Department of Urology, Medical College of Wisconsin, 8701 W. Watertown Plank Road, Milwaukee, WI, 53226, USA.
J Robot Surg. 2021 Dec;15(6):923-928. doi: 10.1007/s11701-021-01191-x. Epub 2021 Jan 25.
Few studies demonstrate the safety and efficacy of postoperative pain regimens that exclude opioids altogether in patients undergoing robot-assisted radical prostatectomy (RARP). To reduce opioid use, we sought to develop an opioid-free regimen for RARP and determine perioperative outcomes before and after implementation. A retrospective, pre-post-interventional study was performed at a single institution between 8/2018 and 10/2019. An opioid-free pain regimen was developed and instituted on 3/7/2019, and all patients received preoperative counseling regarding pain expectations and management. Postoperative pain score was the primary outcome. Secondary outcomes included postoperative opioid use, length of stay, adverse events and unplanned health encounters within 30 days of discharge. Pearson's chi-squared and Student's t-tests were performed on categorical and continuous variables, respectively. Multivariable analysis was performed to determine risk factors for postoperative opioid use in the opioid-free cohort. A total of 89 patients were included for analysis; consisting of 47 (53%) pre-intervention and 42 (47%) post-intervention patients. Baseline characteristics were similar between groups. A significantly lower proportion of patients in the post-intervention group were administered opioids postoperatively (5% vs 53%, p < 0.01), despite having similar postoperative pain scores (2.69 vs 3.11, p = 0.19) and length of stay (1.0 days vs 1.2 days, p = 0.07). The post-intervention group had a significantly lower rate of opioid discharge prescriptions (14% vs 96%, p < 0.01). The rate of ED visits (12% vs 15%, p = 0.68), pain-related phone calls (17% vs 19%, p = 0.76) or adverse events (19% vs 13%, p = 0.42) were similar between groups. Among the opioid-free group, older patients were less likely to be administered postoperative opioids (OR 0.84, p = 0.046). A structured opioid-free pain regimen following RARP is non-inferior compared to traditional opioid-based standard of care. Adoption of similar regimens can help address the ongoing opioid epidemic in the United States and future work is needed to apply these principles broadly.
在接受机器人辅助根治性前列腺切除术 (RARP) 的患者中,很少有研究证明完全排除阿片类药物的术后疼痛方案的安全性和有效性。为了减少阿片类药物的使用,我们试图为 RARP 开发一种无阿片类药物的方案,并在实施前后确定围手术期结果。这是一项在单中心进行的回顾性、干预前后研究,时间为 2018 年 8 月至 2019 年 10 月。2019 年 3 月 7 日制定并实施了一种无阿片类药物的疼痛方案,所有患者均接受了关于疼痛预期和管理的术前咨询。术后疼痛评分是主要结局。次要结局包括术后阿片类药物使用、住院时间、出院后 30 天内的不良事件和计划外健康就诊。分别对分类变量和连续变量进行 Pearson 卡方检验和学生 t 检验。多变量分析用于确定无阿片类药物组术后使用阿片类药物的危险因素。共纳入 89 例患者进行分析;包括 47 例(53%)干预前和 42 例(47%)干预后患者。两组患者的基线特征相似。尽管术后疼痛评分相似(2.69 与 3.11,p=0.19)且住院时间相似(1.0 天与 1.2 天,p=0.07),但干预后组术后给予阿片类药物的患者比例显著降低(5%与 53%,p<0.01)。干预后组阿片类药物出院处方的比例显著降低(14%与 96%,p<0.01)。急诊就诊率(12%与 15%,p=0.68)、与疼痛相关的电话咨询率(17%与 19%,p=0.76)或不良事件发生率(19%与 13%,p=0.42)在两组间相似。在无阿片类药物组中,年龄较大的患者术后更不可能使用阿片类药物(OR 0.84,p=0.046)。与传统基于阿片类药物的标准治疗相比,RARP 后采用结构化无阿片类药物疼痛方案并不劣于后者。采用类似方案可以帮助解决美国正在进行的阿片类药物流行问题,未来需要广泛应用这些原则。