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The use of a natural osteoconductive porous bone mineral (Bio-Oss™) in infrabony periodontal defects

AIM: The aim of the present study was to evaluate the efficacy of a bovine derived xenograft Bio-Oss™ and to compare with open flap debridement in human infrabony periodontal defects. MATERIALS AND METHODS: Twelve healthy patients (5 males, 7 females; aged 30-50 years), with no systemic disease with...

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Autores principales: Gokhale, Shankar T., Dwarakanath, C. D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3459507/
https://www.ncbi.nlm.nih.gov/pubmed/23055593
http://dx.doi.org/10.4103/0972-124X.99270
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author Gokhale, Shankar T.
Dwarakanath, C. D.
author_facet Gokhale, Shankar T.
Dwarakanath, C. D.
author_sort Gokhale, Shankar T.
collection PubMed
description AIM: The aim of the present study was to evaluate the efficacy of a bovine derived xenograft Bio-Oss™ and to compare with open flap debridement in human infrabony periodontal defects. MATERIALS AND METHODS: Twelve healthy patients (5 males, 7 females; aged 30-50 years), with no systemic disease with moderate to severe periodontitis were treated. Surgically defects were included only if presence of two or more vertical osseous defects as verified by radiographs with associated probing pocket depth of ≥5.0 mm following non-surgical therapy. Final selection included 24 defects. The defects were randomly assigned treatment with bovine derived xenograft Bio-Oss™ as experimental sites or open flap debridement as control sites. Soft tissue and hard tissue measurements were recorded on the day of surgery and six months post-operatively. RESULTS: The results showed significant difference statistically between experimental and control sites in all measurements. Soft tissue measurements for the experimental sites included probing pocket depth reduction of 4.33±0.651 mm and attachment gain of 2.92±0.9003 mm, while the control sites showed a probing pocket depth reduction of 2.92±0.669 mm and a attachment gain of 0.583±0.515 mm. Osseous measurements showed bone fill of 1.936±1.046 mm (54.065±12.642%) for experimental sites and 0.02±0.01 mm (0.534±0.384%) for the control sites. Defect resolution was 50.75% for the experimental sites and 5.45% for the control sites. CONCLUSION: Bio-Oss™ is a bone graft material of considerable promise. However, further long term clinical studies with histological evaluation are warranted.
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spelling pubmed-34595072012-10-09 The use of a natural osteoconductive porous bone mineral (Bio-Oss™) in infrabony periodontal defects Gokhale, Shankar T. Dwarakanath, C. D. J Indian Soc Periodontol Original Article AIM: The aim of the present study was to evaluate the efficacy of a bovine derived xenograft Bio-Oss™ and to compare with open flap debridement in human infrabony periodontal defects. MATERIALS AND METHODS: Twelve healthy patients (5 males, 7 females; aged 30-50 years), with no systemic disease with moderate to severe periodontitis were treated. Surgically defects were included only if presence of two or more vertical osseous defects as verified by radiographs with associated probing pocket depth of ≥5.0 mm following non-surgical therapy. Final selection included 24 defects. The defects were randomly assigned treatment with bovine derived xenograft Bio-Oss™ as experimental sites or open flap debridement as control sites. Soft tissue and hard tissue measurements were recorded on the day of surgery and six months post-operatively. RESULTS: The results showed significant difference statistically between experimental and control sites in all measurements. Soft tissue measurements for the experimental sites included probing pocket depth reduction of 4.33±0.651 mm and attachment gain of 2.92±0.9003 mm, while the control sites showed a probing pocket depth reduction of 2.92±0.669 mm and a attachment gain of 0.583±0.515 mm. Osseous measurements showed bone fill of 1.936±1.046 mm (54.065±12.642%) for experimental sites and 0.02±0.01 mm (0.534±0.384%) for the control sites. Defect resolution was 50.75% for the experimental sites and 5.45% for the control sites. CONCLUSION: Bio-Oss™ is a bone graft material of considerable promise. However, further long term clinical studies with histological evaluation are warranted. Medknow Publications & Media Pvt Ltd 2012 /pmc/articles/PMC3459507/ /pubmed/23055593 http://dx.doi.org/10.4103/0972-124X.99270 Text en Copyright: © Journal of Indian Society of Periodontology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Gokhale, Shankar T.
Dwarakanath, C. D.
The use of a natural osteoconductive porous bone mineral (Bio-Oss™) in infrabony periodontal defects
title The use of a natural osteoconductive porous bone mineral (Bio-Oss™) in infrabony periodontal defects
title_full The use of a natural osteoconductive porous bone mineral (Bio-Oss™) in infrabony periodontal defects
title_fullStr The use of a natural osteoconductive porous bone mineral (Bio-Oss™) in infrabony periodontal defects
title_full_unstemmed The use of a natural osteoconductive porous bone mineral (Bio-Oss™) in infrabony periodontal defects
title_short The use of a natural osteoconductive porous bone mineral (Bio-Oss™) in infrabony periodontal defects
title_sort use of a natural osteoconductive porous bone mineral (bio-oss™) in infrabony periodontal defects
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3459507/
https://www.ncbi.nlm.nih.gov/pubmed/23055593
http://dx.doi.org/10.4103/0972-124X.99270
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