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1.
Am J Orthod Dentofacial Orthop ; 162(1): 51-57, 2022 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-35153115

RESUMO

INTRODUCTION: This study aimed to survey retention protocols and retainer characteristics among orthodontists practicing in Canada. METHODS: An online questionnaire was distributed to 576 orthodontists registered with the Canadian Association of Orthodontists. It included respondents' demographic details, preferred orthodontic retainers and prescribed wear protocol, adjunctive retention procedures, the timing of retention follow-ups, retainer choice in specific situations, and retainer characteristics. Chi-square tests and Fisher's exact tests were used to test the associations between variables. RESULTS: An 18% response rate was recorded (n = 101). Vacuum-formed retainers were the most commonly used retainers in the maxilla (50.5%), whereas bonded retainers were preferred in the mandible (54.5%). An initial full-time removable retainer wear period was commonly prescribed (63.0%-67.0%). Retainer checks were carried out by 85.1%-89.1% of orthodontists for 1 or 2 years after the end of active orthodontic treatment. Only 44.6%-56.4% were comfortable with general dentists continuing retainer checks. Most (72.5%-84.1%) retainers were fabricated in the orthodontists' office laboratory. Indefinite retainer wear was commonly suggested and was significantly influenced by the number of years in practice. CONCLUSIONS: Most orthodontists' preferred retainer was the vacuum-formed retainers in the maxilla and the bonded retainers in the mandible. A variety of retention protocols and retainer characteristics was evident among orthodontists that reflect the considerable variation in malocclusion traits we face day-to-day. There seems to be a potential dichotomy between orthodontists being uncomfortable about allowing general dental practitioners to manage retention and orthodontists unwilling to provide retention care indefinitely.


Assuntos
Odontólogos , Ortodontistas , Canadá , Estudos Transversais , Humanos , Desenho de Aparelho Ortodôntico , Contenções Ortodônticas , Padrões de Prática Odontológica , Papel Profissional
2.
Healthcare (Basel) ; 12(10)2024 May 19.
Artigo em Inglês | MEDLINE | ID: mdl-38786456

RESUMO

The aim of this study is to compare the dental profiles of Brazilian patients with rare genetic skeletal disorders and normotypical patients. A cross-sectional study was carried out with 210 individuals aged between 2 and 54 years old [105 with rare diseases (Mucopolysaccharidosis/MPS n = 27 and Osteogenesis Imperfecta/OI n = 78) and 105 without rare diseases] and their parents/caregivers. The parents/caregivers answered a questionnaire about individual aspects of their child and the dental profile was identified from questions related to dental history and the presence/absence of dental problems. The patients' oral cavity was also examined by three examiners for dental caries, malocclusion, gingivitis, and dental anomalies. The average age of individuals with a rare disease was 14.1 years (±12.2) and the median was 9.5 years. Participants who had already used the public health system (SUS) dental care services had a 2.24 times higher chance of belonging to the group with a rare disease (OR = 2.24; 95% CI: 1.07-4.89). Patients with rare diseases are 14.86 times more likely to have difficulty receiving dental treatment (OR = 14.86; 95% CI: 5.96-27.03) and 10.38 times more likely to have one or more dental problems (OR = 10.38; 95% CI: 1.95-35.17). Individuals with rare disorders have a greater history of difficulty in accessing dental treatment, using the SUS, and were diagnosed with more dental problems compared to normotypical individuals.

3.
J Appl Oral Sci ; 31: e20230040, 2023.
Artigo em Inglês | MEDLINE | ID: mdl-37672427

RESUMO

BACKGROUND: Osteogenesis imperfecta (OI) is a rare genetic disorder primarily caused by mutations in the genes involved in the production of type 1 collagen. OI is also known as brittle bone disease. OBJECTIVE: This study aims to describe the prevalence of dental anomalies (except dentinogenesis imperfecta) in individuals with OI, and compare the prevalence of dental anomalies between individuals with and without OI and between individuals with different types of OI. SEARCH METHODS: Searches in PubMed, Web of Science, Scopus, Ovid, and gray literature were performed in October 2022. SELECTION CRITERIA: Observational studies (with or without a comparison group) that evaluated the prevalence of dental anomalies in individuals with OI. Data collection and analysis: Data items were extracted by two authors. Quality assessment employing the Joanna Briggs Institute checklists and meta-analyses was conducted. Results were provided in prevalence values and odds ratio (OR) / 95% confidence interval (CI). Strength of evidence was determined. RESULTS: Eighteen studies were included. Most prevalent dental anomalies in individuals with OI included pulp obliteration (46.4%), dental impaction (33.5%), dental impaction of second molars (27%), and tooth agenesis (23.9%). Individuals with OI type III/IV had 20.16-fold greater chance of exhibiting tooth discoloration in comparison with individuals with OI type I (CI: 1.10-370.98). In comparison with the group without OI, the individuals with OI had 6.90-fold greater chance of exhibiting dental impaction (CI: 1.54-31.00). High methodological quality was found in 47% of the studies. Strength of evidence was low or very low. CONCLUSIONS: Pulp obliteration, dental impaction, and tooth agenesis were the most prevalent dental anomalies in the OI group. Individuals with OI were more likely to have dental impaction than individuals without OI. Individuals with OI type III/IV (severe-moderate) are more likely to have tooth discoloration than individuals with OI type I (mild).


