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Intermittent alpha-blocker therapy in the treatment of men with lower urinary tract symptoms.

机译:间歇性α-受体阻滞剂治疗男性下尿路症状的治疗。

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OBJECTIVES: To determine the safety and efficacy of intermittent alpha-blocker therapy in men with lower urinary tract symptoms (LUTS) in a prospective study. Alpha-blockers have been demonstrated to be safe and effective in the treatment of men with LUTS. To date, the role of varying dosing regimens in responding patients has not been well studied. METHODS: Men with LUTS were entered into this prospective open label, parallel, randomized trial. In phase 1, patients were treated with alfuzosin, 2.5 mg three times daily for 3 months. In phase 2, those patients who had a significant therapeutic response were randomized into one of the following three groups: (1) maintenance of alfuzosin; (2) alfuzosin every other day; and (3) discontinuation of alfuzosin (ie, no treatment). Patients were followed up for a total of 6 months. Parameters of evaluation included the International Prostate Symptom Score (IPSS), global satisfaction, peak urinary flow rate (Qmax), and adverse events. RESULTS: At 3 months, there were 79 patients who were categorized as having obtained a therapeutic response: IPSS decreased to 7.6 +/- 3.2 and Qmax increased to 11.3 +/- 2.9 mL/s. After randomization, IPSS was 7.1 +/- 2.9 and 6.5 +/- 2.5 for group 1; 6.5 +/- 3.2 and 6.7 +/- 2.1 for group 2; and 11.4 +/- 4.8 and 12.3 +/- 4.9 for group 3 at 3 and 6 months, respectively. Qmax was 12.7 +/- 4.8 and 11.7 +/- 5.2 mL/s for group 1; 12.2 +/- 3.9 and 11.9 +/- 3.7 mL/s for group 2; and 9.7 +/- 2.5 and 9.3 +/- 2.1 mL/s for group 3 at 3 and 6 months, respectively. Global satisfaction at 6 months was the same for groups 1 and 2. There were no differences in adverse events among the three groups. CONCLUSIONS: In men with LUTS who responded to alfuzosin, changing the dosing regimen from daily to once every other day resulted in similar efficacy and safety at 3 and 6 months. By contrast, complete cessation of alfuzosin resulted in recurrence of both symptoms and impaired urinary flow. These data provide evidence that in responding patients, intermittent alpha-blocker therapy may be a reasonable therapeutic regimen. The role of intermittent alpha-blocker therapy using other agents, as well as in a large cohort of men with LUTS, remains to be determined.
机译:目的:在一项前瞻性研究中确定间歇性α-受体阻滞剂治疗下尿路症状(LUTS)的男性患者的安全性和有效性。事实证明,α-受体阻滞剂在治疗LUTS的男性中是安全有效的。迄今为止,尚未很好地研究不同的给药方案在反应患者中的作用。方法:将具有LUTS的男性纳入这项前瞻性开放标签,平行,随机试验。在第1阶段,患者每天接受2.5毫克阿夫唑嗪治疗3个月,每天3次。在阶段2中,那些具有显着治疗反应的患者被随机分为以下三组之一:(1)维持阿夫唑嗪; (2)每隔一天一次阿夫唑嗪; (3)终止阿夫唑嗪(即不治疗)。对患者进行了总共6个月的随访。评估参数包括国际前列腺症状评分(IPSS),总体满意度,尿流峰值(Qmax)和不良事件。结果:在3个月时,有79例患者被归类为治疗反应:IPSS降至7.6 +/- 3.2,Qmax升高至11.3 +/- 2.9 mL / s。随机分组后,第1组的IPSS为7.1 +/- 2.9和6.5 +/- 2.5。第2组为6.5 +/- 3.2和6.7 +/- 2.1;第3组在3个月和6个月时分别为11.4 +/- 4.8和12.3 +/- 4.9。第一组的Qmax为12.7 +/- 4.8和11.7 +/- 5.2 mL / s;第2组为12.2 +/- 3.9和11.9 +/- 3.7 mL / s;第3组和第3个月分别为9.7 +/- 2.5和9.3 +/- 2.1 mL / s。 1组和2组在6个月时的总体满意度相同​​。三组之间的不良事件没有差异。结论:对于对阿夫唑嗪有反应的LUTS男性,将给药方案从每天改为每隔一天一次,在3个月和6个月时具有相似的疗效和安全性。相比之下,阿夫唑嗪的完全停止导致两种症状的复发和尿流受损。这些数据提供了证据,表明在有反应的患者中,间歇性α受体阻滞剂治疗可能是一种合理的治疗方案。使用其他药物进行间歇性α受体阻滞剂治疗的作用以及在大量LUTS男性患者中的作用尚待确定。

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