Abstract
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.
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Conceptualization: J. P. and L. C.; methodology: V. F., B. B., I. G., L. C.; formal analysis and investigation: V. F., L. C., B. B., I. G.; writing—original draft preparation: V. F.; writing—original draft review and editing: L. C. and J. P.; supervision: V. F., L. C. All authors approved the final manuscript.
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The research protocol was approved by the Ethics Committee of Rey Juan Carlos University in Madrid, and the procedures involving human participants were in accordance with Declaration of Helsinki. Written informed consent was obtained from all participants prior to starting the treatment.
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The authors declare no competing interests at the time this study was initiated. The author J. P. has recently become a PI of a clinical trial sponsored by 3M Oral Care.
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Fuentes, M.V., Perdigão, J., Baracco, B. et al. Effect of an additional bonding resin on the 5-year performance of a universal adhesive: a randomized clinical trial. Clin Oral Invest 27, 837–848 (2023). https://doi.org/10.1007/s00784-022-04613-8
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DOI: https://doi.org/10.1007/s00784-022-04613-8