Assuntos
Osteogênese Imperfeita , Descoloração de Dente , Humanos , Osteogênese Imperfeita/complicações , Osteogênese Imperfeita/epidemiologia , Prevalência , Descoloração de Dente/epidemiologia
4.
J Appl Oral Sci ; 29: e20200978, 2021.
Artigo em Inglês | MEDLINE | ID: mdl-33886944

RESUMO

Mucopolysaccharidosis (MPS) is a group of rare and inherited metabolic disorders caused by the accumulation of macromolecule glycosaminoglycans inside lysosomes. Affected individuals may have dental and craniofacial tissue alterations, facilitating the development of several oral diseases. OBJECTIVES: To assess, with panoramic radiographic images, the frequency of dental and maxillomandibular incidental findings among MPS individuals and compare them with non-MPS individuals. METHODOLOGY: A cross-sectional study evaluating a sample of 14 MPS individuals and 28 non-MPS individuals aged from 5 to 26 years was carried out. They were matched for sex and age on a 2:1 proportion. Panoramic radiographs were assessed for the presence/absence of the following dental and maxillomandibular alterations: dental anomalies of number (hypodontia/dental agenesis, supernumerary teeth); anomalies of form (microdontia, macrodontia, conoid teeth, taurodontism, and root dilaceration); anomalies of position (impacted tooth, inverted tooth, tooth migration, partially bony teeth, complete bony teeth); periapical alterations (furcation lesion, circumscribed bone rarefaction); other alterations (radiolucent bone lesions, radiopaque bone lesions, radiopacity in the maxillary sinus, condylar hypoplasia). Differences between groups were tested by the Fisher's exact test and chi-square test (p<0.05). RESULTS: For intrarater agreement, Kappa values were 0.76 to 0.85. The presence of supernumerary teeth (p=0.003); conoid teeth (p=0.009); taurodontism (p<0.001); impacted teeth (p<0.001); partial bony teeth (p=0.040); complete bony teeth (p=0.013); and root dilaceration (p=0.047) were statistically more frequent in MPS individuals compared to non-MPS individuals. Bone rarefaction/furcation lesions (p=0.032), condylar hypoplasia (p<0.001), radiolucent bone lesions (p=0.001), and dentigerous cysts (p=0.002) were also more frequent in MPS individuals. CONCLUSION: The presence of specific oral manifestations is more common in MPS individuals than non-MPS individuals.


Assuntos
Mucopolissacaridoses , Anormalidades Dentárias , Dente Supranumerário , Adolescente , Adulto , Criança , Pré-Escolar , Estudos Transversais , Humanos , Achados Incidentais , Mucopolissacaridoses/diagnóstico por imagem , Radiografia Panorâmica , Anormalidades Dentárias/diagnóstico por imagem , Adulto Jovem
5.
Braz Oral Res ; 34: e109, 2020.
Artigo em Inglês | MEDLINE | ID: mdl-32876117

RESUMO

The purpose of the present study was to compare the perceptions of the parents/ caregivers of young people with and without Mucopolysaccharidosis (MPS) with regards to their oral health-related quality of life (OHRQoL). A cross-sectional study was conducted with 29 individuals with MPS and 29 normotypic individuals aged three to 21 years and their parents/caregivers. All parents/caregivers of young people with MPS in follow-up at two reference hospitals in the city of Belo Horizonte, southeastern Brazil, were invited to participate in the study. Individuals without MPS were recruited from the pediatric clinics of both hospitals. Parents/caregivers answered a structured questionnaire addressing the sociodemographic characteristics, behavioral habits and medical and dental history of the children as well as the Brazilian short-form version of the Parental-Caregiver (P-CPQ). The individuals with and without MPS were examined for malocclusion, dental caries and oral hygiene by an examiner who had undergone training and calibration exercises. Mean age of the subjects was 12.1 years (± 4.2). Comparing total P-CPQ scores and scores on the oral symptoms, functional limitations and wellbeing domains, the parents/caregivers individuos with MPS reported a statistically significant greater negative impact on OS domain than their counterparts. Regarding the clinical variables, malocclusion was also associated a greater negative impact on OHRQoL of young people with MPS when compared to those of young people without MPS. Our findings show the great negative impact caused by the malocclusion of young people with MPS.


Assuntos
Mucopolissacaridoses , Adolescente , Adulto , Brasil , Criança , Pré-Escolar , Estudos Transversais , Cárie Dentária , Humanos , Má Oclusão , Saúde Bucal , Pais , Qualidade de Vida , Inquéritos e Questionários , Adulto Jovem
6.
Cien Saude Colet ; 25(2): 533-540, 2020 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-32022193

RESUMO

The present study aimed to analyze factors associated with access of dental care services by Brazilian hemodialysis patients. A cross-sectional study was carried out with 467 hemodialysis patients aging from 19 to 90 years in two renal therapy centers located in the cities of Contagem and Belo Horizonte, Southeastern Brazil. Data were collected through an oral clinical examination of the patients and the application of a structured questionnaire. The dependent variable was the access to dental care, measured by the question "Have you consulted with a dentist in last six months?". The mean age of participants was 49.9 years. The average number of teeth present in the mouth was 19.3. An average of 1.5 teeth with dental caries cavities lesion was diagnosed among hemodialysis patients. One-third of the sample had gone to the dentist in the last six months (27.8%). The access to dental care was associated with formal education (OR = 1.5 [1.1-2.4]), professional advising to consult with a dentist (OR = 2.1 [1.2-3.8]) and prevalence of dental caries (OR = 2.1 [1.3-3.2]). Hemodialysis patients with eight or more years of formal education, who received professional advising to consult with a dentist and without dental caries cavities had higher chances obtaining access to dental care.


