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首页> 外文期刊>Urologic oncology >Prospective implementation of a nonopioid protocol for patients undergoing robot-assisted radical cystectomy with extracorporeal urinary diversion
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Prospective implementation of a nonopioid protocol for patients undergoing robot-assisted radical cystectomy with extracorporeal urinary diversion

机译:对体外尿液转移进行机器人辅助自由基膀胱切除术的患者的非磷酶议定书的预期实施

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摘要

Objectives: To evaluate the feasibility and outcomes of a nonopioid (NOP) perioperative pain management protocol for patients undergoing robot-assisted radical cystectomy (RARC). Materials and Methods: We prospectively included 52 consecutive patients undergoing RARC at our institution for bladder cancer. Patients received a multimodal pain management protocol, including a combination of nonopioid pain medications and regional anesthesia. For comparison, we retrospectively included 41 consecutive patients who received the same procedure before implementation of the NOP protocol. Results: There was no significant difference in demographic and perioperative characteristics between the two groups. Patients included in the NOP protocol received a much lower dose of postoperative morphine milligram equivalents (2.5 [ IQR: 0-23] vs. 44 [ 14.5-128], P < 0.001), with no difference in pain scores. In the NOP protocol, the median time to regular diet was significantly shorter (4 days [ IQR: 3-5] vs. 5 days [ IQR: 4-8], P = 0.002) and the length of stay was 2 days shorter compared to the control group (5 days [ IQR: 4-7] vs. 7 days [ IQR: 6-11], P < 0.001). When evaluating the direct costs within 30 days after initial surgery, the NOP protocol was associated with an 8.6% reduction as compared to the control group (P = 0.032). In multivariate analysis, the receipt of the NOP protocol was a significant predictor of a length of stay < 7 days after RARC (OR: 12.09; 95% CI: 1.70-140; P = 0.023). Conclusions: The prospective implementation of a NOP protocol for patients undergoing RARC is feasible, allowing for minimal narcotic usage and provides benefits to patients, institutions, and population. (C) 2019 Elsevier Inc. All rights reserved.
机译:目的:评估非缺氧(NOP)围手术期疼痛管理方案的可行性和结果,用于接受机器人辅助的自由基膀胱切除术(RARC)的患者。材料和方法:我们预期包括52名膀胱癌机构接受RARC的连续患者。患者接受多峰疼痛管理方案,包括非磷酸疼痛药物和区域麻醉的组合。为了比较,我们回顾性地包括41名在实施NOP议定书之前收到相同程序的连续患者。结果:两组之间的人口统计学和围手术特性没有显着差异。 NOP议定书中包含的患者术后术后毫克毫克等当量的更低剂量(2.5 [IQR:0-23]与44 [14.5-128],P <0.001),疼痛评分没有差异。在NOP协议中,常规饮食的中位时间较短(4天[IQR:3-5]与5天[IQR:4-8],P = 0.002),并且保持时间较短了2天到对照组(5天[IQR:4-7]与7天[IQR:6-11],P <0.001)。当在初始手术后30天内评估直接成本时,与对照组相比,NOP方案与减少8.6%(P = 0.032)相关联。在多变量分析中,NOP协议的收据是RARC后留下长度<7天的重要预测因子(或:12.09; 95%CI:1.70-140; P = 0.023)。结论:接受RARC的患者的NOP议定书的前瞻性实施是可行的,允许对患者,机构和人口提供最小的麻醉剂,为患者,机构和人口提供益处。 (c)2019 Elsevier Inc.保留所有权利。

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