Wolff Bruce G, Weese James L, Ludwig Kirk A, Delaney Conor P, Stamos Michael J, Michelassi Fabrizio, Du Wei, Techner Lee
Division of Colon and Rectal Surgery, Mayo Clinic College of Medicine, Rochester, MN 55905, USA.
J Am Coll Surg. 2007 Apr;204(4):609-16. doi: 10.1016/j.jamcollsurg.2007.01.041.
Postoperative ileus (POI), an interruption of coordinated bowel motility after operation, is exacerbated by opioids used to manage pain. Alvimopan, a peripherally acting mu-opioid receptor antagonist, accelerated gastrointestinal (GI) recovery after bowel resection in randomized, double-blind, placebo-controlled, multicenter phase III POI trials. The effect of alvimopan on POI-related morbidity for patients who underwent bowel resection was evaluated in a post-hoc analysis.
Incidence of POI-related postoperative morbidity (postoperative nasogastric tube insertion or POI-related prolonged hospital stay or readmission) was analyzed in four North American trials for placebo or alvimopan 12 mg administered 30 minutes or more preoperatively and twice daily postoperatively until hospital discharge (7 or fewer postoperative days). GI-related adverse events and opioid consumption were summarized for each treatment. Estimations of odds ratios of alvimopan to placebo and number needed to treat (NNT) to prevent one patient from experiencing an event of POI-related morbidity were derived from the analysis.
Patients receiving alvimopan 12 mg were less likely to experience POI-related morbidity than patients receiving placebo (odds ratio = 0.44, p < 0.001). Fewer patients receiving alvimopan (alvimopan, 7.6%; placebo, 15.8%; NNT = 12) experienced POI-related morbidity. There was a lower incidence of postoperative nasogastric tube insertion, and other GI-related adverse events on postoperative days 3 to 6 in the alvimopan group than the placebo group. Opioid consumption was comparable between groups.
Alvimopan 12 mg was associated with reduced POI-related morbidity compared with placebo, without compromising opioid-based analgesia in patients undergoing bowel resection. Relatively low NNTs are clinically meaningful and reinforce the potential benefits of alvimopan for the patient and health care system.
术后肠梗阻(POI)是术后肠道运动协调性的中断,用于控制疼痛的阿片类药物会使其加重。阿洛司琼是一种外周作用的μ-阿片受体拮抗剂,在随机、双盲、安慰剂对照、多中心III期POI试验中,可加速肠切除术后胃肠道(GI)的恢复。在一项事后分析中评估了阿洛司琼对接受肠切除术患者POI相关发病率的影响。
在四项北美试验中,分析了POI相关术后发病率(术后鼻胃管插入或POI相关的住院时间延长或再次入院),试验中患者术前30分钟或更长时间服用安慰剂或12毫克阿洛司琼,术后每天两次,直至出院(术后7天或更少)。总结了每种治疗的胃肠道相关不良事件和阿片类药物消耗量。通过分析得出阿洛司琼与安慰剂的比值比估计值以及预防一名患者发生POI相关发病事件所需的治疗人数(NNT)。
接受12毫克阿洛司琼的患者比接受安慰剂的患者发生POI相关发病的可能性更小(比值比=0.44,p<0.001)。接受阿洛司琼的患者发生POI相关发病的人数更少(阿洛司琼组为7.6%;安慰剂组为15.8%;NNT=12)。阿洛司琼组术后第3至6天鼻胃管插入的发生率以及其他胃肠道相关不良事件低于安慰剂组。两组之间阿片类药物消耗量相当。
与安慰剂相比,12毫克阿洛司琼可降低POI相关发病率,且不影响接受肠切除术患者基于阿片类药物的镇痛效果。相对较低的NNT在临床上具有意义,并强化了阿洛司琼对患者和医疗保健系统的潜在益处。