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全肩关节置换术后肌间沟神经阻滞与脂质体布比卡因注射的随机试验方案

Randomized trial protocol of interscalene nerve block vs liposomal bupivacaine injection after total shoulder arthroplasty.

作者信息

He Jianbin, Li Yalan

机构信息

Department of Anesthesiology, The Second Clinical Medical College, Jinan University/Shenzhen People's Hospital.

Department of Anesthesiology, The first affiliated hospital of Jinan University, Guangdong Province, China.

出版信息

Medicine (Baltimore). 2020 Jul 10;99(28):e20968. doi: 10.1097/MD.0000000000020968.

Abstract

BACKGROUND

The possibility of local infiltration analgesia (LIA) replacing interscalene blockade (ISB) as an integral component of a multimodal clinical pathway for total shoulder arthroplasty (TSA) needs to be further investigated. We thus further designed a randomized controlled study to compare LIA with ISB in the treatment of TSA.

METHODS

This blinded and randomised study was performed after approval of the institutional review board in the first affiliated hospital of Jinan University. The included patients were all aged over 18 years and underwent shoulder arthroplasty because of osteoarthritis of the shoulder. Subjects were randomized into 2 groups as follows: LIA or ISB. The primary outcome of this noninferiority study is opioid consumption within the first 24 hours following surgery. Secondary outcomes included pain scores, length of hospital stay, complication, and satisfaction score. P value < .05 was considered statistically significant.

RESULTS

For the present trial, we hypothesized that there would be no difference in pain score levels and opioid medication use throughout admission.

TRIAL REGISTRATION

This study protocol was registered in Research Registry (researchregistry5640).

摘要

背景

局部浸润镇痛(LIA)作为全肩关节置换术(TSA)多模式临床路径的一个组成部分,替代肌间沟阻滞(ISB)的可能性需要进一步研究。因此,我们进一步设计了一项随机对照研究,比较LIA和ISB在TSA治疗中的效果。

方法

这项双盲随机研究在暨南大学附属第一医院机构审查委员会批准后进行。纳入的患者均为18岁以上,因肩部骨关节炎接受肩关节置换术。受试者随机分为两组:LIA组或ISB组。这项非劣效性研究的主要结局是术后24小时内的阿片类药物消耗量。次要结局包括疼痛评分、住院时间、并发症和满意度评分。P值<0.05被认为具有统计学意义。

结果

对于本试验,我们假设在整个住院期间疼痛评分水平和阿片类药物使用方面不会有差异。

试验注册

本研究方案已在研究注册库(researchregistry5640)注册。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fbf/7360251/3c05d0683599/medi-99-e20968-g001.jpg

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