ABSTRACT
AIMS: This study aims to provide a comprehensive review and case study about the advantages and disadvantages of the application of digital technologies in presurgical orthopedics in newborns/infants with cleft lip and palate (CLCP). Positive changes in the nasal anatomy, maxillary arch, and cleft width could be achieved. METHODS: Three representative cases of newborns/infants with CLCP were managed using the presurgical newborn/infant orthopedics (PSIO) approach. The patients were diagnosed and treated. Detailed descriptions of the impression procedures and PSIO appliance construction and placement were provided for each case. RESULTS: Case 1 utilized traditional impression techniques, Case 2 employed a semi-digitalized approach with intraoral digital scanning, and Case 3 utilized a completely digitalized method for appliance construction. Positive changes in maxillary arch dimensions and cleft width reduction were observed in all cases. CONCLUSIONS: The management of CLCP in newborns and infants poses a complex challenge with profound implications. The PSIO approach not only facilitates reconstructive surgery but also enhances overall quality of life. Digital tools, like specialized optical scanners and 3D printing, revolutionize the PSIO process, making it more efficient and patient-friendly. Clinical benefits include improved facial morphology, esthetics, feeding, speech, and optimized future surgical results. Despite ongoing efficacy debates, global adoption as the initial surgical approach underscores its value. The integration of digital technologies offers new hope for patients and families, promising a brighter future for those affected by this congenital condition.
Subject(s)
Cleft Lip , Cleft Palate , Nasoalveolar Molding , Humans , Infant , Infant, Newborn , Cleft Lip/surgery , Cleft Palate/surgery , Dental Impression Technique , Preoperative CareABSTRACT
BACKGROUND: Esophageal Atresia (EA) is defined as the congenital interruption of the continuity of the esophagus. Pediatric patients also have other congenital conditions, such as Tracheo-Esophageal Fistula (TEF). CASE REPORT: A 7-year-old male with TEF referred by a Pediatric Cardiologist, with the principal complaint of "severe and generalized tooth wearing". Considering that the patient was systemically stable, it was decided to perform the oral procedures under local anesthesia and rubber-dam isolation with an antimicrobial prophylaxis regimen. The treatment consisted of the extraction of all maxillary primary incisors and canines and both first molars; in the mandibular arch, only the lower second right molar was extracted, and a distal shoe was placed. Pulpotomies were performed and preformed metallic crowns were placed on the remaining second primary molars, on both lower first molars, and on lower canines and lateral incisors. Finally, a fixed prosthesis was positioned in the upper arch, and cemented through orthodontic bands adapted to both crowned second molars. The patient has been maintained under close medical and dental control. The child showed satisfactory oral conditions, and the vomiting episodes had decreased significantly. CONCLUSIONS: Dentists can learn and then participate in the integral health management of infants and young children affected with EA/TEF, particularly those with dental erosion.
Subject(s)
Dental Care , Esophageal Atresia/complications , Gastroesophageal Reflux/complications , Tracheoesophageal Fistula/complications , Child , Humans , MaleABSTRACT
La esclerodermia es una rara enfermedad que afecta los tejidos de origen mesenquimatoso y ectodérmico. Se caracteriza por la aparición de alteraciones inflamatorias y vasculares, además de esclerosis en la piel y órganos de los sistemas respiratorio, cardiovascular y gastrointestinal. El propósito del presente reporte es describir el caso de una niña de 4 años con esclerodermia localizada, sus manifestaciones clínicas, datos epidemiológicos y sugerencias de manejo odontológico de los pacientes pediátricos con esta rara enfermedad.
Scleroderma is a rare disorder that affects mesenchymal and ectodermal tissues. It is characterized of vascular and inflammatory alterations and sclerosis in the skin and organs of respiratory, cardiovascular and gastrointestinal systems. The purpose of this report is to describe the case of a 4 year old girl with localized scleroderma, its clinical manifestations, epidemiological data and recommendations of dental management for the pediatric patients with this rare disease.
Subject(s)
Humans , Female , Child, Preschool , Scleroderma, Localized , Patient Care Management , Case ManagementABSTRACT
El presente es el reporte de un caso de un niño de 5 años 4 meses de edad que exhibía un patrón de caries dental de la infancia temprana severa no tratada oportunamente, debido a ignorancia y posible negligencia por parte de los padres. Se describe el proceso diagnóstico y el tratamiento brindado al paciente y el manejo preventivo que se instituyó a corto, mediano y largo plazo.
This case report is of a 5 years 4 months old male patient who exhibited a pattern of severe dental early caries childhood not treated in a timely manner, due to parent ignorance and possible negligence. The diagnostic process, treatment provided to the patient, and instituted preventive management in the short, medium and long term, are described.
