A 2-year clinical evaluation of direct and semi-direct resin composite restorations in non-carious cervical lesions: a randomized clinical study
Autor(a) principal: | |
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Data de Publicação: | 2019 |
Outros Autores: | , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.1007/s00784-019-03011-x http://hdl.handle.net/11449/190518 |
Resumo: | Objectives: The purpose of this study was to evaluate the 2-year success of resin composite restorations in non-carious cervical lesions (NCCLs) using the direct or semi-direct techniques. Materials and methods: Thirty volunteers presenting with at least two NCCLs were included. Each participant received one restoration using the direct technique and the other using the semi-direct technique, totaling 60 restorations. Time for completing the treatment was computed. Assessments at baseline, 7 days, and 6, 12, and 24 months were performed using the modified United States Public Health Service criteria. Descriptive analysis was reported as a percentage of successful treatments. For inferential analysis, the Student t test was used to evaluate the differences between extension, depth, and time. The chi-square/Fisher tests were used to compare treatment success after each period (α = 0.05). The results were evaluated by using the Kaplan-Meier survival analysis. Results: Differences were detected regarding mean ± standard deviation time, in which direct and semi-direct procedures were accomplished in 21.8 (± 14.5) and 35.3 (± 19.9) min, respectively. Of the 60 restorations placed, 7 failed in the direct group while 8 failed in the semi-direct group up to 2 years. No differences were detected between restorative protocols. The cumulative survival was 88.5% and 88.4% for the direct technique and semi-direct techniques after 24 months, respectively. Conclusion: The tested restorative protocols present similar results for NCCLs within the studied periods. Clinical relevance: The semi-direct technique exhibited clinical performance similar to direct technique for NCCL, demonstrating an alternative for restorations of these lesions. |
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A 2-year clinical evaluation of direct and semi-direct resin composite restorations in non-carious cervical lesions: a randomized clinical studyComposite resinNon-carious cervical lesionsRandomized clinical trialSemi-direct techniqueObjectives: The purpose of this study was to evaluate the 2-year success of resin composite restorations in non-carious cervical lesions (NCCLs) using the direct or semi-direct techniques. Materials and methods: Thirty volunteers presenting with at least two NCCLs were included. Each participant received one restoration using the direct technique and the other using the semi-direct technique, totaling 60 restorations. Time for completing the treatment was computed. Assessments at baseline, 7 days, and 6, 12, and 24 months were performed using the modified United States Public Health Service criteria. Descriptive analysis was reported as a percentage of successful treatments. For inferential analysis, the Student t test was used to evaluate the differences between extension, depth, and time. The chi-square/Fisher tests were used to compare treatment success after each period (α = 0.05). The results were evaluated by using the Kaplan-Meier survival analysis. Results: Differences were detected regarding mean ± standard deviation time, in which direct and semi-direct procedures were accomplished in 21.8 (± 14.5) and 35.3 (± 19.9) min, respectively. Of the 60 restorations placed, 7 failed in the direct group while 8 failed in the semi-direct group up to 2 years. No differences were detected between restorative protocols. The cumulative survival was 88.5% and 88.4% for the direct technique and semi-direct techniques after 24 months, respectively. Conclusion: The tested restorative protocols present similar results for NCCLs within the studied periods. Clinical relevance: The semi-direct technique exhibited clinical performance similar to direct technique for NCCL, demonstrating an alternative for restorations of these lesions.GAPEC - Academic Group of Clinical Research Department of Restorative Dentistry Institute of Science and Technology São Paulo State University (UNESP), Av. Eng. Francisco José Longo, no. 777GAPEC - Academic Group of Clinical Research Department of Restorative Dentistry Institute of Science and Technology São Paulo State University (UNESP), Av. Eng. Francisco José Longo, no. 777Universidade Estadual Paulista (Unesp)Caneppele, Taciana Marco Ferraz [UNESP]Meirelles, Laura Célia Fernandes [UNESP]Rocha, Rafael Santos [UNESP]Gonçalves, Lucélia Lemes [UNESP]Ávila, Daniele Mara Silva [UNESP]Gonçalves, Sérgio Eduardo de Paiva [UNESP]Bresciani, Eduardo [UNESP]2019-10-06T17:15:51Z2019-10-06T17:15:51Z2019-01-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://dx.doi.org/10.1007/s00784-019-03011-xClinical Oral Investigations.1436-37711432-6981http://hdl.handle.net/11449/19051810.1007/s00784-019-03011-x2-s2.0-8506964046336397201554079180000-0001-9299-8792Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengClinical Oral Investigationsinfo:eu-repo/semantics/openAccess2021-10-23T19:23:45Zoai:repositorio.unesp.br:11449/190518Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T22:19:46.915490Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
