阑尾切除术似乎可行且安全,但缺乏高质量的证据,因此需要进行随机试验。本试验旨在证明,就术后第 30 天(D30)的总体死亡率而言,门诊阑尾切除术并不比传统的住院阑尾切除术差。SAMBA 是一项前瞻性、随机对照、多中心非劣效性试验。我们将纳入2023年1月至2025年6月期间在法国15家医院住院的1400名患者。纳入标准为年龄在15至74岁之间、患有急性无并发症阑尾炎、适合接受腹腔镜手术的患者。患者将被随机分配接受门诊治疗(日间手术)或常规住院治疗,并在外科住院一晚。主要结果是第 30 天的术后死亡率。次要结果包括从诊断到阑尾切除术的时间、总住院时间、再次住院时间、介入放射学检查、D30 之前的再次介入治疗、从门诊转为住院、生活质量以及使用有效问卷调查的患者满意度。SAMBA试验验证了以下假设:在拥有支持这种管理策略的技术平台的医疗机构中,无并发症急性阑尾炎的门诊手术(即无需住院过夜)是一种可行且可靠的治疗方法。ClinicalTrials.gov NCT05691348。注册日期:2023 年 1 月 20 日。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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