Examinando por Autor "GIRALDEZ, ISABEL"

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Clinical Evaluation of a Low-shrinkage Composite in Posterior Restorations: One-Year Results
(MERIDIAN ALLEN PRESS, 2012-03) BARACCO, BRUNO; PERDIGAO, JORGE; CABRERA, ELENA; GIRALDEZ, ISABEL; CEBALLOS, LAURA
Objectives: The aim of this study was to compare the one-year clinical performance of three restorative systems, which included a novel low-shrinkage composite and two bonding strategies. Materials and Methods: Twenty-five patients received three Class I (occlusal) or Class II restorations performed with one of three restorative systems: Filtek Silorane Restorative System (FS); Adper Scotchbond 1 XT, a two-step etch-and-rinse adhesive, with Filtek Z250 (XT); and Adper Scotchbond SE, a two-step self-etch adhesive, with Filtek Z250 (SE). All materials were applied following the manufacturer’s instructions. Two independent observers evaluated the restorations at baseline, after six months, and after one year, according to the United States Public Health System modified criteria. The Kruskal-Wallis test and the Mann-Whitney U-test were computed to compare the behavior of the restorative systems; Friedman and Wilcoxon tests were used to analyze the intrasystem data (a=0.05). Results: All restorations were evaluated at one year. FS and XT performed statistically similarly at one year, but marginal staining for SE was statistically worse. Intrasystem comparisons between baseline and one year also showed deterioration of marginal staining for SE, while a deterioration of the marginal adaptation was recorded for both SE and FS. XT was the only system for which there was no statistical change of the parameters measured in this study. Conclusions: Both restorative systems using self-etch adhesives showed a tendency to degradation of marginal adaptation after one year of clinical use, compared to baseline values. Although the clinical performance of FS was deemed acceptable after one year, this study did not find any advantage of the silorane based composite over the methacrylate-based composite. The low-shrinkage associated with FS may not be a determinant factor for clinical success.
Effect of a hydrophobic bonding resin on the 36-month performance of a universal adhesive—a randomized clinical trial
(SPRINGER, 2020) PERDIGAO, JORGE; CEBALLOS, LAURA; GIRALDEZ, ISABEL; BARACCO, BRUNO; FUENTES, M VICTORIA
Objectives To evaluate if the addition of a layer of a hydrophobic bonding resin to the recommended application sequence of a universal adhesive improves the respective clinical behavior in non-carious cervical lesions (NCCLs) after 36 months. Materials and methods Scotchbond Universal Adhesive (SBU, 3M Oral Care) was applied in NCCLs of 39 subjects using four adhesion strategies: (1) three-step ER (etch-and-rinse), (2) two-step ER, (3) two-step SE (self-etch), and (4) one-step SE. An extra layer of a hydrophobic bonding resin was applied for strategies three-step ER and two-step SE. The same composite resin (Filtek Supreme XTE, 3MOral Care) was used for all strategies. Restorations were evaluated at baseline and 18 and 36months using the modified United States Public Health Service (USPHS) criteria. Kruskal–Wallis, Mann–Whitney U, Friedman, and Wilcoxon non-parametric tests were computed. Results The cumulative failure rate was 8.6%. The 36-month retention rates were 100%for both 3-ER and 2-ER, 76.0%for 2-SE, and 86.2% for 1-SE. A lower retention rate was observed for two-step SE at 36 months compared with both three-ER (p < 0.01) and two-ER (p < 0.01). Identical retention rates were measured for the two SE groups. When retention rate was compared at baseline versus 36 months for each adhesion strategy, a significant decrease was observed for 2-SE. The restorations performed with 3-ER, 2-SE, and 1-SE had a significant deterioration in marginal discoloration at the 18-month recall. Conclusions The 36-month clinical performance of Scotchbond Universal Adhesive improved for both etch-and-rinse strategies. Clinical relevance Phosphoric acid etching is still recommended to provide retention to composite restorations in NCCLs.
Effect of an additional bonding resin on the 5‑year performance of a universal adhesive: a randomized clinical trial
(SPRINGER, 2023-02) FUENTES, M VICTORIA; PERDIGAO, JORGE; BARACCO, BRUNO; GIRALDEZ, ISABEL; CEBALLOS, LAURA
Objectives To evaluate the effect of the application of an additional hydrophobic bonding resin on the clinical performance of a universal adhesive applied in etch-and-rinse (ER) or self-etch adhesive (SE) strategy in non-carious cervical lesions (NCCLs) after 5 years. Materials and methods Scotchbond Universal Adhesive (3M Oral Care) was applied in 134 NCCLs of 39 subjects using different adhesion approaches: 3-step ER (3-ER), 2-step ER (2-ER), 2-step SE (2-SE), and 1-step SE (1-SE). Enamel and dentin were acid etched prior to application of the universal adhesive for the 3-ER and 2-ER groups. An extra layer of a hydrophobic bonding resin was applied for groups 3-ER and 2-SE. All lesions were restored with Filtek Supreme XTE resin composite (3M Oral Care). Restorations were evaluated at baseline and at 5 years using the modified USPHS criteria. Mann–Whitney U and Wilcoxon tests were performed, and the survival rates (retention/fracture) were analyzed using Kaplan–Meier and log-rank tests (p < 0.05). Results The recall rate was 66.7% at 5 years. The cumulative survival rate was 96.9% for 3-ER, 96.8% for 2-ER, 71.4% for 2-SE, and 81.3% for 1-SE strategies. The log-rank test was statistically significant (p = 0.006). Retention rates were 100% for both ER groups, 75% for 2-SE and 81.3% for 1-SE. At 5 years, 2- and 1-SE approaches showed similar retention rates, but lower than those for 3- and 2-ER. A significant decrease in retention rate was detected for 2-SE (p = 0.007) and 1-SE (p = 0.014) groups between baseline and 5 years. All groups, except 2-ER, showed an increase in marginal discoloration. For this parameter, significant differences were detected between 2-ER and 1-SE (p = 0.004). Conclusions The addition of a hydrophobic bonding resin to the recommended application sequence of Scotchbond Universal Adhesive did not improve its clinical performance in NCCLs after 5 years. Higher retention rates were measured when this adhesive was applied in ER mode. Trial registration This manuscript is a 5-year follow-up of a randomized clinical trial that started in 2012 when there was no strong recommendation for registration in clinicaltrials.gov. The results after 36 months of clinical service were previously published in this journal.