Department of Urology, Fukushima Medical University School of Medicine, 1 Hikarigaoka, Fukushima, 960-1295, Japan.
Department of Urology, Graduate School of Biomedical Sciences, Hiroshima University, Hiroshima, Japan.
Int Urol Nephrol. 2020 Jan;52(1):67-76. doi: 10.1007/s11255-019-02301-3. Epub 2019 Oct 1.
To assess whether the preoperative 1-h pad test could predict postoperative urinary incontinence and quality of life after robot-assisted radical prostatectomy.
A total of 329 patients who underwent robot-assisted radical prostatectomy between 2013 and 2016 were prospectively enrolled in this study. These patients were divided into the preoperative urinary continence group and the preoperative urinary incontinence group according to the 1-h pad test. The time to achieve urinary continence, lower urinary tract function evaluated by uroflowmetry and post-voided residual urine volume, and quality of life evaluated by King's Health Questionnaire and International Consultation on Incontinence Questionnaire-Short Form were compared between these two groups.
There were 190 patients (58%) in the preoperative urinary continence group (1-h pad test ≤ 2 g) and 139 patients (42%) in the preoperative urinary incontinence group (1-h pad test > 2 g). In the preoperative urinary continence/incontinence groups, 83%/76% of patients achieved continence within 12 months, respectively, and urinary incontinence remained significantly longer in the preoperative incontinence group than in the preoperative continence group (P = 0.042). Although there were no significant differences in all quality of life items between the two groups before surgery, several items were significantly higher in the preoperative urinary continence group.
Achievement of urinary continence and improvement of urinary quality of life are delayed in patients with preoperative urinary incontinence assessed by the 1-h pad test. The preoperative 1-h pad test could be a useful predictor of prolonged urinary incontinence and poor quality of life after robot-assisted radical prostatectomy.
评估术前 1 小时尿垫试验是否可预测机器人辅助前列腺根治术后的尿失禁和生活质量。
本研究前瞻性纳入了 2013 年至 2016 年间接受机器人辅助前列腺根治术的 329 例患者。根据 1 小时尿垫试验,这些患者被分为术前尿控组和术前尿失禁组。比较两组间尿控时间、尿流率和残余尿量等下尿路功能,以及 King 健康问卷和国际尿失禁问卷 - 短表评估的生活质量。
术前尿控组(1 小时尿垫试验≤2 g)有 190 例(58%)患者,术前尿失禁组(1 小时尿垫试验>2 g)有 139 例(42%)患者。术前尿控/失禁组分别有 83%/76%的患者在 12 个月内达到尿控,术前尿失禁组的尿失禁持续时间明显长于术前尿控组(P=0.042)。尽管两组患者术前所有生活质量项目均无显著差异,但术前尿控组的几项评分显著较高。
术前 1 小时尿垫试验评估的尿失禁患者,其尿控的获得和尿质生活质量的改善延迟。术前 1 小时尿垫试验可能是机器人辅助前列腺根治术后尿失禁和生活质量差的有用预测指标。