Park Kwangsung, Park Hyoung Keun, Kim Sae Woong, Yang Dae Yul, Park Jong Kwan, Park Hyun Jun, Moon Ki Hak, Moon Du Geon, Min Kweon Sik, Son Hwancheol, Lee Sung Won, Hyun Jae Seog, Choi Woo Suk, Yang Sang Kuk
Department of Urology, Chonnam National University Medical School, Gwangju, Korea.
Department of Urology, Konkuk University Medical Center, Konkuk University School of Medicine, Seoul, Korea.
World J Mens Health. 2018 Sep;36(3):248-254. doi: 10.5534/wjmh.170003. Epub 2018 May 17.
The purpose of this study was to evaluate the efficacy of treatment in patients with non-bothering nocturia.
In this prospective multicenter study, patients who visited hospitals for treatment of voiding symptoms were enrolled. Inclusion criteria were: 1) men >45 years, and 2) nocturia ≥2 confirmed by a three-day voiding diary. Subjects were divided into non-bothering and bothering groups based on International Consultation on Incontinence Questionnaire Nocturia (ICIQ-N) question 2b. Changes in voiding symptoms, frequency of nocturia, and bothersomeness were evaluated with international prostate symptom score (IPSS), ICIQ-N, and three-day voiding diary at 4 and 12 weeks after treatment.
A total of 48 patients in the non-bothering nocturia group and 50 patients in the bothering nocturia group who completed the 12-week treatment were analyzed. The total IPSS was decreased by 5.8 in the non-bothering group and 5.2 in the bothering group. There was no significant difference in decrease of IPSS between the two groups. Both groups showed significant reduction in discomfort of nocturia. The ICIQ-N 2b score decreased from 3.9 to 2.7 (p=0.01) in the non-bothering group and from 6.9 to 4.6 (p=0.02) in the bothering group. The number of nocturia episodes was significantly decreased in both groups.
Regardless of discomfort associated with nocturia, both groups showed significant improvement in nocturia-related discomfort and voiding symptoms. These results suggest that patients with nocturia who were unaware of its discomfort benefited from treatment.
本研究旨在评估非困扰性夜尿症患者的治疗效果。
在这项前瞻性多中心研究中,纳入了因排尿症状到医院就诊的患者。纳入标准为:1)年龄>45岁的男性,2)通过三天排尿日记确认夜尿症≥2次。根据国际尿失禁咨询委员会夜尿症问卷(ICIQ-N)问题2b将受试者分为非困扰组和困扰组。在治疗后4周和12周,使用国际前列腺症状评分(IPSS)、ICIQ-N和三天排尿日记评估排尿症状、夜尿频率和困扰程度的变化。
对非困扰性夜尿症组的48例患者和困扰性夜尿症组的50例完成12周治疗的患者进行了分析。非困扰组的总IPSS降低了5.8,困扰组降低了5.2。两组之间IPSS降低幅度无显著差异。两组夜尿不适均显著减轻。非困扰组的ICIQ-N 2b评分从3.9降至2.7(p=0.01),困扰组从6.9降至4.6(p=0.02)。两组夜尿发作次数均显著减少。
无论夜尿相关的不适如何,两组在夜尿相关不适和排尿症状方面均有显著改善。这些结果表明,未意识到夜尿不适的夜尿症患者从治疗中获益。