Assuntos
Cárie Dentária/epidemiologia , Serviços de Saúde Bucal/estatística & dados numéricos , Acessibilidade aos Serviços de Saúde , Diálise Renal , Adulto , Idoso , Idoso de 80 Anos ou mais , Brasil/epidemiologia , Estudos Transversais , Assistência Odontológica/estatística & dados numéricos , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Prevalência , Inquéritos e Questionários , Adulto Jovem
7.
Orphanet J Rare Dis ; 14(1): 145, 2019 06 18.
Artigo em Inglês | MEDLINE | ID: mdl-31215497

RESUMO

BACKGROUND: Individuals diagnosed with a rare genetic disease that affects skeletal development often have physical limitations and orofacial problems that exert an impact on oral health. The aim of the present study was to analyze the possible vulnerability to dental caries in individuals with rare genetic diseases that affect skeletal development. METHODS: A paired cross-sectional study was carried out with a sample of 140 individuals [70 with rare genetic diseases affecting skeletal development: mucopolysaccharidosis (MPS) (n = 29) and osteogenesis imperfecta (OI) (n = 41) and 70 without rare diseases] and their parents/caregivers. The participants in the first group were recruited from two reference hospitals specialized in rare genetic diseases in the city of Belo Horizonte, Brazil. All participants were examined for the evaluation of breathing type, malocclusion, dental anomalies, oral hygiene and dental caries. The parents/caregivers answered a structured questionnaire addressing the individual/behavioral characteristics and medical/dental history of the participants. Statistical analysis involved the chi-square test and multiple logistic regression analysis for the dependent variable (dental caries) (α = 5%). This study received approval from the Human Research Ethics Committee of the Universidade Federal de Minas Gerais. RESULTS: The mean age of the individuals was 10.34 ± 6.55 years (median: 9.50 years). Individuals with inadequate oral hygiene were 4.70-fold more likely to have dental caries (95% CI: 2.13-10.40) and those with the rare genetic diseases (MPS/OI) were 2.92-fold more likely to have dental caries (95% CI: 1.38-6.17). CONCLUSION: Individuals with inadequate oral hygiene and those with MPS and OI had a greater chance of belonging to the group with dental caries. Based on the present findings, individuals with the rare genetic diseases may be considered vulnerable to caries.


Assuntos
Cárie Dentária/epidemiologia , Doenças Raras/epidemiologia , Adolescente , Adulto , Criança , Pré-Escolar , Estudos Transversais , Pessoas com Deficiência/estatística & dados numéricos , Feminino , Humanos , Masculino , Saúde Bucal , Adulto Jovem
8.
J. appl. oral sci ; 31: e20230040, 2023. graf
Artigo em Inglês | LILACS-Express | LILACS | ID: biblio-1506565

RESUMO

Abstract Background Osteogenesis imperfecta (OI) is a rare genetic disorder primarily caused by mutations in the genes involved in the production of type 1 collagen. OI is also known as brittle bone disease. Objective This study aims to describe the prevalence of dental anomalies (except dentinogenesis imperfecta) in individuals with OI, and compare the prevalence of dental anomalies between individuals with and without OI and between individuals with different types of OI. Search methods Searches in PubMed, Web of Science, Scopus, Ovid, and gray literature were performed in October 2022. Selection criteria Observational studies (with or without a comparison group) that evaluated the prevalence of dental anomalies in individuals with OI. Data collection and analysis: Data items were extracted by two authors. Quality assessment employing the Joanna Briggs Institute checklists and meta-analyses was conducted. Results were provided in prevalence values and odds ratio (OR) / 95% confidence interval (CI). Strength of evidence was determined. Results Eighteen studies were included. Most prevalent dental anomalies in individuals with OI included pulp obliteration (46.4%), dental impaction (33.5%), dental impaction of second molars (27%), and tooth agenesis (23.9%). Individuals with OI type III/IV had 20.16-fold greater chance of exhibiting tooth discoloration in comparison with individuals with OI type I (CI: 1.10-370.98). In comparison with the group without OI, the individuals with OI had 6.90-fold greater chance of exhibiting dental impaction (CI: 1.54-31.00). High methodological quality was found in 47% of the studies. Strength of evidence was low or very low. Conclusions Pulp obliteration, dental impaction, and tooth agenesis were the most prevalent dental anomalies in the OI group. Individuals with OI were more likely to have dental impaction than individuals without OI. Individuals with OI type III/IV (severe-moderate) are more likely to have tooth discoloration than individuals with OI type I (mild).

9.
Rev. Cient. CRO-RJ (Online) ; 7(1): 16-23, Jan-Apr 2022.
Artigo em Inglês | LILACS, BBO - odontologia (Brasil) | ID: biblio-1382133

RESUMO

Introduction: Children with cerebral palsy (CP) are at high risk of developing oral diseases. Objective: To propose an early dental care protocol for infants with CP. Materials and Methods: A computerized systematic search was performed in the PubMed, Scopus and Embase electronic databases for relevant articles. An early dental care protocol was then proposed for infants with cerebral palsy focused on comprehensive care with a multidisciplinary approach and effective health promotion by caregivers. Results: Fifteen published papers were included in the present literature review and protocol proposal. The protocol comprised the following topics: First dental visit, aspects related to the appointment, oral hygiene recommendations, dietary recommendations and recommendations for the prevention and control of harmful oral habits. The first dental visit should occur prior to the eruption of the teeth. As a special group, it is important to determine the affective bond between the patient and caregiver who will receive the oral health care recommendations. During the clinical examination, the correct positioning and stabilization of the infant is important for the control of involuntary movements and the minimization of swallowing difficulties. Counseling with regards to adequate oral hygiene, a healthy diet and the prevention of harmful oral habits is important to the prevention of dental diseases. Children with oral-motor motility problems and feeding difficulties should be referred to therapeutic follow-up. Due to the neuropsychomotor disorders often found in cerebral palsy, affected children are more vulnerable to oral diseases. Thus, oral health care must be performed as early as possible by the parents/caregivers of these children. Conclusion: Individuals with cerebral palsy are at greater risk of developing oral problems. Thus, oral health programs starting in early childhood and targeting the specificities of these individuals is a strategy for minimizing the occurrence of such problems and the associated burden.


