Department of Anesthesia and Pain Medicine, Mount Sinai Hospital, University of Toronto, Canada.
Department of Anaesthesia and Intensive Care, Post Graduate Institute of Medical Education & Research, Chandigarh, India.
Clin J Pain. 2023 Nov 1;39(11):634-642. doi: 10.1097/AJP.0000000000001147.
Various approaches to quadratus lumborum block (QLB) have been found to be an effective analgesic modality after cesarean delivery (CD). However, the evidence for the superiority of any individual approach still needs to be demonstrated. Therefore, we conducted this network meta-analysis to compare and rank the different injection sites for QLB for pain-related outcomes after CD.
PubMed, EMBASE, SCOPUS, and the Cochrane Central Registers of Controlled Trials (CENTRAL) were searched for randomized controlled trials (RCTs) evaluating the role of any approach of QLB with placebo/no block for post-CD pain. The primary outcome was parenteral consumption of morphine milligram equivalents in 24 postoperative hours. The secondary end points were early pain scores (4 to 6 h), late pain scores (24 h), adverse effects, and block-related complications. We used the surface under cumulative ranking probabilities to order approaches. The analysis was performed using Bayesian statistics (random-effects model).
Thirteen trials enrolling 890 patients were included. The surface under cumulative ranking probability for parenteral morphine equivalent consumption in 24 hours was the highest (87%) for the lateral approach, followed by the posterior and anterior approaches. The probability of reducing pain scores at all intervals was highest with the anterior approach. The anterior approach also ranked high for postoperative nausea and vomiting reduction, the only consistent reported side effect.
The anterior approach QLB had a superior probability for most patient-centric outcomes for patients undergoing CD. The findings should be confirmed through large RCTs.
各种腰方肌阻滞(QLB)方法已被证明是剖宫产(CD)后一种有效的镇痛方式。然而,任何单一方法的优势证据仍有待证明。因此,我们进行了这项网络荟萃分析,以比较和排列不同的 QLB 注射部位,以评估其在 CD 后与疼痛相关的结果。
检索了 PubMed、EMBASE、SCOPUS 和 Cochrane 对照试验中心注册库(CENTRAL),以评估任何一种 QLB 方法与安慰剂/无阻滞在 CD 后疼痛中的作用的随机对照试验(RCT)。主要结局是术后 24 小时内注射吗啡等效剂量。次要终点是早期疼痛评分(4-6 小时)、晚期疼痛评分(24 小时)、不良反应和阻滞相关并发症。我们使用累积排序概率曲线下面积来对方法进行排序。分析采用贝叶斯统计(随机效应模型)。
共纳入了 13 项试验,共 890 名患者。在 24 小时内注射吗啡等效剂量方面,外侧入路的累积排序概率最高(87%),其次是后侧入路和前侧入路。在前侧入路,在所有时间点上降低疼痛评分的概率最高。在前侧入路,术后恶心和呕吐的减少也具有较高的概率,这是唯一一致报告的副作用。
在前侧入路 QLB 方法下,接受 CD 的患者在大多数以患者为中心的结局方面具有更高的概率。这一发现需要通过大型 RCT 来证实。