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1.
Rev. Ciênc. Plur ; 9(3): 32620, 26 dez. 2023. tab, ilus, graf
Artigo em Português | LILACS, BBO | ID: biblio-1524464

RESUMO

Introdução:Sabe-se que a busca pela estética é algo cada vez mais crescente. Dentre os procedimentos mais procurados na odontologia estética, destaca-se o clareamento dental de consultório. Diante disso, ainda são poucos os estudos que avaliam os efeitos dos agentes clareadores de diferentes pHs na efetividade clareadora e na sensibilidade dentária.Objetivo:Avaliar a sensibilidade dentária e a eficácia clareadora de géis clareadores à base de peróxido de hidrogênio a 35% com diferentes pHs.Metodologia:Trata-se de um relato de três casos, descritivo e observacional, do tipo boca dividida (split-mouth) para cada estratégia clareadora (gel clareador com pH básico e gel clareador com pH ácido). Foram avaliados três pacientes de25, 26e 27anos de idade.Realizou-se registro de cor por meio da escala VITAClassical e avaliação da sensibilidade dentária pela escala visual analógica. Resultados:Todos os pacientes avaliados apresentaram cor A3 no registro de cor inicial e, após o clareamento dental,atingiram a cor A1. Todos relataram uma maior sensibilidade no hemiarco direito (local onde foi aplicada o gel clareador Whiteness HP que possui pH ácido. Dois pacientes relataram sensibilidade dentária no hemiarco esquerdo em que foi aplicado o gel clareador de pH básico. Conclusões:Observa-se a eficácia clínica dos géis clareadores de consultório à base de peróxido de hidrogênio a 35% na estabilidade de cor após o tratamento clareador, independente do seu pH. Ademais, nota-se que o gel clareador de pH básico promoveu menor sensibilidade pós-operatória (AU).


Introduction:It is known that the search for aesthetics is something increasingly growing. Among the most sought-after procedures in cosmetic dentistry, in-office tooth bleaching stands out. Therefore, there are still few studies that evaluate the effects of bleaching agents ofdifferent pHs on bleaching effectiveness and tooth sensitivity.Objective:To evaluate tooth sensitivity and bleaching efficacy of 35% hydrogen peroxide-based tooth bleaching gels with different pHs.Methodology:This is a report of three cases, descriptive and observational, of the split-mouth type for each bleaching strategy (bleaching gel with basic pH and bleaching gel with acidic pH). Three patients aged 25, 26 and 27 years were evaluated. Color registration was performed using the VITA Classical scale and tooth sensitivity was evaluated using the visual analogue scale.Results:All evaluated patients presented color A3 in the initial color registration and, after tooth bleaching, reached color A1. All reported greater sensitivity in the right hemi-arch (place where the Whiteness HP bleaching gel with an acid pH was applied. Two patients reported tooth sensitivity in the left hemi-arch where the basic pH bleaching gel was applied.Conclusions:The clinical efficacy of in-office tooth bleaching gels based on 35% hydrogen peroxide in terms of color stability after bleaching treatment is observed, regardless of its pH. In addition, it is noted that the basic pH bleaching gel promoted less postoperative sensitivity (AU).


Introducción: Se sabe que la búsqueda de la estética es algo cada vez más creciente. Entre los procedimientos más populares en odontología estética, se destaca el blanqueamiento dental en consultorio. Ante esto, aún existen pocos estudios que evalúen los efectos de agentes blanqueadores de diferentes pHs sobre la efectividad del blanqueamiento y la sensibilidad dental.Objetivo: Evaluar la sensibilidad dental y la eficacia blanqueadora de geles blanqueadores a base de peróxido de hidrógeno al 35 % con diferentes pH. Metodología: Este es un reporte de tres casos, descriptivo y observacional, del tipo boca partida para cada estrategia de blanqueamiento (gel blanqueador con pH básico y gel blanqueador con pH ácido). Se evaluaron tres pacientes de 25, 26 y 27 años. El registro de color se realizó con la escala clásica VITA y la sensibilidad dental se evaluó con la escala analógica visual.Resultados: Todos los pacientes evaluados presentaron color A3 en el registro de color inicial y, después del blanqueamiento dental, alcanzaron el color A1. Todos refirieron mayor sensibilidad en la hemiarcada derecha (lugar donde se aplicó el gel blanqueador de pH ácido Whiteness HP). Dos pacientes refirieron sensibilidad dental en la hemiarcadaizquierda donde se aplicó el gel blanqueador de pH básico.Conclusiones: Se observala eficacia clínica de los geles blanqueadores de consultorio a base de peróxido de hidrógeno al 35% en cuanto a la estabilidad del color tras el tratamiento blanqueador, independientemente de su pH. Además, se observa que el gel blanqueador de pH básico promovió una menor sensibilidad postoperatoria (AU).


Assuntos
Humanos , Adulto , Cor , Sensibilidade da Dentina/complicações , Clareadores Dentários/efeitos adversos , Peróxido de Hidrogênio , Resultado do Tratamento , Estudo Observacional , Concentração de Íons de Hidrogênio
2.
Braz. dent. j ; Braz. dent. j;32(3): 105-115, May-June 2021. tab, graf
Artigo em Inglês | LILACS, BBO | ID: biblio-1345503

RESUMO

Abstract This clinical trial evaluated the effect of the coadministration of ibuprofen/caffeine on bleaching-induced tooth sensitivity (TS). A triple-blind, parallel-design, randomized clinical trial was conducted on 84 patients who received ibuprofen/caffeine or placebo capsules. The drugs were administered for 48 hours, starting 1 hour before the in-office bleaching. Two bleaching sessions were performed with 35% hydrogen peroxide gel with 1-week interval. TS was recorded up to 48 hours after dental bleaching with a 0-10 visual analogic scale (VAS) and a 5-point numeric rating scale (NRS). The color was evaluated with VITA Classical and VITA Bleachedguide scales (ΔSGU) and VITA Easyshade spectrophotometer (ΔE*ab and ΔE00). The absolute risk of TS in both groups was evaluated using Fischer's exact test. Comparisons of the TS intensity (NRS and VAS data) were performed by using the Mann-Whitney test and a two-way repeated measures ANOVA, respectively. The color alteration between the groups was compared with the Student's t test. The significance level was 5%. There was no statistically significant difference between the groups for the absolute risk of TS (p = 1.00) or for the intensity of TS (p > 0.05). A bleaching of approximately 7 shade guide units was observed on the Vita Classical and Vita Bleachedguide scales, with no statistical difference between the groups. It was concluded that coadministration of ibuprofen and caffeine did not reduce the absolute risk or intensity of TS and did not interfere with the efficacy of dental bleaching.