Introdução: Crianças com Paralisia Cerebral (PC) apresentam um alto risco para o desenvolvimento de doenças bucais. Objetivo: Propor um protocolo de atendimento odontológico precoce para lactentes com PC. Materiais e Métodos: Foi realizada uma busca computadorizada sistemática nas bases de dados eletrônicas PubMed, Scopus e Embase. Também foi desenvolvida uma proposta de protocolo de atendimento a bebês com Paralisia Cerebral com foco no cuidado integral, abordagem transdisciplinar e promoção efetiva da saúde pelos cuidadores. Resultados: Foram incluídos 15 artigos publicados na literatura científica. O protocolo desenvolvido é composto pelos seguintes tópicos: Primeira consulta odontológica, tempo ideal da consulta, recomendações de higiene bucal, recomendações sobre dieta e recomendações sobre prevenção e controle dos hábitos bucais. A primeira visita ao dentista deve ser feita antes da erupção do primeiro dente. Como um grupo especial, é importante determinar o vínculo afetivo entre o paciente e o cuidador que receberá as recomendações de cuidados com a saúde bucal. Durante o exame clínico, a correta posição e estabilização do bebê na cadeira odontológica é importante para controlar os movimentos involuntários e reduzir a dificuldade de deglutição. Recomendações quanto à higiene bucal adequada, alimentação saudável e prevenção de hábitos bucais deletérios são importantes para prevenir o desenvolvimento de doenças bucais. Crianças com problemas de motilidade oral-motora e dificuldades de alimentação devem ser encaminhadas para acompanhamento terapêutico. Devido à presença de distúrbios neuropsicomotores normalmente presentes na Paralisia Cerebral, as crianças afetadas são mais vulneráveis às doenças bucais. Assim, os cuidados com a saúde bucal devem ser realizados o quanto antes pelos pais/responsáveis. Conclusão: Indivíduos com PC apresentam maior risco de desenvolver doenças bucais e programas de saúde bucal iniciados na primeira infância e direcionados às suas especificidades podem ser uma estratégia para minimizar as consequências que possam vir a acontecer.


Assuntos
Humanos , Criança , Paralisia Cerebral/complicações , Saúde Bucal , Assistência Odontológica para a Pessoa com Deficiência , Protocolos Clínicos
10.
Rev. Fac. Odontol. Porto Alegre (Online) ; 62(1): 5-14, jan.-jun. 2021.
Artigo em Inglês | LILACS, BBO - odontologia (Brasil) | ID: biblio-1443182

RESUMO

Introduction: Chronic kidney disease (CKD) is a progres-sive condition characterized by structural or functional abnormalities of the kidney. CKD may be associated with several oral alterations, such as higher prevalence rate of dental caries, periodontal disease, xerostomia, candidiasis and burning mouth. The aim of the study was to identify risk factors associated with edentulism in adults with CKD undergoing hemodialysis. Methods: A cross-sec-tional study was conducted with 650 individuals aged 18 to 90 years undergoing hemodialysis in southeastern Brazil. Oral clinical examination and administration of a questionnaire addressing demographic characteristics and dental history were performed. The study received approval from the Human Research Ethics Committee of UFMG. Findings: A total of 183 participants were eden-tulous (28.2%). Individuals with less schooling (OR = 3.99; 95% CI: 2.34-6.79), those who had not been to a dentist in the previous six months (OR = 2.49; 95% CI: 1.52-4.08), those who rated their own smile as excellent or good (OR = 2.00; 95% CI: 1.35-2.97) and those with some mucosal alteration (OR = 4.17; 95% CI: 2.83-6.13) had a greater chance of belonging to the edentulous group. Discussion: The present findings can contribute to the establishment of public health policies aimed at guiding dental care programs for individuals with chronic kidney disease that take into account the specific needs of this population. Conclusion: Edentulism was associated with low schooling, a lack of dental care in the previous six months, a positive self-perception of one's smile and alterations in the oral mucosa.


Introdução: A doença renal crônica (DRC) é uma condição caracterizada por anormalidades estruturais ou funcionais do rim. A DRC pode estar associada a diversas alterações bucais, como maior prevalência de cárie dentária, doença periodontal, xerostomia, candidíase e queimação bucal. O objetivo deste estudo foi identificar os fatores de risco associados ao edentulismo em indivíduos com DRC em tratamento com hemodiálise. Materiais e Métodos: Foi realizado um estudo transversal com 650 indivíduos de 18 a 90 anos em hemodiálise no sudeste do Brasil. Foi realizado exame clínico oral e aplicação de questionário abordando características demográficas e histórico odontológico. O estudo foi aprovado pelo Comitê de Ética em Pesquisa em Seres Humanos da UFMG. Resultados: Um total de 183 participantes eram edêntulos (28,2%). Indivíduos com menor escolaridade (OR = 3,99; IC 95%: 2,34-6,79), aqueles que não foram ao dentista nos últimos seis meses (OR = 2,49; IC 95%: 1,52-4,08), aqueles que avaliaram o seu próprio sorriso como excelente ou bom (OR = 2,00; IC 95%: 1,35-2,97) e aqueles com alguma alteração de mucosa (OR = 4,17; IC 95%: 2,83-6,13) tiveram maior chance de pertencer ao grupo de edêntulos. Discussão: Os presentes achados podem contribuir para o estabelecimento de políticas públicas de saúde voltadas a nortear programas de atenção odontológica à pessoa com doença renal crônica que atendam às necessidades específicas dessa população. Conclusão: O edentulismo esteve associado à baixa escolaridade, falta de atendimento odontológico nos últimos seis meses, sorriso autoavaliado positivo e alterações mucosas.


