首页> 外文期刊>Journal of Pain Research >Liposome bupivacaine (EXPAREL?) for extended pain relief in patients undergoing ileostomy reversal at a single institution with a fast-track discharge protocol: an IMPROVE Phase IV health economics trial
【24h】

Liposome bupivacaine (EXPAREL?) for extended pain relief in patients undergoing ileostomy reversal at a single institution with a fast-track discharge protocol: an IMPROVE Phase IV health economics trial

机译:布比卡因脂质体(EXPAREL?)可在单一机构通过快速出院方案在回肠造口术逆转患者中延长疼痛缓解时间:一项改进的IV期健康经济学试验

获取原文
       

摘要

Background: Postoperative opioid use following ileostomy reversal procedures contributes to postoperative ileus. We assessed the impact of a liposome bupivacaine-based, opioid-sparing multimodal analgesia regimen versus a standard opioid-based analgesia regimen on postsurgical opioid use. We also assessed health economic outcomes in patients undergoing ileostomy reversal at our institution, which employs an enhanced recovery discharge protocol.Methods: In this single-center, open-label study, patients undergoing ileostomy reversal received postsurgical pain therapy via multimodal analgesia that included a single intraoperative administration of liposome bupivacaine or opioid-based patient-controlled analgesia (PCA) with intravenous morphine or hydromorphone. Rescue analgesia (intravenous [IV] opioids and/or oral opioid + acetaminophen) was available to all patients. Primary efficacy measures included postsurgical opioid use, hospital length of stay (LOS), and hospitalization costs. Secondary measures included: time to first rescue opioid use; patient satisfaction with analgesia; additional medical intervention; and opioid-related adverse events.Results: Forty-three patients were enrolled and met eligibility criteria (IV opioid PCA group = 20; liposome bupivacaine-based multimodal analgesia group = 23). Postsurgical opioid use was significantly less in the multimodal analgesia group compared with the IV opioid PCA group (mean [standard deviation]: 38 mg [46 mg] versus 68 mg [47 mg]; P = 0.004). Postsurgical LOS between-group differences (median: 3.0 days versus 3.8 days) and geometric mean hospitalization costs (US $6,611 versus US$6,790) favored the multimodal analgesic group but did not achieve statistical significance. Median time to first opioid use was 1.1 hours versus 0.7 hours in the multimodal analgesia and IV opioid PCA groups, respectively; P = 0.035. Two patients in the multimodal analgesia group and one in the IV opioid PCA group experienced opioid-related adverse events.Conclusion: A liposome bupivacaine-based multimodal analgesic regimen reduced postoperative opioid consumption in patients undergoing ileostomy reversal under a fast-track discharge protocol. A reduction of 21% in LOS (0.8 days) was noted which, although not statistically significant, may be considered clinically meaningful given the already aggressive fast-track discharge program.
机译:背景:回肠造口术逆转手术后使用阿片类药物会导致术后肠梗阻。我们评估了基于布比卡因脂质体,保留阿片样物质的多峰镇痛方案与基于标准阿片样物质的镇痛方案对术后阿片类药物使用的影响。我们还评估了在我们机构中采用强化恢复出院方案的回肠造口术逆转患者的健康经济结果。方法:在这项单中心,开放标签研究中,进行回肠造口术逆转的患者通过多模式镇痛接受了术后疼痛治疗,包括术中静脉给予吗啡或氢吗啡酮对布比卡因脂质体或基于阿片类药物的患者自控镇痛(PCA)进行单次术中给药。所有患者均可进行抢救性镇痛(静脉注射[IV]阿片类药物和/或口服阿片类药物+对乙酰氨基酚)。主要疗效指标包括术后使用阿片类药物,住院时间(LOS)和住院费用。次要措施包括:首次抢救阿片类药物的时间;患者对镇痛的满意度;额外的医疗干预;结果:43例患者入组并符合入选标准(IV阿片类PCA组= 20;脂质体布比卡因多模镇痛组= 23)。与静脉注射阿片类PCA组相比,多模式镇痛组的术后阿片类药物使用量明显减少(平均[标准偏差]:38 mg [46 mg]对68 mg [47 mg]; P = 0.004)。术后LOS之间的组间差异(中位数:3.0天比3.8天)和几何平均住院费用(6,611美元比6,790美元)偏爱多模态镇痛组,但没有统计学意义。首次使用阿片类药物的中位时间为1.1小时,而多式镇痛和静脉注射阿片类PCA组的中位时间分别为0.7小时; P = 0.035。多模式镇痛组中的2例患者和静脉阿片类PCA组中的1例患者经历了与阿片类药物相关的不良事件。注意到LOS(0.8天)降低了21%,尽管在统计学上不显着,但考虑到已经积极的快速通道放电程序,可能被认为具有临床意义。

著录项

相似文献

  • 外文文献
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号