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dc.contributor.authorSalomó-Coll, O.
dc.contributor.authorMaté-Sánchez de Val, J. E.
dc.contributor.authorRamírez-Fernández, M. P.
dc.contributor.authorSatorres-Nieto, M.
dc.contributor.authorGargallo-Albiol, J.
dc.contributor.authorCalvo-Guirado, J. L.
dc.date.accessioned2024-01-24T09:33:27Z
dc.date.available2024-01-24T09:33:27Z
dc.date.issued2015
dc.identifier.citationSalomó-Coll, O.; Maté-Sánchez de Val, J. E.; Ramírez-Fernández, M. P. [et al.]. Osseoinductive elements for promoting osseointegration around immediate implants: a pilot study in the foxhound dog. Clinical Oral Implants Research, 2015, 27(12), e167-175. Disponible en: <https://onlinelibrary.wiley.com/doi/10.1111/clr.12596>. Fecha de acceso: 24 ene. 2024. DOI: 10.1111/clr.12596ca
dc.identifier.issn0905-7161ca
dc.identifier.urihttp://hdl.handle.net/20.500.12328/3955
dc.description.abstractObjective: The aim of this study was to evaluate the effects of topical applications of melatonin over implant surfaces placed immediately after extraction by means of histological and histomorphometric analysis of peri-implant tissues. Material and methods: Six American foxhound dogs were used in the study; mandibular premolar distal roots were extracted. Thirty-six immediate conical implants were randomly assigned to the distal site on each site of the mandible in three groups: (Group CI) 12 titanium implants alone; (Group MI) 12 titanium implants supplemented with melatonin; and (Group DI) 12 titanium implants supplemented with vitamin D (DI). Prior to implanting test, implants (MI) were submerged in melatonin 5% solution, and implants from (DI) group were submerged in vitamin D 10% solution. No treatment was applied at control implants. After 12 weeks, animals were sacrificed. Block sections were obtained and processed for mineralized ground sectioning. Bone-to-implant contact (total BIC), new bone formation (NBF), inter-thread bone (ITB) and histological linear measurements (HLM) were analyzed. Results: At 12 weeks, all implants were clinically stable and histologically osseointegrated. Total BIC values were 48.36 ± 7.45* for the MI group and 44.82 ± 10.98 for the CI group (P = 0.035) with statistically significant difference between groups. BIC% were 41.36 ± 3.93 for MI and 41.34 ± 9.26 for CI (P > 0.05). Inter-thread bone formation values were MI 15.99 ± 2.43* and CI 14.79 ± 3.62 (P = 0.03), MI showing significantly better results. No statistically significant differences in peri-implant new bone formation could be found between the two groups: MI 25.37 ± 2.32, CI 26.55 ± 7.75 (P > 0.05). Linear measurements showed that the MI group showed significantly less lingual crestal bone loss (CBL) (MI 0.52 ± 0.74*, CI 0.92 ± 1.98) (P = 0.045) and less lingual peri-implant mucosa (PIM) (MI 3.13 ± 1.41*, CI 3.71 ± 1.81) (P = 0.042). No significant differences were observed in the buccal aspect. Conclusions: Within the limitations of this animal study, the topical application of melatonin improved bone formation around immediate implants and reduced lingual bone and lingual peri-implant mucosa, after 12 weeks of osseointegration.ca
dc.format.extent8ca
dc.language.isoengca
dc.publisherWileyca
dc.relation.ispartofClinical Oral Implants Researchca
dc.relation.ispartofseries27;12
dc.rights© 2015 John Wiley & Sons A/S. Published by John Wiley & Sons Ltdca
dc.subject.otherRemodelació òssiaca
dc.subject.otherImplants dentalsca
dc.subject.otherImplants immediatsca
dc.subject.otherMelatoninaca
dc.subject.otherOsteointegracióca
dc.subject.otherRemodelación óseaca
dc.subject.otherImplantes dentalesca
dc.subject.otherImplantes inmediatosca
dc.subject.otherMelatoninaca
dc.subject.otherOsteointegraciónca
dc.subject.otherBone remodelingca
dc.subject.otherDental implantsca
dc.subject.otherImmediate implantsca
dc.subject.otherMelatoninca
dc.subject.otherOsseointegrationca
dc.titleOsseoinductive elements for promoting osseointegration around immediate implants: a pilot study in the foxhound dogca
dc.typeinfo:eu-repo/semantics/articleca
dc.description.versioninfo:eu-repo/semantics/publishedVersionca
dc.rights.accessLevelinfo:eu-repo/semantics/openAccess
dc.embargo.termscapca
dc.subject.udc616.3ca
dc.identifier.doihttps://dx.doi.org/10.1111/clr.12596ca


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