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Bone healing after median sternotomy: A comparison of two hemostatic devices

BACKGROUND: Bone wax is traditionally used as part of surgical procedures to prevent bleeding from exposed spongy bone. It is an effective hemostatic device which creates a physical barrier. Unfortunately it interferes with subsequent bone healing and increases the risk of infection in experimental...

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Autores principales: Vestergaard, Rikke F, Jensen, Henrik, Vind-Kezunovic, Stefan, Jakobsen, Thomas, Søballe, Kjeld, Hasenkam, John M
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3001423/
https://www.ncbi.nlm.nih.gov/pubmed/21106051
http://dx.doi.org/10.1186/1749-8090-5-117
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author Vestergaard, Rikke F
Jensen, Henrik
Vind-Kezunovic, Stefan
Jakobsen, Thomas
Søballe, Kjeld
Hasenkam, John M
author_facet Vestergaard, Rikke F
Jensen, Henrik
Vind-Kezunovic, Stefan
Jakobsen, Thomas
Søballe, Kjeld
Hasenkam, John M
author_sort Vestergaard, Rikke F
collection PubMed
description BACKGROUND: Bone wax is traditionally used as part of surgical procedures to prevent bleeding from exposed spongy bone. It is an effective hemostatic device which creates a physical barrier. Unfortunately it interferes with subsequent bone healing and increases the risk of infection in experimental studies. Recently, a water-soluble, synthetic, hemostatic compound (Ostene(®)) was introduced to serve the same purpose as bone wax without hampering bone healing. This study aims to compare sternal healing after application of either bone wax or Ostene(®). METHODS: Twenty-four pigs were randomized into one of three treatment groups: Ostene(®), bone wax or no hemostatic treatment (control). Each animal was subjected to midline sternotomy. Either Ostene(® )or bone wax was applied to the spongy bone surfaces until local hemostasis was ensured. The control group received no hemostatic treatment. The wound was left open for 60 min before closing to simulate conditions alike those of cardiac surgery. All sterni were harvested 6 weeks after intervention. Bone density and the area of the bone defect were determined with peripheral quantitative CT-scanning; bone healing was displayed with plain X-ray and chronic inflammation was histologically assessed. RESULTS: Both CT-scanning and plain X-ray disclosed that bone healing was significantly impaired in the bone wax group (p < 0.01) compared with the other two groups, and the former group had significantly more chronic inflammation (p < 0.01) than the two latter. CONCLUSION: Bone wax inhibits bone healing and induces chronic inflammation in a porcine model. Ostene(® )treated animals displayed bone healing characteristics and inflammatory reactions similar to those of the control group without application of a hemostatic agent.
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spelling pubmed-30014232010-12-15 Bone healing after median sternotomy: A comparison of two hemostatic devices Vestergaard, Rikke F Jensen, Henrik Vind-Kezunovic, Stefan Jakobsen, Thomas Søballe, Kjeld Hasenkam, John M J Cardiothorac Surg Research Article BACKGROUND: Bone wax is traditionally used as part of surgical procedures to prevent bleeding from exposed spongy bone. It is an effective hemostatic device which creates a physical barrier. Unfortunately it interferes with subsequent bone healing and increases the risk of infection in experimental studies. Recently, a water-soluble, synthetic, hemostatic compound (Ostene(®)) was introduced to serve the same purpose as bone wax without hampering bone healing. This study aims to compare sternal healing after application of either bone wax or Ostene(®). METHODS: Twenty-four pigs were randomized into one of three treatment groups: Ostene(®), bone wax or no hemostatic treatment (control). Each animal was subjected to midline sternotomy. Either Ostene(® )or bone wax was applied to the spongy bone surfaces until local hemostasis was ensured. The control group received no hemostatic treatment. The wound was left open for 60 min before closing to simulate conditions alike those of cardiac surgery. All sterni were harvested 6 weeks after intervention. Bone density and the area of the bone defect were determined with peripheral quantitative CT-scanning; bone healing was displayed with plain X-ray and chronic inflammation was histologically assessed. RESULTS: Both CT-scanning and plain X-ray disclosed that bone healing was significantly impaired in the bone wax group (p < 0.01) compared with the other two groups, and the former group had significantly more chronic inflammation (p < 0.01) than the two latter. CONCLUSION: Bone wax inhibits bone healing and induces chronic inflammation in a porcine model. Ostene(® )treated animals displayed bone healing characteristics and inflammatory reactions similar to those of the control group without application of a hemostatic agent. BioMed Central 2010-11-24 /pmc/articles/PMC3001423/ /pubmed/21106051 http://dx.doi.org/10.1186/1749-8090-5-117 Text en Copyright ©2010 Vestergaard et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Vestergaard, Rikke F
Jensen, Henrik
Vind-Kezunovic, Stefan
Jakobsen, Thomas
Søballe, Kjeld
Hasenkam, John M
Bone healing after median sternotomy: A comparison of two hemostatic devices
title Bone healing after median sternotomy: A comparison of two hemostatic devices
title_full Bone healing after median sternotomy: A comparison of two hemostatic devices
title_fullStr Bone healing after median sternotomy: A comparison of two hemostatic devices
title_full_unstemmed Bone healing after median sternotomy: A comparison of two hemostatic devices
title_short Bone healing after median sternotomy: A comparison of two hemostatic devices
title_sort bone healing after median sternotomy: a comparison of two hemostatic devices
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3001423/
https://www.ncbi.nlm.nih.gov/pubmed/21106051
http://dx.doi.org/10.1186/1749-8090-5-117
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