Negrean Cristina, Ross James, Yu Wenhui, Maciejewski Conrad, Vigil Humberto R, Hickling Duane
Division of Urology, Department of Surgery, University of Ottawa, Ottawa, ON, Canada.
Division of Urology, Department of Surgery, Scarborough Health Network, Toronto, ON, Canada.
Can Urol Assoc J. 2025 Jun;19(6):189-192. doi: 10.5489/cuaj.9011.
Most Canadian urologists use lidocaine solution prior to botulinium toxin (BoNT) administration; however, this requires additional time. Our aim was to compare pain scores in patients undergoing office-based BoNT using lidocaine instillation and lidocaine gel vs. lidocaine gel alone.
All patients undergoing office-based intradetrusor BoNT between March 1 and September 1, 2022, were included. Group 1 received intravesical lidocaine solution (20 ml 2% lidocaine solution + 30 ml 0.9% normal saline) instillation for 30 minutes and lidocaine gel. Group 2 received lidocaine gel only. The Verbal Numeric Rating Scale (VNRS) was used to measure pain. Patient demographics were compared with t-test for continuous and Chi-squared for categorical variables. The Mann-Whitney U test was used to compare pain scores.
A total of 79 patients were included (mean age 61 years, 74.7% female, 58.2% with overactive bladder, and 30.4% receiving first treatment). Group 1 had 39 patients and group 2 had 40. There was no significant difference in pain scores between groups: group 1 median VNRS 3.0 (interquartile range [IQR] 2.5) vs. group 2 median VNRS 4.0 (IQR 2.0) (p=0.11). No significant differences in pain scores were noted between groups based on sex, indication for treatment, or number of previous BoNT treatments (p>0.05). Post-procedural complications were low. Treatment failure did not occur.
Lidocaine gel alone may be an acceptable analgesic alternative while improving availability and efficiency of treatment delivery. Our findings are limited by the retrospective nature of the study and the small sample size.
大多数加拿大泌尿科医生在注射肉毒杆菌毒素(BoNT)之前会使用利多卡因溶液;然而,这需要额外的时间。我们的目的是比较在门诊接受BoNT治疗的患者中,使用利多卡因滴注和利多卡因凝胶与仅使用利多卡因凝胶时的疼痛评分。
纳入2022年3月1日至9月1日期间在门诊接受膀胱逼尿肌内BoNT治疗的所有患者。第1组接受膀胱内利多卡因溶液(20毫升2%利多卡因溶液+30毫升0.9%生理盐水)滴注30分钟,然后使用利多卡因凝胶。第2组仅接受利多卡因凝胶。采用言语数字评定量表(VNRS)来测量疼痛。使用t检验比较连续变量的患者人口统计学数据,使用卡方检验比较分类变量。采用曼-惠特尼U检验比较疼痛评分。
共纳入79例患者(平均年龄61岁,74.7%为女性,58.2%患有膀胱过度活动症,30.4%为首次接受治疗)。第1组有39例患者,第2组有40例。两组之间的疼痛评分无显著差异:第1组VNRS中位数为3.0(四分位间距[IQR]为2.5),第2组VNRS中位数为4.0(IQR为2.0)(p=0.11)。基于性别、治疗指征或既往BoNT治疗次数,两组之间的疼痛评分无显著差异(p>0.05)。术后并发症发生率较低。未发生治疗失败情况。
仅使用利多卡因凝胶可能是一种可接受的镇痛替代方法,同时可提高治疗的可及性和效率。我们的研究结果受到研究的回顾性性质和小样本量的限制。