Ko Kyungtae, Yang Dae Yul, Lee Won Ki, Kim Sae Woong, Moon Du Geon, Moon Ki Hak, Park Nam Cheol, Park Jong Kwan, Son Hwan Cheol, Lee Sung Won, Hyun Jae Seog, Park Kwangsung
Department of Urology, Hallym University College of Medicine, Chuncheon, Korea.
Department of Urology, The Catholic University College of Medicine, Seoul, Korea.
Korean J Urol. 2014 Sep;55(9):608-14. doi: 10.4111/kju.2014.55.9.608. Epub 2014 Sep 5.
To evaluate how much the improvement of lower urinary tract symptoms (LUTS) affects sexual function and which storage symptoms or voiding symptoms have the greatest effect on sexual function.
A total of 187 patients were enrolled in this study. Patients were randomly assigned to receive either tamsulosin 0.2 mg (group A) or tamsulosin 0.2 mg and solifenacin 5 mg (group B). At 4 weeks and 12 weeks, the LUTS and sexual function of the patients were evaluated by use of the International Index of Erectile Function-5 (IIEF5), International Prostate Symptom Score (IPSS), Overactive Bladder Symptom Score (OABSS) questionnaire, uroflowmetry, and bladder scan.
Both groups A and B showed statistically significant improvements in IPSS, OABSS, and quality of life (QoL). Group A showed improved maximum flow rate, mean flow rate, and residual urine volume by time. Group B did not show an improvement in flow rate or residual urine volume but total voiding volume increased with time. The IIEF5 score was not improved in either group. In group A, the IIEF5 score dropped from 13.66 ± 4.97 to 11.93 ± 6.14 after 12 weeks (p=0.072). Group B showed a decline in the IIEF5 score from 13.19 ± 5.91 to 12.45 ± 6.38 (p=0.299). Although group B showed a relatively smaller decrease in the IIEF5 score, the difference between the two groups was not significant (p=0.696).
Tamsulosin monotherapy and combination therapy with solifenacin did not improve erectile function despite improvements in voiding symptoms and QoL. The improvement in storage symptoms did not affect erectile function.
评估下尿路症状(LUTS)的改善对性功能的影响程度,以及哪些储尿症状或排尿症状对性功能影响最大。
本研究共纳入187例患者。患者被随机分配接受坦索罗辛0.2毫克(A组)或坦索罗辛0.2毫克加索利那新5毫克(B组)。在4周和12周时,通过国际勃起功能指数-5(IIEF5)、国际前列腺症状评分(IPSS)、膀胱过度活动症症状评分(OABSS)问卷、尿流率测定和膀胱扫描评估患者的LUTS和性功能。
A组和B组在IPSS、OABSS和生活质量(QoL)方面均有统计学意义的改善。A组随时间推移最大尿流率、平均尿流率和残余尿量均有所改善。B组尿流率或残余尿量未改善,但总排尿量随时间增加。两组的IIEF5评分均未改善。A组12周后IIEF5评分从13.66±4.97降至11.93±6.14(p=0.072)。B组IIEF5评分从13.19±5.91降至12.45±6.38(p=0.299)。虽然B组IIEF5评分下降相对较小,但两组间差异无统计学意义(p=0.696)。
尽管排尿症状和QoL有所改善,但坦索罗辛单药治疗及与索利那新联合治疗均未改善勃起功能。储尿症状的改善未影响勃起功能。