In-office dental bleaching in adolescents using 6% hydrogen peroxide with and without gingival barrier: a randomized double-blind clinical trial

Abstract At low concentrations used for in-office bleaching gels, such as 6% HP, gingival barrier continues to be performed. If we take into account that, in the at-home bleaching technique, no barrier is indicated, it seems that the use of a gingival barrier fails to make much sense when bleaching gel in low concentration is used for in-office bleaching. Objective This double-blind, split-mouth, randomized clinical trial evaluated the gingival irritation (GI) of in-office bleaching using 6% hydrogen peroxide (HP) with and without a gingival barrier in adolescents, as well as color change and the impact of oral condition on quality of life. Methodology Overall, 60 participants were randomized into which side would or would not receive the gingival barrier. In-office bleaching was performed for 50 minutes with 6% HP in three sessions. The absolute risk and intensity of GI were assessed with a visual analogue scale. Color change was assessed using a digital spectrophotometer and color guides. The impact of oral condition on quality of life was assessed using the Brazilian version of the Oral Health Impact Profile (α=0.05). Results The proportion of patients who presented GI for the "with barrier" group was 31.6% and for the "without barrier" group, 30% (p=1.0). There is an equivalence for the evaluated groups regarding GI intensity (p<0.01). Color change was detected with no statistical differences (p>0.29). There was a significant impact of oral condition on quality of life after bleaching (p<0.001). Conclusions The use or not of the gingival barrier for in-office bleaching with 6% HP was equivalent for GI, as well as for bleaching efficacy, with improvement in the impact of oral condition on quality of life.

In-office dental bleaching in adolescents using 6% hydrogen peroxide with different application tips: randomized clinical trial

Abstract Despite the availability of in-office bleaching gels with a 6% concentration of hydrogen peroxide (HP), these gels have not been evaluated in younger patients. They are commercially available with a tip, associated or not with a brush, where the tip with a brush spreads the gel over the entire surface to have a smaller thickness (thin layer) since the manufacturers indicate the application of a thin layer of gel. Objective This randomized, split-mouth, double-blind clinical trial evaluated the efficacy of in-office bleaching with 6% HP in adolescents using different application tips, as well tooth sensitivity (TS) and aesthetic self-perception. Methodology Sixty participants were randomized for 6% HP self-mixing bleaching gel tip design: without brush and with brush. In-office bleaching was performed in 3 sessions of 50 minutes. Color change was evaluated using a digital spectrophotometer (ΔE ab , ΔE 00 , and ΔWI D ) and color guide (ΔSGU), the absolute risk and intensity of TS with a visual analogue scale and aesthetic self-perception with the oral aesthetic scale (a=0.05). Results The groups achieved similar bleaching regardless of the application tip (p>0.05). However, only for ΔWI D , a significant mean difference (MD) was observed in the third week (MD 2.3; 95% CI 1.2 to 3.3; p < 0.001) and at one month (MD 1.6; 95% CI 0.6 to 2.6; p < 0.03) favoring the tip without brush. Regarding TS, 45% in the tip-without-brush group and 33% in the tip-with-brush group reported TS (odds ratio 0.61; 95% CI 0.29 to 1.28; p<0.02), with low TS intensity (MD 0.05; 95% CI -0.06 to 0.17; p>0.36). All patients reported improved aesthetic self-perception after bleaching (MD -1.3; 95% -1.8 to -0.9; p<0.001). Conclusions Regardless of the tip used bleaching with 6% HP achieved a bleaching efficacy and improved the aesthetic self-perception. However, a lower risk of TS for application using the tip with brush was observed.

Can composite packaging and selective enamel etching affect the clinical behavior of bulk-fill composite resin in posterior restorations? 24-month results of a randomized clinical trial

Abstract Objectives This is a double-blind, split-mouth, randomized clinical study that aims to evaluate the influence of bulk-fill composite packaging presented in syringes (BSy) and capsules (BCa), and the effect of selective enamel etching (SEE) on the clinical performance of class I and II bulk-fill resin composite restorations after 24 months. Methodology A total of 295 class I or class II restorations were performed on 70 patients. One universal adhesive was applied in all restorations. SEE was used in 148 restorations and self-etching mode (SET) in 147 restorations. After the adhesive application, cavities were restored with Filtek Bulk-fill Posterior Restorative in syringes (BSy), Filtek One Bulk-fill in capsules (BCa), or Filtek Supreme Ultra in syringes with the incremental technique (In). All restorations were evaluated using the FDI criteria after one week and after six, 12, and 24 months. Kaplan-Meier survival analysis and Pearson's Chi-square test were used (α=0.05) for statistical analysis. Results After 24 months, 62 patients were evaluated and four restorations were lost due to fracture (one for SEEBSy, two for SEEIn, and one for SETIn). No significant differences in the fracture and retention rate were found between groups (p>0.05). SEE showed significantly fewer marginal adaptation defects than SET (p<0.05). BCa and BSy groups showed fewer marginal discrepancies compared to In (p<0.05). Restorations performed with BCa showed less color mismatch than BSy or In (p<0.05). Conclusion Although all restorations exhibited satisfactory clinical performance after 24 months of clinical service, the clinical behavior of class I and II restorations' improved when performed with a bulk-fill composite in capsules, mainly when associated with a universal adhesive applied with SEE.

