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Acupuncture for overactive bladder: a randomized controlled trial.

机译:针刺治疗膀胱过度活动症:一项随机对照试验。

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OBJECTIVE: To compare acupuncture treatment for overactive bladder with urge incontinence with a placebo acupuncture treatment. METHODS: Eighty-five women enrolled in this randomized, placebo-controlled trial. Women were randomly assigned to either receive an acupuncture treatment expected to improve their bladder symptoms, or a placebo acupuncture treatment designed to promote relaxation. They underwent cystometric testing, completed a 3-day voiding diary, and completed the urinary distress inventory and incontinence impact questionnaire, validated quality-of-life inventories, before and after 4 weekly acupuncture treatments. The primary endpoint was number of incontinent episodes over 3 days. Secondary endpoints included voiding frequency and urgency, cystometric bladder capacity, maximum voided volume, and the urinary distress inventory and incontinence impact questionnaire symptom scores. RESULTS: Seventy-four women completed all aspects of the study. Women in both treatment and placebo groups had significant decreases in number of incontinent episodes (59% for treatment, 40% for placebo) without a significant difference in the change between the groups. Women in the treatment group had a 14% reduction in urinary frequency (P = .013), a 30% reduction in the proportion of voids associated with urgency (P = .016), and a 13% increase in both maximum voided volume and maximum cystometric capacity (P = .01). Both groups also had an improvement in the urinary distress inventory and incontinence impact questionnaire scores (54% decrease for treatment, 30% decrease for placebo, P < .001 for the difference in change between the groups). CONCLUSION: Women who received 4 weekly bladder-specific acupuncture treatments had significant improvements in bladder capacity, urgency, frequency, and quality-of-life scores as compared with women who received placebo acupuncture treatments. LEVEL OF EVIDENCE: I.
机译:目的:比较针刺治疗膀胱过度活动症和急迫性尿失禁与安慰剂针刺治疗。方法:八十五名妇女参加了这项随机,安慰剂对照的试验。女性被随机分配接受预期会改善其膀胱症状的针灸治疗,或旨在促进松弛的安慰剂针灸治疗。他们接受了每周4次针灸治疗前后的膀胱测压测试,完成了为期3天的排尿日记,并完成了尿痛检查和尿失禁影响问卷,验证了生活质量库存。主要终点是3天内失禁发作的次数。次要终点包括排尿频率和尿急,膀胱测压膀胱容量,最大排尿量,以及尿痛清单和尿失禁影响问卷症状评分。结果:74名妇女完成了研究的所有方面。在治疗组和安慰剂组中,女性的失禁发作次数均显着减少(治疗组为59%,安慰剂组为40%),两组之间的变化无明显差异。治疗组的妇女尿频减少14%(P = .013),与尿急相关的排尿比例减少30%(P = .016),最大排尿量和排尿量均增加13%最大膀胱测压能力(P = 0.01)。两组的尿痛清单和失禁影响问卷得分也都有改善(治疗组降低54%,安慰剂组降低30%,两组间差异的差异P <.001)。结论:与接受安慰剂针灸治疗的女性相比,接受每周4次膀胱特异性针灸治疗的女性在膀胱容量,尿急,频率和生活质量评分方面均有显着改善。证据级别:I.

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