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超声引导下改良胸椎腰背筋膜间平面阻滞中两种不同局麻药容量的镇痛效果:一项随机对照试验。

Analgesic efficacy of two different volumes of local anaesthetics in ultrasound-guided modified approach to the thoracolumbar interfascial plane block in patients undergoing lumbar spine surgeries: a randomized controlled trial.

机构信息

Department of Anesthesia, Surgical ICU and Pain Management, Kasr-Alainy Faculty of Medicine, Cairo University, Egypt.

Department of Anesthesia, Armed Forces College of Medicine, Egypt.

出版信息

Anaesthesiol Intensive Ther. 2023;55(5):358-365. doi: 10.5114/ait.2023.134196.

Abstract

INTRODUCTION

There is a lack of clarity regarding the ideal local anaesthetic volume for modified thoracolumbar interfascial plane (mTLIP) block. This study was designed to investigate the analgesic efficacy of two different volumes of bupivacaine 0.25% (20 mL, and 10 mL) for ultrasound-guided mTLIP block in patients undergoing lumbar spine surgeries.

MATERIAL AND METHODS

A total of 80 patients received single shot of bilateral mTLIP block at the mid- level of the operative intervention and were randomly allocated into one of the two groups to receive either 10 or 20 mL 0.25% bupivacaine on each side. Total morphine consumption in the first 24 hours postoperative was set as the primary outcome. Time to first rescue analgesia and Numeric Rating Scale (NRS) were set as secondary outcomes.

RESULTS

There was no significant difference in the primary outcome: 6.20 ± 2.18 mg (10 mL Group) vs. 5 ± 0.00 mg (20 mL Group), P = 0.056. The time of first request of rescue morphine was significantly shorter in 10 mL Group (7.80 ± 3.98 hours) as compared to the 20 mL Group (13.23 ± 3.00 hours), P < 0.001. NRS at rest and movement in all time measurements was significantly higher in 10 mL Group.

CONCLUSIONS

Bilateral mTLIP block using 40 mL of 0.25% bupivacaine (20 mL on each side) increased the postoperative total analgesic duration for lumbar spine surgeries, and was associated with a lower postoperative pain scores compared to 20 mL of 0.25% bupivacaine (10 mL on each side).

CLINICAL TRIAL REGISTRATION ID

The study was registered at clinicaltrials.gov (ID: NCT05276908) before patient's enrolment.

摘要

引言

对于改良的胸腰筋膜平面(mTLIP)阻滞,局麻药的理想容量尚不清楚。本研究旨在探讨 0.25%布比卡因(20ml 和 10ml)两种不同容量用于超声引导下 mTLIP 阻滞在腰椎手术患者中的镇痛效果。

材料与方法

共 80 例患者于手术干预中水平接受双侧 mTLIP 单次阻滞,随机分为两组,每组分别接受双侧 10 或 20ml0.25%布比卡因注射。术后 24 小时内的总吗啡消耗量为主要结局。首次解救镇痛时间和数字评分量表(NRS)为次要结局。

结果

主要结局无统计学差异:6.20±2.18mg(10ml 组)与 5±0.00mg(20ml 组),P=0.056。10ml 组首次请求解救吗啡的时间明显短于 20ml 组(7.80±3.98 小时),13.23±3.00 小时),P<0.001。在所有时间测量中,10ml 组的静止和运动时 NRS 评分均明显更高。

结论

双侧 mTLIP 阻滞使用 0.25%布比卡因 40ml(每侧 20ml)可延长腰椎手术的术后总镇痛时间,并与 20ml0.25%布比卡因(每侧 10ml)相比,术后疼痛评分较低。

临床试验注册号

该研究在患者入组前在 clinicaltrials.gov 注册(ID:NCT05276908)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db29/10801459/b05635e7fa74/AIT-55-52200-g001.jpg

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