Effect of nefopam on postoperative catheter-related bladder discomfort after transurethral resection of the bladder under general anesthesia: A randomized controlled trial.

IF 1.8 4区 医学 Q4 MEDICINE, RESEARCH & EXPERIMENTAL
Journal of International Medical Research Pub Date : 2026-10-01 Epub Date: 2026-10-08 DOI:10.1177/03000605261495728
Ji Yong Yeom, Yeong Uk Kim, Jinkyung Kim, Juhee Min, Heewon Ma, Eunkyung Choi
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引用次数: 0

Abstract

ObjectiveCatheter-related bladder discomfort is a common complication following transurethral resection of bladder tumor and may impair postoperative recovery. This study evaluated the effect of intraoperative nefopam on catheter-related bladder discomfort and postoperative recovery quality.MethodsIn this prospective, randomized, double-blind trial, patients undergoing transurethral resection of bladder tumor under general anesthesia were allocated to either Group N (nefopam, 20 mg) or Group S (normal saline). Catheter-related bladder discomfort was assessed using a 4-point scale at multiple postoperative time points. Catheter-related bladder discomfort was defined based on a score ≥1, and moderate-to-severe catheter-related bladder discomfort was defined based on a score ≥2. Postoperative recovery quality was evaluated using the Quality of Recovery 15 questionnaire.ResultsIn total, 72 patients were analyzed. The cumulative incidence of catheter-related bladder discomfort (score ≥1) was 80.6% in Group N and 94.4% in Group S (risk difference, -13.9%; 95% confidence interval, -30.0% to 2.0%; p = 0.076). Longitudinal analysis of catheter-related bladder discomfort severity revealed significant time and group × time interaction effects (both p < 0.001), with lower odds of greater catheter-related bladder discomfort severity in Group N during the early postoperative period. Moderate-to-severe catheter-related bladder discomfort (score ≥2) occurred in 16.7% of the patients in Group N and 58.3% of those in Group S (risk difference, -41.7%; 95% confidence interval, -58.6% to -19.5%; odds ratio, 0.14; 95% confidence interval, 0.05-0.43; p < 0.001). The Quality of Recovery 15 score at 24 h was higher in Group N than in Group S (133.5 ± 11.25 vs. 124.3 ± 14.1; mean difference, 9.2 points; 95% confidence interval, 3.2-15.2; p = 0.003).ConclusionsIntraoperative nefopam did not significantly reduce the cumulative incidence of catheter-related bladder discomfort; however, it was associated with lower early postoperative catheter-related bladder discomfort severity and a lower incidence of moderate-to-severe catheter-related bladder discomfort. Quality of Recovery 15 scores at 24 h were also higher in the nefopam group.Registration: This study was registered with the Clinical Research Information Service (https://cris.nih.go.kr/, KCT0011457).

奈福泮对全麻经尿道膀胱切除术后导管相关性膀胱不适的影响:一项随机对照试验。
目的导管相关性膀胱不适是经尿道膀胱肿瘤切除术后常见的并发症,并可能影响术后恢复。本研究评估术中尼福泮对导尿管相关性膀胱不适和术后恢复质量的影响。方法在本前瞻性、随机、双盲试验中,将全麻下经尿道膀胱肿瘤切除术患者分为N组(奈福泮,20 mg)和S组(生理盐水)。术后多个时间点采用4分制评估导管相关性膀胱不适。导管相关性膀胱不适以≥1分定义,中度至重度导管相关性膀胱不适以≥2分定义。采用恢复质量15问卷对术后恢复质量进行评价。结果共分析72例患者。尿管相关性膀胱不适(评分≥1)的累积发生率N组为80.6%,S组为94.4%(风险差为-13.9%;95%可信区间为-30.0% ~ 2.0%;p = 0.076)。导尿管相关膀胱不适严重程度的纵向分析显示显著的时间和组×时间交互效应(p p p = 0.003)。结论术中奈福泮未显著降低尿管相关性膀胱不适的累积发生率;然而,它与术后早期导管相关性膀胱不适严重程度较低以及中重度导管相关性膀胱不适发生率较低相关。尼福泮组24 h的恢复质量15评分也较高。注册:本研究已在临床研究信息服务中心注册(https://cris.nih.go.kr/, KCT0011457)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
3.20
自引率
0.00%
发文量
555
审稿时长
1 months
期刊介绍: _Journal of International Medical Research_ is a leading international journal for rapid publication of original medical, pre-clinical and clinical research, reviews, preliminary and pilot studies on a page charge basis. As a service to authors, every article accepted by peer review will be given a full technical edit to make papers as accessible and readable to the international medical community as rapidly as possible. Once the technical edit queries have been answered to the satisfaction of the journal, the paper will be published and made available freely to everyone under a creative commons licence. Symposium proceedings, summaries of presentations or collections of medical, pre-clinical or clinical data on a specific topic are welcome for publication as supplements. Print ISSN: 0300-0605
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