Effect of single-dose diode laser photobiomodulation on orthodontic pain following initial archwire placement: a randomized clinical trial.

IF 2.6 2区 医学 Q1 DENTISTRY, ORAL SURGERY & MEDICINE
Amin Golshah, Azadeh Kazemisaleh, Fatemeh Azizi, Amin Hossein Nejad
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引用次数: 0

Abstract

Background: This study assessed the effect of photobiomodulation (PBM) through single-dose diode 940 nm laser on pain after initial archwire placement.

Methods: This parallel-design clinical trial with 1:1 allocation ratio was conducted on 120 orthodontic patients with Class I molar relationship and 3-6 mm crowding, or overbite. Orthodontic brackets had been previously placed by an orthodontist. The patients were randomly assigned to three groups (n = 40) of PBM, placebo (laser in off mode), and control (no intervention). Right after initial archwire placement, patients in PBM group underwent 940 nm laser irradiation with 32 J/cm2 energy density in contact mode, and five areas were irradiated. Laser in off mode was used for the placebo group. The level of pain experienced by patients after archwire placement was recorded subjectively by using a visual analog scale (VAS). The Pain Catastrophizing Scale (PCS) was filled out by patients after 7 days to assess the correlation of personal traits with actual pain. Data were analyzed by the Chi-square test, independent t-test, ANOVA, and ANCOVA (alpha = 0.05).

Results: Type of intervention had no significant effect on VAS pain score (P = 0.654) although slightly lower pain was recorded in the PBM group. Location of orthodontic wire placement (maxilla/mandible) had no significant effect on the pain score (P = 0.780), although the mean pain score in the mandible was slightly higher than that in the maxilla.

Conclusion: In the present study, PBM delivered using a single-session 940 nm diode laser had no significant effect on pain after initial placement of orthodontic archwires.

Trial registration: Trial registration number: IRCT20230603058377N1. Retrospectively registered. Registration date: 08/07/2023.

单剂量二极管激光光生物调节对初始弓丝放置后正畸疼痛的影响:一项随机临床试验。
背景:本研究评估了单剂量940 nm激光光生物调节(PBM)对初置弓丝后疼痛的影响。方法:采用1:1比例的平行设计临床试验,对120例ⅰ类磨牙关系、3 ~ 6 mm拥挤或复咬合的正畸患者进行临床试验。正畸托槽以前由正畸医生放置过。患者被随机分为三组(n = 40): PBM组、安慰剂组(激光关闭模式)和对照组(无干预)。首次放置弓丝后,PBM组患者在接触模式下接受能量密度为32 J/cm2的940 nm激光照射,共照射5个区域。激光关闭模式用于安慰剂组。采用视觉模拟评分法(VAS)主观记录患者放置弓丝后的疼痛程度。7天后,患者填写疼痛灾变量表(PCS),评估个人特征与实际疼痛的相关性。资料分析采用卡方检验、独立t检验、方差分析和方差分析(α = 0.05)。结果:干预方式对VAS疼痛评分无显著影响(P = 0.654), PBM组疼痛评分略低。正畸金属丝放置位置(上颌骨/下颌骨)对疼痛评分无显著影响(P = 0.780),但下颌骨的平均疼痛评分略高于上颌骨。结论:在本研究中,使用940 nm二极管激光单次输送PBM对正畸弓线初始放置后的疼痛无明显影响。试验注册:试验注册号:IRCT20230603058377N1。回顾注册。报名日期:2023年7月8日。
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
BMC Oral Health
BMC Oral Health DENTISTRY, ORAL SURGERY & MEDICINE-
CiteScore
3.90
自引率
6.90%
发文量
481
审稿时长
6-12 weeks
期刊介绍: BMC Oral Health is an open access, peer-reviewed journal that considers articles on all aspects of the prevention, diagnosis and management of disorders of the mouth, teeth and gums, as well as related molecular genetics, pathophysiology, and epidemiology.
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