Departments of Anesthesiology and Critical Care, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Orthopedic Surgery, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Pain Med. 2019 May 1;20(5):1012-1019. doi: 10.1093/pm/pny152.
Pain control after shoulder arthroscopy can be challenging, often relying on opioids. The study aims to measure the quality of recovery (QoR) before and after implementation of a "Multimodal Perioperative Pain Protocol" (MP3) in patients undergoing ambulatory shoulder arthroscopy.
Prospective cohort study.
Free-standing ambulatory surgery facility of a tertiary care academic center.
Patients undergoing ambulatory shoulder arthroscopy.
The primary end point of the study was the QoR-9 score at 24 hours, 48 hours, and one week after surgery. Secondary end points included 1) measuring the quality of pain management using the Revised American Pain Society Patient Oriented Questionnaire (APS-POQ-R) and 2) postoperative opioid requirements.
Data from132 patients in the control group (pre-intervention) and 120 patients in the MP3 group were analyzed. The QoR-9 scores were significantly higher for the MP3 group at all time points, but only met the minimal clinical important difference threshold at 24 hours (13.4 vs 14.9, P < 0.05) and 48 hours (14.0 vs 15.0, P < 0.05) postoperatively. Patients reported better quality of pain management after implementation of the MP3 in the domains of pain intensity, pain interference with activity, and sleep, and they reported the presence of negative emotions up to two days after ambulatory shoulder surgery. In addition, this protocol significantly reduced opioid consumption up to three days after surgery.
Implementation of the MP3 improved the overall QoR and many aspects of postoperative pain relief while reducing total opioid consumption in patients undergoing ambulatory shoulder surgery.
肩关节镜术后的疼痛控制具有挑战性,通常依赖于阿片类药物。本研究旨在测量实施“多模式围手术期疼痛方案”(MP3)前后接受日间肩关节镜手术患者的康复质量(QoR)。
前瞻性队列研究。
三级学术中心的独立日间手术中心。
接受日间肩关节镜手术的患者。
该研究的主要终点是术后 24 小时、48 小时和 1 周时的 QoR-9 评分。次要终点包括:1)使用修订后的美国疼痛学会患者导向问卷(APS-POQ-R)测量疼痛管理质量;2)术后阿片类药物需求。
在对照组(干预前)的 132 例患者和 MP3 组的 120 例患者中,对数据进行了分析。MP3 组在所有时间点的 QoR-9 评分均显著升高,但仅在术后 24 小时(13.4 比 14.9,P < 0.05)和 48 小时(14.0 比 15.0,P < 0.05)达到了最小临床重要差异阈值。患者在疼痛强度、活动干扰和睡眠方面报告了更好的疼痛管理质量,并且在接受日间肩关节手术后两天内报告了存在负面情绪。此外,该方案显著减少了术后三天内的阿片类药物总用量。
实施 MP3 可提高日间肩关节手术患者的整体 QoR 和术后许多缓解疼痛方面的效果,同时减少阿片类药物总用量。