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Objectives: This study aimed to establish a single-session associative protocol for non-restorative management of dentin hypersensitivity (DH). Materials and Methods: Twenty-four individuals with DH and a minimum sensitivity level of 4 on the visual analog scale (VAS) were selected. The study was conducted in a split-mouth design, with each participant (n = 20) having at least 1 affected tooth in all quadrants. The management protocols consisted of control group: universal adhesive, Neural Desensitizing Protocol group: 5% potassium nitrate, Mixed Desensitizing Protocol (PAM) group: 5% sodium fluoride and 5% potassium nitrate, Remineralizing Desensitizing Protocol (PDR) group: surface-partially reacted glass technology photopolymerizable varnish. Evaluations were performed immediately after application, at 1 week, 1 month, 2 months, and 12 months using the VAS sensitivity test. Results: The scores were subjected to statistical analysis using the Friedman test (p < 0.05), Durbin-Conover test (p < 0.05), and Wilcoxon test (p < 0.05). At the 12-month evaluation, all groups showed statistically significant differences compared to the initial assessment. For the evaluation after 12 months, there was a statistically significant difference between the PAM group, the control group, and the PDR group. Conclusions: It can be concluded that all groups were effective in controlling DH, but there were significant results in the control group and PDR group. The clinical relevance of this study is to demonstrate that the application of single-session desensitizing protocols can be effective in controlling DH for up to 12 months. Trial Registration: Brazilian Clinical Trials Registry Identifier: RBR-4r63d7s.

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Introduction: Dentin adhesives provide union between the dental substrate and composite resin, but this union can be influenced by the cleaning agent. Objective: Evaluate the use of ozonated water as a cavity cleaning solution. Material and method: 40 bovine dental crowns were selected, divided into four groups: AD (dentin cleaning with distilled water) and AO (dentin cleaning with ozonized distilled water). Each group was divided into two storage periods (24h and 30 days) kept at 37 °C. The selected universal system adhesive was employed according to the manufacturer's instructions and light cured for 20 seconds. At that time, three cylinders were made (Tygon matrix with an internal diameter of 2 mm and a height of 2 mm) of composite resin in the crowns in the cervical, médium, and incisal regions and light cured for 30 seconds. After storage, the bonding strength was tested by micro-shear, and fracture type analysis was performed. The data were submitted to statistical analysis using the Shapiro-Wilk test with a significance level of 95%, ANOVA, and Turkey. Result: There was a statistically significant difference between the bond strength values, only in the intergroup analysis for the time of 24 hours, between the middle third of the groups (LDAO24 = 2.70 (± 2.39); LDAO30 = 3.82 (± 2.31)). The predominant fracture type for both groups was an adhesive fracture, except in the medium and incisal thirds of the AD, which was a cohesive dentin fracture. Conclusion: The utilization of ozone did not change the bond strength adhesive.

Introdução: Os adesivos dentinários proporcionam união entre o substrato dental e resina composta, porém esta união pode ser influenciada pelo agente de limpeza. Objetivo: Avaliar a influência na resistência de união (RU) de um sistema adesivo universal associado à da água ozonizada como solução de limpeza cavitária. Material e método: Foram selecionadas 40 coroas de dentes anteriores bovinos divididos em 4 grupos: AD (limpeza dentinária com água destilada) e AO (limpeza dentinária com água destilada ozonizada). Cada grupo foi subdividido em outros dois grupos de acordo com o tempo de armazenamento (24h e 30 dias) armazenados a 37ºC. A limpeza dentinária foi realizada por meio de uma seringa de 60mL de cada solução e fricção por 10 segundos. O sistema adesivo universal selecionado foi aplicado de acordo com as instruções do fabricante e fotoativado por 20 segundos. Em seguida, foram confeccionados 3 cilindros (matriz Tygon com um diâmetro interno de 2 mm e 2 mm de altura) de resina composta nas coroas nas regiões cervical, média e incisal e fotoativados por 30 segundos. Após o armazenamento foi realizado o teste de RU por microcisalhamento e análise do tipo de fratura. Os dados coletados foram submetidos a análise estatística através do teste de Shapiro Wilk com nível de significância de 95%, ANOVA e Tukey. Resultado: Houve diferença estatística significativa entre os valores de RU apenas na análise intergrupos para o tempo de 24 horas, entre o terço médio dos grupos (LDAO24 = 2,70 (± 2,39); LDAO30 = 3,82 (± 2,31)). O tipo de fratura predominante para ambos os grupos em todos os tempos foi de fratura adesiva, com exceção ao terço médio e incisal do AD, que foi fratura coesiva de dentina. Conclusão: A utilização do ozônio não alterou a resistência de união adesiva.

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RESUMO

This study evaluated the effect of auricular acupuncture (AA) on physical (PA) and emotional (EA) aspects of patients with temporomandibular disorders (TMDs) and compared the effect of AA with those of Sham and occlusal splints (OS). In accordance with the CONSORT guidelines, patients with TMDs were evaluated by axes I and II of the RDC-TMD. The patients were allocated among three groups: OS, Sham and AA; and followed for 8 weeks. Both intragroup and intergroup evaluation for quantitative variables were analyzed with ANOVA, one-way, followed by the Tukey test. Qualitative variables were analyzed with the Kruskal-Wallis, and Dunn tests (intergroup evaluation) and for intragroup analyses, the Friedman and Wilcoxon tests were applied. At the end of the experiment, the chi-squared test was applied to compare the three groups with respect to the number of variables that had shown improved scores. The adopted level of significance for all tests was α = 5%. Intragroup analysis showed that, in the Sham group, no improvement in performance was seen in either EA and significant was improvements in 5 variables for 9 for PA, while in the AA group, significant improvements were observed in 2 variables for EA and in 9 for PA. In the OS group at the end of this study, significant improvements were observed in 8 and 8 variables for EA and PA, respectively. The analysis of therapies used revealed that the number of variables exhibiting significantly improved outcomes after treatment was similar between the AA and OS groups, whereas the sham group showed statistically significant differences when compared with the other two groups. In conclusion, this study demonstrated that AA applied at a specific TMJ ear point was able to bring about improvements in patients with TMDs, with outcomes similar to those in patients treated with an OS. CLINICAL TRIAL REGISTRATION: RBR-69ynnw (Brazilian Registry of Clinical Trials).

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