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首页> 外文期刊>Archives of surgery. >Gastrointestinal tract recovery in patients undergoing bowel resection: results of a randomized trial of alvimopan and placebo with a standardized accelerated postoperative care pathway.
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Gastrointestinal tract recovery in patients undergoing bowel resection: results of a randomized trial of alvimopan and placebo with a standardized accelerated postoperative care pathway.

机译:接受肠切除术的患者的胃肠道恢复:阿尔维潘和安慰剂的随机试验结果,采用标准化的加速术后护理路径。

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OBJECTIVE: To investigate the efficacy and safety of alvimopan, 12 mg, administered orally 30 to 90 minutes preoperatively and twice daily postoperatively in conjunction with a standardized accelerated postoperative care pathway for managing postoperative ileus after bowel resection. Design, Setting, and PATIENTS: This multicenter, randomized, placebo-controlled, double-blind, phase 3 trial enrolled adult patients undergoing partial bowel resection with primary anastomosis by laparotomy and scheduled to receive intravenous, opioid-based, patient-controlled analgesia. A standardized accelerated postoperative care pathway including early ambulation, oral feeding, and postoperative nasogastric tube removal was used to facilitate gastrointestinal (GI) tract recovery in all of the patients. MAIN OUTCOME MEASURES: The primary end point was time to GI-2 recovery (toleration of solid food and first bowel movement). Secondary end points included time to GI-3 recovery (toleration of solid food and first flatus or bowel movement), hospital discharge order written, and actual hospital discharge. Postoperative length of hospital stay based on calendar day of hospital discharge order written, opioid consumption, and overall postoperative ileus-related morbidity were recorded. RESULTS: Alvimopan, 12 mg, was well tolerated and significantly accelerated GI-2 recovery, GI-3 recovery, and actual hospital discharge compared with a standardized accelerated postoperative care pathway alone (hazard ratio = 1.5, 1.5, and 1.4, respectively; P < .001 for all). Time to hospital discharge order written as measured by hazard ratio (1.4) and by postoperative calendar days (mean for alvimopan, 5.2 days; mean for placebo, 6.2 days) was also accelerated. Opioid consumption was comparable between groups, and alvimopan was associated with reduced postoperative ileus-related morbidity compared with placebo. CONCLUSIONS: Alvimopan, 12 mg, administered 30 to 90 minutes before and twice daily after bowel resection is well tolerated, accelerates GI tract recovery, and reduces postoperative ileus-related morbidity without compromising opioid analgesia.
机译:目的:探讨术前30至90分钟和术后每天两次口服12mg阿尔维莫潘的疗效和安全性,并结合标准化的加速术后护理途径处理肠切除术后肠梗阻。设计,背景和患者:这项多中心,随机,安慰剂对照,双盲,3期试验招募了成年患者,他们接受了部分剖腹手术并通过剖腹手术进行原发性吻合术,并计划接受静脉内,以阿片类药物为基础的,患者控制的镇痛。使用标准化的加速术后护理路径,包括早期移动,口服喂养和术后鼻胃管切除术,以促进所有患者的胃肠道(GI)恢复。主要观察指标:主要终点是恢复GI-2的时间(对固体食物的耐受和首次排便)。次要终点包括恢复GI-3的时间(对固体食物的耐受和第一次肠胃胀气或肠蠕动的时间),书面出院命令以及实际出院时间。根据书面出院日程,阿片类药物的摄入量以及术后总体肠梗阻相关的发病率记录术后住院时间。结果:与单独的标准化术后加速护理途径相比,Alvimopan(12 mg)具有良好的耐受性,并显着加速了GI-2恢复,GI-3恢复和实际出院(危险比分别为1.5、1.5和1.4; P <.001)。还加快了按危险比(1.4)和术后日历天(阿尔维潘平均5.2天;安慰剂平均6.2天)度量的出院时间。阿片类药物的消耗量在两组之间是可比的,与安慰剂相比,阿维莫潘与术后肠梗阻相关的发病率降低有关。结论:Alvimopan,12 mg,在肠切除术之前和之后每天30至90分钟给药,每天两次,耐受性良好,可加速胃肠道恢复,并减少术后肠梗阻相关的发病率,而不会损害阿片类药物的镇痛作用。

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