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A Study of the Influence of Low Intensity Laser Therapy on Painful Temporomandibular Disorder Patients

机译:低强度激光疗法对疼痛性颞下颌关节疾病患者的影响研究

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摘要

A double-blind clinical trial was conducted on 30 female Temporomandibular Disorders (TMD) patients who had pain as a chief complaint. The patients were randomly allocated into three groups based on Low Intensity Laser (LILT) regimes namely 820 nm Gallium Aluminium Arsenide (GaAlAs) laser at energy densities of 21.4J/cm2, 107 J/cm2 and placebo laser. Each patient had three LILT treatments in a week. The pressure pain threshold (PPT) of trigger points in masticatory muscles, unassisted maximum mouth opening without pain (MOSP) and symptom severity index (SSI) were recorded as baseline data and monitored after every treatment. Jaw kinesiology, electromyography (EMG) and pain rating index from McGill pain questionnaire were also recorded as baseline and final results. The analysis of covariance and further analysis showed that the higher energy density laser group had significant increases in PPT and EMG amplitude recorded from voluntary clenching (cEMG) compared with the placebo group at P values 0.0001 and 0.022 respectively. A significantly greater number of patients recovered from myofascial pain and TMJ arthralgia as assessed clinically in the higher energy group compared with the placebo (P value = 0.02 and 0.006 respectively). There was no statistically significant difference in the other parameters of assessment among the groups at a P value 0.05. At a period of 2 to 4 weeks review after LILT, there was an average 52% reduction of pain as assessed by SSI.
机译:一项针对30位女性颞下颌关节疾病(TMD)患者(主要症状为疼痛)进行了一项双盲临床试验。根据低强度激光(LILT)方案将患者随机分为三组,即能量密度分别为21.4J / cm 2 ,107 J / cm 2 和安慰剂激光。每个患者一周内接受三种LILT治疗。将咀嚼肌中触发点的压力疼痛阈值(PPT),无痛无助最大张口(MOSP)和症状严重程度指数(SSI)记录为基线数据,并在每次治疗后进行监测。麦吉尔疼痛问卷中的颚运动学,肌电图(EMG)和疼痛等级指数也记录为基线和最终结果。协方差分析和进一步的分析表明,与安慰剂组相比,较高能量密度的激光组从自愿性握紧(cEMG)记录的PPT和EMG幅度分别显着增加,P值分别为0.0001和0.022。与安慰剂相比,在较高能量组中从临床上评估,从肌筋膜疼痛和TMJ关节痛中康复的患者数量明显更多(分别为P值0.02和0.006)。在P值为0.05时,各组之间的其他评估参数之间无统计学差异。在进行LILT后的2至4周内,通过SSI评估,疼痛平均减少了52%。

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