dc.creator | ABUCHAIM, Clarisse | |
dc.creator | ROTTA, Marina | |
dc.creator | GRANDE, Rosa Helena Miranda | |
dc.creator | LOGUERCIO, Alessandro Dourado | |
dc.creator | REIS, Alessandra | |
dc.date.accessioned | 2012-03-26T20:32:38Z | |
dc.date.accessioned | 2018-07-04T14:21:47Z | |
dc.date.available | 2012-03-26T20:32:38Z | |
dc.date.available | 2018-07-04T14:21:47Z | |
dc.date.created | 2012-03-26T20:32:38Z | |
dc.date.issued | 2010 | |
dc.identifier | Brazilian Oral Research, v.24, n.3, p.361-367, 2010 | |
dc.identifier | 1806-8324 | |
dc.identifier | http://producao.usp.br/handle/BDPI/11257 | |
dc.identifier | 10.1590/S1806-83242010000300017 | |
dc.identifier | http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1806-83242010000300017 | |
dc.identifier | http://www.scielo.br/pdf/bor/v24n3/v24n3a17.pdf | |
dc.identifier.uri | http://repositorioslatinoamericanos.uchile.cl/handle/2250/1609056 | |
dc.description.abstract | The 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.language | eng | |
dc.publisher | Sociedade Brasileira de Pesquisa Odontológica | |
dc.relation | Brazilian Oral Research | |
dc.rights | Copyright Sociedade Brasileira de Pesquisa Odontológica | |
dc.rights | openAccess | |
dc.subject | Dentin-bonding agents | |
dc.subject | Dental caries | |
dc.subject | Dental bonding | |
dc.subject | Clinical trial | |
dc.title | Effectiveness of sealing active proximal caries lesions with an adhesive system: 1-year clinical evaluation | |
dc.type | Artículos de revistas | |