Staskin D, Bavendam T, Miller J, Davila G W, Diokno A, Knapp P, Rappaport S, Sand P, Sant G, Tutrone R
Urodynamics and Incontinence Center, Beth Israel Hospital, Boston, Massachusetts 02215, USA.
Urology. 1996 May;47(5):629-36. doi: 10.1016/s0090-4295(96)00003-9.
The purpose of this study was to test the safety and effectiveness of a urethral insert for managing stress or mixed urinary incontinence.
We performed a prospective, multicenter study of 135 female patients who were treated for 4 months with the Reliance Urinary Control Insert. The effectiveness of the insert was measured objectively at the time of first use and after 4 months' use by standardized pad weight studies. Insert effectiveness was also measured by reports of symptom improvement during patient interviews and on patient diaries. Urine microscopy and culture were obtained monthly; cystoscopy and urodynamics were conducted at study entry and at 4 months.
Significant improvement in involuntary urine loss was observed. Objective measurement of urine loss revealed that 80% of the patients were completely dry, and 95% of the patients achieved greater than an 80% decrease in urine loss. In addition, patients' perceptions of acceptability, incontinence symptom improvement, ease of learning, comfort, and time to habituation also showed improvements. Untoward events reported during the study included hematuria, bacteriuria, and bladder irritation. These events did not require significant medical intervention and did not result in any long-term clinical sequelae.
These preliminary results indicate that the Reliance Urinary Control Insert may be a safe, effective, and well-tolerated alternative to other available methods for the management of stress or mixed incontinence in women. Additional long-term follow-up will be required to substantiate this conclusion.
本研究旨在测试一种尿道插入物用于治疗压力性或混合性尿失禁的安全性和有效性。
我们对135名女性患者进行了一项前瞻性多中心研究,这些患者使用信赖尿控插入物治疗了4个月。在首次使用时和使用4个月后,通过标准化的护垫重量研究客观地测量插入物的有效性。还通过患者访谈期间和患者日记中症状改善的报告来衡量插入物的有效性。每月进行尿液显微镜检查和培养;在研究开始时和4个月时进行膀胱镜检查和尿动力学检查。
观察到不自主漏尿有显著改善。对尿失禁的客观测量显示,80%的患者完全干爽,95%的患者尿失禁减少了80%以上。此外,患者对可接受性、尿失禁症状改善、学习容易程度、舒适度和适应时间的感知也有所改善。研究期间报告的不良事件包括血尿、菌尿和膀胱刺激。这些事件不需要重大医疗干预,也没有导致任何长期临床后遗症。
这些初步结果表明,信赖尿控插入物可能是治疗女性压力性或混合性尿失禁的一种安全、有效且耐受性良好的替代其他现有方法。需要进行更多的长期随访来证实这一结论。