Validation of the brazilian version of the oral health impact profile - Aesthetic questionnaire

Abstract The aim of the study was to develop the Brazilian version of the Oral Health Impact Profile - Aesthetic Questionnaire (OHIP-Aes-Braz) and test its psychometric properties. The questionnaire test versions were developed by a panel of experts and a pre-test was conducted in a focus group. Data used for testing its psychometric properties were obtained from a randomized controlled clinical trial on tooth bleaching. Seventy-nine Brazilian adults were included. The questionnaires were applied before tooth bleaching treatment (baseline), one week (T1), and one month after the intervention (T2). Reliability was assessed in terms of internal consistency and stability, while validity was ascertained by criterion and construct validity. The sensitivity to change was assessed comparing the total scores at baseline and T2, using the Wilcoxon test (α = 0.05). Both stability and internal consistency (intra-class correlation coefficient=0.95, Cronbach's α = 0.92) proved to be adequate. Construct validity was confirmed as the correlation between OHIP-Aes-Braz scores with tooth color satisfaction and self-perceived oral health were in the expected direction. A positive correlation between OHIP-Aes-Braz and OHIP-14 (rs=0.63) and OIDP (rs=0.77) was observed. The instrument was responsive once differences in total scores before and after treatment were statistically significant (p<0.001). The OHIP-Aes-Braz presented good psychometric properties and showed sensitivity to change regarding aesthetics evaluation in Brazilian adults treated with tooth bleaching. A valid and reliable instrument allows a suitable assessment of oral health-related quality of life in Brazilian patients submitted to aesthetics dental interventions.

Resumo O objetivo do estudo foi desenvolver a versão brasileira do Oral Health Impact Profile - Aesthetic Questionnaire (OHIP-Aes-Braz) e testar suas propriedades psicométricas. As versões de teste do questionário foram desenvolvidas por um painel de especialistas e um pré-teste foi realizado em um grupo focal. Os dados usados para testar suas propriedades psicométricas foram obtidos a partir de um ensaio clínico randomizado controlado de clareamento dental. Setenta e nove brasileiros adultos foram incluídos. Os questionários foram aplicados antes do tratamento clareador (baseline), uma semana (T1) e um mês após a intervenção (T2). A confiabilidade foi avaliada em termos de consistência interna e estabilidade, enquanto a validade foi avaliada pela validade de critério e de construto. A sensibilidade à mudança foi avaliada pela comparação entre os escores totais no baseline e T2, usando o teste de Wilcoxon ((=0,05). Tanto a estabilidade quanto a consistência interna (coeficiente de correlação intraclasse=0,95, alfa de Cronbach=0,92) mostraram-se adequadas. A validade de construto foi confirmada uma vez que a correlação dos escores do OHIP-Aes-Braz com a satisfação com a cor dos dentes e a autopercepção da saúde bucal foram na direção esperada. Uma correlação positiva entre OHIP-Aes-Braz e OHIP-14 (r s =0,63) e OIDP (r s =0,77) foi observada. O instrumento foi responsivo uma vez que as diferenças nos escores totais antes e depois do tratamento foram estatisticamente significantes (p<0,001). O OHIP-Aes-Braz apresentou boas propriedades psicométricas e mostrou sensibilidade a mudanças na avaliação estética em adultos brasileiros submetidos ao clareamento dental. Um instrumento válido e confiável permite uma avaliação adequada da qualidade de vida relacionada à saúde bucal em pacientes brasileiros submetidos a intervenções odontológicas estéticas.

A new preheating thermoviscous composite for restoration of non-carious cervical lesions: a 6-month randomized clinical trial / Um novo compósito termoviscoso de pré-aquecimento para restauração de lesões cervicais não cariosas: ensaio clínico randomizado de 6 meses

Objetivo: Este ensaio clínico randomizado, duplo-cego e boca dividida avaliou o desempenho clínico de um novo compósito termoviscoso com pré-aquecimento (PHT) em comparação com uma resina composta sem aquecimento (NHT) em restaurações de lesões cervicais não cariosas (LCNCs) durante um período de 6 meses. Material e Métodos: 120 restaurações foram realizadas em LCNCs com dois materiais restauradores (n = 60). Após a profilaxia, os dentes foram isolados com isolamento de fio retrator/rolos de algodão e um adesivo universal foi aplicado na estratégia de condicionamento seletivo do esmalte. Para o grupo PHT o aquecimento foi realizado a 68°C usando um aquecidor de bancada por 3 min. Por outro lado, para o grupo NHT, nenhum aquecimento foi aplicado. Ambos os materiais restauradores foram colocados no dispensador de cápsulas e inseridos nas LCNCs. Após 6 meses, o desempenho clínico das restaurações foi avaliado de acordo com os critérios FDI. A análise estatística foi realizada com teste Qui-quadrado para todos parâmetros da FDI (α = 0,05). Resultados: Apenas três restaurações no grupo NHT foram perdidas/fraturadas após seis meses de acompanhamento. As taxas de retenção (intervalo confiança 95%) por seis meses foram de 97,5% (88,6% - 99,0%) para o grupo NHT e 100% (93,9% - 100%) para o grupo PHT (p > 0,05). Vinte e duas restaurações (8 para NHT e 14 para PHT) apresentaram pequenos defeitos de adaptação marginal aos seis meses de acompanhamento (p > 0,05). Vinte e seis restaurações apresentaram alguma retenção de biofilme aos seis meses de acompanhamento (11 para NHT e 15 para PHT; p > 0,05). Em relação a todos os outros parâmetros de FDI avaliados, todas as restaurações foram consideradas clinicamente aceitáveis. Conclusão: O desempenho clínico do novo compósito termoviscoso de pré-aquecimento mostrou-se promissor após 6 meses de avaliação clínica quando aplicado em LCNCs.(AU)