Resumo Este ensaio clínico avaliou o efeito da coadministração de ibuprofeno/cafeína na sensibilidade dental decorrente de clareamento (SD). Um estudo clínico randomizado, paralelo, triplo-cego, foi realizado em 84 pacientes que receberam cápsulas de ibuprofeno/cafeína ou placebo. Os fármacos foram administrados por 48 horas, começando 1 hora antes do clareamento em consultório. Duas sessões de clareamento foram realizadas com gel de peróxido de hidrogênio 35% com intervalo de 1 semana. A SD foi registrada até 48 horas após o clareamento dental com uma escala visual analógica (VAS) de 0-10 e uma escala de classificação numérica (NRS) de 5 pontos. A cor foi avaliada com as escalas Vita Classical e Vita Bleachedguide (ΔSGU) e com o espectrômetro Vita Easyshade (ΔE*ab e ΔE00). O risco absoluto de SD em ambos os grupos foi avaliado por meio do teste exato de Fischer. As comparações da intensidade da SD (NRS e VAS) foram realizadas utilizando-se o teste Mann-Whitney e uma ANOVA de dois fatores com medidas repetidas, respectivamente. A alteração de cor entre os grupos foi comparada com a o teste t de Student. O nível de significância foi de 5%. Não houve diferença estatisticamente significante entre os grupos para o risco absoluto de SD (p = 1,00) ou para a intensidade de SD (p > 0,05). Observou-se clareamento de aproximadamente 7 unidades nas escalas Vita Classical e Vita Bleachedguide, sem diferença estatística entre os grupos. Concluiu-se que a coadministração de ibuprofeno e cafeína não reduziu o risco absoluto ou intensidade da SD e não interferiu na eficácia do clareamento dental.


Assuntos
Humanos , Clareamento Dental , Cafeína/uso terapêutico , Ibuprofeno/uso terapêutico , Sensibilidade da Dentina/induzido quimicamente , Clareadores Dentários/efeitos adversos , Resultado do Tratamento , Peróxido de Hidrogênio
3.
J. appl. oral sci ; J. appl. oral sci;28: e20190163, 2020. tab, graf
Artigo em Inglês | LILACS, BBO | ID: biblio-1090782

RESUMO

Abstract Objective This in vitro study evaluated the effect of commercial whitening dentifrices on erosive tooth wear (ETW) of bovine enamel samples, in comparison with commercial regular dentifrices. Methodology Sixty bovine crowns were embedded in acrylic resin, polished and then had their baseline profile determined. They were randomly assigned to 5 groups (n=12/group), according to the type of commercial dentifrice to be tested: GI - Crest Anti-cavity Regular; GII - Crest 3D White; GIII - Colgate Total 12 Clean Mint; GIV - Colgate Optic White; GV - Placebo (negative control, fluoride-free dentifrice). The samples were submitted to daily erosive and abrasive challenges for 3 days. The erosive challenges were performed 3 times a day by immersing the specimens in 0.1% citric acid solution (pH 2.5) for 90 s. Each day after the first and last erosive challenges, the specimens were subjected to the abrasive challenge for 15 s, using a toothbrushing machine (Biopdi, São Carlos, SP, Brazil), soft toothbrushes and slurry (1:3 g/ml) of the tested toothpastes (1.5 N). The specimens were kept in artificial saliva between the challenges. The final profile was obtained and the ETW (µm) was calculated. Data were analyzed by Kruskal-Wallis and Dunn's tests (p<0.05). Results All dentifrices tested significantly reduced the enamel wear in comparison with the Placebo, except GIII. The median (95% CI) ETW was 1.35 (1.25-1.46)bc for GI, 1.17 (1.01-1.34)cd for GII, 1.36 (1.28-1.45)ab for GIII, 1.08 (1.04-1.14)d for GIV and 2.28 (2.18-2.39)a for GV. Conclusion When dentifrices from the same manufacturer were compared, the whitening dentifrices led to similar or less wear than the regular ones.


Assuntos
Animais , Bovinos , Erosão Dentária/induzido quimicamente , Cremes Dentais/efeitos adversos , Esmalte Dentário/efeitos dos fármacos , Clareadores Dentários/efeitos adversos , Propriedades de Superfície , Fatores de Tempo , Escovação Dentária/efeitos adversos , Cremes Dentais/química , Teste de Materiais , Estatísticas não Paramétricas , Esmalte Dentário/química , Clareadores Dentários/química
4.
J. appl. oral sci ; J. appl. oral sci;28: e20190384, 2020. tab, graf
Artigo em Inglês | LILACS, BBO | ID: biblio-1134801

RESUMO

Abstract Objectives This study evaluated if the use of a bioactive glass-ceramic-based gel, named Biosilicate (BS), before, after or mixed with bleaching gel, could influence the inflammation of the dental pulp tissue of rats' molars undergoing dental bleaching with hydrogen peroxide (H2O2). Methodology The upper molars of Wistar rats (Rattus norvegicus, albinus) were divided into Ble: bleached (35% H2O2, 30-min); Ble-BS: bleached and followed by BS-based gel application (20 min); BS-Ble: BS-based gel application and then bleaching; BS/7d-Ble: BS-based gel applications for 7 days and then bleaching; Ble+BS: blend of H2O2 with BS-based gel (1:1, 30-min); and control: placebo gel. After 2 and 30 days (n=10), the rats were euthanized for histological evaluation. The Kruskal-Wallis and Dunn statistical tests were performed (P<0.05). Results At 2 days, the Ble and Ble-BS groups had significant alterations in the pulp tissue, with an area of necrosis. The groups with the application of BS-based gel before H2O2 had moderate inflammation and partial disorganization in the occlusal third of the coronary pulp and were significantly different from the Ble in the middle and cervical thirds (P<0.05). The most favorable results were observed in the Ble+BS, which was similar to the control in all thirds of the coronary pulp (P>0.05). At 30 days, the pulp tissue was organized and the bleached groups presented tertiary dentin deposition. The Ble group had the highest deposition of tertiary dentin, followed by the Ble-BS, and both were different from control (P<0.05). Conclusion A single BS-based gel application beforehand or BS-based gel blended with a bleaching gel minimize the pulp damage induced by dental bleaching.


