Roberts Gregory, Leslie Robert, Robb Sylvia, Siemens D Robert, Beiko Darren
Department of Urology; Queen's University, Kingston, ON, Canada.
Department of Oncology; Queen's University, Kingston, ON, Canada.
Can Urol Assoc J. 2017 Oct;11(10):326-330. doi: 10.5489/cuaj.4408.
Ureteral stent and ureteral manipulation-related pain is a significant complication for patients undergoing ureteroscopy. Herein, we report a phase 2, randomized trial to assess efficacy of direct instillation of intraureteral lidocaine in reducing postoperative pain and ureteral stent symptoms.
We performed a randomized, double-blinded trial of patients undergoing elective ureteroscopy for ureteral calculi. Patients were randomized to direct instillation of 2% lidocaine plus bicarbonate, or to normal saline as control. The primary outcome of interest was early postoperative pain scores. Patients completed10-point visual analog pain scale at one-hour, two-hour, four-hour, 24-hours, four- and seven-day time points. Other outcome measurements collected included a medication diary and voiding questionnaire.
A total of 41 patients were randomized in the study. Mean flank pain scores at one hour were 2.2 (±2.9) vs.1.9 (±2.4) in the intervention and placebo group, respectively (p=0.84). There was no significant difference at any time point between the intervention and placebo groups in patient-reported pain scores. Patients reported lower dysuria scores at all time points in the lidocaine group, however, none reached statistical significance. There was no difference in complication rates or adverse effects between groups.
In this randomized, phase 2 study, direct instillation of lidocaine into the ureter did not appear to significantly improve pain or voiding symptoms following stented ureteroscopy.
输尿管支架及输尿管操作相关疼痛是接受输尿管镜检查患者的一种重要并发症。在此,我们报告一项2期随机试验,以评估输尿管内直接滴注利多卡因在减轻术后疼痛及输尿管支架症状方面的疗效。
我们对因输尿管结石接受择期输尿管镜检查的患者进行了一项随机双盲试验。患者被随机分为直接滴注2%利多卡因加碳酸氢盐组或生理盐水对照组。主要关注的结局是术后早期疼痛评分。患者在1小时、2小时、4小时、24小时、4天和7天时间点完成10分视觉模拟疼痛量表。收集的其他结局测量指标包括用药日记和排尿问卷。
共有41例患者被随机纳入该研究。干预组和安慰剂组1小时时的平均胁腹疼痛评分分别为2.2(±2.9)和1.9(±2.4)(p = 0.84)。干预组和安慰剂组在任何时间点的患者报告疼痛评分均无显著差异。然而,利多卡因组患者在所有时间点的尿痛评分均较低,但均未达到统计学意义。两组之间的并发症发生率或不良反应无差异。
在这项随机2期研究中,输尿管内直接滴注利多卡因似乎并未显著改善输尿管支架置入术后的疼痛或排尿症状。