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The effect of three hemostatic agents on early bone healing in an animal model
BACKGROUND: Resorbable bone hemostasis materials, oxidized regenerated cellulose (ORC) and microfibrillar collagen (MFC), remain at the site of application for up to 8 weeks and may impair osteogenesis. Our experimental study compared the effect of a water-soluble alkylene oxide copolymer (AOC) to O...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3009953/ https://www.ncbi.nlm.nih.gov/pubmed/21167039 http://dx.doi.org/10.1186/1471-2482-10-37 |
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author | Armstrong, Jonathan K Han, Bo Kuwahara, Kenrick Yang, Zhi Magyar, Clara E Dry, Sarah M Atti, Elisa Tetradis, Sotirios Fisher, Timothy C |
author_facet | Armstrong, Jonathan K Han, Bo Kuwahara, Kenrick Yang, Zhi Magyar, Clara E Dry, Sarah M Atti, Elisa Tetradis, Sotirios Fisher, Timothy C |
author_sort | Armstrong, Jonathan K |
collection | PubMed |
description | BACKGROUND: Resorbable bone hemostasis materials, oxidized regenerated cellulose (ORC) and microfibrillar collagen (MFC), remain at the site of application for up to 8 weeks and may impair osteogenesis. Our experimental study compared the effect of a water-soluble alkylene oxide copolymer (AOC) to ORC and MFC versus no hemostatic material on early bone healing. METHODS: Two circular 2.7 mm non-critical defects were made in each tibia of 12 rabbits. Sufficient AOC, ORC or MFC was applied to achieve hemostasis, and effectiveness recorded. An autologous blood clot was applied to control defects. Rabbits were sacrificed at 17 days, tibiae excised and fixed. Bone healing was quantitatively measured by micro-computed tomography (micro-CT) expressed as fractional bone volume, and qualitatively assessed by histological examination of decalcified sections. RESULTS: Hemostasis was immediate after application of MFC and AOC, after 1-2 minutes with ORC, and >5 minutes for control. At 17 days post-surgery, micro-CT analysis showed near-complete healing in control and AOC groups, partial healing in the ORC group and minimal healing in the MFC group. Fractional bone volume was 8 fold greater in the control and AOC groups than in the MFC group (0.42 ± 0.06, 0.40 ± 0.03 vs 0.05 ± 0.01, P < 0.001) and over 1.5-fold greater than in the ORC group (0.25 ± 0.03, P < 0.05). By histology, MFC remained at the application site with minimal healing at the defect margins and early fibrotic tissue within the defect. ORC-treated defects showed partial healing but with early fibrotic tissue in the marrow space. Conversely, control and AOC-treated defects demonstrated newly formed woven bone rich in cellular activity with no evidence of AOC remaining at the application site. CONCLUSIONS: Early healing appeared to be impaired by the presence of MFC and impeded by the presence of ORC. In contrast, AOC did not inhibit bone healing and suggest that AOC may be a better bone hemostatic material for procedures where bony fusion is critical and immediate hemostasis required. |
format | Text |
id | pubmed-3009953 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-30099532010-12-25 The effect of three hemostatic agents on early bone healing in an animal model Armstrong, Jonathan K Han, Bo Kuwahara, Kenrick Yang, Zhi Magyar, Clara E Dry, Sarah M Atti, Elisa Tetradis, Sotirios Fisher, Timothy C BMC Surg Research Article BACKGROUND: Resorbable bone hemostasis materials, oxidized regenerated cellulose (ORC) and microfibrillar collagen (MFC), remain at the site of application for up to 8 weeks and may impair osteogenesis. Our experimental study compared the effect of a water-soluble alkylene oxide copolymer (AOC) to ORC and MFC versus no hemostatic material on early bone healing. METHODS: Two circular 2.7 mm non-critical defects were made in each tibia of 12 rabbits. Sufficient AOC, ORC or MFC was applied to achieve hemostasis, and effectiveness recorded. An autologous blood clot was applied to control defects. Rabbits were sacrificed at 17 days, tibiae excised and fixed. Bone healing was quantitatively measured by micro-computed tomography (micro-CT) expressed as fractional bone volume, and qualitatively assessed by histological examination of decalcified sections. RESULTS: Hemostasis was immediate after application of MFC and AOC, after 1-2 minutes with ORC, and >5 minutes for control. At 17 days post-surgery, micro-CT analysis showed near-complete healing in control and AOC groups, partial healing in the ORC group and minimal healing in the MFC group. Fractional bone volume was 8 fold greater in the control and AOC groups than in the MFC group (0.42 ± 0.06, 0.40 ± 0.03 vs 0.05 ± 0.01, P < 0.001) and over 1.5-fold greater than in the ORC group (0.25 ± 0.03, P < 0.05). By histology, MFC remained at the application site with minimal healing at the defect margins and early fibrotic tissue within the defect. ORC-treated defects showed partial healing but with early fibrotic tissue in the marrow space. Conversely, control and AOC-treated defects demonstrated newly formed woven bone rich in cellular activity with no evidence of AOC remaining at the application site. CONCLUSIONS: Early healing appeared to be impaired by the presence of MFC and impeded by the presence of ORC. In contrast, AOC did not inhibit bone healing and suggest that AOC may be a better bone hemostatic material for procedures where bony fusion is critical and immediate hemostasis required. BioMed Central 2010-12-17 /pmc/articles/PMC3009953/ /pubmed/21167039 http://dx.doi.org/10.1186/1471-2482-10-37 Text en Copyright ©2010 Armstrong et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (<url>http://creativecommons.org/licenses/by/2.0</url>), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Armstrong, Jonathan K Han, Bo Kuwahara, Kenrick Yang, Zhi Magyar, Clara E Dry, Sarah M Atti, Elisa Tetradis, Sotirios Fisher, Timothy C The effect of three hemostatic agents on early bone healing in an animal model |
title | The effect of three hemostatic agents on early bone healing in an animal model |
title_full | The effect of three hemostatic agents on early bone healing in an animal model |
title_fullStr | The effect of three hemostatic agents on early bone healing in an animal model |
title_full_unstemmed | The effect of three hemostatic agents on early bone healing in an animal model |
title_short | The effect of three hemostatic agents on early bone healing in an animal model |
title_sort | effect of three hemostatic agents on early bone healing in an animal model |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3009953/ https://www.ncbi.nlm.nih.gov/pubmed/21167039 http://dx.doi.org/10.1186/1471-2482-10-37 |
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