Evaluation of a novel restorative protocol to treat non-carious cervical lesion associated with gingival recession: a 2-year follow-up randomized clinical trial
Autor(a) principal: | |
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Data de Publicação: | 2023 |
Outros Autores: | , , , , , , , , |
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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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 |
|
_version_ |
1808128305930436608 |