Mohd Rashid Mohd Zaim, Sapuan Jamari, Abdullah Shalimar
Hand and Microsurgery Unit, Department of Orthopedics, Faculty of Medicine, Universiti Kebangsaan Malaysia, Kuala Lumpur, Malaysia.
J Orthop Surg (Hong Kong). 2019 Jan-Apr;27(1):2309499019833002. doi: 10.1177/2309499019833002.
Trigger finger release utilizing wide-awake local anesthesia no tourniquet (WALANT) usage in extremity surgery is not widely used in our setting due to the possibility of necrosis. Usage of a tourniquet is generally acceptable for providing surgical field hemostasis. We evaluate hemostasis score, surgical field visibility, onset and duration of anesthesia, pain score, and the duration of surgery and potential side effects of WALANT.
Eighty-six patients scheduled for trigger finger release between July 2016 and December 2017 were randomized into a control group (1% lignocaine and 8.4% sodium bicarbonate with arm tourniquet; given 10 min prior to procedure) and an intervention group (1% lignocaine, 1:100,000 of adrenaline and 8.4% sodium bicarbonate; given 30 min prior to procedure), with a total of 4 ml of solution injected around the A1 pulley. The onset of anesthesia and pain score upon injection of the first 1 ml were recorded. After the procedure, the surgeon rated for the hemostasis score (1-10: 1 as no bleeding and 10 being profuse bleeding). Duration of surgery and return of sensation were recorded.
Hemostasis score was grouped into visibility score as 1-3: good, 4-6: moderate, and 7-10: poor. The intervention group (with adrenaline) had a 74% of good surgical field visibility compared to 44% from the controlled group (without adrenaline; p < 0.05). Duration of anesthesia was longer in the intervention group (with adrenaline), with a 2.77-h difference.
WALANT provides excellent surgical field visibility and is safe and on par with conventional methods but without the usage of a tourniquet and its associated discomfort.
在肢体手术中,利用清醒局部麻醉无止血带(WALANT)技术进行扳机指松解术在我们的医疗环境中未被广泛应用,原因是存在坏死的可能性。使用止血带通常可接受,用于提供手术视野的止血。我们评估了WALANT的止血评分、手术视野可见度、麻醉起效和持续时间、疼痛评分、手术持续时间以及潜在副作用。
2016年7月至2017年12月计划进行扳机指松解术的86例患者被随机分为对照组(1%利多卡因和8.4%碳酸氢钠,使用臂部止血带;在手术前10分钟给予)和干预组(1%利多卡因、1:100,000肾上腺素和8.4%碳酸氢钠;在手术前30分钟给予),共4毫升溶液注射于A1滑车周围。记录首次注射1毫升时的麻醉起效和疼痛评分。手术后,外科医生对止血评分进行评定(1 - 10分:1分为无出血,10分为大量出血)。记录手术持续时间和感觉恢复情况。
止血评分分为可见度评分1 - 3分:良好,4 - 6分:中等,7 - 10分:差。干预组(使用肾上腺素)手术视野良好可见度的比例为74%,而对照组(未使用肾上腺素)为44%(p < 0.05)。干预组(使用肾上腺素)的麻醉持续时间更长,相差2.77小时。
WALANT提供了极佳的手术视野可见度,安全且与传统方法相当,但无需使用止血带及其相关不适。