Objective: This double-blind, split-mouth randomized clinical trial evaluate the clinical performance of a new preheating (PHT) thermoviscous composite compared to a non-heating (NHT) composite resin in restorations of non-carious cervical lesions (NCCLs) over a period of 6-month. Material and Methods: 120 restorations were performed on NCCLs with two restorative materials (n = 60). After prophylaxis, the teeth were isolated with retraction cord isolation/cotton rolls and one universal adhesive was applied in the selective enamel etching strategy. For the PHT group heating was carried out at 68°C using a heater bench for 3 min. On the other side, for the NHT group, no heating was applied. Both restorative materials were placed in the caps dispenser and inserted in the NCCLs. The restorations were evaluated after 6-month of clinical performance according to the FDI criteria. Statistical analysis was performed with Chi-square test for all FDI parameters (α = 0.05). Results: Three restorations only in the NHT group were lost/fractured after six months follow-up. The retention rates (confidential interval 95%) for six months were 97.5% (88.6% - 99.0%) for the NHT group and 100% (93.9% - 100%) for the PHT group (p > 0.05). Twenty-two restorations (8 for NHT and 14 for PHT) presented small marginal adaptation defects at the six-months follow-up (p > 0.05). Twenty-six restorations were found to have biofilm retention in the six-month recall (11 for NHT and 15 for PHT; p > 0.05). Regarding all others FDI parameters evaluated, all restorations were considered clinically acceptable. Conclusion: The clinical performance of the new preheating thermoviscous was found to be promise after 6-month of clinical evaluation when applied in NCCLs (AU)

Clinical performance of a micro invasive treatment based on demineralization-remineralization for dental fluorosis: case report

Introduction: Dental fluorosis manifests clinically as white to brown spots on the enamel teeth that were exposed to excessive fluoride during the formation process. Esthetic treatments were described in the literature to reduce or eliminate the fluorotic stains on the enamel surface. Objective: The aim of this study is to present an alternative treatment for fluorosis-stained teeth. Case report: This case report describes the clinical performance of a treatment of a 12-year-old male patient whose teeth presented moderate fluorosis. This treatment is based on tooth demineralization and remineralization. The material has an acid phase made by hydrochloric acid with tricarboxylic acid, and an alkaline phase made by Calcium Hydroxide. Results: This pain less and fast treatment presented good results. The treatment eliminated the spots during the follow-up and preserved most of the dental structure, improving the appearance of the patient's teeth. Conclusion: The appearance of the treated enamel showed a surface almost completely free of fluorotic stains, demonstrating the satisfactory results of this treatment.

Introdução: A fluorose dentária manifesta-se clinicamente como manchas brancas a marrons no esmalte de dentes expostos ao excesso de flúor durante o processo de formação. Tratamentos estéticos foram descritos na literatura para reduzir ou eliminar as manchas fluoróticas na superfície do esmalte. Objetivo: Apresentar uma alternativa de tratamento para dentes manchados por fluorose dentária. Relato do caso: Este relato de caso descreve o desempenho clínico do tratamento para dentes com fluorose moderada em um paciente de 12 anos. Esse tratamento foi baseado numa técnica de desmineralização e remineralização do dente. O material possui uma fase ácida composta por ácido clorídrico com ácido tricarboxílico, e uma fase alcalina composta por Hidróxido de Cálcio. Resultados: Observou-se que esse tratamento, sem dor e rápido, apresentou resultados satisfatórios, pois eliminou as manchas durante o acompanhamento. Além disso, preservou ao máximo a estrutura dentária, beneficiando o paciente com uma melhor aparência dos seus dentes. Conclusão: O aspecto do esmalte tratado mostrou uma superfície quase sem manchas fluoróticas, demonstrando resultados satisfatórios deste tratamento.

Influência do ProTaper/ProTaper Next, comparado a outros sistemas rotatórios/reciprocantes, no risco e na intensidade da dor pós-operatória após instrumentação endodôntica em pacientes adultos: uma revisão sistemática e metanálise / Influence of ProTaper/ProTaper Next, compared to other rotatory/reciprocating systems, on the risk and intensity of postoperative pain after endodontic instrumentation in adult patients: a systematic review and meta-analysis

Introdução: O sucesso da terapia endodôntica depende não apenas de sua eficácia e conclusão adequada, mas também do mínimo desconforto do paciente. Objetivo: O objetivo dessa revisão sistemática e metanálise é avaliar o risco e a intensidade da dor endodôntica pós-instrumentação em pacientes adultos. Métodos: Uma pesquisa abrangente foi realizada no MEDLINE via PubMed, Scopus, Web of Science, LILACS, BBO e Cochrane Library e SIGLE, sem restrições. Também foram pesquisadas a conferência anual dos resumos da IADR (1990-2016) e o registro de ensaios não publicados e em andamento. As dissertações e teses foram pesquisadas utilizando-se os bancos de dados das dissertações ProQuest e das bases de teses Periódicos Capes. Apenas ensaios clínicos randomizados que compararam o risco ou a intensidade da dor resultante do tratamento endodôntico em pacientes adultos foram incluídos. Resultados: Após a remoção das duplicatas, 827 artigos foram identificados. Após a triagem do título e resumo, restaram 26 estudos, dos quais 13 foram ainda excluídos, permanecendo 10 para análise qualitativa e 7 para a metanálise. Não foi observada diferença significativa no risco/ intensidade da dor após o tratamento endodôntico nesse estudo. O risco de dor foi de 1,09, com intervalo de confiança de 95%, variando de 0,87 a 1,38 (p=0,45). A diferença padronizada g de Hedges nas médias da intensidade da dor após 24 horas foi de ­ 0,05, com intervalo de confiança variando de ­ 0,21 a 0,11 (p=0,53). Conclusões: Nessa metanálise, não foram encontradas diferenças no risco e na intensidade da dor após o tratamento endodôntico com ProTaper e outros sistemas rotatórios ou reciprocantes (AU).

