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膝关节置换术后围手术期辅助皮质类固醇用于术后镇痛。

Perioperative adjuvant corticosteroids for postoperative analgesia in knee arthroplasty.

机构信息

a Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences (NDORMS) , University of Oxford , Oxford , UK.

b Centre for Statistics in Medicine , University of Oxford , Oxford , UK.

出版信息

Acta Orthop. 2018 Feb;89(1):71-76. doi: 10.1080/17453674.2017.1391409. Epub 2017 Oct 25.

Abstract

Background and purpose - Immediate postoperative pain management offered in knee arthroplasty is suboptimal in up to one-third of patients resulting in high opiate consumption and delayed discharge. In this meta-analysis we investigate the analgesic effect and safety of perioperative adjuvant corticosteroids in knee arthroplasty. Methods - Databases Medline, Embase, and Central were searched for randomized studies comparing the analgesic effect of adjuvant perioperative corticosteroids in knee arthroplasty. Our primary outcome was pain score at 24 hours postoperatively. Secondary outcomes included pain at 12, 48, and 72 hours, opiate consumption, postoperative nausea and vomiting, infection, and discharge time. Systemic (intravenous) and local (intra-articular) corticosteroids were analyzed separately. Results - 14 randomized controlled trials (1,396 knees) were included. Mean corticosteroid dosages were predominantly 50-75mg oral prednisolone equivalents for both systemic and local routes. Systemic corticosteroids demonstrated statistically significant and clinically modest reductions in pain at 12 hours by -1.1 points (95%CI -2.2 to 0.02), 24 hours by -1.3 points (CI -2.3 to -0.26) and 48 hours by -0.4 points (CI -0.67 to -0.04). Local corticosteroids did not reduce pain. Opiate consumption, postoperative nausea and vomiting, infection, or time till discharge were similar between groups. Interpretation - Corticosteroids modestly reduce pain postoperatively at 12 and 24 hours when used systemically without any increase in associated risks for dosages between 50 and 75 mg oral prednisolone equivalents.

摘要

背景与目的-膝关节置换术后的即时疼痛管理在多达三分之一的患者中并不理想,导致阿片类药物消耗增加和出院延迟。在这项荟萃分析中,我们研究了围手术期辅助皮质类固醇在膝关节置换术中的镇痛效果和安全性。

方法-检索 Medline、Embase 和 Central 数据库,以比较膝关节置换术中辅助皮质类固醇的镇痛效果的随机研究。我们的主要结局是术后 24 小时的疼痛评分。次要结局包括 12、48 和 72 小时的疼痛、阿片类药物消耗、术后恶心和呕吐、感染以及出院时间。系统(静脉内)和局部(关节内)皮质类固醇分别进行分析。

结果-纳入了 14 项随机对照试验(1396 个膝关节)。系统和局部途径的皮质类固醇平均剂量主要为 50-75mg 口服泼尼松等效剂量。全身皮质类固醇在 12 小时时疼痛显著降低 -1.1 分(95%CI -2.2 至 0.02),24 小时时疼痛降低 -1.3 分(CI -2.3 至 -0.26),48 小时时疼痛降低 -0.4 分(CI -0.67 至 -0.04)。局部皮质类固醇并未减轻疼痛。阿片类药物消耗、术后恶心和呕吐、感染或直至出院的时间在各组之间相似。

结论-皮质类固醇以 50 至 75mg 口服泼尼松等效剂量使用时,可适度减轻术后 12 和 24 小时的疼痛,而不会增加相关风险。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b9a0/5810836/867305b39d7a/iort-89-71.F01.jpg

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