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肾上腺素在全膝关节置换术后局部浸润镇痛中缓解疼痛和减少阿片类药物消耗的效果:一项随机对照试验。

Efficacy of epinephrine in local infiltration analgesia on pain relief and opioid consumption following total knee arthroplasty: a randomized controlled trial.

机构信息

Department of Orthopaedic Surgery, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.

出版信息

Acta Orthop. 2023 Feb 28;94:97-101. doi: 10.2340/17453674.2023.8482.

DOI:10.2340/17453674.2023.8482
PMID:36856569
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9976710/
Abstract

BACKGROUND AND PURPOSE

Local infiltration analgesia (LIA) is one of the effective regimens to reduce pain after total knee arthroplasty (TKA). Epinephrine is a commonly used sympathetic adjunct in LIA. It is expected to enhance the intensity and extend the duration of LIA. The primary aim of the study was to evaluate the efficacy of epinephrine on postoperative pain control after primary TKA.

PATIENTS AND METHODS

A total of 80 patients who underwent primary TKA were randomized into an epinephrine (EN) and a control (C) group. Postoperative visual analogue pain score (VAPS) and morphine consumption were recorded every 6 hours until 48 hours after operation. The VAPS 6-48 hours were compared using repeated measure statistics. The range of motion (ROM) on discharge and complications were also compared between these 2 groups.

RESULTS

The study showed that although VAPS differed statistically between the 2 groups at 12 hours (C higher) and 48 hours (C lower) postoperatively (p = 0.04 and 0.02, respectively), repeated measures analysis revealed that there were no significant differences in 6-48 hours VAPS (p = 0.6). Total morphine consumption in the EN and C groups was 3.4 (SD 3.7) and 4.2 (SD 4.4) mg, respectively (p = 0.4). ROM on discharge was also similar between the groups. No complications were detected in this study.

CONCLUSION

Our study showed that additional epinephrine in LIA had a statistically significant reduction in VAPS at 12 hours and morphine usage during 6-12 hours when compared with the control group. However, the magnitude of difference did not reach minimal clinically importance difference (MCID) value for TKA.

摘要

背景与目的

局部浸润镇痛(LIA)是减轻全膝关节置换术后疼痛的有效方案之一。肾上腺素是 LIA 中常用的交感神经辅助药物,它有望增强 LIA 的强度并延长其持续时间。本研究的主要目的是评估肾上腺素对初次全膝关节置换术后疼痛控制的疗效。

患者与方法

本研究共纳入 80 例初次接受全膝关节置换术的患者,随机分为肾上腺素(EN)组和对照组(C)。记录术后每 6 小时的视觉模拟疼痛评分(VAPS)和吗啡消耗量,直至术后 48 小时。采用重复测量统计比较 6-48 小时 VAPS。还比较了两组患者的出院时关节活动度(ROM)和并发症。

结果

研究表明,尽管术后 12 小时(C 组较高)和 48 小时(C 组较低)两组间 VAPS 存在统计学差异(分别为 p = 0.04 和 0.02),但重复测量分析显示 6-48 小时 VAPS 无显著差异(p = 0.6)。EN 组和 C 组的吗啡总消耗量分别为 3.4(SD 3.7)mg 和 4.2(SD 4.4)mg(p = 0.4)。两组出院时的 ROM 也相似。本研究未发现任何并发症。

结论

与对照组相比,LIA 中加入肾上腺素可在术后 12 小时时显著降低 VAPS,同时在 6-12 小时时降低吗啡用量。然而,差异的幅度并未达到全膝关节置换术的最小临床重要差异(MCID)值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3a8/9976710/80732ebc23b6/ActaO-94-8482-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3a8/9976710/60646707abbe/ActaO-94-8482-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3a8/9976710/80732ebc23b6/ActaO-94-8482-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3a8/9976710/60646707abbe/ActaO-94-8482-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3a8/9976710/80732ebc23b6/ActaO-94-8482-g002.jpg

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