The use of solvent-preserved human and bovine cancellous bone blocks for lateral defect augmentation - an experimental controlled study in vivo

Abstract Background The aim of this study was to compare new bone formation, resorbed bone matrix, and fibrous enclosed residual bone substitute material in laterally augmented alveolar bone defects using allogeneic, pre-treated and cleaned human bone blocks (tested in dogs, therefore considered to...

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Main Authors: Lara Schorn, Tim Fienitz, Kathrin Berndsen, Norbert R. Kübler, Henrik Holtmann, Daniel Rothamel
Format: Article
Language:English
Published: BMC 2021-06-01
Series:Head & Face Medicine
Subjects:
Online Access:https://doi.org/10.1186/s13005-021-00275-1
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spelling doaj-4da8924d389541fd897becc99574d1f12021-07-04T11:13:36ZengBMCHead & Face Medicine1746-160X2021-06-011711910.1186/s13005-021-00275-1The use of solvent-preserved human and bovine cancellous bone blocks for lateral defect augmentation - an experimental controlled study in vivoLara Schorn0Tim Fienitz1Kathrin Berndsen2Norbert R. Kübler3Henrik Holtmann4Daniel Rothamel5Department of Oral, Maxillofacial and Facial Plastic Surgery, University Hospital DuesseldorfDepartment of Oral Surgery, University Hospital DuesseldorfDepartment of Oral, Maxillofacial and Facial Plastic Surgery, University Hospital CologneDepartment of Oral, Maxillofacial and Facial Plastic Surgery, University Hospital DuesseldorfDepartment of Oral, Maxillofacial and Facial Plastic Surgery, Evangelisches Krankenhaus BethesdaDepartment of Oral, Maxillofacial and Facial Plastic Surgery, University Hospital DuesseldorfAbstract Background The aim of this study was to compare new bone formation, resorbed bone matrix, and fibrous enclosed residual bone substitute material in laterally augmented alveolar bone defects using allogeneic, pre-treated and cleaned human bone blocks (tested in dogs, therefore considered to be xenogeneic), and pre-treated and cleaned bovine cancellous bone blocks, both with and without a collagen membrane in order to evaluate their augmentative potential. Methods Thirty-two critical size horizontal defects were prepared in the mandible of 4 adult foxhound dogs (8 per dog, 4 on each side). After 3 months of healing, the defects were laterally augmented in a split-mouth-design with either human (HXB) or bovine solvent-preserved bone blocks (BXB). Afterwards, defects were randomly covered with a bovine collagenous membrane (HXB + M, BXB + M). After a healing interval of 6 months, percentages of new bone formation, resorbed bone matrix, and fibrous enclosed residual bone substitute material were compared. Results Results showed little new bone formation of up to 3.7 % in human bone blocks (HXB 3.7 % ± 10.2, HXB + M 0.3 %± 0.4, BXB, 0.1 % ± 0.8, BXB + M 2.6 % ± 3.2, p = > 0.05). Percentages of fibrous encapsulation were higher in human bone blocks than in bovine bone blocks (HXB 71.2 % ± 8.6, HXB + M 73.71 % ± 10.6, BXB, 60.5 % ± 27.4, BXB + M 52.5 % ± 28.4, p = > 0.05). Resorption rates differed from 44.8 % in bovine bone blocks covered with a membrane to 17.4 % in human bone blocks (HXB 17.4 % ± 7.4, HXB + M 25.9 % ± 10.7, BXB, 38.4 % ± 27.2, BXB + M 44.8 % ± 29.6, p = > 0.05). The use of additional membranes did not significantly affect results. Conclusions Within its limitations, results of this study suggest that solvent-preserved xenogenic human and bovine bone blocks are not suitable for lateral bone augmentation in dogs. Furthermore, defect coverage with a membrane does not positively affect the outcome.https://doi.org/10.1186/s13005-021-00275-1Lateral bone augmentationHorizontal defectsSolvent-preserved boneXenogeneic bone augmentationCritical size defects
collection DOAJ
language English
