A randomised, placebo-controlled study to assess the efficacy of twice-daily vardenafil in the treatment of lower urinary tract symptoms secondary to benign prostatic hyperplasia

被引:208
作者
Stief, Christian G. [1 ]
Porst, Hartmut [2 ]
Neuser, Dieter [3 ]
Beneke, Manfred [4 ]
Ulbrich, Ernst [4 ]
机构
[1] Univ Munich, Dept Urol, D-81377 Munich, Germany
[2] Private Urol Practice, Hamburg, Germany
[3] Bayer HealthCare, Wuppertal, Germany
[4] Bayer Vital GmbH, Leverkusen, Germany
关键词
benign prostatic hyperplasia; BPH; phosphodiesterase inhibitors; vardenafil; lower urinary tract symptoms; erectile dysfunction; quality of life;
D O I
10.1016/j.eururo.2008.01.075
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Introduction: Benign prostatic hyperplasia (BPH) is associated with bothersome lower urinary tract symptoms (LUTS) and reduced patient quality of life (QoL). Phosphodiesterase (type) 5 (PDE5) inhibitors such as vardenafil are commonly used for the treatment of erectile dysfunction (ED), but have also been shown to improve the symptoms of BPH. This randomised, double-blind, placebo-controlled study investigated the effects of vardenafil on LUTS and QoL in men with BPH/LUTS, with or without concomitant ED. Methods: Men aged 45-64 yr with BPH/LUTS and an International Prostate Symptom Score (IPSS) >= 12 were randomised to receive either 10 mg vardenafil or placebo twice daily. LUTS were assessed with the use of two primary efficacy parameters, IPSS score and maximum urinary flow rate (Q(max)), as well as postvoid residual (PVR) urine volume; ED was measured with the use of the erectile function (EF) domain score of the International Index of Erectile Function (IIEF-EF); and QoL was assessed with the Urolife (TM) QoL-9 questionnaire. Results: After 8 wk of treatment, there was a significant improvement in the IPSS total score in the vardenafil group compared with placebo (-5.9 and -3.6, respectively; p = 0.0013). Nominally significant improvements in irritative and obstructive IPSS subscores (p = 0.0017 and p = 0.0081, respectively), EF (p = 0.0001), and Urolife QoL-9 (p < 0.0001) were also associated with vardenafil treatment. Q(max) and PVR urine volume did not change significantly with treatment, although baseline values were already considered close to normal. Vardenafil was generally well tolerated, with most adverse events considered mild or moderate in severity. Conclusions: Vardenafil treatment significantly improved LUTS, EF, and QoL in men with BPH/LUTS. Vardenafil may be considered a promising treatment option for men with symptoms secondary to BPH. (C) 2008 European Association of Urology. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:1236 / 1244
页数:9
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