Introduction: The success of endodontic therapy depends not merely on their efficacy and proper completion but also on minimal patient discomfort. The purpose of this systematic review and meta-analysis is to evaluate the risk and intensity of post instrumentation endodontic pain in adult patients. Methods: A comprehensive search was performed in the MEDLINE via PubMed, Scopus, Web of Science, LILACS, BBO and Cochrane Library and SIGLE without restrictions. The annual conference of the IADR abstracts (1990-2016), and unpublished and ongoing trials registry were also searched. Dissertations and theses were searched using the ProQuest Dissertations and the Periodicos Capes Theses Databases. Only randomized clinical trials that compared the risk or intensity of pain resulting from endodontic treatment in adult patients were included. Results: After the removal of duplicates, 827 articles were identified. After title and abstract screening, 26 studies remained. Thirteen studies were further excluded while 10 studies remained for qualitative analyses and 7 for the meta-analysis. No significant difference in the risk/intensity of pain after endodontic treatment was observed in this study. The risk of pain ratio was 1.09, with a 95% confidence interval of 0.87 to 1.38 (p = 0.45). The Hedges g standardized difference in means of pain intensity at 24 h was -0.05, with a confidence interval varying from -0.21 to 0.11 (p = 0.53). Conclusions: No differences in risk and intensity of pain after endodontic treatment with ProTaper and other rotatory or reciprocating systems were found in this meta-analysis (AU).

Universal adhesives and dual-cured core buildup composite material: adhesive properties

Abstract Dual-cured buildup composites and simplified light-cured adhesive systems are mixed with a chemical activator to prevent the incompatibility between them. Objective: To evaluate microshear bond strength (μSBS) and nanoleakage (NL) of three universal adhesives used under buildup composites using different curing modes, at baseline and after 6-months (6m). Methodology: Dentin specimens of 55 molars were assigned to: Clearfil Universal Bond[CFU], Prime&Bond Elect[PBE] and One Coat 7 Universal[OCU]. All-Bond Universal[ABU] and Adper Scotchbond Multi-Purpose[SMP] were used as controls. CFU, PBE, and OCU were: light-cured [LC], dual-cured using a self-curing activator [DC], and self-cured, using a self-curing activator and waiting for 20 min [SC]. Upon the application of the adhesive, transparent matrices were filled with a dual-cured buildup composite and light cured, then tested in mSBS. For NL, the specimens were submersed in ammoniacal silver nitrate and sectioned to observe under the SEM. Three-way ANOVA and Tukey's test were applied (α=0.05). Results: OCU/LC-PBE/LC resulted in higher mean μSBS than ABU/LC. For SMP/DC higher mean μSBS were obtained than for both CFU/DC and OCU/DC (baseline). No universal adhesive was significantly affected by curing mode or storage time. CFU, PBE, and OCU did not undergo significant changes in any curing mode (p>0.05). NL (baseline) PBE/LC resulted in higher %NL compared to ABU/LC. SMP/DC resulted in higher %NL than CFU/DC-OCU/DC. CFU/LC/DC resulted in lower %NL than CFU/SC. PBE/SC resulted in lower %NL than PBE/DC. OCU/LC/SC showed lower %NL than OCU/DC. OCU showed significant lower %NL than CFU and PBE. All CFU groups, as well as OCU/SC, resulted in increased %NL at 6m when compared with baseline. Conclusion: For universal adhesives used in etch-and-rinse mode, self-cured activator and different curing modes did not influence μSBS. However, some interactions were observed for NL, but this influence was material-specific.

Evaluation of reservoirs in bleaching trays for at-home bleaching: a split-mouth single-blind randomized controlled equivalence trial

Abstract Objectives This randomized, split-mouth, single-blinded trial assessed whether the use of reservoirs in at-home bleaching trays is equivalent to non-reservoir trays. Our choice of an equivalence trial was based on the expectation that a non-reservoir tray is sufficient to produce a color change. Secondary outcomes such as tooth sensitivity (TS) and gingival irritation (GI) were also assessed. Methodology Forty-six patients were selected with canines shade A2 or darker. In half of the patient's arch, bleaching trays were made with reservoirs and the other half, without reservoirs. At-home bleaching was performed with carbamide peroxide (CP) 10% (3 h daily; 21 days). Color change was evaluated with a digital spectrophotometer (ΔE, ΔE00, and Whiteness Index) and shade guide units (ΔSGU) at baseline, during and one-month post-bleaching. TS and GI were assessed with a numeric scale (NRS) and a visual analog scale (VAS). Results After one month, the equivalence of reservoir and non-reservoir groups were observed in all color instruments (p>0.05). Fifteen and sixteen patients presented pain (absolute risk: 33% and 35%, 95%, confidence interval (CI) 21-46% and 23-49%) in the reservoir and non-reservoir side, respectively. The odds ratio for pain was 0.8 (95%CI 0.2-3.0) and the p-value was non-significant (p=1.0). TS intensity was similar between both groups in any of the pain scales (p>0.05). No difference in the GI was observed (p>0.05). Conclusions The protocol with reservoirs is equivalent in color change to the non-reservoir, although no superiority of the latter was observed in terms of reduced TS and GI with at-home 10% carbamide peroxide bleaching. Clinical Relevance The presence of reservoirs in a bleaching tray did not improve color change or affect tooth sensitivity and gingival irritation.