Assuntos
Animais , Masculino , Pulpite/prevenção & controle , Clareamento Dental/métodos , Polpa Dentária/efeitos dos fármacos , Clareadores Dentários/química , Vidro/química , Peróxido de Hidrogênio/química , Pulpite/induzido quimicamente , Pulpite/patologia , Fatores de Tempo , Clareamento Dental/efeitos adversos , Distribuição Aleatória , Reprodutibilidade dos Testes , Resultado do Tratamento , Ratos Wistar , Polpa Dentária/patologia , Clareadores Dentários/efeitos adversos , Peróxido de Hidrogênio/efeitos adversos , Dente Molar
5.
J. appl. oral sci ; J. appl. oral sci;27: e20180442, 2019. tab, graf
Artigo em Inglês | LILACS, BBO | ID: biblio-1002405

RESUMO

Abstract Objective To assess pulp oxygen saturation levels (SaO2) in maxillary central incisors after dental bleaching. Materials and Methods 80 participants (160 teeth) were randomly allocated to four groups: G1 In-office bleaching with two applications of 35% hydrogen peroxide (HP) (20 minutes), followed by at-home bleaching with 10% carbamide peroxide (CP) (2 hours/day for 16 days); G2 - Same protocol as G1, plus desensitizing toothpaste; G3 - In-office bleaching with 35% HP and one application of placebo gel (20 minutes), followed by at-home bleaching with 10% CP (2 hours/day for 16 days); and G4 - Same protocol as G3, plus desensitizing toothpaste. Pulp SaO2 levels were measured before (T0) and immediately after (T1) in-office bleaching; on the 5th (T2), 8th (T3), 12th (T4), and 16th days of at-home bleaching (T5); and on the 7th (T6) and 30th (T7) days. Mean (SD) pulp SaO2 levels were compared within groups by generalized estimating equations (GEE) and Student's t-test (P<0.05). Results Mean pulp SaO2 at T0 was 84.29% in G1, 84.38% in G2, 84.79% in G3, and 85.83% in G4. At T1, these values decreased to 81.96%, 82.06%, 82.19%, and 81.15% in G1, G2, G3, and G4 respectively, with significant difference in G4 (P<0.05). During home bleaching, pulp SaO2 levels varied in all groups, with 86.55%, 86.60%, 85.71%, and 87.15% means at T7 for G1, G2, G3, and G4, respectively; G2 presented significant difference (P<0.05). Conclusions Pulp SaO2 level in maxillary central incisors was similar at baseline, reducing immediately after in-office bleaching, regardless of using desensitizing toothpaste and increasing at 30 days after dental bleaching.


Assuntos
Humanos , Masculino , Feminino , Adolescente , Adulto , Adulto Jovem , Oxigênio/metabolismo , Clareamento Dental/efeitos adversos , Polpa Dentária/metabolismo , Clareadores Dentários/efeitos adversos , Incisivo/metabolismo , Valores de Referência , Fatores de Tempo , Clareamento Dental/métodos , Cremes Dentais/uso terapêutico , Oximetria/métodos , Resultado do Tratamento , Polpa Dentária/efeitos dos fármacos , Sensibilidade da Dentina/induzido quimicamente , Sensibilidade da Dentina/prevenção & controle , Dessensibilizantes Dentinários/uso terapêutico , Peróxido de Carbamida/efeitos adversos , Peróxido de Hidrogênio/efeitos adversos , Incisivo/efeitos dos fármacos
6.
J. appl. oral sci ; J. appl. oral sci;26: e20170573, 2018. tab, graf
Artigo em Inglês | LILACS, BBO | ID: biblio-954500

RESUMO

Abstract Objectives A single-blinded, randomized, parallel clinical trial evaluated the use of 37% carbamide peroxide (CP) on bleaching effectiveness and tooth sensitivity reported by patients undergoing in-office tooth bleaching, in comparison with the results of using 35% hydrogen peroxide. Material and Methods Forty patients were allocated to receive two sessions of in-office tooth bleaching using either 35% hydrogen peroxide (HP) or 37% CP. Each patient's sensitivity level was evaluated during and up to 24 h after bleaching. The effectiveness of the bleaching procedures was evaluated with a spectrophotometer one week after each session and 30 days after the last session. The impact of tooth bleaching on the patients' perceptions regarding smile changes, in addition to the bleaching procedures and their results, were also recorded. Absolute and relative sensitivity risks were calculated. Data on sensitivity level were analyzed using the Mann-Whitney or T-test, and data from the color evaluation were subjected to 2-way repeated measures ANOVA. Results The use of CP reduced the risk and level of tooth sensitivity to values close to zero, whereas the difference between the bleaching agents disappeared after 24 h. An increased bleaching effect was observed for HP, mainly due to an improved reduction of redness and yellowness. Participants perceived improved tooth bleaching for HP and reduced sensitivity for CP, but no differences regarding the comfort of the techniques were noted. Conclusions In our study, 37% CP resulted in reduced tooth sensitivity but decreased the tooth bleaching effectiveness. However, both bleaching agents resulted in high levels of patient satisfaction.


Assuntos
Humanos , Masculino , Feminino , Adulto , Adulto Jovem , Peróxidos/administração & dosagem , Clareamento Dental/métodos , Ureia/análogos & derivados , Dentina/efeitos dos fármacos , Sensibilidade da Dentina/prevenção & controle , Clareadores Dentários/administração & dosagem , Peróxido de Hidrogênio/administração & dosagem , Peróxidos/efeitos adversos , Fatores de Tempo , Clareamento Dental/efeitos adversos , Ureia/administração & dosagem , Ureia/efeitos adversos , Método Simples-Cego , Reprodutibilidade dos Testes , Fatores de Risco , Análise de Variância , Resultado do Tratamento , Estatísticas não Paramétricas , Medição de Risco , Sensibilidade da Dentina/induzido quimicamente , Clareadores Dentários/efeitos adversos , Escala Visual Analógica , Peróxido de Carbamida , Peróxido de Hidrogênio/efeitos adversos
7.
J. appl. oral sci ; J. appl. oral sci;26: e20170589, 2018. tab, graf
Artigo em Inglês | LILACS, BBO | ID: biblio-954496