format Article
sources DOAJ
author Lara Schorn
Tim Fienitz
Kathrin Berndsen
Norbert R. Kübler
Henrik Holtmann
Daniel Rothamel
spellingShingle Lara Schorn
Tim Fienitz
Kathrin Berndsen
Norbert R. Kübler
Henrik Holtmann
Daniel Rothamel
The use of solvent-preserved human and bovine cancellous bone blocks for lateral defect augmentation - an experimental controlled study in vivo
Head & Face Medicine
Lateral bone augmentation
Horizontal defects
Solvent-preserved bone
Xenogeneic bone augmentation
Critical size defects
author_facet Lara Schorn
Tim Fienitz
Kathrin Berndsen
Norbert R. Kübler
Henrik Holtmann
Daniel Rothamel
author_sort Lara Schorn
title The use of solvent-preserved human and bovine cancellous bone blocks for lateral defect augmentation - an experimental controlled study in vivo
title_short The use of solvent-preserved human and bovine cancellous bone blocks for lateral defect augmentation - an experimental controlled study in vivo
title_full The use of solvent-preserved human and bovine cancellous bone blocks for lateral defect augmentation - an experimental controlled study in vivo
title_fullStr The use of solvent-preserved human and bovine cancellous bone blocks for lateral defect augmentation - an experimental controlled study in vivo
title_full_unstemmed The use of solvent-preserved human and bovine cancellous bone blocks for lateral defect augmentation - an experimental controlled study in vivo
title_sort use of solvent-preserved human and bovine cancellous bone blocks for lateral defect augmentation - an experimental controlled study in vivo
publisher BMC
series Head & Face Medicine
issn 1746-160X
publishDate 2021-06-01
description Abstract Background The aim of this study was to compare new bone formation, resorbed bone matrix, and fibrous enclosed residual bone substitute material in laterally augmented alveolar bone defects using allogeneic, pre-treated and cleaned human bone blocks (tested in dogs, therefore considered to be xenogeneic), and pre-treated and cleaned bovine cancellous bone blocks, both with and without a collagen membrane in order to evaluate their augmentative potential. Methods Thirty-two critical size horizontal defects were prepared in the mandible of 4 adult foxhound dogs (8 per dog, 4 on each side). After 3 months of healing, the defects were laterally augmented in a split-mouth-design with either human (HXB) or bovine solvent-preserved bone blocks (BXB). Afterwards, defects were randomly covered with a bovine collagenous membrane (HXB + M, BXB + M). After a healing interval of 6 months, percentages of new bone formation, resorbed bone matrix, and fibrous enclosed residual bone substitute material were compared. Results Results showed little new bone formation of up to 3.7 % in human bone blocks (HXB 3.7 % ± 10.2, HXB + M 0.3 %± 0.4, BXB, 0.1 % ± 0.8, BXB + M 2.6 % ± 3.2, p = > 0.05). Percentages of fibrous encapsulation were higher in human bone blocks than in bovine bone blocks (HXB 71.2 % ± 8.6, HXB + M 73.71 % ± 10.6, BXB, 60.5 % ± 27.4, BXB + M 52.5 % ± 28.4, p = > 0.05). Resorption rates differed from 44.8 % in bovine bone blocks covered with a membrane to 17.4 % in human bone blocks (HXB 17.4 % ± 7.4, HXB + M 25.9 % ± 10.7, BXB, 38.4 % ± 27.2, BXB + M 44.8 % ± 29.6, p = > 0.05). The use of additional membranes did not significantly affect results. Conclusions Within its limitations, results of this study suggest that solvent-preserved xenogenic human and bovine bone blocks are not suitable for lateral bone augmentation in dogs. Furthermore, defect coverage with a membrane does not positively affect the outcome.
topic Lateral bone augmentation
Horizontal defects
Solvent-preserved bone
Xenogeneic bone augmentation
Critical size defects
url https://doi.org/10.1186/s13005-021-00275-1
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