Valenzuela S, Lopez-Jornet P
Department of Oral Medicine, Faculty of Medicine, University of Murcia, Murcia, Spain.
Medicina Oral, Clínica Odontológica Universitária Hospital Morales Meseguer, Murcia, Spain.
J Oral Rehabil. 2017 Feb;44(2):125-132. doi: 10.1111/joor.12463. Epub 2016 Dec 22.
To investigate low-level laser therapy (LLLT) applied to treat burning mouth syndrome (BMS). This prospective, comparative, partially blinded, single-centre, clinical trial of GaAlAs Laser, with 815 nm wavelength, included 44 BMS patients divided randomly into three groups: Group I (n = 16): GaAlAs laser 815 nm wavelength, 1 W output power, continuous emissions, 4 s, 4 J and fluence rate 133·3 J cm ; Group II (n = 16): GaAlAs infrared laser, 815 nm wavelength, 1 W output power, continuous emissions, 6 s, 6 J and fluence rate 200 J cm ; Group III (n = 12) placebo group, sham laser. All groups received a weekly dose for 4 weeks. Pain intensity was recorded using a 10-cm visual analogue scale; patients responded to the oral health impact profile (OHIP-14), xerostomia severity test and the hospital anxiety-depression scale (HAD). These assessments were performed at baseline, 2 and 4 weeks. LLLT decreased pain intensity and improved OHIP-14 scores significantly from baseline to 2 weeks in groups I and II compared with the placebo group. No statistically significant differences were found from 2 to 4 weeks. Overall improvements in visual analogue scale (VAS) scores from baseline to the end of treatment were as follows: Group I 15·7%; Group II 15·6%; Group III placebo 7·3%. LLLT application reduces symptoms slightly in BMS patients.
探讨低强度激光疗法(LLLT)治疗灼口综合征(BMS)的效果。这项关于波长815nm的砷化镓铝激光的前瞻性、对照、部分盲法、单中心临床试验纳入了44例BMS患者,随机分为三组:第一组(n = 16):波长815nm的砷化镓铝激光,输出功率1W,连续发射,4秒,4焦耳,能量密度133.3焦耳/平方厘米;第二组(n = 16):波长815nm的砷化镓红外激光,输出功率1W,连续发射,6秒,6焦耳,能量密度200焦耳/平方厘米;第三组(n = 12)为安慰剂组,采用假激光。所有组均每周治疗1次,共治疗4周。使用10厘米视觉模拟量表记录疼痛强度;患者对口腔健康影响程度量表(OHIP - 14)、口干严重程度测试及医院焦虑抑郁量表(HAD)进行作答。这些评估在基线、第2周和第4周进行。与安慰剂组相比,第一组和第二组在基线至第2周时,LLLT显著降低了疼痛强度并改善了OHIP - 14评分。在第2周至第4周未发现统计学显著差异。从基线到治疗结束,视觉模拟量表(VAS)评分的总体改善情况如下:第一组15.7%;第二组15.6%;第三组安慰剂组7.3%。应用LLLT可使BMS患者的症状略有减轻。