RESUMEN
Objective: To evaluate the 6-month clinical performance of class I occlusal composite resin restorations through a multicenter, randomized, double-blind, clinical trial. Material and Methods: Two hundred and eighty class I occlusal restorations were performed in 70 patients (aged between 17 to 50 years). The restorations were divided into four groups: G1 (Filtek P60/3M ESPE); G2 (Rok/SDI); G3 (Filtek™ P90/3M ESPE); G4 (Evolux/Dentsply). Two pre-calibrated dental practitioners performed and evaluated the restorative procedures regarding to color match, marginal discoloration, recurrent caries, wear (anatomic form) and marginal integrity according to the USPHS criteria. Results: In 85.8% of the evaluated restorations was observed the ideal score (A) for color match; 91.4% for marginal discoloration; 100% for recurrent caries; 87.7% for wear (anatomic form) and 99.3% for marginal integrity. Conclusion: The composite resins used in this study presented satisfactory and similar clinical performance in a 6-month clinical evaluation. (AU)
Objetivos: Avaliar através de um ensaio clínico randomizado duplo-cego e multicêntrico o desempenho clínico de restaurações classe I oclusais realizadas em dentes posteriores. Material e Métodos: Foram realizadas duzentas e oitenta restaurações em 70 pacientes dos gêneros masculino e feminino (entre 17 e 50 anos). As restaurações foram divididas em 4 grupos: G1 (Filtek P60/3M ESPE); G2 ( Rok/SDI); G3 Filtek TM P90/3M ESPE); G4 (Evolux/Dentsply). Dois operadores précalibrados avaliaram os procedimentos restauradores em relação a reprodução da cor, descoloração marginal, incidência de cárie, desgaste e integridade marginal de acordo com os critérios da USPHS. Resultados: De um total de restaurações avaliadas, 85,8% receberam score ideal (A) para reprodução da cor; 91,4% para descoloração marginal; 100% para incidência de cárie; 87,7% para contorno e 99,3% para integridade marginal. Conclusão: Os materiais empregados neste estudo apresentaram desempenho clínico satisfatório e semelhante após avaliação clínica de 06 meses. (AU)
Asunto(s)
Humanos , Masculino , Femenino , Adolescente , Adulto , Persona de Mediana Edad , Diente Premolar , Resinas Compuestas , Restauración Dental Permanente , Odontología , Maloclusión Clase I de Angle , Diente Molar , Ensayo Clínico Controlado AleatorioRESUMEN
INTRODUCTION: A mandibular setback reduces space in the pharyngeal airway, and it has been suggested that it might induce sleep-disordered breathing. OBJECTIVES: An evidence-based literature review was conducted to identify the effect of mandibular setback on the respiratory function during sleep. METHODS: The authors performed a systematic review of pertinent literature published up to 2014. A structured search of literature was performed, with predefined criteria. A survey of the PubMed, ScienceDirect, and Cochrane database was performed. A manual search of oral and maxillofacial surgery-related journals was accomplished. Potentially relevant studies then had their full-text publication reviewed. RESULTS: A total of 1,780 publications were evaluated, through which nine papers (seven case series and two case-control studies) were selected for the final review. No evidence of sleep disorder after six months was related in 223 patients. In one study, two patients developed obstructive sleep apnea syndrome after surgery, and in another two studies, seven patients presented an increase of obstructive apneas/hypopneas events and oxygen desaturation index. Most of the patients analyzed were young and thin. CONCLUSION: There was no evidence of postoperative sleep apnea syndrome after a mandibular setback surgery. However, one should always consider a potential reduction of the upper airway space during the treatment plan. Obese patients and those submitted to large amounts of mandibular setbacks present a higher chance to develop obstructive sleep apnea syndrome.