Preemptive use of piroxicam on tooth sensitivity caused by in-office bleaching: a randomized clinical trial

Abstract This clinical trial evaluated the effect of preemptive use of the non-steroidal anti-inflammatory drug piroxicam in a single dose 30 min prior to in-office bleaching on the prevention of tooth sensitivity (TS) reported by patients. Fifty patients were submitted to two sessions of in-office tooth bleaching with 35% hydrogen peroxide used for 2 sessions, each consisting of a single 45-min application, with an interval of 7 days between session. Thirty minutes prior to the procedure, the patient randomly received a single dose of piroxicam (200 mg) or placebo in a double-blind, randomized, crossover design. The TS was evaluated using verbal rate (VRS) and visual analog (VAS) scales during the bleaching procedure and at 24 h after each session. The color changes were assessed by the Vita Bleachedguide scale 1 week after each bleaching session. Risk of TS was calculated from the VRS and analyzed by the McNemar test, while the level of TS was analyzed by the Mann-Whitney test. For the VAS, t-tests were used to compare data from the treatments at each assessment time. Data regarding color changes were subjected to Wilcoxon and Mann-Whitney tests (α=0.05). The preemptive administration of piroxicam did not affect the risk and level of TS compared to placebo, irrespective of the assessment time. The treatment sequence did not affect bleaching effectiveness. In conclusion, the administration of a single dose of piroxicam prior to in-office tooth bleaching was unable to significantly reduce the risk and level of TS.

Resumo Este ensaio clínico avaliou o efeito do uso preemptivo do anti-inflamatório não-esteroidal piroxicam em dose única 30 minutos antes do clareamento de consultório na prevenção de sensibilidade dentária (SD) relatada pelos pacientes. Cinquenta pacientes foram submetidos a duas sessões de clareamento dental em consultório com peróxido de hidrogênio a 35% por 2 sessões, consistindo de aplicação única de 45 minutos, com um intervalo de 7 dias entres as sessões. Trinta minutos antes do procedimento, o paciente recebia aleatoriamente dose única de piroxicam (200 mg) ou do placebo em um desenho duplo-cego, randomizado e cruzado. A SD foi avaliada usando a escalas de gradação verbal (EGV) e visual analógica (EVA) durante o procedimento clareador e 24h após o procedimento. As mudanças de cor foram avaliadas usando a escala Vita Bleachedguide uma semana após cada sessão de clareamento. O risco de SD foi calculado a partir de EGV a analisado pelo teste de McNemar, enquanto o nível de SD foi analisada pelo teste de Mann-Whitney. Para EVA, testes T foram usados para comparar dados dos tratamentos em cada tempo de avaliação. Dados de mudança de cor foram submetidos aos testes de Wilcoxon e Mann-Whitney (α=0.05). A administração preemptiva de piroxicam não afetou o risco e nível de SD quando comparado ao placebo, independentemente do tempo de avaliação. A sequencia de tratamento não afetou a efetividade do clareamento. Como conclusão, a administração de dose única de piroxicam previamente ao clareamento dental de consultório não foi efetiva em reduzir significantemente o risco e nível de SD.

Does the use of reservoirs have any impact on the efficacy of at-home bleaching? a systematic review

Abstract To answer the following focused question through a systematic review: "Are the risk and intensity of tooth sensitivity (TS) and bleaching efficacy different between adult patients who undergo at-home bleaching using trays with reservoirs and those who use trays without reservoirs?". A comprehensive search was performed in the MEDLINE via PubMed, Scopus, Web of Science, Latin American and Caribbean Health Sciences Literature database, Brazilian Library in Dentistry, Cochrane Library, and grey literature without restrictions. Abstracts from conferences; unpublished and ongoing trial registries, dissertations and theses (ProQuest Dissertations and Periódicos Capes Theses databases) were searched. Only randomized clinical trials (RCTs) were included. We used the Risk of Bias tool (RoB) from the Cochrane Collaboration for quality assessment. After the removal of duplicates, title and abstract screening and full-text examination, nine RCTs remained for qualitative analyses. The great majority of the studies did not report the method of randomization, allocation concealment, and examiner blinding during color assessment. From the nine studies, eight were at unclear risk of bias. In regard to color change, four studies reported no change and two reported improved color change with reservoirs. Only four studies recorded tooth sensitivity and they reported no significant differences. Only one study reported greater gingival irritation with reservoirs. Lack of data reporting prevented us from running a meta-analysis. Further well-designed RCT should be conducted to answer this research question. So far there is not evidence to support that reservoirs in bleaching trays improve color change. PROSPERO - CRD42016037628

