Combination of two desensitizing protocols to control dentin hypersensitivity in non-carious lesions: a randomized, double-blind clinical trial

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Autor(es): dc.contributorUniversidade Federal do Pará (UFPA)-
Autor(es): dc.contributorUniversidade Estadual Paulista (UNESP)-
Autor(es): dc.creatorBarros, Antonia Patricia Oliveira-
Autor(es): dc.creatorde Melo Alencar, Cristiane [UNESP]-
Autor(es): dc.creatorde Melo Pingarilho Carneiro, Alexandra-
Autor(es): dc.creatorda Silva Pompeu, Danielle-
Autor(es): dc.creatorBarbosa, Gabriela Monteiro-
Autor(es): dc.creatorAraújo, Jesuína Lamartine Nogueira-
Autor(es): dc.creatorSilva, Cecy Martins-
Data de aceite: dc.date.accessioned2022-08-04T22:11:31Z-
Data de disponibilização: dc.date.available2022-08-04T22:11:31Z-
Data de envio: dc.date.issued2022-04-28-
Data de envio: dc.date.issued2022-04-28-
Data de envio: dc.date.issued2022-01-31-
Fonte completa do material: dc.identifierhttp://dx.doi.org/10.1007/s00784-021-04104-2-
Fonte completa do material: dc.identifierhttp://hdl.handle.net/11449/222135-
Fonte: dc.identifier.urihttp://educapes.capes.gov.br/handle/11449/222135-
Descrição: dc.descriptionObjectives: This study evaluated the effect of photobiomodulation (PBM) combined with 8% strontium acetate (SA8%) in the treatment of dentin hypersensitivity (DH) in non-carious lesions and analyzed the risk factors with the patient’s quality of life. Methods: Eighty teeth with DH were randomly allocated into four treatment groups (n = 20): G1, PBM imitation + toothpaste with no active ingredient; G2, PBM imitation + toothpaste with SA8%; G3, PBM + toothpaste without the active ingredient; and G4, PBM + toothpaste with SA8%. Participants were provided with a questionnaire on the experience of dentin hypersensitivity (QEDH) to assess the impact of desensitizing treatment on health-related quality of life (HRQL). Friedman and Kruskal–Wallis tests were used for intra- and intergroup comparisons, and Wilcoxon and Mann–Whitney tests were used to analyze HRQL. All analyses used significance levels of 5%. Results: Intergroup comparisons revealed a significant difference (p < 0.05); G4 had the best response in terms of HD reduction in G4 compared to the other groups on the 7th day of assessment (T3). Only G4 showed a statistically significant difference (p < 0.05) in the reduction of EDH for intragroup analysis. Conclusion: The combination of therapies was more effective in reducing DH than the isolated use of these strategies. Clinical relevance: The combination of therapies is effective in the treatment of DH.-
Descrição: dc.descriptionPró-Reitoria de Pesquisa e Pós-Graduação, Universidade Federal do Pará-
Descrição: dc.descriptionUniversidade Federal do Pará-
Descrição: dc.descriptionSchool of Dentistry Federal University of Pará, Pará-
Descrição: dc.descriptionAraraquara School of Dentistry Paulista State University, SP-
Descrição: dc.descriptionDental Materials Laboratory of the Postgraduate Program in Dentistry Federal University of Pará, Pará-
Descrição: dc.descriptionAraraquara School of Dentistry Paulista State University, SP-
Formato: dc.format1299-1307-
Idioma: dc.languageen-
Relação: dc.relationClinical Oral Investigations-
???dc.source???: dc.sourceScopus-
Palavras-chave: dc.subjectDentin hypersensitivity-
Palavras-chave: dc.subjectQuality of life-
Palavras-chave: dc.subjectRisk factors-
Palavras-chave: dc.subjectTherapy-
Título: dc.titleCombination of two desensitizing protocols to control dentin hypersensitivity in non-carious lesions: a randomized, double-blind clinical trial-
Tipo de arquivo: dc.typelivro digital-
Aparece nas coleções:Repositório Institucional - Unesp

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