Treatment of Urinary Urgency Incontinence Using a Rechargeable SNM System: 6-Month Results of the ARTISAN-SNM Study

医学 骶神经电刺激 尿失禁 膀胱过度活动 生活质量(医疗保健) 神经调节 尿急 泌尿系统 患者满意度 指南 大便失禁 泌尿科 外科 物理疗法 内科学 护理部 替代医学 病理 刺激
作者
Rebecca McCrery,Felicia Lane,Kevin Benson,C. B. Taylor,Osvaldo F. Padron,Bertil Blok,Stefan De Wachter,Andrea Pezzella,Jennifer Gruenenfelder,Mahreen Pakzad,M.-A. Perrouin-Verbe,L. Le Normand,Philip Van Kerrebroeck,Jeffrey Mangel,Kenneth M. Peters,Michael Kennelly,A. M. James Shapiro,Una Lee,Craig V. Comiter,Margaret Mueller,Howard B. Goldman
出处
期刊:The Journal of Urology [Lippincott Williams & Wilkins]
卷期号:203 (1): 185-192 被引量:22
标识
DOI:10.1097/ju.0000000000000458
摘要

Sacral neuromodulation is a guideline recommended treatment of urinary dysfunction and fecal incontinence in patients in whom conservative treatments have failed. Historically sacral neuromodulation has been delivered using a nonrechargeable device with an average life span of 4.4 years. Surgery is required to replace the implanted neurostimulator due to battery depletion. Implantation of a long-lived implanted neurostimulator can eliminate the need for replacement surgeries, potentially reducing patient surgical risks and health care costs. The Axonics r-SNM System™ is a miniaturized, rechargeable sacral neuromodulation system designed to deliver therapy for at least 15 years. The ARTISAN-SNM (Axonics® Sacral Neuromodulation System for Urinary Urgency Incontinence Treatment) study is a pivotal study using rechargeable sacral neuromodulation therapy to treat urinary urgency incontinence. Six-month results are presented.A total of 129 eligible patients with urinary urgency incontinence were treated. All participants were implanted with a tined lead and the rechargeable sacral neuromodulation system in a nonstaged procedure. Efficacy data were collected using a 3-day bladder diary, the validated ICIQ-OABqol (International Consultation on Incontinence Questionnaire Overactive Bladder quality of life) questionnaire and a participant satisfaction questionnaire. Therapy responders were identified as participants with a 50% or greater reduction in urinary urgency incontinence episodes compared to baseline. We performed an as-treated analysis in all implanted participants.At 6 months 90% of participants were therapy responders. The mean ± SE number of urinary urgency incontinence episodes per day was reduced from 5.6 ± 0.3 at baseline to 1.3 ± 0.2. Participants experienced a clinically meaningful 34-point improvement on the ICIQ-OABqol questionnaire. There were no serious device related adverse events.The Axonics r-SNM System is safe and effective with 90% of participants experiencing clinically and statistically significant improvements in urinary urgency incontinence symptoms.

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