Lazovic Milica, Ilic-Stojanovic Olivera, Kocic Mirjana, Zivkovic Vesna, Hrkovic Marija, Radosavljevic Natasa
1 Institute for Rehabilitation , Belgrade, Serbia, Medical Faculty Belgrade, Serbia .
Photomed Laser Surg. 2014 Jun;32(6):336-44. doi: 10.1089/pho.2013.3563.
This study investigated the short-term efficacy of low-level laser therapy (LLLT) in patients with mild to moderate carpal tunnel syndrome (CTS), lasting for <1 year.
Seventy-nine patients with CTS were included in this double-blind, placebo-controlled study, and randomly divided in two treatment groups: Experimental group (EG), active laser group (40 patients); and control group (CG), placebo (sham) laser group (39 patients). A GaAlAs diode laser [780 nm, 30 mW continuous wave (CW), 0.785 cm(2), 38.2 mW/cm(2)] was applied in contact with four points perpendicularly to the skin over the carpal tunnel area for 90 sec per point (2.7 J, 3.4 J/cm(2)/point). Both groups were treated five times per week, once a day over 2 weeks, followed by 10 treatments every other day for 3 weeks, that is, for a total of 20 treatments. Clinical assessment, including visual analogue scale (VAS) pain rating, Tinel's sign, and median nerve conduction studies (NCSs) were evaluated before, and 3 weeks after, the last LLLT treatment.
Significant reduction in pain, reduction in the percentage of patients with a positive Tinel's sign, and shortening of sensory and motor latency time in the NCS examination was observed in the experimental LLLT group (but not in the control group).
This study has observed and documented the statistically significant short-term effects of LLLT on CTS patients in comparison with a placebo group. The results support this conclusion, especially if the LLLT is applied in the earlier stages of CTS, and with mild to moderate cases.
本研究调查了低强度激光疗法(LLLT)对病程小于1年的轻至中度腕管综合征(CTS)患者的短期疗效。
79例CTS患者纳入本双盲、安慰剂对照研究,并随机分为两个治疗组:实验组(EG),即活性激光组(40例患者);对照组(CG),即安慰剂(假)激光组(39例患者)。使用砷化镓铝二极管激光[780纳米,30毫瓦连续波(CW),0.785平方厘米,38.2毫瓦/平方厘米]垂直于腕管区域皮肤接触四个点,每点照射90秒(2.7焦耳,3.4焦耳/平方厘米/点)。两组均每周治疗5次,每天1次,共2周,随后每隔一天治疗10次,持续3周,即总共治疗20次。在最后一次LLLT治疗前和治疗后3周进行临床评估,包括视觉模拟量表(VAS)疼痛评分、Tinel征和正中神经传导研究(NCS)。
在实验性LLLT组中观察到疼痛显著减轻、Tinel征阳性患者百分比降低以及NCS检查中感觉和运动潜伏期缩短(对照组未观察到)。
本研究观察并记录了与安慰剂组相比,LLLT对CTS患者具有统计学意义的短期疗效。这些结果支持这一结论,特别是在CTS早期且为轻至中度病例时应用LLLT。