Comparative Efficacy of Ultrasound-Guided Quadratus Lumborum Block Versus Alternative Fascial Plane Blocks for Postoperative Analgesia Following Hysterectomy: A Systematic Review and Meta-Analysis.

IF 1.5 Q2 ANESTHESIOLOGY
Anesthesiology Research and Practice Pub Date : 2026-05-17 eCollection Date: 2026-01-01 DOI:10.1155/anrp/5760922
Priyanka Dwivedi, Tejas K Patel, Vijeta Bajpai, Chanchal Goyal, Ankita Kabi, Santosh Kumar Sharma, Hari Shanker Joshi, Pratibha Singh
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引用次数: 0

Abstract

Objective: The primary aim was to compare the efficacy of the quadratus lumborum (QL) block with alternative fascial plane blocks for postoperative analgesia following hysterectomy, while secondary aims were to compare total 24-h analgesic consumption, postoperative pain scores at different time intervals, and the incidence of postoperative nausea and vomiting (PONV) between the QL block and comparator groups.

Methods: Electronic databases were systematically searched for studies that compared bilateral ultrasound-guided single-injection QL block to no block or other fascial plane blocks in hysterectomy surgeries. The QL block was compared with other fascial plane blocks, including transversus abdominis plane (TAP), oblique subcostal TAP (OSTAP), erector spinae plane (ESP), and combined TAP with ilioinguinal/iliohypogastric nerve block. The methodological quality of the included studies was assessed using the RoB 2.0 risk-of-bias tool. All outcomes were pooled using the Mantel-Haenszel method and random-effect model.

Results: After screening 946 relevant articles, 15 RCTs were included in this meta-analysis. The QL block significantly prolonged the time to first rescue analgesic request compared to the TAP block in the abdominal hysterectomy subgroup (MD 244.77 [95% CI: 191.98 to 297.56], I 2 = 89%; GRADE evidence-"high") and the laparoscopic hysterectomy subgroup (MD 443.15 [95% CI: 56.37 to 829.93], I 2 = 98%; GRADE evidence-"high"). Regarding the 24-h total analgesic requirement, the QL block significantly reduced its consumption than the TAP block in both the abdominal (MD -2.64 [95% CI: -4.19 to -1.09], I 2 = 93%; GRADE evidence-"moderate") and the laparoscopic hysterectomy subgroup (MD -6.65 [95% CI: -7.39 to -5.91], I 2 = NA due to n = 1; GRADE evidence-"moderate"). The risk of PONV did not differ significantly between the QL block and placebo in abdominal hysterectomy (RR 2.48 [95% CI: 0.50 to -12.35], I 2 = 0%; GRADE evidence: "moderate") and laparoscopic hysterectomy arm (RR 0.78 [95% CI: 0.50 to -1.22], I 2 = 44%; GRADE evidence: "moderate"). The QL block did not show significant difference in risk of PONV than the TAP block across both the abdominal (RR 0.59 [95% CI: 0.25 to 1.40], I 2 = 0%; GRADE evidence: "moderate") and laparoscopic hysterectomy subgroups (RR 0.86 [95% CI: 0.30 to 2.45], I 2 = 0%; GRADE evidence: "moderate").

Conclusion: The QL block provides superior postoperative analgesia compared with the TAP block in patients undergoing abdominal and laparoscopic hysterectomy.

超声引导腰方肌阻滞与替代筋膜平面阻滞用于子宫切除术后镇痛的疗效比较:系统回顾和荟萃分析。
目的:主要目的是比较腰方肌(QL)阻滞与其他筋膜平面阻滞对子宫切除术后术后镇痛的效果,次要目的是比较腰方肌阻滞与对照组之间24小时总镇痛消耗、不同时间间隔的术后疼痛评分和术后恶心呕吐(PONV)发生率。方法:系统检索电子数据库,比较双侧超声引导下单次注射QL阻滞与无阻滞或其他筋膜面阻滞在子宫切除术中的研究。将QL阻滞与其他筋膜平面阻滞进行比较,包括腹横平面(TAP)、斜肋下平面(OSTAP)、竖脊平面(ESP),以及TAP联合髂腹股沟/髂腹下神经阻滞。使用RoB 2.0风险偏倚工具评估纳入研究的方法学质量。所有结果采用Mantel-Haenszel方法和随机效应模型进行汇总。结果:在筛选了946篇相关文章后,本meta分析纳入了15项rct。与TAP阻滞相比,QL阻滞显著延长了腹部子宫切除术亚组(MD 244.77 [95% CI: 191.98至297.56],I 2 = 89%;等级证据-“高”)和腹腔镜子宫切除术亚组(MD 443.15 [95% CI: 56.37至829.93],I 2 = 98%;等级证据-“高”)第一次抢救镇痛请求的时间。关于24小时总镇痛需求,QL阻滞在腹部(MD -2.64 [95% CI: -4.19至-1.09],I 2 = 93%;等级证据-“中等”)和腹腔镜子宫切除术亚组(MD -6.65 [95% CI: -7.39至-5.91],I 2 = NA,因为n = 1;等级证据-“中等”)均显著低于TAP阻滞。在腹式子宫切除术中,QL阻断组和安慰剂组发生PONV的风险无显著差异(RR 2.48 [95% CI: 0.50 ~ -12.35],ⅱ= 0%;分级证据:“中度”)和腹腔镜子宫切除术组(RR 0.78 [95% CI: 0.50 ~ -1.22],ⅱ= 44%;分级证据:“中度”)。QL阻滞与TAP阻滞相比,在腹部发生PONV的风险无显著差异(RR 0.59 [95% CI: 0.25 ~ 1.40],ⅱ= 0%;分级证据:“中度”)和腹腔镜子宫切除术亚组(RR 0.86 [95% CI: 0.30 ~ 2.45],ⅱ= 0%;分级证据:“中度”)。结论:与TAP阻滞相比,QL阻滞在腹部和腹腔镜子宫切除术患者中具有更好的术后镇痛效果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
3.10
自引率
0.00%
发文量
29
审稿时长
18 weeks
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