Assuntos
Humanos , Masculino , Feminino , Adolescente , Adulto , Pessoa de Meia-Idade , Idoso , Idoso de 80 Anos ou mais , Adulto Jovem , Fatores de Risco , Diálise Renal , Arcada Edêntula/etiologia , Insuficiência Renal Crônica , Estudos Transversais
11.
J. appl. oral sci ; 29: e20200978, 2021. tab, graf
Artigo em Inglês | LILACS | ID: biblio-1286913

RESUMO

Abstract Mucopolysaccharidosis (MPS) is a group of rare and inherited metabolic disorders caused by the accumulation of macromolecule glycosaminoglycans inside lysosomes. Affected individuals may have dental and craniofacial tissue alterations, facilitating the development of several oral diseases. Objectives To assess, with panoramic radiographic images, the frequency of dental and maxillomandibular incidental findings among MPS individuals and compare them with non-MPS individuals. Methodology A cross-sectional study evaluating a sample of 14 MPS individuals and 28 non-MPS individuals aged from 5 to 26 years was carried out. They were matched for sex and age on a 2:1 proportion. Panoramic radiographs were assessed for the presence/absence of the following dental and maxillomandibular alterations: dental anomalies of number (hypodontia/dental agenesis, supernumerary teeth); anomalies of form (microdontia, macrodontia, conoid teeth, taurodontism, and root dilaceration); anomalies of position (impacted tooth, inverted tooth, tooth migration, partially bony teeth, complete bony teeth); periapical alterations (furcation lesion, circumscribed bone rarefaction); other alterations (radiolucent bone lesions, radiopaque bone lesions, radiopacity in the maxillary sinus, condylar hypoplasia). Differences between groups were tested by the Fisher's exact test and chi-square test (p<0.05). Results For intrarater agreement, Kappa values were 0.76 to 0.85. The presence of supernumerary teeth (p=0.003); conoid teeth (p=0.009); taurodontism (p<0.001); impacted teeth (p<0.001); partial bony teeth (p=0.040); complete bony teeth (p=0.013); and root dilaceration (p=0.047) were statistically more frequent in MPS individuals compared to non-MPS individuals. Bone rarefaction/furcation lesions (p=0.032), condylar hypoplasia (p<0.001), radiolucent bone lesions (p=0.001), and dentigerous cysts (p=0.002) were also more frequent in MPS individuals. Conclusion The presence of specific oral manifestations is more common in MPS individuals than non-MPS individuals.


Assuntos
Humanos , Pré-Escolar , Criança , Adolescente , Adulto , Adulto Jovem , Anormalidades Dentárias/diagnóstico por imagem , Dente Supranumerário , Mucopolissacaridoses/diagnóstico por imagem , Radiografia Panorâmica , Estudos Transversais , Achados Incidentais
12.
Artigo em Inglês | LILACS, BBO - odontologia (Brasil) | ID: biblio-1346672

RESUMO

ABSTRACT Objective: To analyze the perception of mothers of children with Cerebral Palsy (CP) on the diagnosis moment and the child's health. Material and Methods: Research with a qualitative approach, carried out with 19 mothers of children with CP, in a public higher education institution, in the state of Minas Gerais, Brazil. For data collection, the interview was used and for data interpretation, content analysis. Results: Mothers reported that the diagnosis of a child with CP resulted in major changes in the family's daily life, increasing their responsibility and demands. After the diagnosis, mothers revealed oscillating feelings, with progressively replaced by her motherly ability to take care, reestablishing the psychic balance. The health associated with the absence of disease and curative practices was frequently observed. Mothers reported a great concern with oral hygiene habits and frequent visits to the dentist. Conclusion: The diagnosis of a child with CP led to changes in the family's priorities and routine. After the moment of anguish, uncertainty and fear, the mothers accepted the reality. The biomedical principle significantly influenced the mother´s perception of health, being health perceived as the absence of disease and curative practices. In relation to oral health, practices widely spread and recommended by the media and health services, such as correct tooth brushing, showed an orientation of patients to maintain oral health.


Assuntos
Humanos , Feminino , Higiene Bucal/educação , Paralisia Cerebral/diagnóstico , Saúde Bucal/educação , Serviços de Saúde para Pessoas com Deficiência , Mães , Brasil/epidemiologia , Criança , Pesquisa Qualitativa
13.
Braz. oral res. (Online) ; 34: e109, 2020. tab, graf
Artigo em Inglês | LILACS, BBO - odontologia (Brasil) | ID: biblio-1132694

RESUMO

Abstract The purpose of the present study was to compare the perceptions of the parents/ caregivers of young people with and without Mucopolysaccharidosis (MPS) with regards to their oral health-related quality of life (OHRQoL). A cross-sectional study was conducted with 29 individuals with MPS and 29 normotypic individuals aged three to 21 years and their parents/caregivers. All parents/caregivers of young people with MPS in follow-up at two reference hospitals in the city of Belo Horizonte, southeastern Brazil, were invited to participate in the study. Individuals without MPS were recruited from the pediatric clinics of both hospitals. Parents/caregivers answered a structured questionnaire addressing the sociodemographic characteristics, behavioral habits and medical and dental history of the children as well as the Brazilian short-form version of the Parental-Caregiver (P-CPQ). The individuals with and without MPS were examined for malocclusion, dental caries and oral hygiene by an examiner who had undergone training and calibration exercises. Mean age of the subjects was 12.1 years (± 4.2). Comparing total P-CPQ scores and scores on the oral symptoms, functional limitations and wellbeing domains, the parents/caregivers individuos with MPS reported a statistically significant greater negative impact on OS domain than their counterparts. Regarding the clinical variables, malocclusion was also associated a greater negative impact on OHRQoL of young people with MPS when compared to those of young people without MPS. Our findings show the great negative impact caused by the malocclusion of young people with MPS.


