Efficacy of 660 nm Photobiomodulation in Burning Mouth Syndrome Management: A Single-Blind Quasi-Experimental Controlled Clinical Trial.

IF 1.8 Q2 SURGERY
Bruno Munhoz Marotta, Norberto Nobuo Sugaya, Reem Hanna, Camila de Barros Gallo
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Abstract

Background: Burning mouth syndrome (BMS) is characterized by a burning sensation of the oral mucosa without any evidence of clinical signs or underlining condition. Several treatment modalities have been utilized with various results and levels of evidence. Lately, photobiomodulation (PBM) has emerged as a noninvasive effective therapy due to its anti-inflammatory and biostimulatory effects, especially the low-power laser setting of red wavelength. Objective: This single-blind quasi-experimental controlled clinical trial aimed to evaluate the PBM effectiveness at a low level of red laser light in patients with BMS compared with sham control. Materials and methods: Thirty patients diagnosed with BMS were consecutively assigned to intervention (PBM therapy) and control (sham) groups. The protocol for PBM dosimetry was as follows: laser 660 nm; spot size: 0.04 cm2; power output: 100 mW; emission mode: continuous wave; power density: 6 J/cm2; irradiation time: 10 sec per point within 1 cm2 surface area of the symptomatic area. The treatment protocol was based on once a week for a total of 10 sessions. Results: Our results showed no statistically significant difference in reduction of pain intensity between the two groups at all the evaluated timepoints during the course of treatment. However, in both groups, we observed a statistically significant reduction of maximum pain intensity of 50% compared with patient-self reporting before the treatment. Conclusions: Further randomized clinical trials to validate our positive results with a large sample size with a long-term follow-up and understanding further the sham placebo effect are warranted.

660 纳米光生物调节治疗烧灼口腔综合征的疗效:单盲准实验对照临床试验。
背景:烧灼感口腔综合征(BMS)的特征是口腔黏膜有烧灼感,但没有任何临床症状或基本病症。目前已采用多种治疗方法,但效果和证据水平各不相同。最近,光生物调制(PBM)因其抗炎和生物刺激作用,尤其是红色波长的低功率激光设置,已成为一种非侵入性的有效疗法。研究目的本单盲准实验对照临床试验旨在评估低强度红色激光与假对照相比,PBM 对 BMS 患者的疗效。材料与方法:将 30 名确诊为 BMS 的患者连续分配到干预组(PBM 治疗)和对照组(假对照)。PBM 剂量测定方案如下:激光波长:660 nm;光斑大小:0.04 cm2;输出功率:100 mW;发射模式:连续发射:100 mW;发射模式:连续波;功率密度:6 J/cm2;照射时间:症状区域 1 cm2 表面积内的每个点 10 秒。治疗方案为每周一次,共 10 次。结果显示结果显示,在治疗过程中的所有评估时间点上,两组在减轻疼痛强度方面没有明显的统计学差异。不过,与治疗前患者的自我报告相比,我们观察到两组患者的最大疼痛强度均有统计学意义的50%的降低。结论:我们有必要进一步开展随机临床试验,通过大样本量的长期随访来验证我们的积极结果,并进一步了解假安慰剂效应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
4.10
自引率
0.00%
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0
期刊介绍: Photobiomodulation, Photomedicine, and Laser Surgery Editor-in-Chief: Michael R Hamblin, PhD Co-Editor-in-Chief: Heidi Abrahamse, PhD
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