Evaluation of a novel restorative protocol to treat non-carious cervical lesion associated with gingival recession: a 2-year follow-up randomized clinical trial

Detalhes bibliográficos
Autor(a) principal: Mathias-Santamaria, Ingrid Fernandes [UNESP]
Data de Publicação: 2023
Outros Autores: Santamaria, Mauro Pedrine [UNESP], Silveira, Camila Augusto [UNESP], Martinho, Frederico Canato, de Melo, Mary Anne Sampaio, De Marco, Andrea Carvalho [UNESP], Augusto, Marina Gullo, de Andrade, Guilherme Schmitt, Roulet, Jean-François, Bresciani, Eduardo [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1007/s00784-022-04806-1
http://hdl.handle.net/11449/249430
Resumo: Objective: To compare 2 different resin composites and 2 adhesive systems used in a new restorative protocol (partial restoration) to treat non-carious cervical lesions associated with gingival recession type 1 (RT1). Material and methods: Eighty combined defects (CDs) were treated with a partial restoration and periodontal plastic surgery for root coverage. The CDs were randomly assigned to one of the following groups: NP + TE (n = 20), nanofilled composite and 2-step total-etch adhesive system; NP + UA (n = 20), nanofilled composite and universal adhesive system; MH + TE (n = 20), microhybrid composite and 2-step total-etch adhesive; MH + UA (n = 20), microhybrid composite and universal adhesive. Restorations were assessed using the United States Public Health Service (USPHS) criteria at 1 week (baseline) and 6, 12, and 24 months. Survival rate, periodontal parameters, dentin hypersensitivity (DH), and aesthetics were also evaluated. Results: After 24 months, only the MH + TE group did not lose any restoration, with no significant differences between groups. For surface roughness parameter, MH presented 83.3% of the restorations scoring Bravo, whereas NP presented 48.5% of the restorations scoring Bravo. All groups presented restorations with marginal discoloration. All periodontal parameters behaved similarly, regardless of the restorative material. All groups presented significant reductions of dentin hypersensitivity and improved aesthetic perceptions (p < 0.05). Conclusion: Both resin composites and adhesives tested can be combined for partial restorations to treat CDs. Clinical relevance: This new restorative-surgical protocol to treat CDs presents satisfactory outcomes. The partial restorations can be successfully executed with both combinations of adhesives and resin composites evaluated in this investigation. TRN: ClinicalTrial.gov: NCT03215615; registration date July 12, 2017.
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spelling Evaluation of a novel restorative protocol to treat non-carious cervical lesion associated with gingival recession: a 2-year follow-up randomized clinical trialComposite resinDental restoration wearGingival recessionTooth cervixTooth wearObjective: To compare 2 different resin composites and 2 adhesive systems used in a new restorative protocol (partial restoration) to treat non-carious cervical lesions associated with gingival recession type 1 (RT1). Material and methods: Eighty combined defects (CDs) were treated with a partial restoration and periodontal plastic surgery for root coverage. The CDs were randomly assigned to one of the following groups: NP + TE (n = 20), nanofilled composite and 2-step total-etch adhesive system; NP + UA (n = 20), nanofilled composite and universal adhesive system; MH + TE (n = 20), microhybrid composite and 2-step total-etch adhesive; MH + UA (n = 20), microhybrid composite and universal adhesive. Restorations were assessed using the United States Public Health Service (USPHS) criteria at 1 week (baseline) and 6, 12, and 24 months. Survival rate, periodontal parameters, dentin hypersensitivity (DH), and aesthetics were also evaluated. Results: After 24 months, only the MH + TE group did not lose any restoration, with no significant differences between groups. For surface roughness parameter, MH presented 83.3% of the restorations scoring Bravo, whereas NP presented 48.5% of the restorations scoring Bravo. All