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腹横肌平面阻滞与第 2 型腰方肌阻滞用于肾移植术后镇痛的随机对照试验。

Transversus abdominis plane block versus quadratus lumborum block type 2 for analgesia in renal transplantation: A randomised trial.

机构信息

From the I Department of Anesthesiology and Intensive Care, Medical University of Warsaw, Warsaw (MK, MJ, KZ, BB, JT) and Department of Anesthesiology and Intensive Care, Collegium Medicum, University of Warmia and Mazury in Olsztyn, Olsztyn, Poland (MM, MW-D, DO).

出版信息

Eur J Anaesthesiol. 2020 Sep;37(9):773-789. doi: 10.1097/EJA.0000000000001193.

Abstract

BACKGROUND

Several studies have shown an analgesic efficacy of a transversus abdominis plane block (TAPB) in reducing opioid requirements during and after cadaveric renal transplantation surgery, but the effect of a quadratus lumborum block (QLB) in this type of surgery is unclear.

OBJECTIVES

The main objective of this prospective, randomised, double-centre clinical study was to compare the analgesic efficacy of a one-sided lateral approach TAPB with a unilateral QLB type 2 in cadaveric renal transplantation surgery.

DESIGN

Randomised, single-blinded trial.

SETTING

Two University-affiliated tertiary care hospitals between April 2016 and May 2017.

PATIENTS

A total of 101 patients aged more than 18 years, scheduled for cadaveric renal transplantation.

INTERVENTIONS

On receiving ethical board approval and individual informed consent, consecutive patients were allocated randomly to receive either an ultrasound-guided single-shot lateral TAPB or an ultrasound-guided single-shot QLB type 2 on the surgical side using 20 ml of bupivacaine 0.25% with adrenaline after a standardised induction of general anaesthesia. All patients on surgical completion and recovery from general anaesthesia were admitted to the postanaesthesia care unit for 24 h. They received standardised intravenous patient-controlled analgesia with fentanyl, and their pain scores were noted at regular intervals.

MAIN OUTCOME MEASURES

The primary endpoint was total cumulative fentanyl dose used per kg body mass in the first 24 h after surgery. Secondary outcomes were the need to start a continuous infusion of fentanyl in addition to patient-controlled analgesia boluses during the stay in post-anaesthesia care unit, postoperative pain severity measured using a numerical rating scale, patient satisfaction with analgesic treatment, evidence of postoperative nausea and vomiting, pruritus and sedation level.

RESULTS

The 49 patients allocated to the QLB type 2 group used significantly less fentanyl per kg in the first 24 h after surgery than the 52 patients who received a TAPB (median [IQR] 4.2 [2.3 to 8.0] μg kg versus 6.7 [3.5 to 10.7] μg kg, P = 0.042). No statistically significant differences were noted in the secondary endpoints within the study, including the frequency of adverse effects of opioids.

CONCLUSION

The reduction of fentanyl consumption in the first 24 h after renal transplantation with no difference in pain intensity and patient satisfaction shows a beneficial effect of one-sided QLB type 2 over a one-sided TAPB in regards to postoperative analgesia. However, the reduction in opioid consumption did not affect the frequency of opioid-related adverse effects.

TRIAL REGISTRATION

ClinicalTrials.gov ID: NCT02783586.

摘要

背景

多项研究表明,在尸体肾移植手术中,腹横肌平面阻滞(TAPB)可减少阿片类药物的需求,具有镇痛效果,但关于后路竖脊肌阻滞(QLB)在这种手术中的效果尚不清楚。

目的

本前瞻性、随机、双中心临床研究的主要目的是比较单侧外侧入路 TAPB 与单侧 QLB 2 型在尸体肾移植手术中的镇痛效果。

设计

随机、单盲试验。

地点

2016 年 4 月至 2017 年 5 月期间的两家大学附属三级护理医院。

患者

年龄大于 18 岁,计划接受尸体肾移植的 101 例患者。

干预措施

在获得伦理委员会批准和个人知情同意后,连续患者被随机分配接受超声引导下单次外侧 TAPB 或单侧 QLB 2 型阻滞,在全身麻醉诱导后使用 20ml 0.25%布比卡因加肾上腺素。所有患者在手术完成并从全身麻醉中恢复后,均在麻醉后监护病房(PACU)入住 24 小时。他们接受芬太尼标准化静脉患者自控镇痛(PCIA),并定期记录疼痛评分。

主要观察指标

主要终点是手术后 24 小时内每公斤体重使用的芬太尼总累积剂量。次要结局是在 PACU 住院期间,除了 PCIA 推注外,是否需要开始持续输注芬太尼、术后疼痛严重程度(用数字评分量表测量)、患者对镇痛治疗的满意度、术后恶心和呕吐、瘙痒和镇静水平的证据。

结果

QLB 2 组的 49 例患者术后 24 小时内每公斤使用的芬太尼明显少于接受 TAPB 的 52 例患者(中位数[IQR]4.2[2.3 至 8.0]μg/kg 比 6.7[3.5 至 10.7]μg/kg,P=0.042)。在研究的次要终点中,包括阿片类药物不良反应的频率,均未观察到统计学差异。

结论

肾移植后 24 小时内芬太尼消耗量的减少,而疼痛强度和患者满意度没有差异,表明单侧 QLB 2 型在术后镇痛方面优于单侧 TAPB。然而,阿片类药物消耗的减少并未影响阿片类药物相关不良反应的频率。

试验注册

ClinicalTrials.gov 标识符:NCT02783586。

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