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连续关节内注射布比卡因用于全髋关节置换术后镇痛:一项随机、安慰剂对照、双盲研究。

Continuous intra-articular infusion of bupivacaine for post-operative pain relief after total hip arthroplasty: a randomized, placebo-controlled, double-blind study.

机构信息

Department of Orthopedics, Chang Gung Memorial Hospital, Taoyuan, Taiwan.

出版信息

Eur J Pain. 2010 May;14(5):529-34. doi: 10.1016/j.ejpain.2009.08.008. Epub 2009 Sep 24.

DOI:10.1016/j.ejpain.2009.08.008
PMID:19781964
Abstract

BACKGROUND

Instillation of local anesthetics into a surgical site has been gaining popularity in post-operative pain management.

AIM

To determine whether continuous intra-articular infusion of bupivacaine via pain-control infusion pumps (PCIP) enhances and sustains analgesia after total hip arthroplasty (THA).

METHODS

Ninety-two patients undergoing THA were randomized to receive continuous intra-articular infusion of either 0.5% bupivacaine or 0.9% normal saline at a flow rate of 2 mL/h via a PCIP for 48 h. The primary outcome measure was pain intensity on Visual Analogue Scale (VAS) scores in the first 72 h. Other measures included time to first rescue dose of narcotics, amount of narcotic use, presence of adverse events, length of hospital stay, and hip function evaluated with the Western Ontario and McMaster Universities Osteoarthritis (WOMAC) index.

RESULTS

Despite a longer time to first narcotic rescue (56 versus 21 min, p<0.0001) in patients receiving bupivacaine, the two groups did not differ significantly in overall pain relief (p=0.54). A lower VAS score was found only at time 0 and 2 h; no difference in VAS score was noted at any other time point. Additionally, no difference was found in terms of amount of narcotic use, incidence of adverse events, hospitalization days, and the WOMAC score.

CONCLUSION

Continuous intra-articular infusion of 0.5% bupivacaine at 2 mL/h via a PCIP does not provide sustained post-operative pain relief in patients undergoing THA.

摘要

背景

局部麻醉剂在手术部位的滴注在术后疼痛管理中越来越受欢迎。

目的

确定通过疼痛控制输注泵(PCIP)持续关节内输注布比卡因是否能增强并维持全髋关节置换术(THA)后的镇痛效果。

方法

92 例行 THA 的患者随机分为两组,每组 46 例,分别通过 PCIP 以 2 mL/h 的流速持续关节内输注 0.5%布比卡因或 0.9%生理盐水,共 48 小时。主要观察指标为术后 72 小时内视觉模拟评分(VAS)的疼痛强度。其他观察指标包括首次使用麻醉性镇痛药的时间、麻醉性镇痛药的使用量、不良反应的发生情况、住院时间和采用 Western Ontario 和 McMaster 大学骨关节炎(WOMAC)指数评估的髋关节功能。

结果

尽管接受布比卡因的患者首次使用麻醉性镇痛药的时间更长(56 分钟 vs. 21 分钟,p<0.0001),但两组在总体疼痛缓解方面无显著差异(p=0.54)。仅在 0 小时和 2 小时时 VAS 评分较低;在其他任何时间点均未发现 VAS 评分有差异。此外,两组在麻醉性镇痛药使用量、不良反应发生率、住院天数和 WOMAC 评分方面均无差异。

结论

通过 PCIP 以 2 mL/h 的流速持续关节内输注 0.5%布比卡因不能为接受 THA 的患者提供持续的术后镇痛效果。

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