Resumo Para responder a seguinte questão de pesquisa através de uma revisão sistemática: "O risco e a intensidade de sensibilidade dentária (SD) e eficácia de clareamento são diferentes entre pacientes adultos que realizam clareamento caseiro usando moldeiras com reservatórios e aqueles que usam moldeiras sem reservatórios?". Uma pesquisa abrangente foi realizada no MEDLINE via PubMed, Scopus, Web of Science, Literatura Latino-Americana e do Caribe em Ciências da Saúde (LILACS), Biblioteca Cochrane e literatura cinzenta, sem restrições. Os resumos da conferência anual da Associação Internacional para Pesquisa Dental além de estudos registrados ou em andamento também foram pesquisados. Dissertações e Teses foram pesquisados utilizando o Capes Journal Dissertações e Teses ProQuest. Apenas ensaios clínicos randomizados (ECR) foram incluídos. Usamos a ferramenta Risk of Bias (RoB) da Cochrane para avaliação de qualidade. Após a remoção de duplicatas, triagem de título e resumo e exame de texto completo, nove ECRs permaneceram para análises qualitativas. A grande maioria dos estudos não relatou o método de randomização, ocultação de alocação e cegamento do examinador durante a avaliação de cores. Dos nove estudos, oito estavam sob risco claro de viés. Em relação à mudança de cor, quatro estudos não relataram nenhuma mudança e dois relataram melhora na mudança de cor com reservatórios. Apenas quatro estudos registraram a sensibilidade dentária e não relataram diferenças significativas. Apenas um estudo relatou maior irritação gengival com reservatórios. A falta de relatórios de dados nos impediu de executar uma meta-análise. Outros ECR bem desenhados devem ser conduzidos para responder a esta questão de pesquisa. Até agora não há evidências que sustentem que reservatórios em moldeiras de clareamento melhorem a mudança de cor. PROSPERO - CRD42016037628

Effect of grape seed extract-containing phosphoric acid formulations on bonding to enamel and dentin

Abstract The aim was to evaluate the effect of 2% grape seed extract (GSE) containing phosphoric acid (PhA) on the bond strength to enamel and dentin. The control group was 37% PhA. The following three PhA formulations with 2% GSE and 20% ethanol were obtained: GSE5 = 5% PhA; GSE10 = 10% PhA; and GSE20 = 20% PhA. The enamel and dentin surfaces of molars were etched with the acid solutions, followed by Scotchbond Multi-Purpose adhesive and composite resin application. The tensile bond strength (TBS) test evaluated the bond to enamel after 24 h, and the microtensile bond strength (μTBS) test evaluated the bond to dentin after 24 h and 12-month water storage. Etched enamel and dentin were observed by scanning electron microscopy (SEM) and atomic force microscopy (AFM), respectively. The TBS data were submitted to one-way ANOVA, while µTBS data were submitted to two-way ANOVA and Tukey's test (α = 0.05). The TBS (MPa) to enamel did not significantly differ among the control (48.1 ± 15.7), GSE5 (46.1 ± 9.6), GSE10 (49.8 ± 13.6) and GSE20 (44.1 ± 11.9) groups (p = 0.537). The µTBS (MPa) to dentin of the control (28.4 ± 14.4) and GSE20 (24.1 ± 8.1) groups were significantly higher than those of the GSE5 (16.8 ± 7.4) and GSE10 (17.5 ± 6.6) groups at 24 h (p < 0.006). After 12-month storage, only GSE5 (21.0 ± 7.8) and GSE10 (17.6 ± 8.0) did not show significantly decreased μTBS (p > 0.145). SEM micrographs showed a shallower enamel etching pattern for GSE5. AFM images showed the formation of collagenous globular structures for GSE5 and GSE10. The different acid solutions did not influence the TBS to enamel, and the µTBS to dentin was stable over time when dentin was etched with GSE5 and GSE10.

Preemptive use of etodolac on tooth sensitivity after in-office bleaching: a randomized clinical trial

Abstract Purpose: This study determined the effectiveness of the preemptive administration of etodolac on risk and intensity of tooth sensitivity and the bleaching effect caused by in-office bleaching using 35% hydrogen peroxide. Material and methods: Fifty patients were selected for this tripleblind, randomized, crossover, and placebo-controlled clinical trial. Etodolac (400 mg) or placebo was administrated in a single-dose 1 hour prior to the bleaching procedure. The whitening treatment with 35% hydrogen peroxide was carried out in two sessions with a 7-day interval. Tooth sensitivity was assessed before, during, and 24 hours after the procedure using the analog visual scale and the verbal rating scale. Color alteration was assessed by a bleach guide scale, 7 days after each session. Relative risk of sensitivity was calculated and adjusted by session, while overall risk was compared by the McNemar's test. Data on the sensitivity level of both scales and color shade were subjected to Friedman, Wilcoxon, and Mann-Whitney tests, respectively (α=0.05). Results: The preemptive administration of etodolac did not affect the risk of tooth sensitivity and the level of sensitivity reported, regardless of the time of evaluation and scale used. The sequence of treatment allocation did not affect bleaching effectiveness, while the second session resulted in additional color modification. The preemptive administration of etodolac in a single dose 1 hour prior to in-office tooth bleaching did not alter tooth color, and the risk and intensity of tooth sensitivity reported by patients. Conclusion: A single-dose preemptive administration of 400 mg of etodolac did not affect either risk of tooth sensitivity or level of sensitivity reported by patients, during or after the in-office tooth bleaching procedure.

Randomized clinical trials of dental bleaching - Compliance with the CONSORT Statement: a systematic review

Abstract We reviewed the literature to evaluate: a) The compliance of randomized clinical trials (RCTs) on bleaching with the CONSORT; and b) the risk of bias of these studies using the Cochrane Collaboration risk of bias tool (CCRT). We searched the Cochrane Library, PubMed and other electronic databases, to find RCTs focused on bleaching (or whitening). The articles were evaluated in compliance with CONSORT in a scale: 0 = no description, 1 = poor description and 2 = adequate description. Descriptive analyses of the number of studies by journal, follow-up period, country and quality assessments were performed with CCRT for assessing risk of bias in RCTs. 185 RCTs were included for assessment. More than 30% of the studies received score 0 or 1. Protocol, flow chart, allocation concealment and sample size were more critical items, as 80% of the studies scored 0. The overall CONSORT score for the included studies was 16.7 ± 5.4 points, which represents 52.2% of the maximum CONSORT score. A significant difference among journal, country and period of time was observed (p < 0.02). Only 7.6% of the studies were judged at "low" risk; 62.1% were classified as "unclear"; and 30.3% as "high" risk of bias. The adherence of RCTs evaluating bleaching materials and techniques to the CONSORT is still low with unclear/high risk of bias.

