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关节镜肩关节手术后连续输注导管行肩峰下镇痛与安慰剂对照的系统评价和荟萃分析。

Subacromial analgesia via continuous infusion catheter vs. placebo following arthroscopic shoulder surgery: a systematic review and meta-analysis of randomized trials.

机构信息

Department of Orthopaedic Surgery, Royal Prince Alfred Hospital, Camperdown, NSW, Australia.

Department of Orthopaedic Surgery, Royal Prince Alfred Hospital, Camperdown, NSW, Australia.

出版信息

J Shoulder Elbow Surg. 2020 Mar;29(3):471-482. doi: 10.1016/j.jse.2019.11.010.

Abstract

BACKGROUND

Subacromial analgesia (SAA) is hypothesized to reduce pain after arthroscopic shoulder surgery by delivering a continuous infusion of local anesthetic directly to the surgical site. The purpose of this systematic review and meta-analysis was to evaluate the efficacy of SAA vs. placebo for pain relief after arthroscopic subacromial shoulder procedures.

METHODS

MEDLINE, Embase, PubMed, and the Cochrane Central Register of Controlled Trials were searched for randomized controlled trials comparing SAA with placebo after arthroscopic shoulder surgery. Outcomes collected included pain scores (converted to equivalent ordinal visual analog scores; minimal clinically important difference 1.4 cm), oral morphine equivalents used postoperatively, and catheter-related complications. Meta-analysis was performed via a random-effects model. Included trials underwent a risk of bias and quality of evidence assessment.

RESULTS

Nine studies involving 459 participants were included. There were no clinically significant changes for pain scores in SAA at 6-, 12-, 24-, and 48-hour postoperative timepoints. Patients receiving SAA used less morphine equivalents of pain medication at 12 hours only (-0.37 mg, 95% confidence interval: -0.63 to -0.11), but there was no significant difference at 24 and 48 hours. There were no major complications (infection or reoperation). Included trials demonstrated a moderate risk-of-bias, and low to very low quality of evidence for primary outcomes.

CONCLUSION

Subacromial continuous infusion of local anesthetic does not provide a clinically significant benefit compared with placebo as part of a multimodal analgesia regime after arthroscopic subacromial surgical procedures. Future, high-quality trials are required to further assess the efficacy of SAA against placebo.

摘要

背景

肩峰下局部镇痛(SAA)通过将局部麻醉剂直接输送到手术部位,被假设为可以减少关节镜肩手术后的疼痛。本系统评价和荟萃分析的目的是评估 SAA 与安慰剂在关节镜下肩峰下手术治疗后缓解疼痛的效果。

方法

通过 MEDLINE、Embase、PubMed 和 Cochrane 中央对照试验注册库,检索比较关节镜肩手术后 SAA 与安慰剂的随机对照试验。收集的结果包括疼痛评分(转换为等效的数字模拟评分;最小临床重要差异 1.4cm)、术后使用的口服吗啡等效物和导管相关并发症。采用随机效应模型进行荟萃分析。纳入的试验进行了风险偏倚和证据质量评估。

结果

纳入了 9 项涉及 459 名参与者的研究。在术后 6、12、24 和 48 小时的时间点,SAA 对疼痛评分没有明显的临床改善。接受 SAA 的患者仅在 12 小时时使用的吗啡等效物止痛药较少(-0.37mg,95%置信区间:-0.63 至 -0.11),但在 24 和 48 小时时没有显著差异。没有重大并发症(感染或再次手术)。纳入的试验显示,在主要结局方面,存在中度偏倚,证据质量为低至极低。

结论

与安慰剂相比,关节镜下肩峰下手术后,作为多模式镇痛方案的一部分,肩峰下连续输注局部麻醉剂并没有提供明显的临床益处。需要未来进行高质量的试验,以进一步评估 SAA 与安慰剂的疗效。

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