Davila G W, Neal D, Horbach N, Peacher J, Doughtie J D, Karram M
Colorado Gynecology and Continence Center, Denver 80220, USA.
Obstet Gynecol. 1999 Jun;93(6):938-42. doi: 10.1016/s0029-7844(99)00240-9.
To evaluate the safety and efficacy of a bladder-neck support prosthesis, a vaginal device designed to support the bladder neck, in women with genuine stress and mixed incontinence.
For enrollment, incontinent women underwent a history, physical examination including cotton-swab test, urinalysis, postvoid residual urine, and multichannel urodynamic testing. Those with genuine stress incontinence or mixed incontinence and urethral hypermobility completed 7-day bladder diaries, the Incontinence Impact Questionnaire, and underwent standardized pad tests. They were fitted with a prosthesis and seen weekly to optimize fit and efficacy. At week 5, they underwent repeat evaluations with the best-fitting prosthesis in place.
Seventy women were enrolled and 53 completed the 1-month study (29 genuine stress incontinence, 24 mixed incontinence). The mean ages were 50.4 years for genuine stress incontinence (range 24-76) and 55.7 years for mixed incontinence (range 30-88). A statistically significant reduction in incontinence was noted on pad testing (genuine stress incontinence, mean 46.6-16.6 g; mixed incontinence, mean 31.9-6.8 g) and in the bladder diary (genuine stress incontinence, mean 28.6-7.8 losses per week; mixed incontinence, mean 30.2-15 losses per week). Quality-of-life scores improved in both groups. With the device in place, urodynamic testing indicated normalization of urethral function without evidence of outflow obstruction. Subjects found the device comfortable, easy to use, and convenient. Side effects included five urinary tract infections and 23 cases of vaginal mucosal soreness or mild irritation.
The bladder-neck support prosthesis significantly reduced involuntary urine loss in women with stress and mixed incontinence.
评估一种膀胱颈支撑假体(一种用于支撑膀胱颈的阴道装置)对真性压力性尿失禁和混合性尿失禁女性的安全性和有效性。
入组时,尿失禁女性接受病史采集、体格检查(包括棉拭子试验)、尿液分析、排尿后残余尿量测定以及多通道尿动力学检测。患有真性压力性尿失禁或混合性尿失禁且尿道活动过度的女性完成7天膀胱日记、尿失禁影响问卷,并接受标准化的护垫试验。为她们安装假体,并每周进行检查以优化贴合度和疗效。在第5周时,使用最合适的假体对她们进行重复评估。
70名女性入组,53名完成了为期1个月的研究(29例真性压力性尿失禁,24例混合性尿失禁)。真性压力性尿失禁患者的平均年龄为50.4岁(范围24 - 76岁),混合性尿失禁患者的平均年龄为55.7岁(范围30 - 88岁)。护垫试验显示尿失禁有统计学意义的显著减少(真性压力性尿失禁,平均从46.6克降至16.6克;混合性尿失禁,平均从31.9克降至6.8克),膀胱日记结果也显示减少(真性压力性尿失禁,平均每周漏尿次数从28.6次降至7.8次;混合性尿失禁,平均每周漏尿次数从30.2次降至15次)。两组的生活质量评分均有所改善。使用该装置时,尿动力学检测表明尿道功能恢复正常,且无流出道梗阻迹象。受试者认为该装置舒适、易于使用且方便。副作用包括5例尿路感染和23例阴道黏膜酸痛或轻度刺激。
膀胱颈支撑假体可显著减少压力性和混合性尿失禁女性的不自主尿失禁。