A 2-year clinical evaluation of direct and semi-direct resin composite restorations in non-carious cervical lesions: a randomized clinical study

Detalhes bibliográficos
Autor(a) principal: Caneppele, Taciana Marco Ferraz [UNESP]
Data de Publicação: 2019
Outros Autores: 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]
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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spelling 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
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