布比卡因脂质体用于腹腔镜肾切除术后腰方肌外侧弓形上韧带阻滞的镇痛效果:一项单中心、三盲、随机对照试验。

IF 2.5 3区 医学 Q2 CLINICAL NEUROLOGY
Journal of Pain Research Pub Date : 2025-09-26 eCollection Date: 2025-01-01 DOI:10.2147/JPR.S550175
Hanwei Gong, Zifei Wang, Guangrui Kou, Zichen Zheng, Li Xu, Beining Hang, Yan Peng, Qianwei Sun, Mengxing Jia
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引用次数: 0

摘要

目的:腰方肌阻滞外侧弓上韧带(QLB-LSAL)已被证明对腹腔镜肾切除术患者术后疼痛管理有效。布比卡因脂质体,一种新型的缓释局部麻醉剂,提供长达72小时的镇痛作用。然而,其在QLB-LSAL中的镇痛作用尚未确定。本随机对照试验旨在比较布比卡因脂质体与盐酸布比卡因在腹腔镜肾切除术后接受QLB-LSAL患者的术后镇痛效果。患者和方法:116例患者在全麻下行择期腹腔镜肾切除术。患者按1:1的比例随机分为两组。布比卡因脂质体组(n = 53)给予布比卡因脂质体(133mg) 10 mL与生理盐水10 mL混合,共20 mL;盐酸布比卡因组(n = 53)给予0.375%盐酸布比卡因20 mL。术后给予患者控制的舒芬太尼镇痛。主要观察指标为术后48小时内吗啡当量总消耗量。结果:布比卡因脂质体组术后48 h内吗啡当量总消耗量显著低于盐酸布比卡因组(mean±SD: 31.8±2.3 vs 20.7±2.8,95%可信区间:10.1 ~ 12.1,P < 0.001)。布比卡因脂质体组术后恢复质量较好(P < 0.05),超过最小临床重要差异(P < 0.05),两组不良事件发生率无显著差异(P < 0.05)。结论:研究结果表明,在QLB-LASL患者中给予布比卡因脂质体可显著减少术后阿片类药物的消耗,同时提高腹腔镜肾切除术患者的恢复质量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Liposomal Bupivacaine for Quadratus Lumborum Block at the Lateral Supra-Arcuate Ligament in the Analgesic Effect After Laparoscopic Nephrectomy: A Single-Centre, Triple-Blind, Randomized Controlled Trial.

Liposomal Bupivacaine for Quadratus Lumborum Block at the Lateral Supra-Arcuate Ligament in the Analgesic Effect After Laparoscopic Nephrectomy: A Single-Centre, Triple-Blind, Randomized Controlled Trial.

Liposomal Bupivacaine for Quadratus Lumborum Block at the Lateral Supra-Arcuate Ligament in the Analgesic Effect After Laparoscopic Nephrectomy: A Single-Centre, Triple-Blind, Randomized Controlled Trial.

Liposomal Bupivacaine for Quadratus Lumborum Block at the Lateral Supra-Arcuate Ligament in the Analgesic Effect After Laparoscopic Nephrectomy: A Single-Centre, Triple-Blind, Randomized Controlled Trial.

Purpose: Quadratus lumborum block at the lateral supra-arcuate ligament (QLB-LSAL) has demonstrated efficacy in postoperative pain management for laparoscopic nephrectomy patients. Liposomal bupivacaine, a novel sustained-release local anesthetic, provides analgesia lasting up to 72 hours. However, its analgesic effect in QLB-LSAL remains undetermined. This randomized controlled trial aimed to compare the postoperative analgesic efficacy of liposomal bupivacaine versus bupivacaine hydrochloride in patients receiving QLB-LSAL after laparoscopic nephrectomy.

Patients and methods: A total of 116 patients were scheduled to undergo elective laparoscopic nephrectomy under general anesthesia. Patients were randomly assigned to two groups in a 1:1 ratio. The liposomal bupivacaine group (n = 53) received a mixture of 10 mL of liposomal bupivacaine (133mg) and 10 mL of normal saline, totaling 20 mL, while the bupivacaine hydrochloride group (n = 53) received 20 mL of 0.375% bupivacaine hydrochloride. Post-surgical patient-controlled sufentanil analgesia was provided. The primary outcome was total morphine equivalent consumption within the first 48 hours postoperatively.

Results: The total consumption of morphine equivalents within 48 hours postoperatively was significantly lower in the liposomal bupivacaine group than in the bupivacaine hydrochloride group (mean ± SD: 31.8 ± 2.3 vs 20.7 ± 2.8, 95% Confidence Intervals: 10.1 to 12.1, P < 0.001). The liposomal bupivacaine group demonstrated superior postoperative recovery quality (P < 0.05), exceeding the minimal clinically important difference, whereas no significant difference in the incidence of adverse events (P > 0.05) was observed between the two groups.

Conclusion: The findings demonstrated that administration of liposomal bupivacaine in QLB-LASL significantly reduced postoperative opioid consumption while concurrently improving recovery quality in patients undergoing laparoscopic nephrectomy.

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来源期刊
Journal of Pain Research
Journal of Pain Research CLINICAL NEUROLOGY-
CiteScore
4.50
自引率
3.70%
发文量
411
审稿时长
16 weeks
期刊介绍: Journal of Pain Research is an international, peer-reviewed, open access journal that welcomes laboratory and clinical findings in the fields of pain research and the prevention and management of pain. Original research, reviews, symposium reports, hypothesis formation and commentaries are all considered for publication. Additionally, the journal now welcomes the submission of pain-policy-related editorials and commentaries, particularly in regard to ethical, regulatory, forensic, and other legal issues in pain medicine, and to the education of pain practitioners and researchers.
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