上肢骨科手术处方指南的实施:对术后阿片类药物消费和满意度的前瞻性分析

The Hand Pub Date : 2019-08-23 DOI:10.1177/1558944719867122
Jenna R. Adalbert, A. Ilyas
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引用次数: 9

摘要

背景:由于缺乏既定的阿片类药物处方指南,最近的研究提出了初步指南,以减轻无意中的过量用药、转移和滥用。我们研究的目的是通过对患者消费和满意度的前瞻性评估来评估一套特定阿片类药物处方指南的疗效。方法:在连续的一段时间内,所有接受门诊上肢手术的患者都根据公布的特定解剖位置和手术指南,在术后服用阿片类药物。在术后第一次就诊时,记录手术细节、阿片类药物消耗模式、处方疗效和满意度。结果:共有201名患者报告了任何剂量的处方使用,导致平均服用5.5粒药丸。与接受骨折修复(6.7粒)或关节镜和关节成形术/融合手术(8.7粒)的患者相比,接受软组织手术的患者报告的需求最低(4.2粒)。与接受手腕(6.3粒)或肘部(8.1粒)手术的患者相比,接受手部手术的患者消耗更少的阿片类药物(3.9粒)。在需要阿片类药物的患者中,82%的患者表示对处方量满意或至少中立(P<.001),92%的患者表示满意或至少对处方阿片类镇痛效果中立(P<.001)。总体而言,研究补充请求率为13%。结论:尽管拟议的指南往往超出了患者的需求,但该研究证实了患者的强烈满意度,总体补充请求率仅为13%。我们得出的结论是,遵循解剖学和特定程序的阿片类药物处方指南是上肢术后开具阿片类物质处方的有效方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Implementing Prescribing Guidelines for Upper Extremity Orthopedic Procedures: A Prospective Analysis of Postoperative Opioid Consumption and Satisfaction
Background: A lack of established opioid-prescribing guidelines has prompted recent studies to propose preliminary guidelines to mitigate inadvertent overprescribing, diversion, and abuse. The purpose of our study was to assess the efficacy of a specific set of opioid-prescribing guidelines by prospective evaluation of patient consumption and satisfaction. Methods: During a consecutive period, all patients undergoing outpatient upper extremity surgical procedures were postoperatively prescribed opioids based on published guidelines that were specific to the anatomical location and procedure being performed. At the first postoperative visit, surgical details, opioid consumption patterns, and prescription efficacy and satisfaction were recorded. Results: A total of 201 patients reported any amount of prescription use, resulting in a mean consumption of 5.5 pills. Patients who underwent soft tissue procedures reported the lowest requirement (4.2 pills) compared with those who underwent fracture repairs (6.7 pills) or arthroscopy and arthroplasty/fusion procedures (8.7 pills). Patients undergoing hand procedures consumed fewer opioids (3.9 pills) compared with those undergoing wrist (6.3 pills) or elbow (8.1 pills) procedures. Of the patients requiring opioids, 82% reported being satisfied or at least neutral to the prescribed quantity (P < .001), and 92% reported being satisfied or at least neutral to the prescribed opioid analgesic efficacy (P < .001). Overall, the study refill request rate was 13%. Conclusions: Although the proposed guidelines tended to exceed patient need, the study confirmed strong patient satisfaction and an overall refill request rate of only 13%. We conclude that following anatomical and procedure-specific opioid-prescribing guidelines is an effective method of prescribing opioids postoperatively after upper extremity.
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