Özel Silivri Anadolu Hastanesi Ortopedi ve Travmatoloji Bölümü, 34570 Silivri, İstanbul, Türkiye.
Jt Dis Relat Surg. 2022;33(2):367-373. doi: 10.52312/jdrs.2022.664. Epub 2022 Jul 6.
The issue of performing a hallux valgus operation with the wide-awake local anesthesia with no tourniquet (WALANT) technique has not been evaluated before. The objective of this study was to compare the clinical results of patients who underwent the WALANT technique during hallux valgus operation and patients who underwent the procedure with traditional anesthesia (TA).
In this cross-sectional, retrospective study, 34 patients (17 males, 17 females; mean age: 46.1±8.3 years; range, 36 to 62 years) who underwent first metatarsal osteotomy with the diagnosis of hallux valgus disease between November 1, 2018, and June 1, 2020, were divided into two groups according to the surgical approach determined by patient choice: the WALANT group and the TA group. Demographic characteristics, Visual Analog Scale (VAS) scores for pain and anxiety, postoperative satisfaction levels, and complications were recorded.
There was no significant difference between the groups in terms of demographic characteristics. The VAS pain score during needle insertion was significantly higher in the WALANT group compared to the TA group (p<0.001). Conversely, the VAS anxiety score was significantly higher in the WALANT group compared to the TA group (p<0.001). The median follow-up time was 5.4 months (interquartile range, 5-6 months).
This is the first study demonstrating that adequate anesthetic efficacy can be achieved with the WALANT technique for the hallux valgus operation. Acceptable pain scores can be achieved with this technique, and costs are reduced.
采用清醒局部麻醉无止血带(WALANT)技术行踇外翻手术的问题尚未得到评估。本研究的目的是比较 WALANT 技术组和传统麻醉(TA)组行踇外翻手术患者的临床结果。
在这项横断面、回顾性研究中,根据患者选择的手术方法将 2018 年 11 月 1 日至 2020 年 6 月 1 日期间诊断为踇外翻疾病而行第一跖骨截骨术的 34 例患者(男 17 例,女 17 例;平均年龄:46.1±8.3 岁;年龄范围 36 岁至 62 岁)分为两组:WALANT 组和 TA 组。记录了人口统计学特征、疼痛和焦虑的视觉模拟量表(VAS)评分、术后满意度和并发症。
两组患者的人口统计学特征无显著差异。与 TA 组相比,WALANT 组在进针时的 VAS 疼痛评分显著更高(p<0.001)。相反,WALANT 组的 VAS 焦虑评分显著高于 TA 组(p<0.001)。中位随访时间为 5.4 个月(四分位间距,5-6 个月)。
这是第一项表明 WALANT 技术在踇外翻手术中可获得足够的麻醉效果的研究。该技术可获得可接受的疼痛评分,并降低成本。