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腕部局部麻醉下上肢远端手术与腋路阻滞术后患者满意度:一项倾向匹配比较队列研究。

Patient satisfaction after distal upper limb surgery under WALANT versus axillary block: A propensity-matched comparative cohort study.

作者信息

Meunier V, Mares O, Gricourt Y, Simon N, Kouyoumdjian P, Cuvillon P

机构信息

Department of Anesthesiology and Pain Management, Centre Hospitalo-Universitaire (CHU) Carémeau, Place du Professeur Debré, Nîmes, and Montpellier University 1, Montpellier, France.

Department of Traumatology and Orthopedic Surgery, Centre Hospitalo-Universitaire (CHU) Carémeau, Place du Professeur Debré, Nîmes, and Montpellier University 1, Montpellier, France.

出版信息

Hand Surg Rehabil. 2022 Oct;41(5):576-581. doi: 10.1016/j.hansur.2022.06.005. Epub 2022 Jul 6.

Abstract

Distal upper limb surgery is performed under WALANT (Wide Awake Local Anesthesia No Tourniquet) in many outpatient centers because the benefits are numerous: simple, low-cost technique, with fast turnover and short length of stay. In view of a paucity of data concerning patient satisfaction, this non-randomized cohort study was designed to compare EVAN-LR anesthesia satisfaction questionnaire results (information, pain, expectation, attention, discomfort: 0-100 points) between patients receiving WALANT or axillary nerve block (AxB). After IRB approval, patients (>18 years, stable ASA 1-3) scheduled for outpatient distal upper limb surgery were prospectively enrolled in the two groups. At discharge, patients in both groups received standard information on postoperative recovery and care, with a multimodal analgesic regime (acetaminophen and ketoprofen for 5 days). The primary endpoint was EVAN-LR score before discharge. Secondary endpoints were pain relief and side-effects over a 7-day period. Results were recorded as median and 25-75% interquartile range. Propensity-score-matched analysis was performed. Over the study period, from October 2019 to November 2020, 183 patients were included; 48 WALANT patients were propensity-score matched to 48 AxB patients. Pre-procedural APAIS anxiety score was lower in the WALANT than the AxB group: 9 (IQR, 6-12) vs 12 (IQR, 8-14) (p = 0.01). EVAN-LR scores were similar between the WALANT (78 [72-82]) and the AxB group (73 [67-80]). Incidences of paresthesia and of pain (NRS pain score, opioid rescue) were similar. WALANT patients had shorter length of stay: 135 (110-175) min vs 170 (110-250) min (p = 0.01). The present study demonstrated that WALANT was associated with a high level of patient satisfaction. For clinical relevance and quality of care, WALANT should be proposed in first line for distal limb surgery.

摘要

在许多门诊中心,上肢远端手术是在清醒局部麻醉无止血带(WALANT)技术下进行的,因为其优点众多:技术简单、成本低,周转快且住院时间短。鉴于关于患者满意度的数据较少,这项非随机队列研究旨在比较接受WALANT或腋神经阻滞(AxB)的患者的EVAN-LR麻醉满意度问卷结果(信息、疼痛、期望、注意力、不适:0至100分)。经机构审查委员会批准后,计划进行门诊上肢远端手术的患者(年龄>18岁,美国麻醉医师协会身体状况分级1至3级且病情稳定)被前瞻性纳入这两组。出院时,两组患者均收到关于术后恢复和护理的标准信息,采用多模式镇痛方案(对乙酰氨基酚和酮洛芬连用5天)。主要终点是出院前的EVAN-LR评分。次要终点是7天内的疼痛缓解情况和副作用。结果记录为中位数及25%至75%四分位数间距。进行了倾向评分匹配分析。在2019年10月至2020年11月的研究期间,共纳入183例患者;48例接受WALANT的患者与48例接受AxB的患者进行了倾向评分匹配。WALANT组术前的APAI S焦虑评分低于AxB组:9分(四分位数间距,6至12分)对12分(四分位数间距,8至14分)(p = 0.01)。WALANT组(78分[72至82分])和AxB组(73分[67至80分])的EVAN-LR评分相似。感觉异常和疼痛的发生率(数字评分量表疼痛评分、阿片类药物解救情况)相似。接受WALANT的患者住院时间较短:135分钟(110至175分钟)对170分钟(110至250分钟)(p = 0.01)。本研究表明,WALANT与较高的患者满意度相关。就临床相关性和医疗质量而言,对于上肢远端手术,应首选WALANT。

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