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Objective: This randomized controlled trial aimed to compare nanohydroxyapatite with fluoride on managing post ultrasonic scaling Dentine hypersensitivity (DH). Material and Methods: Thirty patients (aged 20-50 years) with post ultrasonic-scaling DH were included in this study. The sample was randomly divided into three equal groups of 60 teeth each: the first group received nanohydroxyapatite material, the second group received fluoride material and the third group received sterile water as a placebo (controls). The materials were applied once for each patient. All patients were instructed to rate the level of pain before treatment, and after 1 hour, 24 hours, 2 weeks and 1 month on the numerical rating scale (NRS). The Kruskal-Wallis test, Mann-Whitney tests, linear regression analysis were used for the statistical analysis. Significance level was set at 0.05. Results: Both nanohydroxyapatite and fluoride were successful in reducing pain associated with DH when compared with the placebo in subsequent follow-ups (p < 0.05). However, one-hour and one-day post application, nanohydroxyapatite could reduce hypersensitivity pain moreeffectively than fluoride (p < 0.05). Conclusion: Nanohydroxyapatite material was found to besignificantly more effective in reducing the DH that followed ultrasonic scaling one-hour and one-day post application as compared to fluoride and sterile water. Both fluoride and nanohydroxyapatite had similar effect on DH after two-weeks and one-month after application. (AU)
Objetivo: Este ensaio clínico randomizado teve como objetivo comparar a nano-hidroxiapatita com o flúor no manejo da hipersensibilidade dentinária (HD) pós-raspagem ultrassônica. Material e Métodos: Trinta pacientes (com idades entre 20-50 anos) com HD pós-raspagem ultrassônica foram incluídos neste estudo. A amostra foi dividida aleatoriamente em três grupos iguais com 60 dentes cada: o primeiro grupo recebeu material de nano-hidroxiapatita, o segundo grupo recebeu material de flúor e o terceiro grupo recebeu água esterilizada como placebo (controle). Os materiais foram aplicados uma vez para cada paciente. Todos os pacientes foram instruídos a avaliar o nível de dor antes do tratamento, e após 1 hora, 24 horas, 2 semanas e 1 mês na escala de avaliação numérica (NRS). Os testes de Kruskal-Wallis, Mann-Whitney e análise de regressão linear foram usados para a análise estatística. O nível de significância foi estabelecido em 0,05. Resultados: Tanto a nano- hidroxiapatita quanto o flúor foram bem-sucedidos na redução da dor associada à HD quando comparados ao placebo em acompanhamentos subsequentes (p <0,05). No entanto, 1 hora e 1 dia após a aplicação, a nano-hidroxiapatita pode reduzir a dor de hipersensibilidade de forma mais eficaz do que o flúor (p <0,05). Conclusão: O material da nano-hidroxiapatita foi significativamente mais eficaz na redução da HD que se seguiu à raspagem ultrassônica, 1 hora e 1 dia após a aplicação, em comparação com o flúor e a água estéril. Tanto o flúor, quanto a nano-hidroxiapatita apresentou efeito semelhante na HD após 2 semanas e 1 mês após a aplicação (AU)
Subject(s)
Durapatite , Dentin Sensitivity , Dentin Desensitizing Agents , FluoridesABSTRACT
<p><b>OBJECTIVE</b>This review aims to identify the dimensional structure of the shortened dentine hypersensitivity experience questionnaire (DHEQ-15) using confirmatory factor analysis (CFA).</p><p><b>METHODS</b>The Chinese language version of DHEQ-15 was applied to 210 patients with dentine hypersensitivity aged 18-70 years old. The three-dimensional construct was confirmed by CFA.</p><p><b>RESULTS</b>All the questionnaires were fully completed. The item "Because of the sensations, I take longer to finish a meal than others" was the most frequently reported by the parents. The modified three-factor model is suitable for the data. The chi-square fit statistics/degree of freedom was 2.213, the goodness-of-fit index was 0.905, the adjusted goodness-of-fit index was 0.872, the normed fit index was 0.845, the incremental fit index was 0.962, the Tucker-Lewis index was 0.969, the comparative fit index was 0.977, and the root mean square error of approximation was 0.068.</p><p><b>CONCLUSIONS</b>Our findings generally support the three-dimensional construct of the DHEQ-15. Thus, DHEQ-15 can be used as a valid instrument in patients with dentine hypersensitivity in China.</p>