RESUMO

Abstract High concentrations of hydrogen peroxide can cause adverse effects on composition and structure of teeth. However, the addition of calcium and fluoride in bleaching agents may reduce enamel demineralization. Objective: To evaluate chemical changes of sound and demineralized enamels submitted to high concentrations of hydrogen peroxide containing fluoride (F) or calcium (Ca). Material and Methods: Enamel blocks of bovine incisors with standard dimensions were obtained and half of them were submitted to pH-cycling to promote initial enamel caries lesions. Sound and demineralized enamel samples were divided into (n=10): (C) Control (no whitening treatment); (HP) 35% hydrogen peroxide; and two experimental groups: (HPF) 35% HP+0.2% F and (HPC) 35% HP+0.2% Ca. Experimental groups were submitted to two in-office bleaching sessions and agents were applied 3 times for 15 min to each session. The control group was kept in remineralizing solution at 37°C during the bleaching treatment. The surface mineral content of sound and demineralized enamels was determined through Fourier Transform Raman spectroscopy (FT-Raman), Energy dispersive Micro X-ray fluorescence spectroscopy (μ-EDXRF); and the subsurface, through cross-sectional microhardness (CSMH). In addition, polarized light microscopy (PLM) images of enamel subsurface were observed. Results: According to three-way (FT-Raman and μ-EDXRF analyses) or two-way analysis of variance (ANOVA) (CSMH) and Tukey test (α=5%), the calcium or fluoride added to high-concentrated bleaching agents increased phosphate and carbonate concentrations on sound and demineralized enamels (p<0.05). However, HPC and HPF were unable to completely reverse the subsurface mineral loss promoted by bleaching on sound and demineralized enamels. The calcium/ phosphate (Ca/P) ratio of sound enamel decreased after HP treatment (p<0.001). Conclusion: Even though experimental bleaching agents with Ca or F reduced mineral loss for both sound and demineralized enamel surfaces, these agents were unable to reverse the enamel subsurface demineralization.


Assuntos
Animais , Bovinos , Cálcio/química , Desmineralização do Dente/induzido quimicamente , Esmalte Dentário/efeitos dos fármacos , Clareadores Dentários/química , Fluoretos/química , Peróxido de Hidrogênio/química , Fosfatos/química , Valores de Referência , Espectrometria por Raios X , Análise Espectral Raman , Propriedades de Superfície/efeitos dos fármacos , Fatores de Tempo , Clareamento Dental/efeitos adversos , Clareamento Dental/métodos , Teste de Materiais , Carbonatos/química , Reprodutibilidade dos Testes , Esmalte Dentário/química , Clareadores Dentários/efeitos adversos , Testes de Dureza , Microscopia de Polarização
8.
J. appl. oral sci ; J. appl. oral sci;26: e20170043, 2018. tab, graf
Artigo em Inglês | LILACS, BBO | ID: biblio-893713

RESUMO

Abstract Objective This study verified the occurrence of dental sensitivity in patients submitted to a 35% hydrogen peroxide based product (Whiteness HP Maxx 35% - FGM), skin cold sensation threshold (SCST) and its influence on dental sensitivity. Material and Methods Sixty volunteers were divided into 4 groups (n = 15), according to SCST (low: GI and GIII, and high: GII and IV) and bleaching treatment (hydrogen peroxide: GI and GII, and placebo: GIII and GIV). SCST was determined in the inner forearm for 6 different times using a neurosensory analyzer, the TSA II (Medoc Advanced Medical Systems, Ramat Yishai, Northern District, Israel). Dental sensitivity measurements were performed 10 different times using a thermal stimulus and an intraoral device attached to TSA II, positioned in the buccal surface of the upper right central incisor. Spontaneous dental sensitivity was also determined using the Visual Analogue Scale (VAS). Data were submitted to Student's t-test and Pearson's Correlation Test (α=0.05). SCST remained the same during bleaching treatment. Results Distinct responses of dental sensitivity were found in patients with low and high SCST during the first and third bleaching session (p≤0.05). The teeth submitted to the bleaching treatment became more sensitive to cold than those treated with placebo. Moreover, data obtained with TSA and VAS presented moderate correlation. Conclusions Bleaching treatment increased dental sensitivity and skin cold sensation threshold might represent a determining factor in this occurrence, since low and high SCST patients had different responses to the thermal stimulus in the teeth.


Assuntos
Humanos , Masculino , Adolescente , Adulto , Adulto Jovem , Temperatura Cutânea/efeitos dos fármacos , Clareamento Dental/efeitos adversos , Sensibilidade da Dentina/induzido quimicamente , Clareadores Dentários/efeitos adversos , Peróxido de Hidrogênio/efeitos adversos , Valores de Referência , Limiar Sensorial , Fatores de Tempo , Medição da Dor , Efeito Placebo , Resultado do Tratamento , Temperatura Baixa
9.
J. appl. oral sci ; J. appl. oral sci;26: e20160473, 2018. tab, graf
Artigo em Inglês | LILACS, BBO | ID: biblio-893702

RESUMO

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.


Assuntos
Humanos , Masculino , Feminino , Adolescente , Adulto , Adulto Jovem , Clareamento Dental/efeitos adversos , Etodolac/uso terapêutico , Sensibilidade da Dentina/induzido quimicamente , Sensibilidade da Dentina/prevenção & controle , Dessensibilizantes Dentinários/uso terapêutico , Clareadores Dentários/efeitos adversos , Peróxido de Hidrogênio/efeitos adversos , Fatores de Tempo , Índice de Gravidade de Doença , Medição da Dor , Reprodutibilidade dos Testes , Resultado do Tratamento , Cor , Estatísticas não Paramétricas , Medição de Risco , Inibidores de Ciclo-Oxigenase 2/uso terapêutico
10.
J. appl. oral sci ; J. appl. oral sci;26: e20170284, 2018. tab, graf
Artigo em Inglês | LILACS, BBO | ID: biblio-893698

RESUMO

Abstract Objective The objective of this study was to evaluate dental sensitivity using visual analogue scale, a Computerized Visual Analogue Scale (CoVAS) and a neurosensory analyzer (TSA II) during at-home bleaching with 10% carbamide peroxide, with and without potassium oxalate. Materials and Methods Power Bleaching 10% containing potassium oxalate was used on one maxillary hemi-arch of the 25 volunteers, and Opalescence 10% was used on the opposite hemi-arch. Bleaching agents were used daily for 3 weeks. Analysis was performed before treatment, 24 hours later, 7, 14, and 21 days after the start of the treatment, and 7 days after its conclusion. The spontaneous tooth sensitivity was evaluated using the visual analogue scale and the sensitivity caused by a continuous 0°C stimulus was analyzed using CoVAS. The cold sensation threshold was also analyzed using the TSA II. The temperatures obtained were statistically analyzed using ANOVA and Tukey's test (α=5%). Results The data obtained with the other methods were also analyzed. 24 hours, 7 and 14 days before the beginning of the treatment, over 20% of the teeth presented spontaneous sensitivity, the normal condition was restored after the end of the treatment. Regarding the cold sensation temperatures, both products sensitized the teeth (p<0.05) and no differences were detected between the products in each period (p>0.05). In addition, when they were compared using CoVAS, Power Bleaching caused the highest levels of sensitivity in all study periods, with the exception of the 14th day of treatment. Conclusion We concluded that the bleaching treatment sensitized the teeth and the product with potassium oxalate was not able to modulate tooth sensitivity.


