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酚嗪吡啶用于评估输尿管通畅性的随机对照试验。

Phenazopyridine for Evaluation of Ureteral Patency: A Randomized Controlled Trial.

机构信息

Department of Women's Health, Female Pelvic Medicine and Reconstructive Surgery and Research Administration, Hartford Hospital, Harford, Connecticut.

出版信息

Obstet Gynecol. 2016 Aug;128(2):348-355. doi: 10.1097/AOG.0000000000001472.

Abstract

OBJECTIVE

To evaluate the usefulness of phenazopyridine for confirmation of ureteral patency during intraoperative cystoscopy.

METHODS

We conducted a randomized controlled trial comparing use of phenazopyridine with no medications for evaluation of ureteral patency during intraoperative cystoscopy in women undergoing pelvic surgery. The primary study outcome was time to visualize ureteral urine efflux. To detect a 3-minute difference with α of 0.05 using a two-sided, two-sample t test and β 0.80 required 98 patients equally divided into two groups.

RESULTS

A total of 104 women were randomized from April to December 2015. Patients in the treatment group tended to be older (P=.02); otherwise, study groups were similar. Time to visualize ureteral urine efflux did not differ between study groups with a mean time of 2 minutes 40 seconds (±2 minutes 38 seconds) in the control group and 2 minutes 53 seconds (±4 minutes 35 seconds) in the treatment group (P=.77). Regarding the surgeon survey, surgeons felt less frustrated and impatient in visualization of ureteral urine efflux in the treatment group compared with the control group (mean response 1.5±0.8 in treatment compared with 2.0±1.0 in control, P=.007), and surgeons felt that the cystoscopy took too long more often in the control than in the treatment group (1.7±0.9 in treatment compared with 2.1±1.0 in control, P=.02). Trial of void result differed significantly between groups with fewer patients in the treatment group failing a void trial (P=.04). There were no adverse events related to phenazopyridine use.

CONCLUSION

Preoperative phenazopyridine is a useful and cost-saving medication for use in planned cystoscopy for evaluation of ureteral patency.

CLINICAL TRIAL REGISTRATION

ClinicalTrials.gov, https://clinicaltrials.gov/, NCT02424149.

摘要

目的

评估在术中膀胱镜检查期间使用 phenazopyridine 来确认输尿管通畅性的有效性。

方法

我们进行了一项随机对照试验,比较了在接受盆腔手术的女性中,在术中膀胱镜检查期间使用 phenazopyridine 与不使用任何药物来评估输尿管通畅性的效果。主要研究结果是可视化输尿管尿液流出的时间。使用双侧、两样本 t 检验和 β 0.80,检测到 3 分钟差异,需要每组 98 名患者。

结果

2015 年 4 月至 12 月期间共随机分配了 104 名女性患者。治疗组的患者年龄较大(P=.02);否则,研究组之间相似。在对照组中,可视化输尿管尿液流出的时间平均为 2 分 40 秒(±2 分 38 秒),在治疗组中为 2 分 53 秒(±4 分 35 秒),两组之间没有差异(P=.77)。关于外科医生的调查,与对照组相比,治疗组的外科医生在可视化输尿管尿液流出时感到不那么沮丧和不耐烦(治疗组的平均反应为 1.5±0.8,对照组为 2.0±1.0,P=.007),并且治疗组的外科医生经常觉得膀胱镜检查时间过长(治疗组为 1.7±0.9,对照组为 2.1±1.0,P=.02)。两组之间的试排空结果有显著差异,治疗组中有较少的患者试排空失败(P=.04)。使用 phenazopyridine 没有相关的不良反应。

结论

术前 phenazopyridine 是一种有用且节省成本的药物,可用于计划中的膀胱镜检查以评估输尿管通畅性。

临床试验注册

ClinicalTrials.gov,https://clinicaltrials.gov/,NCT02424149。

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