Efficacy of light-emitting diode (LED) photobiomodulation in pain management, facial edema, trismus, and quality of life after extraction of retained lower third molars : A randomized, double-blind, placebo-controlled clinical trial

• Autor(a) principal: Tenis, Carlos Alberto
• Data de Publicação: 2018
• Outros Autores: Martins, Manoela Domingues, Gonçalves, Marcela Leticia Leal, Silva, Daniela de Fátima Teixeira da, Cunha Filho, João Julio da, Martins, Marco Antonio Trevizani, Mesquita-Ferrari, Raquel Agnelli, Bussadori, Sandra Kalil, Fernandes, Kristianne Porta Santos
• Tipo de documento: Artigo
• Idioma: eng
• Título da fonte: Repositório Institucional da UFRGS
• Texto Completo: http://hdl.handle.net/10183/206451
• topic: Método duplo-cego; Edema; Face; Lasers semicondutores; Terapia com luz de baixa intensidade; Dente serotino; Manejo da dor; Qualidade de vida; Projetos de pesquisa; Extração dentária; Trismo; Double-Blind Method; Lasers, Semiconductor; Low-Level Light Therapy; Molar, Third; Pain Management; Quality of Life; Research Design; Tooth Extraction; Trismus

Background: In dentistry, one of the most common surgical procedures is the removal of retained third molars. This surgery generates great morbidity to the participants for causing pain, edema, and trismus due to surgical trauma. The objective of the present study is to evaluate the efficacy of photobiomodulation with light emitting diode (LED) in the control of pain, facial edema, trismus, and quality of life resulting from the extraction of retained lower third molars. Methods:A randomized, double-blind, placebo-controlled clinical trial involving 38 adult participants, who meet the criteria of eligibility and agree to participate in the study. Before the surgeries are performed, the facial and mouth opening measures of all the participants will be taken. Immediately after the surgeries, participants will be randomized into 2 groups. In the LED group, participants will receive LED applications (intra oral with 660 nm, 12J and extraoral with 850 nm, 108J) in the immediate postoperative, first and second days after the surgical procedure. In the control group, the participants will be attended in the same way as in the LED group, however, the person in charge of the application will simulate the irradiation. Pain (EVA and NRS-101), postoperative edema, trismus, temperature, dysphagia, and hematoma will be evaluated after 1, 2, 5, and 7 days. The oral health impact profile (OHIP-14 Questionnaire) and anxiety analysis (Beck anxiety inventory -BAI) questionnaires will be applied preoperatively and 7 days after treatment. The appropriate statistical tests will be applied for each specific analysis in a significance level of 5%. Discussion: Although the use of low-power laser in the postoperative has shown good results in the control of postoperative sequelae, this is the first study on the efficacy of the use of LED in this situation. Abbreviations: BAI = Beck anxiety inventory, LED = light emitting diode, NRS-101 = numerical rating scale 101, OHIP-14 = oral health impact profile, PBM = pohotobiomodulation, VAS = visual analog scale.