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萘哌地尔治疗女性尿道综合征的临床体会
引用本文:黄后宝,姜书传,董昌斌,钱立新. 萘哌地尔治疗女性尿道综合征的临床体会[J]. 医学研究生学报, 2005, 18(9): 821-823
作者姓名:黄后宝  姜书传  董昌斌  钱立新
作者单位:1. 南京医科大学第一附属医院泌尿外科,江苏,南京,210029
2. 皖南医学院附属弋矶山医院泌尿外科,安徽,芜糊,241001
摘    要:目的:探讨萘哌地尔(Naftopidil)治疗女性尿道综合征的有效性和安全性。方法:38例患者采用自身对照试验,洗脱期1周,治疗期4周,应用萘哌地尔片25mg,每晚口服。以尿道综合征症状评分(FUSS)为主要疗效指标,以生活质量评分(QOL)为次要观察指标。结果:治疗2周后患者症状开始好转,4周后疗效显著。治疗前后的FUSS、QOL相比较,差异显示均有统计学意义(P〈0.01及P〈0.05),总有效率为76.31%。结论:萘哌地尔治疗女性尿道综合征有效、安全。

关 键 词:萘哌地尔 尿道综合征 有效性 安全性
文章编号:1008-8199(2005)09-0821-03
收稿时间:2005-04-03
修稿时间:2005-06-24

The efficacy of naftopidil in treatment of female urethral syndrome
HUANG Hou-bao,JIANG Shu-chuan,DONG Chang-bin,QIAN Li-xin. The efficacy of naftopidil in treatment of female urethral syndrome[J]. Bulletin of Medical Postgraduate, 2005, 18(9): 821-823
Authors:HUANG Hou-bao  JIANG Shu-chuan  DONG Chang-bin  QIAN Li-xin
Abstract:Objective: To evaluate the efficacy and safety of Naftopidil on patients with female urethral syndrome (FUS). Methods: Self-controlled clinical trial was performed in patients with FUS. Thirty-eight patients were treated with naftopidil tablet 25mg/po/qn for 4 weeks after one-week washout period. The effects were evaluated mainly by female urethral syndrome score (FUSS) and quality of life (QOL). Results: FUSS began to decrease after 2 (week's) administration and decreased significantly after 4 weeks' treatment. It had statistically significant difference of FUSS and QOL after treatment compared with control (P<0.01 or P<0.05). The total effective rate was 76.31%. Conclusion:Naftopidil was safe and effective in treating FUS.
Keywords:Naftopidil   Female urethral syndrome    Efficacy    Safety
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