Assuntos
Humanos , Masculino , Feminino , Adolescente , Adulto , Adulto Jovem , Peróxidos/efeitos adversos , Clareamento Dental/efeitos adversos , Ureia/análogos & derivados , Medição da Dor/métodos , Sensibilidade da Dentina/diagnóstico , Sensibilidade da Dentina/induzido quimicamente , Clareadores Dentários/efeitos adversos , Ácido Orótico/uso terapêutico , Peróxidos/química , Fatores de Tempo , Ureia/efeitos adversos , Ureia/química , Índice de Gravidade de Doença , Análise de Variância , Resultado do Tratamento , Limiar da Dor , Escala Visual Analógica , Peróxido de Carbamida
11.
J. appl. oral sci ; J. appl. oral sci;25(3): 335-340, May-June 2017. tab, graf
Artigo em Inglês | LILACS, BBO | ID: biblio-893618

RESUMO

Abstract Objective This randomized, controlled, double-blind clinical study evaluated the effect of calcium sodium phosphosilicate (NovaMin) and casein phosphopeptide-amorphous calcium phosphate with fluoride (CPP-ACPF) on the prevention of post-operative sensitivity and on the effects of clinical bleaching treatment. Material and Methods Sixty volunteers were selected according to inclusion and exclusion criteria and were randomly assigned into three groups (n=20): CG (control group) patients, who were treated with 35% hydrogen peroxide; NOVAG (NovaMin group) patients, who were treated with 35% hydrogen peroxide followed by the application of NovaMin; and CPPG (CPP group) patients, who were treated with 35% hydrogen peroxide followed by the application of CPP-ACPF. Both bioactive agents were applied for five minutes. An evaporative stimulus associated with a modified visual scale was used to analyze sensitivity 24 hours after each bleaching session. The color evaluation was performed on the maxillary central incisors using a spectrophotometer. Associations between the intervention group, bleaching session, and reported sensitivity were tested using Chi-square partitioning. Results Color change values (ΔE) were analyzed using analysis of variance (ANOVA). The significance level used for both tests was 5%. In the intragroup assessment, the Friedman test showed that only the CPP-ACPF group showed no statistically significant difference (p<0.05) between baseline and first bleaching session. In the intergroup assessment, the Kruskal-Wallis test showed that the CPPG had less postoperative sensitivity after the first session, when compared to the other groups (p<0.05). Color change analysis (ΔE) showed a significant difference between the means obtained in the different bleaching sessions in all groups (p<0.05). Conclusions This study showed that the combination of CPP-ACPF with 35% hydrogen peroxide significantly reduced post-operative sensitivity in the first session, compared with the other evaluated treatments. The association of CPP-ACPF and NovaMin did not affect the color change induced by tooth bleaching.


Assuntos
Humanos , Masculino , Feminino , Adolescente , Adulto , Adulto Jovem , Clareamento Dental/efeitos adversos , Caseínas/uso terapêutico , Sensibilidade da Dentina/prevenção & controle , Dessensibilizantes Dentinários/uso terapêutico , Fluoretos/uso terapêutico , Vidro/química , Período Pós-Operatório , Espectrofotometria , Fatores de Tempo , Método Duplo-Cego , Reprodutibilidade dos Testes , Análise de Variância , Resultado do Tratamento , Cor , Esmalte Dentário/efeitos dos fármacos , Quimioterapia Combinada , Clareadores Dentários/efeitos adversos , Peróxido de Hidrogênio/efeitos adversos
12.
Rio de janeiro; s.n; 2017. 124 p. ilus.
Tese em Português | BBO, LILACS | ID: biblio-1015198

RESUMO

As técnicas clareadoras são consideradas seguras, simples e não invasivas. Assim, ganharam popularidade entre profissionais e pacientes. No entanto, o livre acesso do gel à estrutura dentária e o contato direto com a superfície do esmalte levantam dúvidas sobre seus reais impactos. Novas preocupações surgiram com os chamados produtos de bancada e a possibilidade de auto-aplicação, inclusive com consumo exagerado e/ou sem orientação e acompanhamento. Sendo assim, buscou-se avaliar, os efeitos de produtos clareadores caseiros sobre microestrutura, rugosidade, composição, nanodureza e módulo de elasticidade do esmalte dentário humano, em protocolos de uso normal ou excessivo. Amostras obtidas de 10 terceiros molares foram divididas em 4 grupos: grupo I ­ armazenamento em saliva artificial, grupo II ­ utilização de peróxido de carbamida (PC) 10%, grupo III ­ utilização de peróxido de hidrogênio (H2O2) 10%, grupo IV ­ utilização de tiras clareadoras (H2O2 10%). Cada dente forneceu quatro fragmentos de esmalte para cada um dos grupos. Foram realizadas aplicações diárias de acordo com a recomendação dos fabricantes, e foi adotada simulação de escovação duas vezes ao dia com escova elétrica. Todas as amostras foram armazenadas em saliva artificial e passaram por análises antes do início da terapia, após 4 e 8 semanas de intervenção. A escolha por técnicas não-destrutivas permitiu que cada amostra fosse seu próprio controle. Desse modo, a microscopia confocal por varredura a laser e microscopia de força atômica avaliaram alterações na microestrutura da superfície e foram coletados dados de rugosidade (Sa e Sq) para análise estatística. Os espécimes passaram por testes de nanoindentação para avaliação de nanodureza e módulo de elasticidade. Essas informações foram correlacionadas com as alterações de composição por microespectroscopia Raman. O clareamento com PC não apresentou alterações significativas nas amostras de esmalte, seguindo o padrão de comportamento daquelas escovadas e armazenadas em saliva artificial, tendo se mostrado segura. No entanto, os grupos que passaram por intervenção com H2O2 (III e IV) apresentaram modificações significativas em suas propriedades após 4 e 8 semanas de utilização. A alteração na superfície com aparência mais exposta foi associada a maior detecção de proteínas após as primeiras 4 semanas de utilização, especialmente para o grupo III. Após 8 semanas, a superfície apareceu mais suave, com perda do padrão prismático e queda no conteúdo orgânico, sugerindo uma perda de camadas superficiais desorganizadas. Do mesmo modo, o aumento dos valores de dureza e módulo de elasticidade para essas amostras pareceu derivar do efeito remineralizador da saliva e do papel positivo das proteínas mais expostas nas propriedades mecânicas permitindo maior deslizamento dos cristais e acomodação frente às cargas. Conclui-se que o uso de géis a base de H2O2 deve ser cauteloso, seguindo as recomendações profissionais e que são necessários testes in situ e in vivo para confirmar as tendências observadas.


