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A randomised trial of the bone formation after maxillary sinus floor augmentation with bovine hydroxyapatite (Cerabone®) and Photobiomodulation: histomorphometric and immunohistochemical analysis

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A randomised trial of the bone formation after maxillary sinus floor augmentation with bovine hydroxyapatite (Cerabone®) and Photobiomodulation: histomorphometric and immunohistochemical analysis

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dc.contributor.author Klassmann, Fabio-André es
dc.contributor.author Ervolino, Edilson es
dc.contributor.author Klüppel, Leandro Eduardo es
dc.contributor.author Theodoro, Letícia H. es
dc.contributor.author Mulinari-Santos, Gabriel es
dc.contributor.author Garcia, Valdir G. es
dc.date.accessioned 2023-09-25T11:11:33Z
dc.date.available 2023-09-25T11:11:33Z
dc.date.issued 2023 es
dc.identifier.citation Klassmann, F., Ervolino, E., Klüppel, L. E., Theodoro, L. H., Mulinari-Santos, G., & Garcia, V. G. (2023). A randomised trial of the bone formation after maxillary sinus floor augmentation with bovine hydroxyapatite (cerabone®) and photobiomodulation: Histomorphometric and immunohistochemical analysis. Journal of Clinical and Experimental Dentistry, 15(7), 542-550 es
dc.identifier.uri https://hdl.handle.net/10550/89582
dc.description.abstract The use of non-autogenous biomaterial to increase bone height in the maxillary sinus has been shown to be effective, but the results are still inconclusive.Eight participants were selected and included in the research. After surgical access with osteotomy on the lateral wall of both maxillary sinuses, these were filled with Cerabone®. Then, by blind randomization, they received one of the following treatments: Filling with Cerabone® (Control group); treatment with Photobiomodulation (PBM), filling with Cerabone® and treatment with low-power laser (PBM group). Biopsies were obtained 30 days after the surgery, using a 2.8 mm internal diameter trephine bur. Qualitative and quantitative histological analyzes were performed and immunohistochemical analyzes of osteocalcin (OCN) and tartrate-resistant acid phosphatase (TRAP) were performed with scores for each of the biological events.The Cerabone® biomaterial demonstrated a high degree of biocompatibility. New bone formation was observed in both groups. In the PBM group, there was greater bone formation and newly formed tissue in an advanced state of bone maturation. The immunostaining of OCN was greater at 30 days in the PBM group than in the control. There was no significant difference in TRAP immunostaining at 30 days between the groups.Low-power laser-mediated by PBM promoted greater bone formation; the newly formed tissue showed a more advanced state of bone maturation in maxillary sinuses filled with Cerabone® biomaterial and treatment with PBM, within the 30-day evaluation period. es
dc.subject Sinus floor augmentation es
dc.subject dental implants es
dc.subject bone and bones es
dc.subject low-level light therapy es
dc.title A randomised trial of the bone formation after maxillary sinus floor augmentation with bovine hydroxyapatite (Cerabone®) and Photobiomodulation: histomorphometric and immunohistochemical analysis es
dc.type journal article es_ES
dc.subject.unesco UNESCO:CIENCIAS MÉDICAS es
dc.identifier.doi 10.4317/jced.60594 es
dc.type.hasVersion VoR es_ES
dc.identifier.url http://www.medicinaoral.com/medoralfree01/aop/60594.pdf

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