Foster N E, Baxter F, Walsh D M, Baxter G D, Allen J M
Rehabilitation Sciences Research Group, School of Biomedical Sciences, University of Ulster at Jordanstown, County Antrim, Northern Ireland.
Clin J Pain. 1996 Dec;12(4):301-10. doi: 10.1097/00002508-199612000-00009.
Two separate studies investigated the hypoalgesic effect of manipulation of Transcutaneous Electrical Nerve Stimulation (TENS) parameters on two models of experimental pain: the Submaximal Effort Tourniquet Technique and cold-pressor pain. For the first study, 32 healthy subjects (16 male and 16 female) attended once for the purpose of cold-pressor pain induction that involved immersion of the nondominant hand in a water bath at 0 degree C. Subjects were allocated to Control, Placebo, or 1 of 2 treatment groups (110 or 4-Hz TENS). Pain threshold measurements (time to withdrawal of hand in seconds) were obtained over six standardised cold pain cycles (i.e., two before stimulation onset, three during stimulation, and one cycle after stimulation). In the second study, 48 healthy volunteers (24 male and 24 female) attended on two occasions, 48 h apart, for the purposes of ischaemic pain induction. On the first attendance, baseline data were obtained and on the second, subjects were randomly allocated to Control, Placebo, or one of four treatment groups with different combinations of stimulation frequencies and pulse durations (4 or 110 Hz and 50 or 200 microseconds). Measurements of "current pain intensity" and "worst pain experienced" were obtained via the Visual Analogue Scale (VAS) and the McGill Pain Questionnaire (MPQ), respectively. Analysis of variance performed on both sets of collected data revealed no significant differences between any of the groups, thus indicating no apparent relevance of manipulation of TENS parameters using these models of pain. Several hypotheses are suggested to explain these findings.
两项独立研究调查了经皮电神经刺激(TENS)参数操作对两种实验性疼痛模型(次最大用力止血带技术和冷压痛)的镇痛效果。在第一项研究中,32名健康受试者(16名男性和16名女性)参加了一次实验,目的是诱导冷压痛,即将非优势手浸入0摄氏度的水浴中。受试者被分配到对照组、安慰剂组或两个治疗组之一(110赫兹或4赫兹TENS)。在六个标准化的冷痛周期内(即刺激开始前两个周期、刺激期间三个周期和刺激后一个周期)测量疼痛阈值(手抽出的时间,单位为秒)。在第二项研究中,48名健康志愿者(24名男性和24名女性)分两次参加实验,两次间隔48小时,目的是诱导缺血性疼痛。第一次参加时获取基线数据,第二次时,受试者被随机分配到对照组、安慰剂组或四个治疗组之一,这些治疗组具有不同的刺激频率和脉冲持续时间组合(4或110赫兹以及50或200微秒)。分别通过视觉模拟量表(VAS)和麦吉尔疼痛问卷(MPQ)获取“当前疼痛强度”和“经历的最严重疼痛”的测量值。对两组收集的数据进行方差分析显示,各实验组之间无显著差异,因此表明使用这些疼痛模型操作TENS参数没有明显关联。文中提出了几种假设来解释这些发现。