Assuntos
Humanos , Pré-Escolar , Criança , Adolescente , Adulto , Adulto Jovem , Mucopolissacaridoses , Pais , Qualidade de Vida , Brasil , Saúde Bucal , Estudos Transversais , Inquéritos e Questionários , Cárie Dentária , Má Oclusão
14.
Ciênc. Saúde Colet. (Impr.) ; 25(2): 533-540, Feb. 2020. tab
Artigo em Inglês | LILACS | ID: biblio-1055816

RESUMO

Abstract The present study aimed to analyze factors associated with access of dental care services by Brazilian hemodialysis patients. A cross-sectional study was carried out with 467 hemodialysis patients aging from 19 to 90 years in two renal therapy centers located in the cities of Contagem and Belo Horizonte, Southeastern Brazil. Data were collected through an oral clinical examination of the patients and the application of a structured questionnaire. The dependent variable was the access to dental care, measured by the question "Have you consulted with a dentist in last six months?". The mean age of participants was 49.9 years. The average number of teeth present in the mouth was 19.3. An average of 1.5 teeth with dental caries cavities lesion was diagnosed among hemodialysis patients. One-third of the sample had gone to the dentist in the last six months (27.8%). The access to dental care was associated with formal education (OR = 1.5 [1.1-2.4]), professional advising to consult with a dentist (OR = 2.1 [1.2-3.8]) and prevalence of dental caries (OR = 2.1 [1.3-3.2]). Hemodialysis patients with eight or more years of formal education, who received professional advising to consult with a dentist and without dental caries cavities had higher chances obtaining access to dental care.


Resumo Este estudo objetivou analisar os fatores associados ao uso de serviços odontológicos por pacientes em hemodiálise. Foi realizado um estudo transversal com 467 pacientes em hemodiálise, na faixa etária de 19 a 90 anos, de Contagem e Belo Horizonte, região Sudeste do Brasil. Os dados foram coletados por meio de exame clínico bucal dos participantes e da aplicação de um questionário estruturado. A variável dependente foi o acesso odontológico, mensurado pela pergunta "Você foi ao dentista nos últimos seis meses?". A média de idade dos participantes foi de 49,9 anos. A média de dentes presentes na boca foi de 19,3. Uma média de 1,5 dentes com lesão de cárie cavitada foi diagnosticada entre os pacientes em hemodiálise. Um terço da amostra afirmou ter ido ao dentista nos últimos seis meses (27,8%). O acesso odontológico dos pacientes em hemodiálise foi associado à escolaridade (OR = 1,5 [1,1-2,4]), orientação profissional para ir ao dentista (OR = 2,1 [1,2-3,8]) e prevalência de cárie dentária (OR = 2,1 [1,3-3,2]). Os pacientes em hemodiálise com oito anos ou mais de escolaridade, que receberam orientação profissional para ir ao dentista e sem cárie dentária apresentaram maior chance de terem acesso odontológico.


Assuntos
Humanos , Masculino , Feminino , Adulto , Idoso , Idoso de 80 Anos ou mais , Adulto Jovem , Diálise Renal , Cárie Dentária/epidemiologia , Serviços de Saúde Bucal/estatística & dados numéricos , Acessibilidade aos Serviços de Saúde , Brasil/epidemiologia , Prevalência , Estudos Transversais , Inquéritos e Questionários , Assistência Odontológica/estatística & dados numéricos , Pessoa de Meia-Idade
15.
Belo Horizonte; s.n; 2020. 108 p. ilus.
Tese em Português | LILACS, BBO - odontologia (Brasil) | ID: biblio-1292769

