体表肌电刺激治疗女性压力性尿失禁

G. Kolb, E. Kolb, Cherrilyn Richmond, Craig Hanson
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引用次数: 3

摘要

背景:盆底物理疗法是治疗女性压力性尿失禁的有效方法。然而,治疗师使用的许多设备都需要阴道插入,许多女性认为这是侵入性的。Elitone装置为骨盆底肌电刺激提供了一种无创的替代方法,这可能会促进这种治疗方式的广泛应用。此外,该装置的配置允许家庭使用,可用于补充临床治疗。目的:本研究探讨表面肌电刺激治疗女性压力性尿失禁的安全性和有效性。研究设计:无对照组的队列研究。方法:20例轻/中度应激性尿失禁女性患者每日自行使用Elitone装置治疗6周。参与者在每日日志中记录尿失禁事件和吸水垫的使用情况。研究前和研究后的问卷被用来评估生活质量、参与者满意度和产品可用性。结果:失禁发作频率、尿垫使用和生活质量测量分别有75%、85%和67%的参与者改善到临床显著程度。研究前后3个指标的变化均有统计学意义(P < 0.001)。83%的参与者对治疗感到满意。结论:接受保守、无创Elitone装置治疗的参与者在多个以患者为中心的结果测量中获得了有意义的尿失禁症状改善。改善程度与更具侵入性的阴道内治疗的历史表现一致。这种疗法可能特别有利于那些反对使用阴道插入装置的妇女。此外,尽管本研究评估了作为独立在家治疗的疗效,但物理治疗师可能会通过使用该设备作为在家治疗的补充而获得额外的好处。
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Surface-Applied Electrical Muscle Stimulation for Self-administered Treatment of Female Stress Urinary Incontinence
Background: Female stress urinary incontinence is effectively treated with pelvic floor physical therapy. However, many of the devices available to therapists necessitate vaginal insertion, which many women perceive as invasive. The Elitone device delivers a noninvasive alternative for delivering electrical muscle stimulation to the pelvic floor, which may promote broader access to this therapeutic modality. Further, the device's configuration enables home use, which may be used to complement in-clinic therapy sessions. Objective: This research investigates the safety and efficacy of surface-applied electrical muscle stimulation in the treatment of female stress urinary incontinence in an at-home, patient-administered use case. Study Design: Cohort study without control group. Methods: Twenty female participants with mild/moderate stress urinary incontinence self-administered daily treatments with the Elitone device for 6 weeks. Participants recorded incontinence episodes and absorbent pad use in a daily log. Pre- and poststudy questionnaires were used to assess quality of life, participant satisfaction, and product usability. Results: Incontinence episode frequency, pad usage, and quality-of-life measures improved to a clinically significant degree for 75%, 85%, and 67% of participants, respectively. The pre- to poststudy changes were statistically significant (P < .001) for all 3 measures. Eighty-three percent of participants were satisfied with the treatment. Conclusion: Participants receiving treatment with the conservative, noninvasive Elitone device achieved meaningful improvement in incontinence symptoms across multiple, patient-centric outcome measures. The degree of improvement aligned with historical performance of more invasive, intravaginal therapies. The therapy may particularly benefit those women who oppose use of vaginally inserted devices. Further, although this study evaluated efficacy as a stand-alone, at-home treatment, physical therapists may realize additional benefits by using the device as an at-home complement to in-office therapy sessions.
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