The bleaching techniques are considered safe, simple and non-invasive and thus have gained popularity among professionals and patients. However, the free access of the gel to dental structures and the direct contact with the surface of the enamel, during the whole treatment raises doubts, about its possible impacts. Concerns were also raised about the emergence of so-called over-the-counter products and the possibility of self-application that could lead to excessive consumption and / or lack of guidance and monitoring. The aim of this study was to evaluate the effects of home bleaching products on the microstructure, roughness, composition, nanohardness and elastic modulus of human dental enamel in protocols of normal or excessive use. Samples were obtained from 10 third molars and divided into 4 groups: group I - storage in artificial saliva, group II - treatment with 10% carbamide peroxide, group III - treatment with 10% hydrogen peroxide, group IV - treatment with whitening strips (10% hydrogen peroxide). Each tooth provided four enamel fragments for treatment in each one of the groups. Daily applications were performed according to the manufacturers' recommendations, and a brushing simulation was used twice a day with an electric brush. All samples were stored in artificial saliva at the treatment intervals and were analyzed before the start of therapy, after 4 and 8 weeks of intervention. The choice by non-destructive techniques allowed each sample to be its own control. Qualitative analyzes of microstructure alteration were carried out using confocal laser scanning microscopy and atomic force microscopy. Roughness data (Sa and Sq) were also obtained for statistical analysis. Nanoindentation tests were used to determine changes in the nanohardness and elastic modulus. All of this information was correlated with composition changes by Raman micro-spectroscopy. Carbamide peroxide bleaching showed no significant changes in enamel samples, following the behavior pattern of those brushed and stored in artificial saliva, and therefore considered safe. However, the groups treated with hydrogen peroxide (III and IV) showed significant modifications in their properties after 4 and 8 weeks of treatment. The change in surface with more exposed appearance was associated with greater protein detection after the first month of treatment, especially for group III. After 8 weeks, the surface appeared smoother, with reduction of prismatic pattern and drop in organic content, suggesting a loss of disorganized mineral surface layers. Likewise, the increase in hardness and elastic modulus values for these samples seems to derive from the remineralizing effect of saliva and the positive role of the most exposed proteins in the mechanical properties, allowing greater slip of the crystals and accommodation with the loads. These changes may not reach clinically perceptible patterns but reinforce the importance of dentists' supervision and monitoring, since in-vivo the patient may be exposed to other challenges that may worsen the impacts. It is concluded that the use of hydrogen peroxide gels in bleaching therapies should be under professional supervision and that in situ and in vivo tests are required to confirm the observed trends.


Assuntos
Humanos , Clareamento Dental/efeitos adversos , Esmalte Dentário/efeitos dos fármacos , Clareadores Dentários/efeitos adversos , Peróxido de Hidrogênio/efeitos adversos , Análise Espectral Raman , Propriedades de Superfície , Microscopia Confocal
13.
Braz. oral res. (Online) ; 30(1): e82, 2016. tab, graf
Artigo em Inglês | LILACS | ID: biblio-952033

RESUMO

Abstract The aim of this clinical study was to evaluate tooth color changes (ΔE) and tooth sensitivity (TS) associated with whitening dentifrices. Sixty participants were selected according to inclusion and exclusion criteria and then allocated to three groups (n = 20): Colgate Luminous White (G1), Close Up White Now (G2) and Sorriso dentifrice (G3-control). The participants were instructed to use only the provided dentifrice and toothbrush in standardized oral hygiene procedures for 4 weeks. ΔE was assessed by spectrophotometry (CIELab System) whereas TS was determined by a visual analog scale at baseline and weekly using four assessment points. The data were analyzed by two-way ANOVA and Tukey's post-hoc test and Friedman test (α = 0.05). ΔE (baseline-assessment point 4) showed no significant difference (p>0.05) across the groups: G1 (ΔE = 5.1), G2 (ΔE = 6.8), and G3 (ΔE = 4.4). Δb (baseline-assessment point 4) was significantly different (p < 0.05) in G2 (3.8) when compared to G1 (-0.2) and G3 (0.3). There was no significant difference (p > 0.05) in TS at baseline. Both the control and whitening dentifrices caused similar tooth color changes (ΔE). There was no significant TS during the study period.


Assuntos
Humanos , Masculino , Feminino , Adulto , Clareamento Dental/métodos , Dentifrícios/farmacologia , Sensibilidade da Dentina/induzido quimicamente , Clareadores Dentários/farmacologia , Espectrofotometria , Fatores de Tempo , Método Duplo-Cego , Análise de Variância , Resultado do Tratamento , Cor , Dentifrícios/efeitos adversos , Clareadores Dentários/efeitos adversos , Escala Visual Analógica
14.
Braz. j. oral sci ; 14(4): 262-266, Oct.-Dec. 2015. ilus, tab
Artigo em Inglês | LILACS | ID: lil-778241

RESUMO

To evaluate the effect of different in-office bleaching agents on the permeability, roughness and surface microhardness of human enamel. Methods: For evaluation of roughness and microhardness, 40 hemi-faces of 20 premolars were subjected to initial roughness (Ra parameter) and microhardness (VHN) measurements. Thirty-two premolar's crowns were used for permeability test. Then, all specimens were randomly divided into four groups: C - without bleaching (control), HP35 - bleaching with 35% hydrogen peroxide (HP), HPF38 - 38% HP+fluoride, HPC35 - 35% HP+calcium. Final roughness (FR) and microhardness (FM) measurements were evaluated. For permeability, the 32 crowns were immersed in 1% sodium hypochlorite (20 min) and silver nitrate solutions (2 h) and subjected to developing solution under fluorescent light (16 h). Three sections from the crowns were analyzed in light microscope (100x) to evaluate the scores of permeability: Score 0 - no tracer agent penetration; Score 1 - less than half the thickness of enamel penetration; Score 2 - tracer agent reaching half the enamel thickness; Score 3 - entire enamel depth penetration, without reaching dentin and Score 4 - tracer agent reaching dentin. For roughness and microhardness evaluation were used one-way ANOVA and Dunnet post-test for independent samples, and t test for paired samples. For permeability, the data were analyzed by Kruskal Wallis and Dunn tests. Results: A significantly higher permeability and surface roughness were observed in groups HP35, HPF38 and HPC35 compared to the C group, as well as decreased microhardness (p<0.05). Conclusions: All bleaching agents increased permeability and surface roughness, and decreased microhardness of human enamel; thus, the addition of fluoride or calcium was not beneficial...


