第二十条

M. Hamza, P. White, W. F. Craig, El‐sayed A. Ghoname, H. E. Ahmed, Timothy J. Proctor, C. Noe, Akshay S. Vakharia, N. Gajraj
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引用次数: 13

摘要

研究设计和方法:共有50名患有2型糖尿病和持续时间超过6个月的下肢周围神经性疼痛的成年患者被随机分配接受主动PENS(频率为15和30 Hz的电刺激针)和假(仅针)治疗3周。每组疗程30分钟,每周3次。在1周的洗脱期后,所有患者随后切换到另一种模式。在每次治疗前,采用10cm视觉模拟量表(VAS)评估疼痛、身体活动和睡眠质量。在每3周的治疗期间,测定VAS评分和每日口服镇痛药物需用量的变化。患者在完成每种治疗方式前后完成了MOS 36项简短健康调查(SF-36)、贝克抑郁量表(BDI)和心境状态量表(POMS)。在交叉研究结束时,使用患者偏好问卷来比较两种治疗方式的有效性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Article 20
RESEARCH DESIGN AND METHODS -A total of 50 adult patients with type 2 diabetes and peripheral neuropathic pain of [greater than]6 months duration involving the lower extremities were randomly assigned to receive active PENS (needles with electrical stimulation at an alternating frequency of 15 and 30 Hz) and sham (needles only) treatments for 3 weeks. Each series of treatments was administered for 30 min three times a week according to a standardized protocol. After a 1-week washout period, all patients were subsequently switched to the other modality A 10-cm visual analog scale (VAS) was used to assess pain, physical activity and quality of sleep before each session. The changes in VAS scores and daily requirements for oral analgesic medication were determined during each 3-week treatment period. Patients completed the MOS 36-Item Short-Form Health Survey (SF-36), the Beck Depression Inventory (BDI), and the Profile of Mood States (POMS) before and after completion of each treatment modality At the end of the crossover study a patient preference questionnaire was used to compare the effectiveness of the two modalities.
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