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一项随机对照试验研究了肛门直肠手术多模式强化康复方案对阿片类药物使用的影响。

A Randomized Controlled Trial Examining the Impact of an Anorectal Surgery Multimodal Enhanced Recovery Program on Opioid Use.

机构信息

Division of Colorectal Surgery, Department of Surgery, New York Presbyterian Hospital-Columbia University Medical Center, New York, New York.

Center for Innovation and Outcomes Research, Columbia University Medical Center, New York, New York.

出版信息

Ann Surg. 2022 Jan 1;275(1):e22-e29. doi: 10.1097/SLA.0000000000004701.

Abstract

BACKGROUND

Anorectal cases may be a common gateway to the opioid epidemic. Opioid reduction is inherent in enhanced recovery after surgery (ERAS) protocols, but little work has evaluated ERAS in these cases.

OBJECTIVE

To determine if ERAS could reduce postoperative opioid utilization in ambulatory anorectal surgery without sacrificing patient pain or satisfaction.

METHODS

A randomized controlled trial assigned ambulatory anorectal patients to ERAS (experimental) or routine care (surgeon's choice) for pain management (control) over 30-days postoperatively. Primary outcome was overall days of opioid use. Secondary outcomes included pain and satisfaction scores over multiple time points and new persistent opioid use. The Visual Analog Scale, Functional Pain Scale, and EQ-5D-3L measured patient-reported pain and satisfaction. Univariate analysis compared outcomes overall and at individual time points. Two-way mixed ANOVA evaluated pain and satisfaction measures between groups and over time.

RESULTS

Thirty-two patients were randomized into each arm (64 total). The control group consumed significantly more opioids after discharge (median 121.3MME vs 23.5MME, P < 0.001). Significantly more control patients requested additional narcotics (P  =  0.004), made unplanned calls (P = 0.009), and had unplanned clinic visits (P = 0.003). The control group had significantly more days on opioids (mean 14.4 vs 2.2, P < 0.001). Three control patients (9.4%) versus no experimental patients had new persistent opioid use. The mean global health, EQ5D-3L, Visual Analog Scale, and Functional Pain scores were comparable between groups over time.

CONCLUSIONS

An ERAS protocol in ambulatory anorectal surgery is feasible, and resulted in reduced opioid use, and healthcare utilization, with no difference in pain or patient satisfaction. This challenges the paradigm that extended opioids are needed for effective postoperative pain management.

摘要

背景

肛肠病例可能是阿片类药物流行的常见途径。减少阿片类药物的使用是增强术后恢复(ERAS)方案的固有内容,但很少有研究评估这些病例中的 ERAS。

目的

确定 ERAS 是否可以减少门诊肛肠手术患者术后阿片类药物的使用,同时又不影响患者的疼痛或满意度。

方法

一项随机对照试验将门诊肛肠患者分为 ERAS(实验组)或常规护理(医生选择)进行疼痛管理(对照组),随访 30 天。主要结局是总用阿片类药物天数。次要结局包括多个时间点的疼痛和满意度评分以及新的持续性阿片类药物使用。视觉模拟量表、功能疼痛量表和 EQ-5D-3L 测量患者报告的疼痛和满意度。单变量分析比较了总体和各个时间点的结果。双因素混合方差分析评估了组间和随时间的疼痛和满意度测量。

结果

每组随机分配 32 名患者(共 64 名)。对照组在出院后阿片类药物的使用明显更多(中位数 121.3MME 比 23.5MME,P < 0.001)。对照组中有更多的患者要求额外的麻醉药(P = 0.004)、计划外电话咨询(P = 0.009)和计划外就诊(P = 0.003)。对照组的阿片类药物使用天数明显更多(平均 14.4 天比 2.2 天,P < 0.001)。对照组中有 3 名患者(9.4%)出现新的持续性阿片类药物使用,而实验组没有。两组患者的全球健康状况、EQ5D-3L、视觉模拟量表和功能疼痛评分在随访期间总体上相似。

结论

门诊肛肠手术中的 ERAS 方案是可行的,可减少阿片类药物的使用和医疗保健的利用,而在疼痛或患者满意度方面没有差异。这对延长阿片类药物用于有效术后疼痛管理的观点提出了挑战。

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