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Objective@#To study the blocking effect and abrasion resistance of hydroxyapatite (HA) with different particle sizes and morphologyies on dentinal tubules from the qualitative and quantitative aspects. @*Methods @# Dentin discs were etched and divided into 4 groups randomly: 20 nm HA group; 30 nm HA group; 12 μm HA group; control group (without any experimental treatment). Each group was brushed with correspondent materials for 7 days. Then, the dentin disk was divided into two parts, the one was detected by the scanning electron microscopy (SEM); the other was observed by SEM after toothbrush abrasion test. The Image-Pro Plus 6.0 image analysis software was used to calculate the plugging rate of dentinal tubules. @*Results @#SEM showed that the blockage is granular, the plugging rate of the dentinal tubules were about 82% to 96%. 30 nm HA group (short rod) range the first in the average plugging rate, followed by the 20 nm HA group (needles) and 12 μm HA group (spherical). After mechanical brushing for 7 days, SEM images showed that deposited layer in each group was smooth and compact, and more than 63% of the tubules still had been blocked. @* Conclusion @#HA with different particle sizes and morphologies had good plugging effect and abrasion resistance on dentine tubules. The blocking effect of HA was affected not only by particle size but also by the morphology.
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Objetivo: avaliar o número de aplicações necessárias para a completa obliteração dos túbulos dentinários utilizando diferentes agentes dessensibilizantes. Material e Métodos: a porção do esmalte coronário da face vestibular de 40 incisivos bovinos foi removida com auxílio de lixas para expor a dentina superficial da junção amelo-cementária. Em seguida, as raízes e a porção coronária referente ao terço médio-incisal dos dentes foram removidas. A seguir foi realizada a completa remoção de smear layer, evidenciando os túbulos dentinários. As amostras foram divididas em quatro grupos experimentais conforme o agente dessensibilizante utilizado: verniz fluoretado, adesivo dentinário, dessensibilizante dentinário e creme dental. Os produtos foram aplicados de acordo com as recomendações do fabricante. As amostras foram avaliadas previamente e após o uso dos agentes por microscopia eletrônica de varredura de baixo vácuo. A aplicação do agente e a análise foram realizadas até a completa obliteração dos túbulos dentinários. Os dados foram avaliados estatisticamente em relação ao número de aplicações necessárias utilizando os testes de Kruskal-Wallis e Mann-Whitney (p < 0,05). Resultados: o verniz fluoretado foi o mais eficaz dos agentes avaliados, sendo necessária uma aplicação para a completa obliteração dos túbulos. Para o adesivo dentinário foram necessárias duas aplicações e para o dessensibilizante e o creme dental foram necessárias cinco aplicações. Conclusão: os agentes dessensibilizantes testados necessitam de um número variado de aplicações, sendo o mais eficaz o verniz fluoretado, onde apenas uma aplicação possibilitou a completa obliteração dos túbulos.
Objective: The aim of this study was to evaluate the number of applications necessary for the complete obliteration of dentinal tubules using different desensitizing agents. Materials and Methods: A portion of coronary enamel of the buccal surface of 40 bovine incisors was removed with the aid of sandpaper in order to expose the superficial dentin at the dentin-enamel junction. The roots and the coronary portions of the mesial-incisal third of the teeth were also removed. Complete smear-layer removal was performed, exposing the dentinal tubules. Samples were divided into four experimental groups according to the desensitizing agents used: fluoride varnish; dentin adhesive; dentin desensitizing; and toothpaste. The products were applied in accordance with the manufacturer's recommendations. Samples were evaluated before and after the application of different agents by scanning electronic microscopy of low vacuum. The application of the products and analyses were carried out until complete obliteration of dentinal tubules. Data were evaluated statistically in relation to the required number of applications, using Kruskal-Wallis and Mann-Whitney tests (p < 0.05). Results: The results showed that fluoride varnish was the most efficient of the tested agents, requiring a single application for the complete obliteration of the dentinal tubule. For the dentin adhesive, two applications were necessary and for the dentin desensitizing and toothpaste, five applications were required. Conclusion: The desensitizing agents tested required a distinct number of applications, and the fluoride varnish was the most effective agent, with a single application resulting in the complete obliteration of the dentin tubule.