Assuntos
Humanos , Masculino , Feminino , Clareadores Dentários/efeitos adversos , Esmalte Dentário , Permeabilidade do Esmalte Dentário , Peróxido de Hidrogênio/efeitos adversos , Peróxido de Hidrogênio/uso terapêutico , Propriedades de Superfície , Clareamento Dental
15.
Braz. dent. j ; Braz. dent. j;26(3): 242-248, May-Jun/2015. tab, graf
Artigo em Inglês | LILACS | ID: lil-751867

RESUMO

This study evaluated a whitening effect and the likely side effect (tooth sensitivity and pulp response) of human teeth subjected to different in-office bleaching (IOB) techniques and materials, mainly the presence of calcium in the IOB materials. A calcium-free (CF) and a calcium-containing (CC) 35% hydrogen peroxide (HP) gels were evaluated. The CF was refreshed every 15 minutes, three times (CF 3-15) or in a single 45-min application (CF 1-45) at one bleaching appointment. The CC was used only in a single 45-min application (CC 1-45). Each technique was applied in 5 mandibular incisors scheduled for extraction for different patients. In control group, no tooth bleaching was performed. The tooth colour (TC) and tooth sensitivity (TS) were recorded at baseline and after IOB. The teeth were extracted 2 days after the application of IOB and subjected to histological analysis. The data was submitted to appropriate statistical analysis (α=0.05). The changes of TC were similar between groups and statistically different from the control (p<0.05). However, TS of groups bleached with CF was statistically higher than that recorded for CC and the control (p<0.05). In CF 3-15 and CF 1-45 groups, the coronal pulp tissue exhibited partial necrosis associated with tertiary dentin deposition. In CC 1-45 group smaller area of necrosis occurred only in three bleached teeth in which tertiary dentin deposition was observed. The calcium-containing 35%HP gel could be preferable for in-office bleaching because it caused less tooth sensibility and pulp damage.


O objetivo do estudo foi avaliar o efeito clareador e seus efeitos adversos (sensibilidade e resposta pulpar) de dentes humanos submetidos a diferentes técnicas e materiais para o clareamento em consultório (CLCO), principalmente a presença de cálcio nos materiais para CLCO. Um agente clareador a base de peróxido de hidrogênio (PH) a 35% sem cálcio (SC) e com cálcio (CC) foram avaliados. O agente clareador SC foi usado em duas técnicas de aplicação: o gel clareador foi reaplicado a cada 15 minutos, três vezes (SC 3-15) ou 1 x 45-min por aplicação (SC 1-45) em uma sessão clínica. O agente clareador CC foi usado apenas em 1 x 45-min por aplicação (CC 1-45). Cada técnica foi aplicada em 5 incisivos inferiores indicados para extração de pacientes diferentes. No grupo controle, o clareamento não foi realizado. O efeito clareador (EC) e a sensibilidade dental (SD) foram registrados inicialmente e após o CLCO. Os dentes foram extraídos após 2 dias da aplicação do CLCO e foram submetidos ao análise histológica. Os dados foram submetidos a análise estatística apropriada (α=0.05). As mudanças foram semelhantes entre os grupos e significativamente diferentes do controle (p<0.05). Entretanto, a SD nos grupos clareados com SC foi estatisticamente maior do que a registrada nos grupos CC e do grupo controle (p<0.05). Nos grupos SC 3-15 e SC CF 1-45, o tecido pulpar da região coronária exibia necrose parcial associada a deposição de dentina terciária. No grupo CC 1-45, pequenas áreas de necrose ocorreram somente em 3 dentes clareados, nos quais deposição de dentina terciária também foi observada. O gel CC de HP a 35%HP gel poderia ser preferível para a realização de CLCO devido ao fato de causar menos danos ao tecido pulpar.


Assuntos
Humanos , Polpa Dentária , Clareamento Dental , Cor , Sensibilidade da Dentina , Clareadores Dentários/efeitos adversos , Clareamento Dental/efeitos adversos
16.
Braz. j. oral sci ; 14(2): 154-158, Apr.-June 2015. tab, ilus
Artigo em Inglês | LILACS | ID: lil-755043

RESUMO

Aim: To evaluate enamel microhardness and morphology after bleaching with hydrogen peroxide containing calcium in different concentrations. Methods: One hundred specimens of human teeth were ground and polished and had the initial microhardness evaluated. The specimens were randomly assigned into five groups (n=20): Group 1 - Control group (no treatment); Group 2 - Home Peroxide 6% (without calcium); Group 3 - Home Peroxide 7.5% (without calcium); Group 4 - White Class 6% (with calcium); Group 5 - White Class 7.5% (with calcium). For each group, the bleaching was performed according to the manufacturer's specifications. The specimens were bleached once a day for 5 days and subjected to pH cycling. Microhardness and scanning electron microscopy (SEM) analysis were performed before and after bleaching. Results: The results showed that groups submitted to bleaching treatment presented hardness loss compared to the control group. The group of 7.5% hydrogen peroxide with calcium showed a lower percentage of hardness loss in relation to other groups. Conclusion: Calcium in association with a higher hydrogen peroxide concentration may decrease microhardness changes on enamel.


Assuntos
Humanos , Masculino , Feminino , Cálcio/efeitos adversos , Clareadores Dentários/efeitos adversos , Esmalte Dentário/anatomia & histologia , Peróxido de Hidrogênio/efeitos adversos , Peróxido de Hidrogênio/uso terapêutico , Clareamento Dental , Oxidantes/uso terapêutico
17.
Braz. oral res. (Online) ; 29(1): 1-6, 2015. tab, ilus
Artigo em Inglês | LILACS | ID: lil-777173

RESUMO

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.


Assuntos
Humanos , Adulto , Adulto Jovem , Polpa Dentária/irrigação sanguínea , Sensibilidade da Dentina/induzido quimicamente , Peróxido de Hidrogênio/efeitos adversos , Fluxometria por Laser-Doppler/métodos , Clareadores Dentários/efeitos adversos , Clareamento Dental/efeitos adversos , Polpa Dentária/efeitos dos fármacos , Valores de Referência , Fluxo Sanguíneo Regional/efeitos dos fármacos , Fluxo Sanguíneo Regional/fisiologia , Fatores de Tempo , Clareamento Dental/métodos , Resultado do Tratamento
18.
Braz. oral res. (Online) ; 29(1): 1-7, 2015. tab, ilus
Artigo em Inglês | LILACS | ID: lil-777205

RESUMO

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.