RESUMO

As mucopolissacaridoses (MPS) caracterizam-se por um grupo de doenças genéticas metabólicas raras, com manifestações multissistêmicas progressivas. Acarretam diversas alterações físicas, motoras e intelectuais. Dentre as alterações físicas, muitas estão presentes na face e na cavidade bucal. Na área odontológica ainda são poucos os estudos dedicados à MPS, sendo insuficientes as informações sobre as características orofaciais presentes nas pessoas acometidas por essa anomalia. O presente estudo objetivou identificar as características orofaciais de indivíduos com MPS e comparar com um grupo de indivíduos sem MPS. Foi realizado um estudo observacional transversal com uma amostra pareada de 14 indivíduos com MPS e 28 sem MPS, na faixa etária de 5 a 26 anos, pareados por sexo e idade. Os participantes com MPS e sem MPS são atendidos em dois hospitais públicos de Belo Horizonte, região sudeste do Brasil. Em ambos os grupos foi realizada a análise facial e a análise cefalométrica (medidas angulares e lineares). Além disso, também foram identificadas a presença ou ausência de alterações dentárias e maxilomandibulares por meio de radiografias panorâmicas. Previamente ao estudo principal, a examinadora passou pelo processo de calibração prática. Foram obtidos valores kappa entre 0,76 e 0,98. Para as variáveis cefalométricas, não foram observados erros sistemáticos significativos (p> 0,05). Os erros aleatórios para as medidas lineares e angulares foram baixos. A análise estatística entre os grupos foi realizada por meio do teste qui-quadrado e teste t independente. O estudo foi aprovado pelo Comitê de Ética em Pesquisa da Universidade Federal de Minas Gerais. A média de idade dos 42 participantes foi de 13,9 anos (± 7,2). Em relação às alterações faciais e cefalométricas, observou-se que quando comparados com indivíduos sem MPS, a maioria dos indivíduos com MPS apresentou perfil dolicofacial, alteração nas proporções faciais, com aumento da altura facial anterior inferior (AFAI) e incompetência labial (todos p<0,05). Seis medidas angulares foram significativamente maiores entre os indivíduos com MPS: 1s.Na, 1s.NB, FMA, IMPA, AFI e Po.Or_Go.Me; todos p <0,05. Duas medidas angulares apresentaram-se significativamente reduzidas nos indivíduos com MPS: 1s.1i, Ba.N-Ptm.Gn; p <0,05. Quatro medidas lineares apresentaram-se aumentadas entre os indivíduos com MPS: 1s-NA, 1i-NB, S-UL e S-LL; todos p<0,05. E, cinco medidas lineares (PogN-Perp, Co-A, Co-Gn, Nfa-Nfp e overbite; todos p<0,05) apresentaram-se reduzidas entre os indivíduos com MPS. Em relação à presença/ausência de alterações dentárias e maxilomandibulares, observou-se que a presença de dentes supranumerários (p=0,003); dentes conóides (p = 0,009); taurodontismo (p<0,001); dentes impactados (p<0,001); dentes semi-inclusos (p=0,040); dentes inclusos (p=0,013); e dilaceração radicular (p=0,047) foi estatisticamente mais frequente nos indivíduos com MPS quando comparados aos sem MPS. Além disso, a presença de rarefação óssea/ lesão de furca óssea (p=0,032), hipoplasia condilar (p<0,001), lesões ósseas radiolúcidas (p=0,001) e cistos dentígeros (p=0,001) também foram mais frequentes em indivíduos com MPS. Conclui-se que a maioria dos indivíduos com MPS apresentou perfil dolicofacial com aumento da altura facial anteroinferior. Os indivíduos com MPS foram identificados com incisivos superiores e inferiores vestibularizados, espaço nasofaríngeo reduzido e overbite reduzido. A presença de alterações dentárias e maxilomandibulares também foram frequentes nos indivíduos com MPS, ressaltando assim a importância do conhecimento a cerca das manifestações clínicas orais e faciais que podem ser herdadas através da MPS, a fim de se realizar um atendimento odontológico preventivo e eficaz.


Mucopolysaccharidosis (MPS) are characterized as a group of rare metabolic genetic diseases, with progressive multisystemic manifestations. There are several physical, motor and intellectual alterations. Among the physical alterations, many are presented in the face and oral cavity. In the the area of dentistry, there are still few studies dedicated to MPS, with insufficient information about the orofacial characteristics presented in individuals affected by this anomaly. Therefore, the aim of the present study was to evaluate the orofacial features of individuals with Mucopolysaccharidosis (MPS) and to compare the characteristics of those individuals with a group of non-MPS individuals. A cross-sectional study was carried out with a paired sample of 14 MPS individuals and 28 non-MPS individuals between five and 26 years old matched for sex and age. Participants with and without MPS are patients attended at two public hospitals in Belo Horizonte, southeastern region of Brazil. Facial and cephalometric analysis (angular and linear measurements) was performed for both groups. Besides that, the presence/absence of dental and maxillomandibular alterations were assessed through panoramic radiographs. Prior to the main study, the examiner went through practical calibration process. Kappa scores for categorical variables obtained were 0.76 to 0.98. For the cephalometric variables, no systematic errors were observed (p>0.05). Random errors for linear and angular measurements were low. Statistical analysis between groups was performed by means of chi-square test and independent t test. The study was approved by the Research Ethics Committee of the Universidade Federal de Minas Gerais. The mean age of the 42 participants was 13.9 years (±7.2). Regarding facial and cephalometric measures, it was observed that when compared to non-MPS individuals, most MPS individuals were dolichofacial, with facial proportions alterations, increased ALFH, and no passive lip sealing (all p<0.05). Six angular measurements (1s.Na, 1s.NB, FMA, IMPA, AFI, and Po.Or_Go.Me; all p<0.05) were significantly increased among MPS individuals. Two angular measurements (1s.1i, Ba.N-Ptm.Gn; all p<0.05) were significantly decreased among MPS individuals. Four linear measurements were significantly increased among MPS individuals (1s-NA, 1i-NB, S-UL and S-LL; all p<0.05). Five linear measurements (PogN-Perp, Co-A, Co-Gn, Nfa-Nfp and overbite; all p<0.05) were significantly decreased among MPS individuals. It can be concluded that, most MPS individuals were dolichofacial with increased anterior lower facial height. MPS individuals also present pro-inclined upper and lower incisors, reduced nasopharyngeal space and reduced overbite. The presence of dental and maxillomandibular alterations were also more frequent in MPS individuals, highlighting the importance of the knowledge about the oral and facial clinical manifestations that can be inherited with the MPS disease, in order to provide preventive and effective dental care.