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Background: Periodontal attachment loss could be an earlier indicator or a possible risk factor of dentine hypersensitivity (DH). Thus, there is a need for diagnosing this condition both by questionnaire and by clinical examination before rendering both home care and in‑office treatment modalities. Aims: To investigate the relationship between various demographic factors and DH and to detect the percentage of patients using desensitizing agents. Materials and Methods: In this cross‑sectional study, 2051 patients were evaluated till the required sample size of 1000 patients was achieved who were evaluated both by questionnaire and clinical test. Association between DH clinical attachment level and apparent recession was established. Results: This study found that the prevalence of dentine hypersensitivity in chronic periodontitis patients was 37.2% according to questionnaire and 47.8% according to the results of clinical test. Various demographic factors were found to affect dentine hypersensitivity such as age, gender, education, diet, and locality. Conclusion: The prevalence of dentine hypersensitivity in chronic periodontitis patients was 37.2% according to questionnaire and 47.8% according to the results of clinical test. Periodontal attachment loss could be an earlier indicator or a possible risk factor of DH. Only 14.36% of the patients with sensitive teeth used desensitizing paste. This could be due to the fact that either the patients did not consider the condition bad enough to warrant treatment or it was not being diagnosed.
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Objective:To observe the clinical effect of Desensitizer Oravive combined Er:YAG laser irradiation on dentin hypersen-sitivity.Methods:240 molars in 86 patients with dentin hypersensitivity were divided into 2 groups(n =1 20).In control group De-sensitizer Oravive was applied to the teeth surface for 30 s;in combination group the teeth surfaces were treated by Er:YAG laser irra-diation for 60 s,and then by Desensitizer oravive for 30 s.Each tooth was treated only once.Pain and pain relief were evaluated by VAS before treatment and immediately,4,8 and 1 2 weeks after treatment.Data were statistically analyzed.Results:Before treat-ment,VAS showed no significant difference between the groups(P >0.05).Both groups exhibited lower VAS after treatment(P <0. 05),VAS values were lower(P <0.05)and the effective rate was higher in the combination group than those in the control group at each treatment stage(P <0.05).Conclusion:Desensitizer Oravive combined with Er:YAG laser is more effective than Desensitizer Oravive in the treatment of dentin hypersensitivity.
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Background: Many patients visit dentists as a result of pain. It may have nonodontogenic causes such as lesions of vascular, neurologic/psychological, muscular, bone structures or referred from surrounding structures, or odontogenic, in which case the cause of the pain is the tooth and/or tooth supporting structures. Non odontogenic pain is often challenging to diagnose with consequent inappropriate treatment, leading to frustration of the patients and loss of confidence in the managing physician. Hence, attention on the pattern of distribution of these groups of facial pain would assist in their management. Aims: To describe the pattern of presentation of non-odontogenic pain among patients who attend oral medicine clinic in LUTH Methodology: A retrospective review of all cases of non odontogenic pain seen in oral medicine clinic of Lagos University Teaching Hospital (LUTH) between May 2010 and May 2011 was done using the clinic records and patients’ case notes. The recorded parameter includes patients' age, sex and the clinical diagnosis. The results were analysed with SPSS software Results: A total number of 221 patients were seen, 144 (65%) were diagnosed with one form of non-odontogenic pain. The age distribution of subjects with non odontogenic pain ranged from 15 to 85 yrs (45yr+13.8) with the peak age of occurrence at 51-55yrs. On the other hand, those with odontogenic pain were most prevalent at the peak age of 21- 40yr, mean age of 37.3+13.6. Female predilection was observed in all subjects. Dentine hypersensitivity, pulpitis and periodontits were some of the odontogenic pain diagnosed while the various non odontogenic pain diagnosed includes burning mouth 34(23.6%), Aphthous ulceration 28(19.4%), Trigeminal neuralgia 16(11.1%), Candidiasis 11(7.4%), Lichen planus 7(4.6%), Erythemamultiforme 7(4.6%), and Herpes zoster 3(1.9%). Others include mucous membrane pemphigoid and traumatic ulcer. Conclusion: Non-odontogenicpain is relatively common presentations in oral medicine. Burning mouth sensation due to herbal toothpaste use was the most prevalent.
