dc.creatorABUCHAIM, Clarisse
dc.creatorROTTA, Marina
dc.creatorGRANDE, Rosa Helena Miranda
dc.creatorLOGUERCIO, Alessandro Dourado
dc.creatorREIS, Alessandra
dc.date.accessioned2012-03-26T20:32:38Z
dc.date.accessioned2018-07-04T14:21:47Z
dc.date.available2012-03-26T20:32:38Z
dc.date.available2018-07-04T14:21:47Z
dc.date.created2012-03-26T20:32:38Z
dc.date.issued2010
dc.identifierBrazilian Oral Research, v.24, n.3, p.361-367, 2010
dc.identifier1806-8324
dc.identifierhttp://producao.usp.br/handle/BDPI/11257
dc.identifier10.1590/S1806-83242010000300017
dc.identifierhttp://www.scielo.br/scielo.php?script=sci_arttext&pid=S1806-83242010000300017
dc.identifierhttp://www.scielo.br/pdf/bor/v24n3/v24n3a17.pdf
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1609056
dc.description.abstractThe objective of this study was to evaluate the effectiveness of a therapeutic sealant to arrest non-cavitated proximal carious lesion progression. The study population comprised 44 adolescents who had bitewing radiographs taken for caries diagnosis. Non-cavitated lesions extending up to half of dentin thickness were included in the sample. In the experimental group (n = 33), the proximal caries-lesion surfaces were sealed with an adhesive (OptiBond Solo, Kerr) after tooth separation. The control group (n = 11) received no treatment, except for oral hygiene instructions including use of dental floss. Follow-up radiographs were taken after one year and were analyzed in comparison with baseline radiographs. In a blind study setting, visual readings were performed by two examiners, blinded to whether the examined radiograph was baseline or follow-up, and whether it concerned a test or control lesion. The efficacy of sealing treatment was evaluated by the McNemar test (0.05). About 22% of the sealed lesions showed reduction, 61% showed no change and 16% showed progression. For the control lesions, the corresponding values were 27%, 36% and 36% respectively. The number of lesions that showed reduction and no changes were merged and therefore 83.3% of the sealed lesions and 63.6% of the control lesions were considered clinically successful. No statistical significance was detected (p > 0.05). In the course of 1 year, sealing proximal caries lesions was not shown to be superior to lesion monitoring.
dc.languageeng
dc.publisherSociedade Brasileira de Pesquisa Odontológica
dc.relationBrazilian Oral Research
dc.rightsCopyright Sociedade Brasileira de Pesquisa Odontológica
dc.rightsopenAccess
dc.subjectDentin-bonding agents
dc.subjectDental caries
dc.subjectDental bonding
dc.subjectClinical trial
dc.titleEffectiveness of sealing active proximal caries lesions with an adhesive system: 1-year clinical evaluation
dc.typeArtículos de revistas


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