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首页> 外文期刊>International Urology and Nephrology >Zolpidem pharmacotherapy combined with alpha-blocker therapy for nocturia unresponsive to alpha-blocker monotherapy in men with lower urinary tract symptoms: a preliminary study.
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Zolpidem pharmacotherapy combined with alpha-blocker therapy for nocturia unresponsive to alpha-blocker monotherapy in men with lower urinary tract symptoms: a preliminary study.

机译:唑吡坦药物治疗联合α-受体阻滞剂治疗夜尿症患者对下尿路症状的男性对α-受体阻滞剂单一疗法无反应:一项初步研究。

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AIM: The aim of the present study was to determine whether administration of zolpidem, a nonbenzodiazepine sedative-hypnotic agent, at night would improve the frequency of nocturia unresponsive to alpha-blocker monotherapy in men with lower urinary tract symptoms (LUTS). MATERIALS AND METHODS: The study inclusion criteria were: age >/=50 years, nocturia twice or more per night (International Prostate Symptom Score [IPSS] question 7) after taking alpha-blockers for more than eight weeks, and incomplete frequency-flow chart (FVC). A total of 18 patients met the criteria and constituted the study cohort. Three patients were given 0.2 mg tamsulosin once daily and others were given 4 mg terazosin once daily. All patients were additionally administered 10 mg zolpidem once at night for the eight weeks. RESULTS: There were no serious side-effects in any patient. Nocturia decreased from a baseline median (25-75th percentiles) of 3 (3-5) to 3 (3-4.5) episodes after taking alpha-blockers (p = 0.129) and to 2 (1-3) episodes after taking zolpidem and alpha-blockers (p = 0.001) on the IPSS. After treatment, the scores of uroflowmetry values did not significantly changed. However, at eight weeks, voiding symptoms (p = 0.041) and total IPSS scores (p = 0.028) significantly decreased compared with those at baseline. Median (25-75th percentiles) quality-of-life (QoL) index changed from 5 (4-5) at baseline to 3 (3-3) after eight weeks of treatment (p = 0.005). CONCLUSION: Our results indicate that zolpidem resulted in a subjective reduction in nocturia episodes when given to some men with LUTS.
机译:目的:本研究的目的是确定夜间使用非苯二氮卓类镇静催眠药唑吡坦是否可以提高夜尿症的发生频率,该夜尿症对低尿路症状(LUTS)的男性对α-受体阻滞剂单一疗法无反应。材料与方法:研究纳入标准为:年龄> / = 50岁,夜尿症两次或两次以上(国际前列腺症状评分[IPSS]问题7),服用α受体阻滞剂超过八周,且频率不完全图表(FVC)。共有18名患者符合标准,构成了研究队列。三名患者每天一次接受0.2 mg坦索罗辛治疗,其他患者每天一次接受4 mg特拉唑嗪。在八周的晚上,所有患者另外一次接受10 mg唑吡坦治疗。结果:任何患者均无严重副作用。夜尿症从接受α-受体阻滞剂(p = 0.129)的基线中位数(25-75%)发作3(3-5)减少至3(3-4.5)发作,以及服用唑吡坦和苯丙胺氮芥后降至2(1-3)发作IPSS上的α受体阻滞剂(p = 0.001)。治疗后,尿流率值得分没有明显变化。但是,与基线时相比,排尿症状(p = 0.041)和IPSS总评分(p = 0.028)在第8周时显着降低。治疗八周后,中位(25-75个百分点)生活质量(QoL)指数从基线的5(4-5)变为3(3-3)(p = 0.005)。结论:我们的结果表明,将唑吡坦给予某些患有LUTS的男性后,其夜尿症发作主观减少。

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