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La hipersensibilidad dentinaria (HD) posterior al raspado y alisado radicular (RAR) ha sido poco estudiada desde una perspectiva preventiva a pesar de su relevancia clínica. El objetivo de esta investigación fue evaluar el efecto de las cremas desensibilizantes en pacientes con indicaciones de raspado y alisado radicular. Para ello, se realizó un estudio longitudinal cuasi-experimental con una muestra no probabilística de 18 pacientes (hombres y mujeres) entre 20 y 50 años de edad, que requerían tratamiento con RAR en dientes posteriores (premolares y primer molar), quienes fueron asignados al azar en cada uno de los tres grupos a evaluar. Las cremas desensibilizantes utilizadas en esta investigación contienen citrato de potasio, nitrato de potasio, fluoruro de sodio y triclosan estas se indicaron un mes antes de realizar los RAR en todos los grupos. Para medir la presencia de hipersensibilidad dentinaria se aplicaron estímulos táctiles y térmicos a los 8, 15 y 22 días posteriores al tratamiento de RAR y se usó la Escala Visual Análoga Graduada (EVAG) para evaluar el dolor. Como resultado se obtuvo menor presencia de HD en el grupo que utilizó citrato de potasio 5.04% y monofluorfosfato 1.1%, aun cuando en los tres grupos se observó disminución de HD durante los tres periodos de medición. Llegando a la conclusión que es pertinente prescribir cremas desensibilizantes con citrato de potasio 5.04% y monofluorfosfato 1.1% a los pacientes con necesidades clínicas similares a los de este estudio un mes antes de planificar los RAR.
The presence of dentine hypersensitivity (DH) after scaling and root planning treatment (RPT) has been scarcely studied from a preventive perspective in spite the clinical relevance of the issue. The aim of this research was to evaluate the preventive effect of some desensitizing dentifrices in patients previous to a RPT. In this sense, a cuasi-experimental, longitudinal study was performed. The non probabilistic sample was constituted by 18 patients (women and men) aged between 20 and 50; all of them diagnosed as requiring scaling and root planning treatment for posterior teeth (premolars and first molars). Subjects were randomly assigned to one of the three groups. The desensitizing toothpaste used in the study contained potassium citrate, potassium nitrate, sodium fluoride and triclosan. These paste were prescribed for patients a month before the RPT. Dentine hypersensitivity was evaluated by using tactile and thermal stimuli applied 8, 25 and 22 days after RPT; the Visual Analogue Scale (VSA) was used to assess pain. Results showed lower presence DH in the 5.04% potassium citrate group and 1.1% monofluor fosfate, even when there was a decrease of DH for the three measurement periods. It was concluded that it would be good to prescribe 5.04% potassium citrate group and 1.1% monofluorfosfate desensitizing agents to patients with clinical needs similar to the ones described in this study, a month before the RPT.
Subject(s)
Humans , Male , Adult , Middle Aged , Female , Bicuspid , Subgingival Curettage , Dentin Sensitivity , Molar , Pain , Dental Scaling , Triclosan/therapeutic use , Dentistry , Pain MeasurementABSTRACT
OBJECTIVES: The purpose of this study was to develop a dentine hypersensitivity (DH) manual for a dental hospital. METHODS: The records of all DH patients who presented between 2005 to 2010 were analyzed to determine their age group, awareness of DH, and DH distribution before and after dental treatment. RESULTS: Out of 953,272 patients, data of 4,646 were analyzed. The male to female ratio of DH patients was found to be 1:1:1. The prevalence of DH was highest in patients in the age group of 40-49 years. The DH awareness rate was high to time, temperature and after dental treatment factor in the middle-age group. CONCLUSIONS: Since DH is widely prevalent and common, systematic screening is essential to ensure good oral health.