A 2-year clinical evaluation of direct and semi-direct resin composite restorations in non-carious cervical lesions: a randomized clinical study |
title |
A 2-year clinical evaluation of direct and semi-direct resin composite restorations in non-carious cervical lesions: a randomized clinical study |
spellingShingle |
A 2-year clinical evaluation of direct and semi-direct resin composite restorations in non-carious cervical lesions: a randomized clinical study Caneppele, Taciana Marco Ferraz [UNESP] Composite resin Non-carious cervical lesions Randomized clinical trial Semi-direct technique |
title_short |
A 2-year clinical evaluation of direct and semi-direct resin composite restorations in non-carious cervical lesions: a randomized clinical study |
title_full |
A 2-year clinical evaluation of direct and semi-direct resin composite restorations in non-carious cervical lesions: a randomized clinical study |
title_fullStr |
A 2-year clinical evaluation of direct and semi-direct resin composite restorations in non-carious cervical lesions: a randomized clinical study |
title_full_unstemmed |
A 2-year clinical evaluation of direct and semi-direct resin composite restorations in non-carious cervical lesions: a randomized clinical study |
title_sort |
A 2-year clinical evaluation of direct and semi-direct resin composite restorations in non-carious cervical lesions: a randomized clinical study |
author |
Caneppele, Taciana Marco Ferraz [UNESP] |
author_facet |
Caneppele, Taciana Marco Ferraz [UNESP] Meirelles, Laura Célia Fernandes [UNESP] Rocha, Rafael Santos [UNESP] Gonçalves, Lucélia Lemes [UNESP] Ávila, Daniele Mara Silva [UNESP] Gonçalves, Sérgio Eduardo de Paiva [UNESP] Bresciani, Eduardo [UNESP] |
author_role |
author |
author2 |
Meirelles, Laura Célia Fernandes [UNESP] Rocha, Rafael Santos [UNESP] Gonçalves, Lucélia Lemes [UNESP] Ávila, Daniele Mara Silva [UNESP] Gonçalves, Sérgio Eduardo de Paiva [UNESP] Bresciani, Eduardo [UNESP] |
author2_role |
author author author author author author |
dc.contributor.none.fl_str_mv |
Universidade Estadual Paulista (Unesp) |
dc.contributor.author.fl_str_mv |
Caneppele, Taciana Marco Ferraz [UNESP] Meirelles, Laura Célia Fernandes [UNESP] Rocha, Rafael Santos [UNESP] Gonçalves, Lucélia Lemes [UNESP] Ávila, Daniele Mara Silva [UNESP] Gonçalves, Sérgio Eduardo de Paiva [UNESP] Bresciani, Eduardo [UNESP] |
dc.subject.por.fl_str_mv |
Composite resin Non-carious cervical lesions Randomized clinical trial Semi-direct technique |
topic |
Composite resin Non-carious cervical lesions Randomized clinical trial Semi-direct technique |
description |
Objectives: The purpose of this study was to evaluate the 2-year success of resin composite restorations in non-carious cervical lesions (NCCLs) using the direct or semi-direct techniques. Materials and methods: Thirty volunteers presenting with at least two NCCLs were included. Each participant received one restoration using the direct technique and the other using the semi-direct technique, totaling 60 restorations. Time for completing the treatment was computed. Assessments at baseline, 7 days, and 6, 12, and 24 months were performed using the modified United States Public Health Service criteria. Descriptive analysis was reported as a percentage of successful treatments. For inferential analysis, the Student t test was used to evaluate the differences between extension, depth, and time. The chi-square/Fisher tests were used to compare treatment success after each period (α = 0.05). The results were evaluated by using the Kaplan-Meier survival analysis. Results: Differences were detected regarding mean ± standard deviation time, in which direct and semi-direct procedures were accomplished in 21.8 (± 14.5) and 35.3 (± 19.9) min, respectively. Of the 60 restorations placed, 7 failed in the direct group while 8 failed in the semi-direct group up to 2 years. No differences were detected between restorative protocols. The cumulative survival was 88.5% and 88.4% for the direct technique and semi-direct techniques after 24 months, respectively. Conclusion: The tested restorative protocols present similar results for NCCLs within the studied periods. Clinical relevance: The semi-direct technique exhibited clinical performance similar to direct technique for NCCL, demonstrating an alternative for restorations of these lesions. |
publishDate |
2019 |
dc.date.none.fl_str_mv |
2019-10-06T17:15:51Z 2019-10-06T17:15:51Z 2019-01-01 |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1007/s00784-019-03011-x Clinical Oral Investigations. 1436-3771 1432-6981 http://hdl.handle.net/11449/190518 10.1007/s00784-019-03011-x 2-s2.0-85069640463 3639720155407918 0000-0001-9299-8792 |
url |
http://dx.doi.org/10.1007/s00784-019-03011-x http://hdl.handle.net/11449/190518 |
identifier_str_mv |
Clinical Oral Investigations. 1436-3771 1432-6981 10.1007/s00784-019-03011-x 2-s2.0-85069640463 3639720155407918 0000-0001-9299-8792 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Clinical Oral Investigations |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.source.none.fl_str_mv |
Scopus reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
Repositório Institucional da UNESP |
collection |
Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
|
_version_ |
1808129415661486080 |