groups presented restorations with marginal discoloration. All periodontal parameters behaved similarly, regardless of the restorative material. All groups presented significant reductions of dentin hypersensitivity and improved aesthetic perceptions (p < 0.05). Conclusion: Both resin composites and adhesives tested can be combined for partial restorations to treat CDs. Clinical relevance: This new restorative-surgical protocol to treat CDs presents satisfactory outcomes. The partial restorations can be successfully executed with both combinations of adhesives and resin composites evaluated in this investigation. TRN: ClinicalTrial.gov: NCT03215615; registration date July 12, 2017.Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Department of General Dentistry School of Dentistry University of Maryland Baltimore, 650 West Baltimore StreetDepartment of Restorative Dentistry Institute of Science and Technology UNESP - São Paulo State UniversityDepartment of Diagnosis and Surgery Institute of Science and Technology UNESP - São Paulo State UniversityCenter for Oral Health Research College of Dentistry University of KentuckyDepartment of Advanced Oral Sciences and Therapeutics School of Dentistry University of Maryland BaltimoreDepartment of Dentistry School of Dentistry Western Paraná State UniversityDepartment of Restorative Dental Sciences College of Dentistry University of FloridaDepartment of Restorative Dentistry Institute of Science and Technology UNESP - São Paulo State UniversityDepartment of Diagnosis and Surgery Institute of Science and Technology UNESP - São Paulo State UniversityCAPES: Finance Code 001BaltimoreUniversidade Estadual Paulista (UNESP)University of KentuckyWestern Paraná State UniversityUniversity of FloridaMathias-Santamaria, Ingrid Fernandes [UNESP]Santamaria, Mauro Pedrine [UNESP]Silveira, Camila Augusto [UNESP]Martinho, Frederico Canatode Melo, Mary Anne SampaioDe Marco, Andrea Carvalho [UNESP]Augusto, Marina Gullode Andrade, Guilherme SchmittRoulet, Jean-FrançoisBresciani, Eduardo [UNESP]2023-07-29T15:34:55Z2023-07-29T15:34:55Z2023-04-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article1781-1792http://dx.doi.org/10.1007/s00784-022-04806-1Clinical Oral Investigations, v. 27, n. 4, p. 1781-1792, 2023.1436-37711432-6981http://hdl.handle.net/11449/24943010.1007/s00784-022-04806-12-s2.0-85143205766Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengClinical Oral Investigationsinfo:eu-repo/semantics/openAccess2023-07-29T15:34:55Zoai:repositorio.unesp.br:11449/249430Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T14:01:28.137387Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Evaluation of a novel restorative protocol to treat non-carious cervical lesion associated with gingival recession: a 2-year follow-up randomized clinical trial
title Evaluation of a novel restorative protocol to treat non-carious cervical lesion associated with gingival recession: a 2-year follow-up randomized clinical trial
spellingShingle Evaluation of a novel restorative protocol to treat non-carious cervical lesion associated with gingival recession: a 2-year follow-up randomized clinical trial
Mathias-Santamaria, Ingrid Fernandes [UNESP]
Composite resin
Dental restoration wear
Gingival recession
Tooth cervix
Tooth wear
title_short Evaluation of a novel restorative protocol to treat non-carious cervical lesion associated with gingival recession: a 2-year follow-up randomized clinical trial
title_full Evaluation of a novel restorative protocol to treat non-carious cervical lesion associated with gingival recession: a 2-year follow-up randomized clinical trial
title_fullStr Evaluation of a novel restorative protocol to treat non-carious cervical lesion associated with gingival recession: a 2-year follow-up randomized clinical trial
title_full_unstemmed Evaluation of a novel restorative protocol to treat non-carious cervical lesion associated with gingival recession: a 2-year follow-up randomized clinical trial
title_sort Evaluation of a novel restorative protocol to treat non-carious cervical lesion associated with gingival recession: a 2-year follow-up randomized clinical trial
