Feasibility of Self-administered Neuromodulation for Neurogenic Bladder in Spinal Cord Injury

医学 抗胆碱能 脊髓损伤 尿失禁 随机对照试验 不利影响 膀胱过度活动 生活质量(医疗保健) 麻醉 物理疗法 导尿 内科学 泌尿系统 泌尿科 脊髓 替代医学 护理部 病理 精神科
作者
Argyrios Stampas,Rose Khavari,Joel Frontera,Suzanne L. Groah
出处
期刊:International Neurourology Journal [Korean Continence Society]
卷期号:23 (3): 249-256 被引量:10
标识
DOI:10.5213/inj.1938120.060
摘要

To determine if self-administered transcutaneous tibial nerve stimulation (TTNS) is a feasible treatment option for neurogenic bladder among people with spinal cord injury (SCI) who utilize intermittent catheterization for bladder management.Four-week observational trial in chronic SCI subjects performing intermittent catheterization with incontinence episodes using TTNS at home daily for 30 minutes. Those using anticholinergic bladder medications were given a weaning schedule to begin at week 2. Primary outcomes were compliance and satisfaction. Secondary outcomes included change in bladder medications, efficacy based on bladder diary, adverse events, and incontinence quality of life (I-QoL) survey.All 16 subjects who started the study completed the 4-week trial rating TTNS with high satisfaction and easy to use, without discomfort. Twelve of 14 patients (86%) using anticholinergic bladder medications reduced their dosage and maintained similar frequency and volumes of bladder catheterization and incontinence episodes. Bladder medication reduced by approximately 3.2 mg weekly (95% confidence interval, -5.9 to -0.4) and anticholinergic side effects of dry mouth and drowsiness decreased more than 1 level of severity from baseline (P=0.027, P=0.015, respectively). At 4 weeks, total I-QoL score improved by an average of 3.2 points compared to baseline in all domains.This pilot trial suggests TTNS is feasible to be performed at home in people with chronic SCI. Participants were able to reduce anticholinergic medication dosage and anticholinergic side effects while maintaining continence, subsequently improving QoL scores. These results advocate for further randomized, controlled trials with longer duration and urodynamic evaluation to assess long-term efficacy.
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