骨科手术(OREOS)中阿片类药物减少和增强康复:一项膝关节置换术患者的可行性随机对照试验。

IF 2 Q3 CLINICAL NEUROLOGY Canadian Journal of Pain-Revue Canadienne de la Douleur Pub Date : 2022-10-04 eCollection Date: 2022-01-01 DOI:10.1080/24740527.2022.2102465
Sushmitha Pallapothu, Kim Madden, Anthony Adili, Adrijana Krsmanovic, Matilda Nowakowski, Tara Packham, Sidra Shoaib, Lehana Thabane, Jean-Eric Tarride, Daniel Tushinski, Harsha Shanthanna
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引用次数: 0

摘要

背景:全膝关节置换术是加拿大第二大常见手术。大多数患者恢复良好,但20%或更多的患者仍然遭受持续疼痛和阿片类药物的困扰。虽然阿片类药物是围手术期疼痛管理的重要组成部分,但其潜在的长期不良反应是公认的。限制阿片类药物可能不足以克服阿片类药物过度使用的问题。疼痛和阿片类药物的使用是高度相关的,所以一个有效的替代方案需要同时解决这两个问题。目的:本试验的主要目的是评估可行性。临床目的是确定多组分护理途径对无阿片类药物疼痛控制、持续疼痛和阿片类药物使用、膝关节功能结局、生活质量和功能恢复的影响。方法:我们将纳入预定进行初级选择性全膝关节置换术的成年患者。干预组的患者将接受多组分干预途径,干预协调员将每位患者及其手术/围手术期团队联系起来。介入途径将包括(1)术前关于疼痛和阿片类药物使用的教育,(2)术前使用认知行为技能识别和缓解风险,(3)个性化出院后镇痛处方,以及(4)持续支持长达8周的疼痛控制和恢复。对照组患者将在其所在机构接受常规护理。讨论:总体目标是实施和评估一种协调的临床护理方法,以改善疼痛控制和减少伤害,强调以患者为中心的护理和共同决策。试验注册号:NCT04968132(知情同意/研究伦理委员会声明)。
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Opioid reduction and enhanced recovery in orthopaedic surgery (OREOS): A feasibility randomized controlled trial in knee replacement patients.

Background: Total knee arthroplasties are the second most common surgery in Canada. Most patients recover well, but 20% or more still suffer from persistent pain and opioid use. Though opioids are an important part of perioperative pain management, their potential for long-term adverse effects is well recognized. Limiting opioids may be insufficient to overcome the issue of opioid overuse. Pain and opioid use are highly linked, so an effective alternative needs to address both issues.

Objectives: The principal objective of this pilot trial is to assess the feasibility. The clinical objectives are to determine the effects of a multicomponent care pathway on opioid-free pain control, persisting pain and opioid use, functional knee outcomes, quality of life, and return to function.

Methods: We will include adult patients scheduled for primary elective total knee arthroplasty. Patients in the intervention group will undergo a multicomponent intervention pathway that will be facilitated by an intervention coordinator linking each patient and their surgical/ perioperative team. The interventional pathway will include (1) preoperative education on pain and opioid use, (2) preoperative risk identification and mitigation using cognitive behavioral skills, (3) personalized postdischarge analgesic prescriptions, and (4) continued support for pain control and recovery up to 8 weeks. Patients in the control group will receive the usual care at their institution.

Discussion: The overarching goal is to implement and evaluate a coordinated approach to clinical care to improve pain control and reduce harms, with an emphasis on patient-centered care and shared decision making.Trial Registration Number: NCT04968132 (informed consent/ research ethics board statement).

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CiteScore
3.70
自引率
12.50%
发文量
36
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