RESUMEN
INTRODUCTION: This microsurgical clinical study evaluated if teeth that have undergone endodontic retreatment are associated with more dentinal defects than primary root canal-treated teeth. METHODS: One hundred fifty-five patients who underwent periapical microsurgery treatment in a private practice setting were evaluated. The root ends were resected, and the roots were inspected for the presence of dentinal defects through the surgical operating microscope with the help of a 0.8-mm-diameter light-emitting diode probe light and methylene blue dye. The root canal treatment history (primary vs retreatment) of the teeth was documented and related to the presence or absence of dentinal defects. Bivariate analysis was performed using the chi-square test, and a multivariate analysis was performed using logistic regression to evaluate possible confounding effects of patient age, sex, and tooth location on the association between treatment and the presence of dentinal defects. RESULTS: Of the 155 treated teeth, 33 were excluded (3 fractured and 30 missing treatment history). Of the remaining 122 included teeth, 73 (59.8%) had undergone primary root canal treatment and 49 (40.2%) retreatment. Sixteen teeth (22.5%) of the primary root canal group versus 33 (64.7%) of the retreatment group had dentinal defects. The proportion of retreated teeth with dentinal defects compared with primary treatment was statistically significant (P < .001) with a higher proportion of retreated teeth having dentinal defects. In the multivariate analysis, only the type of treatment was statistically significant (P < .001). CONCLUSIONS: This clinical study showed that root canal-retreated teeth are associated with more dentinal defects than primary root canal-treated teeth.
Asunto(s)
Displasia de la Dentina/epidemiología , Displasia de la Dentina/etiología , Dentina/lesiones , Dentina/patología , Microcirugia , Retratamiento/efectos adversos , Tratamiento del Conducto Radicular/efectos adversos , Ápice del Diente/cirugía , Diente no Vital/patología , Adulto , Femenino , Humanos , Masculino , Materiales de Obturación del Conducto Radicular/efectos adversosRESUMEN
BACKGROUND: Dentinogenesis imperfecta (DGI) is a heritable disorder of dentin. Genetic analyses have found two subgroups in this disorder: DGI type I, a syndromic form associated with osteogenesis imperfecta (OI), and DGI type II, a non-syndromic form. The differential diagnosis between types I and II is often challenging. Thus, the present cross-sectional study had two aims: to (i) investigate the prevalence and incidence of DGI type II among Swedish children and adolescents and (ii) search out undiagnosed cases of DGI type I by documenting the prevalence of clinical symptoms of OI in these individuals. We invited all public and private specialist pediatric dental clinics (n = 47) in 21 counties of Sweden to participate in the study. We then continuously followed up all reported cases during 2014-2017 in order to identify all children and adolescents presenting with DGI type II. Using a structured questionnaire and an examination protocol, pediatric dentists interviewed and examined patients regarding medical aspects such as bruising, prolonged bleeding, spraining, fractures, hearing impairment, and family history of osteoporosis and OI. Joint hypermobility and sclerae were assessed. The clinical oral examination, which included a radiographic examination when indicated, emphasized dental variables associated with OI. RESULTS: The prevalence of DGI type II was estimated to be 0.0022% (95% CI, 0.0016-0.0029%) or 1 in 45,455 individuals. Dental agenesis occurred in 9% of our group. Other findings included tooth retention (17%), pulpal obliteration (100%), and generalized joint hypermobility (30%). Clinical and radiographic findings raised a suspicion of undiagnosed OI in one individual, a 2-year-old boy; he was later diagnosed with OI type IV. CONCLUSIONS: These results show a significantly lower prevalence of DGI type II than previously reported and point to the importance of excluding OI in children with DGI.
Asunto(s)
Dentinogénesis Imperfecta/epidemiología , Adolescente , Adulto , Niño , Preescolar , Tejido Conectivo/patología , Estudios Transversales , Displasia de la Dentina/epidemiología , Displasia de la Dentina/metabolismo , Dentinogénesis Imperfecta/metabolismo , Proteínas de la Matriz Extracelular/metabolismo , Femenino , Enfermedades Genéticas Congénitas/epidemiología , Enfermedades Genéticas Congénitas/metabolismo , Humanos , Incidencia , Lactante , Masculino , Osteogénesis Imperfecta/epidemiología , Osteogénesis Imperfecta/metabolismo , Fosfoproteínas/metabolismo , Sialoglicoproteínas/metabolismo , Encuestas y Cuestionarios , Suecia , Adulto JovenRESUMEN
Se realizó un estudio de prevalencia de anomalías de número de piezas dentarias, con 348 pacientes del Servicio de Ortodoncia del Hospital Base de Los Angeles. Los objetivos planteados fueron: conocer la prevalencia de agenesias y supernumerarios y su distribución según sexo en los pacientes estudiados. En relación a esto, se obtuvo un 8,9 por ciento de anomalías de número y se encontraron proporciones de 7 mujeres por cada 2 hombres en cuanto a la aparición de agenesias y 6 mujeres por cada 4 hombres presentaron supernumerarios, encontrándose cifras similares a las de otros estudios