Assuntos
Adulto , Feminino , Humanos , Masculino , Adulto Jovem , Fosfatos de Cálcio/administração & dosagem , Dessensibilizantes Dentinários/administração & dosagem , Sensibilidade da Dentina/induzido quimicamente , Peróxido de Hidrogênio/administração & dosagem , Nitratos/administração & dosagem , Compostos de Potássio/administração & dosagem , Clareadores Dentários/administração & dosagem , Clareamento Dental/efeitos adversos , Fosfatos de Cálcio/efeitos adversos , Método Duplo-Cego , Peróxido de Hidrogênio/efeitos adversos , Nitratos/efeitos adversos , Compostos de Potássio/efeitos adversos , Clareadores Dentários/efeitos adversos , Clareamento Dental/métodos , Descoloração de Dente/tratamento farmacológico
19.
Braz. oral res ; 27(6): 517-523, Nov-Dec/2013. tab, graf
Artigo em Inglês | LILACS | ID: lil-695984

RESUMO

The purpose of this study was to evaluate whether the use of desensitizing dentifrices used 15 days prior to and after in-office tooth bleaching could eliminate or reduce tooth sensitivity. After institutional review board approval and informed consent, 45 subjects were selected and divided into 3 groups according to the dentifrice selected: Colgate Total (CT), Colgate Sensitive Pro-Relief (CS) or Sensodyne ProNamel (SP). The subjects used toothpaste and a toothbrush provided to them for 15 days prior to bleaching. They were then submitted to two in-office bleaching sessions (Whiteness HP Blue Calcium). Their tooth sensitivity was assessed using the Visual Analog Scale (VAS) for a week after each session. Their tooth shade alteration was measured with a Vitapan Classical shade guide to determine if the dentifrices could influence the effectiveness of the bleaching agent. The data were submitted to Wilcoxon, Kruskal-Wallis and Mann-Whitney tests (α = 0.05). The use of desensitizing dentifrices did not affect the bleaching efficacy. In regard to tooth sensitivity, there was a statistically significant difference between the results of the Control Group and Group T2 after the first session (p = 0.048). There was no statistically significant difference in the results for the other groups after the first session. In regard to the second session, there was no statistically significant difference in the results for all the groups. The use of a desensitizing dentifrice containing nitrate potassium reduced tooth sensitivity during the bleaching regimen. Dentifrices containing arginine and calcium carbonate did not reduce tooth sensitivity. Color change was not influenced by the dentifrices used.


Assuntos
Adolescente , Adulto , Feminino , Humanos , Masculino , Adulto Jovem , Dentifrícios/uso terapêutico , Dessensibilizantes Dentinários/uso terapêutico , Sensibilidade da Dentina/tratamento farmacológico , Clareamento Dental/efeitos adversos , Odontalgia/tratamento farmacológico , Cor , Misturas Complexas/uso terapêutico , Combinação de Medicamentos , Dentifrícios/farmacologia , Fluoretos/uso terapêutico , Nitratos/uso terapêutico , Pré-Medicação , Fosfatos/uso terapêutico , Compostos de Potássio/uso terapêutico , Distribuição Aleatória , Estatísticas não Paramétricas , Ácido Silícico/efeitos adversos , Fatores de Tempo , Resultado do Tratamento , Clareadores Dentários/efeitos adversos , Cremes Dentais/efeitos adversos
20.
Dental press j. orthod. (Impr.) ; 18(6): 5-12, Nov.-Dec. 2013. ilus
Artigo em Inglês | LILACS | ID: lil-697724

RESUMO

It all began in Ancient Egypt where people used to bleach their teeth with antiseptic mouthwashes made of urea from human urine. Teeth harmony is promoted by expression of feelings, communication, a real window of the brain and its content! Tooth bleaching products are medicines, not cosmetics! Mouth washing with hydrogen peroxide is an illogical and dangerous procedure! Hydrogen peroxide must be used in one's mouth only when employed by a dentist who has been properly instructed to protect the mucosa, preventing it from receiving these products. How and for how long these products are going to be used require caution in order to avoid or decrease any adverse effects on the tissues. Many websites instruct people on how to purchase and prepare hydrogen peroxide so that it is used as an antiseptic mouthwash and tooth bleaching agent. Some websites even refer to dentists as "exploiters", accusing them of not instructing patients properly. In this article, we aim at providing evidence and information upon which dentists and assistants may base their thinking as well as their opinion and procedures regarding "the indiscriminate and free use of hydrogen peroxide in the mouth, on teeth and oral mucosa". Those websites, blogs and social network profiles trespass the limits of public trust and should be immediately sued by the government for committing a crime against public health.


Tudo começou no Egito antigo, onde procurava-se clarear os dentes com bochechos antissépticos com ureia da urina humana. Os dentes se harmonizam com expressões de sentimentos, na comunicação, como uma verdadeira vitrine do cérebro e seus conteúdos! Clareadores dentários são medicamentos, e não cosméticos! Bochecho com água oxigenada representa um procedimento improcedente e perigoso! O uso do peróxido de hidrogênio ou água oxigenada na boca deve ser feito diretamente pelo profissional da Odontologia, treinado para proteger as mucosas contra o contato desses produtos. O tempo e a forma de uso requerem cuidados, para se proteger ou diminuir os efeitos indesejáveis sobre os tecidos. Vários websites "ensinam" como adquirir e preparar água oxigenada para fazer bochechos antissépticos e clarear os dentes. Alguns websites se referem ao profissional da Odontologia como um "explorador", por não ensinar isso ao paciente. No presente artigo, procuraremos informar e dar fundamentos para que os profissionais da Odontologia e auxiliares possam embasar suas reflexões, opiniões e condutas relacionadas ao tema "uso indiscriminado e livre de peróxido de hidrogênio na boca sobre os dentes e mucosa bucal". Esses websites, blogs e perfis em redes sociais abusam da fé pública e deveriam ser acionados judicialmente, imediatamente, pelas autoridades públicas, pelo crime contra a saúde das pessoas.


Assuntos
Animais , Humanos , Carcinógenos , Comunicação , Peróxido de Hidrogênio/efeitos adversos , Internet , Antissépticos Bucais/efeitos adversos , Oxidantes/efeitos adversos , Clareadores Dentários/efeitos adversos , Carcinogênese , Cocarcinogênese , Relações Dentista-Paciente , Progressão da Doença , Mucosa Gástrica/efeitos dos fármacos , Mucosa Intestinal/efeitos dos fármacos , Mucosa Bucal/efeitos dos fármacos , Neoplasias/induzido quimicamente , Educação de Pacientes como Assunto , Automedicação , Dente/efeitos dos fármacos , Cremes Dentais/efeitos adversos
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