Colorectal Unit, Department of Surgery, Royal Adelaide Hospital, Adelaide, South Australia, Australia.
Adelaide Medical School, Faculty of Health and Medical Sciences, University of Adelaide, Adelaide, South Australia, Australia.
Br J Surg. 2024 May 3;111(5). doi: 10.1093/bjs/znae121.
Postoperative ileus, driven by the cholinergic anti-inflammatory pathway, is the most common complication in patients undergoing colorectal surgery. By inhibiting acetylcholinesterase, pyridostigmine can potentially modulate the cholinergic anti-inflammatory pathway and accelerate gastrointestinal recovery. This study aimed to assess the efficacy of pyridostigmine in improving gastrointestinal recovery after colorectal surgery.
This double-blinded RCT enrolled adult patients undergoing elective colorectal surgery at two hospitals in South Australia. Patients were randomized to 60 mg oral pyridostigmine or placebo twice daily starting 6 h after surgery until the first passage of stool. The primary outcome was GI-2, a validated composite measure of time to first stool and tolerance of oral diet. Secondary outcomes included incidence of postoperative ileus (defined as GI-2 greater than 4 days), duration of hospital stay, and 30-day complications, evaluated by intention-to-treat univariate analysis.
Of 130 patients recruited (mean(s.d.) age 58.4(16.4) years; 73 men, 56%), 65 were allocated to each arm. The median GI-2 was 1 day shorter with pyridostigmine compared with placebo (2 (i.q.r. 1-3) versus 3 (2-4) days; P = 0.015). However, there were no significant differences in postoperative ileus (17.2 versus 21.5%; P = 0.532) or duration of hospital stay (median 5 (i.q.r. 4-8.75) versus 5 (4-7.5) days; P = 0.921). Similarly, there were no significant differences in overall complications, anastomotic leak, cardiac complications, or patient-reported side effects.
Pyridostigmine resulted in a quicker return of GI-2 and was well tolerated. Larger multicentre studies are required to determine the optimal dosing and evaluate the impact of pyridostigmine in different surgical settings. Registration number: ACTRN12621000530820 (https://anzctr.org.au).
术后肠麻痹是结直肠手术后最常见的并发症,其受胆碱能抗炎途径驱动。吡啶斯的明通过抑制乙酰胆碱酯酶,可能调节胆碱能抗炎途径并加速胃肠道恢复。本研究旨在评估吡啶斯的明改善结直肠手术后胃肠道恢复的疗效。
这是一项在澳大利亚南澳大利亚的两家医院进行的成人择期结直肠手术的双盲 RCT。患者在手术后 6 小时开始每天口服 60mg 吡啶斯的明或安慰剂两次,直到首次排便。主要结局是 GI-2,这是一种经过验证的综合测量指标,用于衡量首次排便时间和口服饮食耐受情况。次要结局包括术后肠麻痹(定义为 GI-2 大于 4 天)的发生率、住院时间和 30 天并发症,通过意向治疗的单变量分析进行评估。
共招募了 130 名患者(平均年龄为 58.4(16.4)岁;73 名男性,56%),每组 65 名患者。与安慰剂相比,吡啶斯的明组的中位 GI-2 缩短了 1 天(2(IQR 1-3)天 vs 3(2-4)天;P = 0.015)。然而,两组术后肠麻痹发生率(17.2% vs 21.5%;P = 0.532)或住院时间(中位数 5(IQR 4-8.75)天 vs 5(4-7.5)天;P = 0.921)无显著差异。同样,两组总体并发症、吻合口漏、心脏并发症或患者报告的副作用发生率也无显著差异。
吡啶斯的明可使 GI-2 更快恢复,且耐受性良好。需要更大规模的多中心研究来确定最佳剂量,并评估吡啶斯的明在不同手术环境中的影响。注册号:ACTRN12621000530820(https://anzctr.org.au)。