Assuntos
Mucopolissacaridoses , Anormalidades Craniofaciais , Doenças Raras , Anormalidades Maxilomandibulares , Má Oclusão , Odontologia Preventiva , Estudo Observacional
16.
Belo Horizonte; s.n; 2016. 80 p. ilus.
Tese em Inglês, Português | BBO - odontologia (Brasil) | ID: biblio-946367

RESUMO

As mucopolissacaridoses (MPS) são um grupo de doenças hereditárias causadas pela falta de enzimas lisossomais específicas responsáveis pela degradação de glicosaminoglicanos (GAG). Por meio do Senso de Coerência (SOC), é possível compreender a razão de algumas pessoas adoecerem após a ocorrência de uma situação estressante e outras não. Este estudo objetivou testar a associação entre o Senso de Coerência Materno (SOC) Materno e a presença de MPS, bem como entre o SOC Materno e a saúde bucal de crianças/adolescentes com e sem MPS. Foi realizado um estudo transversal pareado, com uma amostra de 58 crianças/adolescentes, sendo 29 com MPS e 29 sem MPS, entre 3 e 21 anos, e suas respectivas mães. Os participantes dos dois grupos foram pareados por sexo e idade. Os dados foram coletados em uma das clínicas da Faculdade de Odontologia da Universidade Federal de Minas Gerais, localizada na cidade de Belo Horizonte, região sudeste do Brasil. As crianças/adolescentes com e sem MPS, bem como as respectivas mães, foram selecionadas em um hospital universitário. As mães que concordaram em participar do estudo responderam o questionário de Antonovsky SOC (SOC-13) e seus filhos tiveram a cavidade bucal examinada para cárie dentária, higiene bucal, defeito de desenvolvimento de esmalte e má oclusão. Esta pesquisa foi aprovada pelo Comitê de Ética em Pesquisa com Seres Humanos da UFMG. As mães de crianças/adolescentes com MPS apresentaram menores valores de SOC [média: 33,3 (+4,0)/mediana: 32,0] quando comparadas com as mães de crianças/adolescentes sem MPS [média: 36,9 (+4,5) /mediana: 37,0] (p<0,001). As mães de crianças/adolescentes com MPS apresentaram menores valores de SOC quando os filhos apresentavam um ou mais dentes cariados [31,5 (+3,2)] quando comparados com aqueles sem dentes cariados [35,7 (+3,8)] (p=0,004). As mães de crianças/adolescentes com MPS apresentaram menores valores de SOC quando os filhos apresentavam um ou mais dentes perdidos [30,2 (+0,9)], quando comparados com aqueles sem nenhum dente perdido [33,8 (+4,1)] (p=0,046). As mães de crianças/adolescentes com MPS apresentaram valores menores de SOC. As mães de filhos com MPS e 10 cárie dentária e/ou dentes perdidos foram identificadas com valores menores de SOC. O estudo do Senso de Coerência Materno e saúde bucal de crianças/adolescentes com MPS permite uma abordagem multidisciplinar mais adequada para as famílias, especialmente as mães, e os profissionais de saúde que os assistem. Dessa forma, é possível promover uma melhor qualidade de vida e saúde bucal para essa parcela da população


Mucopolysaccharidosis (MPS) are a group of inherited diseases caused by enzyme inadequacy of lysosomes, responsible for the degradation of glycosaminoglycans (GAG). Sense of Coherence (SOC) is a theoretical construct used to understand why some people fall ill after the occurance of a stressful situation and some not .This study aimed to assess the association between the presence of MPS in children/adolescents and the mother?s sense of coherence (SOC), as well as the association between mother?s SOC and the oral health status of children/adolescents with and without MPS. A paired cross-sectional study was carried out with a convenience sample of 29 children/adolescents with MPS and 29 children/adolescents without MPS, with age ranging from of 3 to 21 years, and their mothers. They were individually matched by sex and age. Data was collected at a clinic of the School of Dentistry of the Universidade Federal de Minas Gerais, in the city of Belo Horizonte, in the southeast of Brazil. Mothers who agreed to participate completed the Antonovsky?s SOC instrument (SOC-13) and had their child?s oral cavity examined for caries experience, oral hygiene, developmental defects of enamel, and occlusal problems. This study was approved by the Human Research Ethics Committee of the Universidade Federal de Minas Gerais. The children/adolescents with and without MPS and their mothers were selected in a university hospital. Mothers of children with MPS had lower SOC values [mean: 33.3 (+4.0)/median: 32.0] compared with mothers of children without MPS [mean: 36.9 (+4.5) /median: 37.0] (p<0.001). In the group of children/adolescents with MPS, the mother's SOC values were lower for those children with one or more decayed teeth [31.5 (+3.2)] than for those children/adolescents without decayed teeth [35.7 (+3.8)] (p=0.004). Mother´s SOC values in the group with MPS were lower for those children/adolescents with one or more missing teeth [30.2 (+0.9)] than for those children/adolescents identified without missing teeth [33.8 (+4.1)] (p=0.046). Mothers of children with MPS had lower mother's SOC values. Mother´s of children/adolescents with MPS and dental caries and/or missing teeth had SOC lower values. The study of Mother´s SOC 12 and oral health status of children/adolescents with MPS allows an appropriate approach to the families, especially mothers, and the health professionals who assist them, leading to a better quality of life for these population


Assuntos
Humanos , Masculino , Feminino , Criança , Adolescente , Inquéritos de Saúde Bucal/estatística & dados numéricos , Crianças com Deficiência/estatística & dados numéricos , Pessoas com Deficiência/estatística & dados numéricos , Mucopolissacaridoses/história , Senso de Coerência/classificação , Distribuição por Idade e Sexo , Associação , Estudos Transversais/estatística & dados numéricos , Interpretação Estatística de Dados , Inquéritos e Questionários/estatística & dados numéricos
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