Stergioulas Apostolos
Laboratory of Health, Fitness, and Rehabilitation Management, Faculty of Humam Movement and Quality of Life, Peloponnese University, Sparta, Greece.
Photomed Laser Surg. 2008 Apr;26(2):99-105. doi: 10.1089/pho.2007.2138.
In this study I sought to test the efficacy of low-power laser therapy (LLLT) in patients with frozen shoulder.
The use of low-level laser energy has been recommended for the management of a variety of musculoskeletal disorders.
Sixty-three patients with frozen shoulder were randomly assigned into one of two groups. In the active laser group (n = 31), patients were treated with a 810-nm Ga-Al-As laser with a continuous output of 60 mW applied to eight points on the shoulder for 30 sec each, for a total dose of 1.8 J per point and 14.4 J per session. In the placebo group (n = 32), patients received placebo laser treatment. During 8 wk of treatment, the patients in each group received 12 sessions of laser or placebo, two sessions per week (for weeks 1-4), and one session per week (for weeks 5-8).
Relative to the placebo group, the active laser group had: (1) a significant decrease in overall, night, and activity pain scores at the end of 4 wk and 8 wk of treatment, and at the end of 8 wk additional follow-up (16 wk post-randomization); (2) a significant decrease in shoulder pain and disability index (SPADI) scores and Croft shoulder disability questionnaire scores at those same intervals; (3) a significant decrease in disability of arm, shoulder, and hand questionnaire (DASH) scores at the end of 8 wk of treatment, and at 16 wk posttreatment; and (4) a significant decrease in health-assessment questionnaire (HAQ) scores at the end of 4 wk and 8 wk of treatment. There was some improvement in range of motion, but this did not reach statistical significance.
The results suggested that laser treatment was more effective in reducing pain and disability scores than placebo at the end of the treatment period, as well as at follow-up.
在本研究中,我试图测试低功率激光疗法(LLLT)对肩周炎患者的疗效。
低强度激光能量已被推荐用于治疗多种肌肉骨骼疾病。
63例肩周炎患者被随机分为两组。在主动激光组(n = 31)中,患者接受波长810 nm的镓铝砷激光治疗,连续输出功率为60 mW,照射肩部8个点,每个点照射30秒,每点总剂量为1.8 J,每次治疗总剂量为14.4 J。在安慰剂组(n = 32)中,患者接受安慰剂激光治疗。在8周的治疗期间,每组患者接受12次激光或安慰剂治疗,每周2次(第1 - 4周),每周1次(第5 - 8周)。
与安慰剂组相比,主动激光组有:(1)在治疗4周和8周结束时,以及8周额外随访结束时(随机分组后16周),总体、夜间和活动疼痛评分显著降低;(2)在相同时间间隔,肩部疼痛和功能障碍指数(SPADI)评分以及克罗夫特肩部功能障碍问卷评分显著降低;(3)在治疗8周结束时和治疗后16周,手臂、肩部和手部功能障碍问卷(DASH)评分显著降低;(4)在治疗4周和8周结束时,健康评估问卷(HAQ)评分显著降低。活动范围有一定改善,但未达到统计学意义。
结果表明,在治疗期结束时以及随访时,激光治疗在降低疼痛和功能障碍评分方面比安慰剂更有效。