Mokhtar B, Baxter G D, Walsh D M, Bell A J, Allen J M
Department of Occupational Therapy and Physiotherapy, University of Ulster, Jordanstown, Northern Ireland, U.K.
Lasers Surg Med. 1995;17(1):74-81. doi: 10.1002/lsm.1900170109.
This study assessed the putative analgesic effect of combined monochromatic light/laser irradiation at low intensity (660-950 nm; 31.9 J/cm2; pulsed at 16 or 73 Hz).
STUDY DESIGN/MATERIALS AND METHODS: The investigation was completed under double-blind conditions using a standardised form of the submaximal effort tourniquet technique. Healthy male volunteers naive to the experimental conditions (n = 45) attended on two occasions for the purposes of pain induction, the first during which baseline data were obtained and on a second occasion during which they were randomly allocated to one of two treatments or a placebo condition. For the treatment conditions, irradiation was applied to the ipsilateral Erb's point at the parameters stated; for the placebo condition, sham "irradiation" was delivered using a dummy unit. Pain was measured using computerised visual analogue scales and McGill Pain Questionnaires (MPQ) to assess "current pain intensity" and "worst pain experienced," respectively.
Analysis of variance and appropriate post hoc tests demonstrated only a weak (but significant) hypoalgesic effect compared to placebo (P < 0.05) in the treatment group irradiated at 16Hz for the sensory component of the MPQ; other comparisons were found to be nonsignificant.
These results do not provide convincing evidence for the hypoalgesic potential of combined monochromatic light/laser irradiation, at least at the parameters used here, and thus indicate the necessity of additional work to investigate this modality further in order to assess the potential benefit, if any, of such treatment in the clinical setting.
本研究评估了低强度(660 - 950纳米;31.9焦耳/平方厘米;以16或73赫兹脉冲)的单色光/激光联合照射的假定镇痛效果。
研究设计/材料与方法:本研究在双盲条件下,采用标准化的次最大努力止血带技术完成。对实验条件不知情的健康男性志愿者(n = 45)分两次前来进行疼痛诱发,第一次获取基线数据,第二次将他们随机分配至两种治疗之一或安慰剂组。对于治疗组,按照所述参数对同侧的Erb点进行照射;对于安慰剂组,使用假装置进行假“照射”。分别使用计算机化视觉模拟量表和麦吉尔疼痛问卷(MPQ)测量疼痛,以评估“当前疼痛强度”和“经历的最严重疼痛”。
方差分析及适当的事后检验表明,在MPQ的感觉成分方面,与安慰剂相比,仅在以16赫兹照射的治疗组中显示出微弱(但显著)的镇痛效果(P < 0.05);其他比较均无统计学意义。
这些结果并未为单色光/激光联合照射的镇痛潜力提供令人信服的证据,至少在此处使用的参数下如此,因此表明有必要开展更多工作以进一步研究这种治疗方式,从而评估其在临床环境中可能存在的益处(若有的话)。