利多卡因和罗哌卡因混合作为WALANT手术的局麻药:一项前瞻性随机研究。

IF 2.1 2区 医学 Q2 ORTHOPEDICS
Yann Gricourt, Bob-Valery Occean, Amélie Favrelle, Thierry Chevallier, Olivier Mares, Philippe Cuvillon
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引用次数: 0

摘要

目的:采用利多卡因进行全清醒局麻无止血带(WALANT)技术,提供有效的麻醉效果。然而,这种技术的镇痛时间也很短(3小时)。本研究分析了当罗哌卡因(一种长效局麻药,8-12小时)加入利多卡因后的疼痛缓解和恢复质量。方法:这项前瞻性、双盲随机研究纳入了计划在WALANT下进行上肢远端手术的患者。患者被随机分为两组:利多卡因组(1%利多卡因20 mL, 1:10万肾上腺素浓度)或利多卡因-罗哌卡因组(1%利多卡因18 mL, 1:10万肾上腺素浓度,0.75%罗哌卡因2 mL)。主要终点是第2天的术后恢复质量(QoR)-40评分。次要终点是术后前7天的疼痛评分、抢救性镇痛、不良医疗和手术事件以及3个月时的慢性疼痛。结果:在研究期间,91例患者被随机分组。利多卡因组QoR评分为187分(182 ~ 190分),利多卡因-罗哌卡因组QoR评分为186分(180 ~ 188分)。利多卡因组中位镇痛时间为8(4-12)小时,利多卡因-罗哌卡因组中位镇痛时间为8(4-10)小时。在3个月时,两组在镇痛、疼痛评分、不良事件或慢性疼痛发生率方面没有差异。结论:在利多卡因中加入罗哌卡因治疗WALANT并不能改善患者术后恢复。研究类型/证据水平:治疗性Ib。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mixture of Lidocaine and Ropivacaine as a Local Anesthetic in WALANT Surgery: A Prospective Randomized Study.

Purpose: With lidocaine, the wide awake local anesthesia no tourniquet (WALANT) technique provides effective anesthesia. However, analgesia is also short with this technique (3 hours). This study analyzed pain relief and quality of recovery when ropivacaine (a long-acting local anesthetic, 8-12 hours) was added to lidocaine.

Methods: This prospective, double-blinded randomized study included patients scheduled for distal upper limb surgery under WALANT. Patients were randomly assigned to a group: the lidocaine group (20 mL of 1% lidocaine at 1:100,000 epinephrine) or the lidocaine-ropivacaine group (18 mL of 1% lidocaine at 1:100,000 epinephrine and 2 mL of 0.75% ropivacaine). The primary end point was the postoperative Quality of Recovery (QoR)-40 score at Day 2. Secondary end points were the pain score for the first 7 days postsurgery, rescue analgesia, adverse medical and surgical events, and chronic pain at 3 months.

Results: Over the study period, 91 patients were randomized. The QoR score was 187 (182-190) in the lidocaine group and 186 (180-188) for lidocaine-ropivacaine group. The median duration of analgesia was 8 (4-12) hours for the lidocaine group and 8 (4-10) hours for the lidocaine-ropivacaine group. No difference was observed between groups regarding rescue analgesia, pain score, adverse events, or incidence of chronic pain at 3 months.

Conclusions: Adding ropivacaine to lidocaine for WALANT did not improve patient recovery after surgery.

Type of study/level of evidence: Therapeutic Ib.

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来源期刊
CiteScore
3.20
自引率
10.50%
发文量
402
审稿时长
12 weeks
期刊介绍: The Journal of Hand Surgery publishes original, peer-reviewed articles related to the pathophysiology, diagnosis, and treatment of diseases and conditions of the upper extremity; these include both clinical and basic science studies, along with case reports. Special features include Review Articles (including Current Concepts and The Hand Surgery Landscape), Reviews of Books and Media, and Letters to the Editor.
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