Department of Pediatric Surgery, Children's Hospital, University of Helsinki, Helsinki, Finland; Department of Psychology and Logopedics, Åbo Akademi University, Turku (PS), Finland.
Department of Pediatric Surgery, Children's Hospital, University of Helsinki, Helsinki, Finland; Department of Psychology and Logopedics, Åbo Akademi University, Turku (PS), Finland.
J Urol. 2015 Jul;194(1):195-9. doi: 10.1016/j.juro.2015.01.098. Epub 2015 Jan 30.
Bladder exstrophy and epispadias complex is a rare congenital malformation that may have detrimental effects on sexual function. We evaluated sexual function of patients with bladder exstrophy and epispadias complex using validated questionnaires and compared the results with age matched controls.
Patients with bladder exstrophy and epispadias complex treated between 1956 and 1992 were identified from our hospital operative database. A total of 63 patients were mailed questionnaires up to 3 times, resulting in 32 replies (51%). Men were mailed the International Index of Erectile Function-15 questionnaire and women were mailed the Female Sexual Function Index questionnaire, and all patients were asked auxiliary questions regarding children, satisfaction with external genitalia and urinary continence.
There were no differences in sexual function between sexually active men with bladder exstrophy and epispadias complex and age matched controls on different erectile function domain scores according to the International Index of Erectile Function-15 questionnaire. The Female Sexual Function Index questionnaire among women yielded comparable results on different domain scores, except for median total score, which was higher in patients (33.6, IQR 29.4 to 34.9) than in controls (30.1, IQR 26.4 to 32.4, p = 0.049), suggesting better sexual function in patients with bladder exstrophy and epispadias complex. A greater proportion of patients with bladder exstrophy and epispadias complex had not become sexually active, compared to controls (35% vs 11%, p = 0.008). Patients with bladder exstrophy and epispadias complex were less likely to have children than controls (22% vs 45%, p = 0.021).
Men and women with bladder exstrophy and epispadias complex had good long-term outcomes on erectile and general sexual function tests. However, there is a likelihood that these individuals start their sexual life later than the general population, and fewer have children compared to controls.
膀胱外翻和尿道上裂复合畸形是一种罕见的先天性畸形,可能对性功能有不良影响。我们使用经过验证的问卷评估了膀胱外翻和尿道上裂复合畸形患者的性功能,并将结果与年龄匹配的对照组进行了比较。
从我们的医院手术数据库中确定了 1956 年至 1992 年间治疗的膀胱外翻和尿道上裂复合畸形患者。共向 63 名患者邮寄了问卷,最多邮寄了 3 次,共收到 32 份回复(51%)。男性患者邮寄国际勃起功能指数-15 问卷,女性患者邮寄女性性功能指数问卷,所有患者均被问及关于孩子、对外生殖器满意度和尿控的辅助问题。
根据国际勃起功能指数-15 问卷,在不同的勃起功能域评分上,活跃的膀胱外翻和尿道上裂复合畸形男性患者与年龄匹配的对照组之间的性功能没有差异。女性性功能指数问卷在不同的域评分上得出了类似的结果,除了中位数总分,患者(33.6,IQR 29.4 至 34.9)高于对照组(30.1,IQR 26.4 至 32.4,p = 0.049),提示患者的性功能更好。与对照组相比,膀胱外翻和尿道上裂复合畸形患者的性活跃比例较低(35%比 11%,p = 0.008)。与对照组相比,膀胱外翻和尿道上裂复合畸形患者生育子女的可能性较小(22%比 45%,p = 0.021)。
膀胱外翻和尿道上裂复合畸形患者在勃起和一般性功能测试方面有良好的长期结果。然而,这些个体开始性生活的可能性比一般人群晚,与对照组相比,生育子女的可能性较小。