Subject(s)
Female , Humans , Male , Dentin Sensitivity , Dentin , Mass Screening , Oral Health , PrevalenceABSTRACT
Background: Dentin hypersensitivity is a recurrent condition causing discomfort and sometimes pain to the patient, which also deters him from maintaining adequate oral hygiene. Home care and office measures are used for treatment of this malady. Aim: To evaluate and compare the efficacy of 2 treatment modalities for dentinal hypersensitivity, iontophoresis with acidulated phosphate gel (APF) gel, and dentin-bonding agent application. Materials and Methods: This split mouth randomized clinical study recruited subjects with a history of hypersensitivity with at least 2 teeth, verified by a light stroke with a dental explorer along the cervical third of the teeth. The patients were subjected to a 1-s air blast and cold water stimuli and their responses were recorded on a verbal rating scale. A total of 30 sites from 15 patients were divided into Group A-1.23% APF gel iontophoresis; and Group B-aqueous solution of hydroxyl-ethyl-methacrylate and glutaraldehyde. The teeth were evaluated immediately after the treatment and at the end of 2 weeks. In case of failure, the tooth was retreated with the same agent as before. Results: The results were statistically analyzed using Kruskal-Wallis analysis of variance and Mann-Whitney U tests. There was no statistically significant difference between the groups at the end of 2 weeks. However, Group A was more effective clinically, with fewer number of failures compared with Group B. Conclusion: Both the agents showed a statistically significant reduction in sensitivity compared with baseline; however, APF gel iontophoresis was more effective in reducing hypersensitivity over a longer time period.
Subject(s)
Acidulated Phosphate Fluoride/therapeutic use , Cross-Linking Reagents/therapeutic use , Dentin Desensitizing Agents/therapeutic use , Dentin Sensitivity/drug therapy , Dentin-Bonding Agents/therapeutic use , Gels , Glutaral/therapeutic use , Humans , Iontophoresis/methods , Methacrylates/therapeutic use , Resin Cements/therapeutic use , Treatment OutcomeABSTRACT
PURPOSE: The aim of this study was to compare the effectiveness of hydroxyapatite containing toothpaste with positive control toothpastes in reducing dentine hypersensitivity. MATERIALS AND METHODS: This clinical trial was a double-blind, randomized, parallel group comparison of two, namely hydroxyapatite containing toothpaste and strontium chloride containing toothpaste. A total of 55 subjects were included in this study. The subjects were given randomly assigned one of the two toothpastes after received tooth brushing instruction at baseline. Some clinical indices(PI, GI, PD), verbal rating score(VRS) for sensitivity to stimulus, the effect in relieving sensitivity and visual analogue scale(VAS) for sensitivity at baseline, week 2, week 4 and week 8 were assessed. All data were evaluated by intention-to-treat analysis. RESULTS: Overall, PI and GI scores were significantly reduced compare baseline in all groups(p0.05). CONCLUSION: This study demonstrated that the new hydroxyapatite containing toothpaste was similarly effective in reducing dentine hypersensitivity with pre-existing benchmark toothpaste.
Subject(s)
Dentin , Dentin Sensitivity , Durapatite , Strontium , Tooth , ToothpastesABSTRACT
OBJECTIVE:To observe the clinical efficacy of herbal desensitizer in the treatment of dentine hypersensitivity. METHODS: 126 patients with dentine hypersensitivity were enrolled: 64(a total of 172 diseased teeth) were randomly assigned to trial group to be treated with herbal desensitizer,and 62(158 diseased teeth) to control group to be treated with sodium fluoride glycerin. The clinical effects observation was scheduled immediately,3 and 6 months after the treatment. Then the results were analyzed using statistics software.RESULTS: Significant differences were found between the trial group and the control group in clinical effects (P
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Objective:To investigate the effect of self-made herbal desensitizer in the treatment of dentine hypersensitivity. Methods:Herbal desensitizer was made of corydalis tuber, asarum herb, long pepper, galangal rhizom and prepared wild aconite root into three different forms:gargle(GG), embrocation(EC) and cataplasm(CP). 750 g/L sodium fluoride paste(SFP) was used as the control. 765 teeth with dentine hypersensitivity in 216 patients were treated with GG,CP,EC and SFP respectively at random. In group CP dental tray was used to carry the desensitizer.The clinical effects were observed in the following 6 months. The effects of the drugs on the obstruction of detinal tubules were observed with scanning electron micoscope(SEM) in the in vitro experiment on 12 extracted teeth.Results:The clinical immediate effective rate(%)of GG,CP,EC and SFP was 57.3(110/192),91.8(179/195),86.9(166/191) and 63.6(119/187) (CP vs GG,EC or SFP P