David S Han, Ezra J Margolin, Miyad Movassaghi, Jeffrey P Johnson, Mahveesh Chowdhury, Srinath-Reddi Pingle, Michael L Schulster, David M Weiner, Ojas Shah
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The primary outcome was Ureteral Stent Symptoms Questionnaire urinary symptoms and pain scores with stent in situ immediately before stent removal; groups were compared using the Student <i>t</i> test. Higher scores represented increasing symptom severity.</p><p><strong>Results: </strong>Of 73 patients (37 study arm, 36 control arm), mean age was 52 years old, and the majority were male (60%). Mean stone burden (10 mm) and median time to stent removal (9 days) were similar between groups. With stent in situ, there were no differences in urinary symptoms or pain scores between study and control groups (28 vs 29, <i>P</i> = .85 and 14 vs 17, <i>P</i> = .25); moreover, there were no differences between arms in any Ureteral Stent Symptoms Questionnaire domain at this timepoint (<i>P</i> > .05). 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引用次数: 0
摘要
导言:鉴于抗组胺药对膀胱疼痛综合征和肾绞痛的疗效,我们评估了抗组胺药对输尿管支架相关症状的影响。材料和方法:我们进行了一项双盲、随机对照试验,成人接受单侧输尿管镜检查并放置支架治疗尿石症。所有手术均使用康乐保Imajin®硅胶支架(康乐保A/S, Humlebaek,丹麦)。除了用于控制疼痛的非甾体抗炎药物外,患者还随机接受10天疗程的非索非那定(180mg /天)口服(研究组)或安慰剂(对照组)。主要结局是输尿管支架症状问卷(USSQ)泌尿系统症状和支架原位取出前的疼痛评分;各组间比较采用学生t检验。分数越高,症状越严重。结果:73例患者(研究组37例,对照组36例),平均年龄52岁,男性居多(60%)。两组间平均结石负荷(10mm)和支架取出的中位时间(9天)相似。在支架原位放置的情况下,研究组和对照组在泌尿系统症状或疼痛评分方面没有差异(28 vs. 29, p=0.85; 14 vs. 17, p=0.25);此外,在此时间点,各军种在USSQ域中均无差异(p < 0.05)。研究组和对照组在出院后麻醉性镇痛的使用(5% vs. 14%, p=0.26)、办公室电话总次数(5 vs. 9, p=0.61)或急诊总次数(2 vs. 3, p=0.67)方面均无差异。结论:术后抗组胺药耐受性良好,但不能显著减少输尿管支架相关症状。
Effect of Antihistamine on Ureteral Stent-Related Symptoms: A Double-Blind Randomized Controlled Trial.
Introduction: Given evidence of antihistamine's efficacy in bladder pain syndrome and renal colic, we evaluated the effect of antihistamine on ureteral stent-related symptoms.
Methods: We performed a double-blind, randomized controlled trial of adults undergoing unilateral ureteroscopy with stent placement for urolithiasis treatment. Coloplast Imajin silicone stents (Coloplast A/S, Humlebaek, Denmark) were used for all procedures. Alongside nonsteroidal anti-inflammatory medications for pain control, patients were randomly prescribed a 10-day course of either fexofenadine 180 mg oral daily (study arm) or placebo (control). The primary outcome was Ureteral Stent Symptoms Questionnaire urinary symptoms and pain scores with stent in situ immediately before stent removal; groups were compared using the Student t test. Higher scores represented increasing symptom severity.
Results: Of 73 patients (37 study arm, 36 control arm), mean age was 52 years old, and the majority were male (60%). Mean stone burden (10 mm) and median time to stent removal (9 days) were similar between groups. With stent in situ, there were no differences in urinary symptoms or pain scores between study and control groups (28 vs 29, P = .85 and 14 vs 17, P = .25); moreover, there were no differences between arms in any Ureteral Stent Symptoms Questionnaire domain at this timepoint (P > .05). There were no differences between study and control groups in postdischarge narcotic analgesia use (5% vs 14%, P = .26), total number of office phone calls (5 vs 9, P = .61), or total number of emergency department visits (2 vs 3, P = .67).
Conclusions: Postoperative antihistamines were well tolerated but did not significantly reduce ureteral stent-related symptoms.