author Mathias-Santamaria, Ingrid Fernandes [UNESP]
author_facet Mathias-Santamaria, Ingrid Fernandes [UNESP]
Santamaria, Mauro Pedrine [UNESP]
Silveira, Camila Augusto [UNESP]
Martinho, Frederico Canato
de Melo, Mary Anne Sampaio
De Marco, Andrea Carvalho [UNESP]
Augusto, Marina Gullo
de Andrade, Guilherme Schmitt
Roulet, Jean-François
Bresciani, Eduardo [UNESP]
author_role author
author2 Santamaria, Mauro Pedrine [UNESP]
Silveira, Camila Augusto [UNESP]
Martinho, Frederico Canato
de Melo, Mary Anne Sampaio
De Marco, Andrea Carvalho [UNESP]
Augusto, Marina Gullo
de Andrade, Guilherme Schmitt
Roulet, Jean-François
Bresciani, Eduardo [UNESP]
author2_role author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Baltimore
Universidade Estadual Paulista (UNESP)
University of Kentucky
Western Paraná State University
University of Florida
dc.contributor.author.fl_str_mv Mathias-Santamaria, Ingrid Fernandes [UNESP]
Santamaria, Mauro Pedrine [UNESP]
Silveira, Camila Augusto [UNESP]
Martinho, Frederico Canato
de Melo, Mary Anne Sampaio
De Marco, Andrea Carvalho [UNESP]
Augusto, Marina Gullo
de Andrade, Guilherme Schmitt
Roulet, Jean-François
Bresciani, Eduardo [UNESP]
dc.subject.por.fl_str_mv Composite resin
Dental restoration wear
Gingival recession
Tooth cervix
Tooth wear
topic Composite resin
Dental restoration wear
Gingival recession
Tooth cervix
Tooth wear
description Objective: To compare 2 different resin composites and 2 adhesive systems used in a new restorative protocol (partial restoration) to treat non-carious cervical lesions associated with gingival recession type 1 (RT1). Material and methods: Eighty combined defects (CDs) were treated with a partial restoration and periodontal plastic surgery for root coverage. The CDs were randomly assigned to one of the following groups: NP + TE (n = 20), nanofilled composite and 2-step total-etch adhesive system; NP + UA (n = 20), nanofilled composite and universal adhesive system; MH + TE (n = 20), microhybrid composite and 2-step total-etch adhesive; MH + UA (n = 20), microhybrid composite and universal adhesive. Restorations were assessed using the United States Public Health Service (USPHS) criteria at 1 week (baseline) and 6, 12, and 24 months. Survival rate, periodontal parameters, dentin hypersensitivity (DH), and aesthetics were also evaluated. Results: After 24 months, only the MH + TE group did not lose any restoration, with no significant differences between groups. For surface roughness parameter, MH presented 83.3% of the restorations scoring Bravo, whereas NP presented 48.5% of the restorations scoring Bravo. All groups presented restorations with marginal discoloration. All periodontal parameters behaved similarly, regardless of the restorative material. All groups presented significant reductions of dentin hypersensitivity and improved aesthetic perceptions (p < 0.05). Conclusion: Both resin composites and adhesives tested can be combined for partial restorations to treat CDs. Clinical relevance: This new restorative-surgical protocol to treat CDs presents satisfactory outcomes. The partial restorations can be successfully executed with both combinations of adhesives and resin composites evaluated in this investigation. TRN: ClinicalTrial.gov: NCT03215615; registration date July 12, 2017.
publishDate 2023
dc.date.none.fl_str_mv 2023-07-29T15:34:55Z
2023-07-29T15:34:55Z
2023-04-01
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/s00784-022-04806-1
Clinical Oral Investigations, v. 27, n. 4, p. 1781-1792, 2023.
1436-3771
1432-6981
http://hdl.handle.net/11449/249430
10.1007/s00784-022-04806-1
2-s2.0-85143205766
url http://dx.doi.org/10.1007/s00784-022-04806-1
http://hdl.handle.net/11449/249430
identifier_str_mv Clinical Oral Investigations, v. 27, n. 4, p. 1781-1792, 2023.
1436-3771
1432-6981
10.1007/s00784-022-04806-1
2-s2.0-85143205766
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.format.none.fl_str_mv 1781-1792
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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