Department of Gastroenterological Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan.
Department of Anesthesiology and Resuscitology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan.
BJS Open. 2024 Jan 3;8(1). doi: 10.1093/bjsopen/zrad161.
BACKGROUND: Epidural analgesia (EDA) is a main modality for postoperative pain relief in major open abdominal surgery within the Enhanced Recovery After Surgery protocol. However, it remains unclear whether EDA is an imperative modality in laparoscopic gastrectomy (LG). This study examined non-inferiority of patient-controlled intravenous analgesia (PCIA) to EDA in terms of postoperative pain and recovery in patients who underwent LG. METHODS: In this open-label, non-inferiority, parallel, individually randomized clinical trial, patients who underwent elective LG for gastric cancer were randomized 1:1 to receive either EDA or PCIA after surgery. The primary endpoint was pain score using the Numerical Rating Scale at rest 24 h after surgery, analysed both according to the intention-to-treat (ITT) principle and per protocol. The non-inferiority margin for pain score was set at 1. Secondary outcomes were postoperative parameters related to recovery and adverse events related to analgesia. RESULTS: Between 3 July 2017 and 29 September 2020, 132 patients were randomized to receive either EDA (n = 66) or PCIA (n = 66). After exclusions, 64 patients were included in the EDA group and 65 patients in the PCIA group for the ITT analysis. Pain score at rest 24 h after surgery was 1.94 (s.d. 2.07) in the EDA group and 2.63 (s.d. 1.76) in the PCIA group (P = 0.043). PCIA was not non-inferior to EDA for the primary endpoint (difference 0.69, one side 95% c.i. 1.25, P = 0.184) in ITT analysis. Postoperative parameters related to recovery were similar between groups. More EDA patients (21 (32.8%) versus 1 (1.5%), P < 0.001) developed postoperative hypotension as an adverse event. CONCLUSIONS: PCIA was not non-inferior to EDA in terms of early-phase pain relief after LG.Registration number: UMIN000027643 (https://www.umin.ac.jp/ctr/index-j.htm).
背景:硬膜外镇痛(EDA)是加速康复外科方案中大型开腹腹部手术后缓解术后疼痛的主要方式。然而,在腹腔镜胃切除术(LG)中,EDA 是否是必需的方式仍不清楚。本研究旨在检查患者自控静脉镇痛(PCIA)在 LG 术后患者的术后疼痛和恢复方面是否不劣于 EDA。
方法:这是一项开放标签、非劣效性、平行、个体随机临床试验,入组了接受择期 LG 治疗胃癌的患者,术后随机接受 EDA 或 PCIA。主要终点是术后 24 小时静息时的数字评分量表(NRS)疼痛评分,根据意向治疗(ITT)原则和方案进行分析。疼痛评分的非劣效性边界设定为 1。次要结局是与恢复相关的术后参数和与镇痛相关的不良事件。
结果:2017 年 7 月 3 日至 2020 年 9 月 29 日,共有 132 名患者被随机分为 EDA 组(n = 66)或 PCIA 组(n = 66)。排除后,64 名患者被纳入 EDA 组,65 名患者被纳入 PCIA 组进行 ITT 分析。术后 24 小时静息时的疼痛评分在 EDA 组为 1.94(标准差 2.07),在 PCIA 组为 2.63(标准差 1.76)(P = 0.043)。PCIA 在 ITT 分析中对主要终点(差值 0.69,单侧 95%可信区间 1.25,P = 0.184)不劣于 EDA。两组间与恢复相关的术后参数相似。更多的 EDA 患者(21 例[32.8%]与 1 例[1.5%],P < 0.001)发生术后低血压作为不良事件。
结论:在 LG 术后早期缓解疼痛方面,PCIA 不劣于 EDA。注册号:UMIN000027643(https://www.umin.ac.jp/ctr/index-j.htm)。
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