Efeito da Temperatura de Evaporação do Solvente na Longevidade da Adesão de Adesivos Autocondicionantes à Dentina / Effect of Solvent Evaporation Temperature on Bonding Longevity of All-In-One Adhesives to Dentin

Avaliou-se a durabilidade da adesão de adesivos autocondicionantes à dentina após evaporação dos solventes com jato de ar frio e quente. Os sistemas adesivos Clearfil 3S Bond e OptiBond All-In-One foram aplicados em superfícies planas de dentina, a evaporação dos solventes feita com ar quente (60±2 o C) ou ar frio (20±2 o C), seguindo-se fotoativação (600mW/cm2 por 10 s) e restauração com compósito (3 x 2 mm). Após armazenagem em água destilada (24 horas / 37 o C), as amostras foram seccionadas para obtenção de paralelogramos de 0,8 mm2 para testar em tração (0,5mm/min) em 24 horas e 6 meses. Dois paralelogramos de cada grupo experimental foram preparados para observar a nanoinfiltração na interface com a dentina. Os valores médios da resistência adesiva (em MPa) de cada grupo foram tratados por Análise de Variância de três fatores e teste de Tukey (5%), sendo o dente a unidade experimental. Foi observada maior adesão após evaporação dos solventes com ar quente (p=0.000) no tempo de 24 horas de armazenagem (0.003). Não houve diferenças para o tipo de adesivo (p=0.343) e nem para a interação adesivo X tempo X temperatura de evaporação do solvente (p>0,05). Concluiu-se que a durabilidade da adesão foi influenciada pela temperatura de evaporação do jato de ar

To evaluate the bonding longevity of one-step self-etch adhesive systems to dentin, after solvent evaporation with warm or cold airstream. Clearfil 3S Bond and OptiBond All-In-One adhesives were applied on flat dentin surfaces, solvent evaporation was performed with a warm (60±2 o C) or cold air (20±2 o C), the surfaces were light cured (600mW/cm2 during 10 s), and blocks of compositeres min were built (3 x 2mm). After storage in distilled water (24-hour at 37 o C), the samples were sectioned into 0.8 mm2 sticks and tested in tensile (0.5 mm/min) at 24-hour and 6-month periods. Two sticks from each experimental group were prepared for nanoleakage observation of the bond interface. The mean bond strength values of experimental groups (in MPa) were subjected to a three- way Analysis of Variance and post-hoc Tukey´s test (5%), using tooth as the experimental unit. Higher bond strength was observed with warm air (p=0.000) for solvent evaporation, and 24 hour of water storage (0.003. No significant differences were observed for both the adhesive systems (p=0.343) and interactions.The bonding durability was influenced by the air temperature for solvent evaporation

Protocolo das possibilidades técnicas de aplicação dos sistemas adesivos universais: revisão de literatura com relato de caso / Clinical strategies using universal adhesive systems: literature review with case report

Este relato de caso demonstra a utilização clínica de um novo sistema adesivo universal, Xeno Universal (Dentsply DeTrey, Alemanha) descrevendo quatro formas possíveis de aplicação: autocondicionante, com ou sem condicionamento seletivo do esmalte, ou com condicionamento ácido total, seguido da aplicação do adesivo sobre dentina seca ou úmida. Os adesivos universais de uma maneira geral são de fácil aplicação e versáteis, uma vez que o mesmo produto pode ter várias formas de aplicação, reduzindo o tempo clínico e em muitas situações a sensibilidade técnica. No entanto, mais estudos laboratoriais e clínicos que comprovem a eficácia deste novo adesivo universal em particular são necessários, antes que seu uso seja bem indicado aos cirurgiões-dentistas.

This case report describes the clinical application of a new universal adhesive system, Xeno Universal (Dentsply DeTrey, Germany) describing four application modes: self-etching, with or without selective enamel etching, or total etching followed by adhesive application on dry or moist dentin. Universal adhesive systems usually are versatile and easy to use, facilitating the operator, since the same product has several technical possibilities, thus reducing the operating time and the technique sensitivity. However, long-term laboratory studies and more clinical reports and/or clinical trials are needed to prove the quality of this new universal adhesive system, before dentists can start using them in their dental offices.

In-office bleaching effects on the pulp flow and tooth sensitivity – case series

Laser Doppler flowmetry (LDF) is a noninvasive method capable of evaluating variations in pulp blood flow (PBF) and pulp vitality. This method has thus far not been used to assess changes in blood flow after in-office bleaching. The aim of this case series report was to measure changes in PBF by LDF in the upper central incisor of three patients submitted to in-office bleaching. The buccal surfaces of the upper arch were bleached with a single session of 35% hydrogen peroxide gel with three 15-min applications. The color was recorded using a value-oriented Vita shade guide before in-office bleaching and one week after the procedure. The tooth sensitivity (TS) in a verbal scale was reported, and PBF was assessed by LDF before, immediately, and one week after the bleaching session. The lower arch was submitted to dental bleaching but not used for data assessment. A whitening degree of 3 to 4 shade guide units was detected. All participants experienced moderate to considerable TS after the procedure. The PBF readings reduced 20% to 40% immediately after bleaching. One week post-bleaching, TS and PBF were shown to be equal to baseline values. A reversible decrease of PBF was detected immediately after bleaching, which recovered to the baseline values or showed a slight increase sooner than one week post-bleaching. The LDF method allows detection of pulp blood changes in teeth submitted to in-office bleaching, but further studies are still required.

