Clinical evaluation of a polyacid-modified resin composite in class V carious lesions: 3-year results.

This study evaluated the three-year clinical performance of Class V restorations made of a polyacid-modified resin composite, Dyract. Ninety-two Class V carious lesions in 28 patients were restored with Dyract. Restorations were clinically evaluated at baseline, first, second, and third year recall visits, according to the modified Ryge criteria by two experienced, calibrated examiners. Retention rate after three years in Class V carious restorations was 92.4%, with only seven failed restorations. Color change and marginal discoloration in restorations were found to be statistically significant (p = 0.013 and p < 0.001, respectively) at the end of third year, but none of the affected restorations required replacement. The results of this study revealed that at the end of three years, Dyract exhibited good clinical success rate but significant color change and marginal discoloration in Class V carious lesions.

Clinical evaluation of a polyacid-modified resin composite (Dyract) in class III cavities: three-year results.

This study evaluated the three-year clinical performance of a polyacid-modified resin composite material, Dyract (DeTrey/Dentsply, Konstanz, Germany), in Class III cavities. Sixty-two Class III cavities in 30 patients were restored with Dyract. Restorations were clinically evaluated at baseline, one-, two- and three-year recalls according to the modified Ryge criteria by two experienced, calibrated examiners. After three years, the retention rate was 96.7%. At the one-year interval, one restoration had to be replaced due to sensitivity. At the two-year recall, one restoration, with a caries lesion adjacent to its margin, was clinically unacceptable and had to be replaced. Except for these two restorations, all other restorations were clinically acceptable in regard to color match, marginal discoloration, wear or loss of anatomical form, caries, marginal adaptation and surface texture after three years. At the end of three years, marginal discoloration was statistically significant (p=0.017) but did not require replacement of any of the restorations. Dyract exhibited significant marginal discoloration after three-year clinical performance in Class III cavities.

Two-year clinical evaluation of Dyract in small Class I cavities.

PURPOSE: To evaluate the 2-year clinical performance of Dyract in small Class I cavities in non stress-bearing areas. MATERIALS AND METHODS: On 36 patients, 87 small cavity preparations were performed. The lesions were diagnosed macroscopically with a probe. They involved fissures, were shallow and had reached dentin but the lateral spread was limited and localized in dentin. Cavities were designed to be on non stress bearing areas. Cavities' average faciolingual widths were prepared to be 1/3 or less than the intercuspal width. At baseline, 1- and 2-year recalls, the restorations were evaluated according to the modified Ryge criteria by two calibrated, experienced examiners. RESULTS: None of the restorations was lost and retention rate was 100% at the end of 1 year. After 2 years, one restoration (1.1%) had to be replaced due to caries lesion adjacent to its margin and the rate of retention was 98.9%. At the 2-year recall, marginal discoloration (rated Bravo) was observed in 19.8% of the restorations but did not require the replacement of any restorations. Except the failed restoration, no other was clinically unacceptable in regard to color match, wear or loss of anatomic form, marginal discoloration, caries, marginal adaptation and surface texture.