Preoperative Risk Factors for Opioid Use Predict Self-Reported Health and Function Up to 6 Months After Anterior Cruciate Ligament Reconstruction.

Q3 Medicine
Arthroscopy Sports Medicine and Rehabilitation Pub Date : 2026-09-06 eCollection Date: 2026-10-01 DOI:10.1002/ars2.70066
Eric V Neufeld, William DeGouveia, Camille Pinpin, Matthew Zinner, Michael J Sayegh, Michael J Meade, Steven E Rokito
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Abstract

Purpose: To identify risk factors that predict the need for rescue opioid use and patient-reported outcomes following an opioid-limiting postoperative analgesia protocol after anterior cruciate ligament reconstruction.

Methods: This prospective cohort study recruited 44 patients undergoing primary arthroscopic-assisted anterior cruciate ligament reconstruction. Preoperatively, patients completed questionnaires including demographics, medical history, Visual Analog Scale (VAS), Brief Resilience Scale, Six-Item State-Trait Anxiety Inventory, Patient Health Questionnaire-2, Single Assessment Numeric Evaluation score, and patient-reported outcome measures (PROMs) including Patient-Reported Outcomes Measurement Information System physical component. Postoperatively, patients received acetaminophen, meloxicam, tramadol, gabapentin, and oxycodone. Morphine milligram equivalents (MMEs) and VAS were assessed at multiple timepoints through 6 months. PROMs were completed at 3 and 6 months. Patients were analyzed as a single group and partitioned by Brief Resilience Scale and Six-Item State-Trait Anxiety Inventory scores into low-normal (1.00-4.30) and high (4.31-5.00) resilience, and low (20-37) and moderate-high (38-80) anxiety groups, respectively.

Results: Prior opioid use positively predicted VAS and MME at 48 to 72 hours and MME at 6 weeks. Body mass index positively predicted MME at 2 weeks. Surgical history negatively predicted VAS at 48 to 72 hours, but positively predicted change in Single Assessment Numeric Evaluation score at 3 and 6 months and Patient-Reported Outcomes Measurement Information System physical component score at 6 months.

Conclusions: Only 4.8% of patients required opioid medications more than 2 weeks postoperatively. Patients with prior opioid use exhibited greater postoperative pain and narcotic consumption. Higher body mass index linked to increased opioid use at 2 weeks, whereas individuals with prior surgical history reported less pain and improved PROMs postoperatively. Measurements of patient resilience and anxiety show little effect on postoperative pain, opioid consumption, and PROMs requiring further study.

Level of evidence: Level III, retrospective prognostic case series.

术前阿片类药物使用的危险因素预测前交叉韧带重建后6个月的自我报告健康和功能
目的:确定预测前交叉韧带重建术后阿片类药物限制术后镇痛方案后阿片类药物使用需求的危险因素和患者报告的结果。方法:这项前瞻性队列研究招募了44例接受初级关节镜辅助前交叉韧带重建的患者。术前,患者完成包括人口统计学、病史、视觉模拟量表(VAS)、简短恢复力量表、六项状态-特质焦虑量表、患者健康问卷-2、单一评估数字评估评分和患者报告结果测量(PROMs)(包括患者报告结果测量信息系统物理成分)在内的问卷。术后给予对乙酰氨基酚、美洛昔康、曲马多、加巴喷丁和羟考酮。在6个月内的多个时间点评估吗啡毫克当量(MMEs)和VAS。在3个月和6个月时完成PROMs。采用简易心理弹性量表和六项状态-特质焦虑量表评分将患者分为低正常(1.00-4.30)和高焦虑(4.31-5.00)、低焦虑(20-37)和中高焦虑(38-80)组。结果:既往阿片类药物使用对48 ~ 72小时的VAS和MME以及6周的MME有正向预测作用。体重指数正预测2周时的MME。手术史对48 ~ 72小时的VAS评分有负相关预测,但对3个月和6个月的单一评估数值评估评分和6个月患者报告结果测量信息系统物理成分评分的变化有正向预测。结论:只有4.8%的患者术后2周以上需要阿片类药物治疗。既往使用阿片类药物的患者表现出更大的术后疼痛和麻醉消耗。2周时,较高的体重指数与阿片类药物使用增加有关,而有既往手术史的个体术后疼痛减轻,PROMs改善。患者恢复力和焦虑的测量显示,对术后疼痛、阿片类药物消耗和PROMs的影响很小,需要进一步研究。证据等级:III级,回顾性预后病例系列。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
2.70
自引率
0.00%
发文量
218
审稿时长
45 weeks
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