Effectiveness of nano-calcium phosphate paste on sensitivity during and after bleaching: a randomized clinical trial

The study aimed to evaluate the effectiveness of in-office bleaching and associated tooth sensitivity on application of nano-calcium phosphate paste as desensitizing agent. Bleaching was performed with 35% hydrogen peroxide gel in 40 patients who were randomly divided into placebo and nano-calcium phosphate paste groups. Bleaching efficacy (BE) was evaluated using a value-oriented Vita shade guide. Tooth sensitivity was recorded using a numeric rating scale (0–4) during bleaching and up to 48 h after each session. The primary outcome of absolute risk of tooth sensitivity was compared using the Fisher’s exact test (α = 0.05). The intensity of tooth sensitivity and the efficacy of in-office bleaching were also statistically evaluated. No significant differences in absolute risk and intensity of tooth sensitivity were detected between the groups (p = 1.0 and p = 0.53, respectively). BE was also found to be similar between the groups (p = 0.67). Although the use of a nano-calcium phosphate paste associated with fluoride and potassium nitrate did not influence the whitening outcome, but it also did not reduce bleaching-induced tooth sensitivity.

Genotoxic potential of 10% and 16% Carbamide Peroxide in dental bleaching

Dental bleaching has become one of the most frequently requested esthetic treatments in dental offices. Despite the high clinical success observed with this procedure, some adverse effects have been reported, including a potential for developing premalignant lesions, root resorption and tooth sensitivity, especially when misused. The aim of this study was to evaluate the genotoxic response using a micronucleus (MN) assay, after the application of two concentrations of carbamide peroxide. Thirty-seven patients were divided into two groups and randomly received either a 10% carbamide peroxide (CP) (19) or a 16% carbamide peroxide (18) concentration for 21 days in individual dental trays. Gingival margin cells were collected immediately before the first use (baseline), and then 15 and 45 days after baseline. The cells were placed on a histological slide, stained by the Feulgen technique, and evaluated by an experienced blinded examiner. One thousand cells per slide were counted, and the MN rate was determined. The two groups were analyzed by the Wilcoxon rank-sum test and the Kruskal-Wallis equality-of-populations rank test. A slight increase in MN was observed for both groups, in comparison with the baseline, at 15 days. However, no difference was observed between the two groups (10% and 16%), at either 15 or 45 days (p = 0.90). When bleaching is not prolonged or not performed very frequently, bleaching agents containing carbamide peroxide alone will not cause mutagenic stress on gingival epithelial cells.

Corantes com e sem açúcar versus efetividade do clareamento dental: estudo ex vivo / Dyes with and without sugar versus effectiveness of dental bleaching: an ex vivo study

As descolorações dos dentes e restaurações podem estar relacionadascom o tipo de corante presente nos alimentos, o pH e a presença de açúcar. Objetivo: Avaliar ex vivo a influência de bebidas contendo corantes, com e sem a adição de açúcar, na efetividade do clareamento dental caseiro em dentes humanos expostos a bebidas contendo corantes com e sem adição de açúcar durante o tratamento clareador. Material e método: Setenta pré-molares humanos foram divididos em 7 grupos (n=10) de acordo com a solução corante: água destilada (A), café (C), café com açúcar (CA), chá preto (CH), chá preto com açúcar (CHA), suco de uva(U) e suco de uva com açúcar (UA). O clareamento dental caseiro foi realizado com peróxido de carbamida (PC) 16% (Whiteness Perfect 16%, FGM) por 3 horas diárias durante 3 semanas, para todos os grupos. A cor foi mensurada com Espectrofotômetro Vita Easyshade, nos períodos: inicial, ao término do clareamento (3ª semana) e pós-clareamento (1 semana). Para a avaliação de cor, os dados foram submetidos à análise não paramétrica de Kruskal-Wallis (?=0,05). Resultados: Não houve diferença estatisticamente significante entre os grupos analisados (p<0,001). Conclusões: O clareamento dental caseiro foi efetivo mesmo napresença dos corantes alimentares durante o tratamento clareador, independentemente da presença do açúcar.

The discoloration of teeth and esthetic restorations may be related to the type of colorant present in food, pH and the presence of sugar. Objective: Evaluate ex vivo the effectiveness of dental bleaching exposed in a dye-containing beverages with and without addition of sugar during the bleaching treatment. Material e Methods: Seventy human premolars were divided into 7 groups (n = 10) according to the dye solution: distilled water (W), coffee (C), coffee with sugar (CS), black tea (T), black tea with sugar(TS), grape juice (G) and grape juice with sugar (GS). The home bleaching was performed with carbamide peroxide (PC) 16% (Whiteness Perfect, FGM) for 3 hours daily during 3 weeks for all groups. The color was measured with spectrophotometer Vita Easyshade in the periods: baseline, at the end of bleaching (3rd week) and post-bleaching (1 week after). Evaluation of color, data were analyzed by nonparametric Kruskal-Wallis test (? = 0.05). Results: There was no statistically significant difference between the groups (p <0.001). Conclusion: It was concluded that the bleaching was effective even in the presence of food colors during the at home dental bleaching, regardless of the presence of sugar.