الفهرس | Only 14 pages are availabe for public view |
Abstract The continuous research of dental materials resulted in the evolution of bioactive materials over the past three decades from just relatively specialized, highly biocompatible but low strength materials to the currently known products with advanced formulations for expanded clinical uses in restorative dentistry. BiodentineTM was one of those products. It is classified as a calcium silicate based material and is considered to be the newer sister product of MTA which somehow is categorized similarly. The use of BiodentineTM in pediatric dentistry was just vague prior to the initiation of this study. Its similarity to MTA was a motive for us as researchers to investigate its performance as a pulp dressing in primary teeth. Moreover, partial pulpotomy technique in primary molars was revisited using BiodentineTM. The current study was composed of two corresponding, in vivo and in vitro studies. In the in vivo study, a total of twenty seven patients between ages of 4-7 years old were selected from the outpatient clinic of Pediatric Dentistry Department, Faculty of Dentistry, Ain Shams University from which 45 teeth were recruited following the inclusion criteria adopted by the study. Teeth were randomly allocated into four groups and received treatment accordingly. group (I) -BiodentineTM Partial Pulpotomy group (II) -Calcium Hydroxide Partial Pulpotomy group (III)-Formocresol Complete Pulpotomy group (IV)-BiodentineTM Complete Pulpotomy Follow up appointments were given at 6 months, 12 months, and 18 months to evaluate the clinical and radiographic success according to the criteria proposed by Agamy et al. and Vargas et al. 98, 102 A binary scoring system was employed to record any failures. Statistical analysis of the tabulated scores was performed using Kruskal–Wallis followed by Mann-Whitney U, revealing the superiority of BiodentineTM in both complete and partial pulpotomy in primary teeth versus FC complete pulpotomy and CH partial pulpotomy. Steep deterioration in the clinical performance of the CH partial pulpotomy group was detected at 6, 12, and 18 months. In the in vitro study, a total of fifteen sound human premolars which were freshly extracted for orthodontic reasons were collected from the Department of Maxillo-facial and Oral surgery, Faculty of Dentistry, Ain shams University and were utilized in this study. Teeth were divided into two groups and restored by BiodentineTM and glass ionomer. They were stored in distilled water for 24 hours and then dyed using 1% methylene blue solution. Teeth were sectioned bucco-lingually and examined for microleakage implementing Ghasemi et al. criteria, using a stereo light microscope.103 Scores were tabulated and statistically analyzed. The results revealed that there was no significant difference between both BiodentineTM and conventional glass ionomer as a dentine replacement material. |