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dc.contributor.authorTenis, Carlos Albertopt_BR
dc.contributor.authorMartins, Manoela Dominguespt_BR
dc.contributor.authorGonçalves, Marcela Leticia Lealpt_BR
dc.contributor.authorSilva, Daniela de Fátima Teixeira dapt_BR
dc.contributor.authorCunha Filho, João Julio dapt_BR
dc.contributor.authorMartins, Marco Antonio Trevizanipt_BR
dc.contributor.authorMesquita-Ferrari, Raquel Agnellipt_BR
dc.contributor.authorBussadori, Sandra Kalilpt_BR
dc.contributor.authorFernandes, Kristianne Porta Santospt_BR
dc.date.accessioned2020-03-05T04:15:19Zpt_BR
dc.date.issued2018pt_BR
dc.identifier.issn0025-7974pt_BR
dc.identifier.urihttp://hdl.handle.net/10183/206451pt_BR
dc.description.abstractBackground: 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.en
dc.format.mimetypeapplication/pdfpt_BR
dc.language.isoengpt_BR
dc.relation.ispartofMedicine (Baltimore). Hagerstown. Vol. 97, no. 37 (Sept. 2018), p. 1-6, e12264pt_BR
dc.rightsOpen Accessen
dc.subjectDouble-Blind Methoden
dc.subjectMétodo duplo-cegopt_BR
dc.subjectEdemapt_BR
dc.subjectLasers, Semiconductoren
dc.subjectFacept_BR
dc.subjectLow-Level Light Therapyen
dc.subjectMolar, Thirden
dc.subjectLasers semicondutorespt_BR
dc.subjectTerapia com luz de baixa intensidadept_BR
dc.subjectPain Managementen
dc.subjectQuality of Lifeen
dc.subjectDente serotinopt_BR
dc.subjectResearch Designen
dc.subjectManejo da dorpt_BR
dc.subjectTooth Extractionen
dc.subjectQualidade de vidapt_BR
dc.subjectTrismusen
dc.subjectProjetos de pesquisapt_BR
dc.subjectExtração dentáriapt_BR
dc.subjectTrismopt_BR
dc.titleEfficacy 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 trialpt_BR
dc.typeArtigo de periódicopt_BR
dc.identifier.nrb001112878pt_BR
dc.type.originEstrangeiropt_BR


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