[Efficacy of naftopidil in patients with overactive bladder associated with benign prostatic hyperplasia: prospective randomized controlled study to compare differences in efficacy between morning and evening medication].
[Efficacy of naftopidil in patients with overactive bladder associated with benign prostatic hyperplasia: prospective randomized controlled study to compare differences in efficacy between morning and evening medication].
复制标题
萘哌地尔对良性前列腺增生相关膀胱过度活动症患者的疗效:比较早晚用药疗效差异的前瞻性随机对照研究
DOI:
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复制
发表时间:
2011
期刊:
影响因子:
--
通讯作者:
H. Kanetake
中科院分区:
文献类型:
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作者:
H. Sakai;T. Igawa;T. Onita;M. Furukawa;T. Hakariya;M. Hayashi;F. Matsuya;Y. Shida;N. Nishimura;Y. Yogi;T. Tsurusaki;K. Takehara;Koichiro Nomata;Kazutaka Shiraishi;T. Shono;Daiyu Aoki;H. Kanetake
A total of 100 patients with benign prostatic hyperplasia (BPH) and overactive bladder (OAB) symptoms (BPH/OAB), enrolled between June 2006 to March 2008, were randomly divided into 2 groups of morning medication (M) and evening medication (E) groups, then 50 mg of naftopidil was given once a day after breakfast or supper for 8 weeks. Data were available for efficacy analysis on 80 patients (M group ; 43, E group ; 37). Naftopidil significantly improved the overall international prostatic symptom score ; from 19.2±7.9 to 11.7±5.8 in the M group and from 19.4±6.4 to 12.3±6.8 in the E group (p<0.0001), QOL score from 4.9±0.8 to 3.2±1.4 in the M group and from 5.0±0.8 to 3.6±1.3 in the E group (p<0.0001), and OAB symptom score from 7.8±2.6 to 5.0±2.5 in the M group (p<0.0001) and from 8.6±2.9 to 5.8± 3.3 in the E group (p<0.0001). There was no significant difference in the incidence of adverse effects between the M group (6.1%) and E group (2.2%). These results suggest that naftopidil improves storage symptoms as well as voiding symptoms regardless of timing of administration.
DOI:
10.1016/s0169-328x(98)00287-3
发表时间:
1999
期刊:
Brain research. Molecular brain research
影响因子:
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作者:
Smith,MS;Schambra,UB;Wilson,KH;Page,SO;Schwinn,DA
通讯作者:
Schwinn,DA