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Increased bone formation in a rabbit long-bone defect model after single local and single systemic application of erythropoietin

BACKGROUND AND PURPOSE: Delayed bone healing with non-union is a common problem. Further options to increase bone healing together with surgery are needed. We therefore evaluated a 1-dose single application of erythropoietin (EPO), applied either locally to the defect or systemically during surgery,...

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Autores principales: Omlor, Georg W, Kleinschmidt, Kerstin, Gantz, Simone, Speicher, Anja, Guehring, Thorsten, Richter, Wiltrud
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4967288/
https://www.ncbi.nlm.nih.gov/pubmed/27348783
http://dx.doi.org/10.1080/17453674.2016.1198200
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author Omlor, Georg W
Kleinschmidt, Kerstin
Gantz, Simone
Speicher, Anja
Guehring, Thorsten
Richter, Wiltrud
author_facet Omlor, Georg W
Kleinschmidt, Kerstin
Gantz, Simone
Speicher, Anja
Guehring, Thorsten
Richter, Wiltrud
author_sort Omlor, Georg W
collection PubMed
description BACKGROUND AND PURPOSE: Delayed bone healing with non-union is a common problem. Further options to increase bone healing together with surgery are needed. We therefore evaluated a 1-dose single application of erythropoietin (EPO), applied either locally to the defect or systemically during surgery, in a critical-size rabbit long-bone defect. MATERIAL AND METHODS: 19 New Zealand White rabbits received a 15-mm defect in the radius diaphysis. An absorbable gelatin sponge was soaked with saline (control group and systemic treatment group) or EPO (local treatment group) and implanted into the gap. The systemic treatment group received EPO subcutaneously. In vivo micro-CT analysis was performed 4, 8, and 12 weeks postoperatively. Vascularization was evaluated histologically. RESULTS: Semiquantitative histomorphometric and radiological evaluation showed increased bone formation (2.3- to 2.5-fold) in both treatment groups after 12 weeks compared to the controls. Quantitative determination of bone volume and tissue volume showed superior bone healing after EPO treatment at all follow-up time points, with the highest values after 12 weeks in locally treated animals (3.0- to 3.4-fold). More vascularization was found in both EPO treatment groups. INTERPRETATION: Initial single dosing with EPO was sufficient to increase bone healing substantially after 12 weeks of follow-up. Local application inside the defect was most effective, and it can be administered directly during surgery. Apart from effects on ossification, systemic and local EPO treatment leads to increased callus vascularization.
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spelling pubmed-49672882017-01-11 Increased bone formation in a rabbit long-bone defect model after single local and single systemic application of erythropoietin Omlor, Georg W Kleinschmidt, Kerstin Gantz, Simone Speicher, Anja Guehring, Thorsten Richter, Wiltrud Acta Orthop Articles BACKGROUND AND PURPOSE: Delayed bone healing with non-union is a common problem. Further options to increase bone healing together with surgery are needed. We therefore evaluated a 1-dose single application of erythropoietin (EPO), applied either locally to the defect or systemically during surgery, in a critical-size rabbit long-bone defect. MATERIAL AND METHODS: 19 New Zealand White rabbits received a 15-mm defect in the radius diaphysis. An absorbable gelatin sponge was soaked with saline (control group and systemic treatment group) or EPO (local treatment group) and implanted into the gap. The systemic treatment group received EPO subcutaneously. In vivo micro-CT analysis was performed 4, 8, and 12 weeks postoperatively. Vascularization was evaluated histologically. RESULTS: Semiquantitative histomorphometric and radiological evaluation showed increased bone formation (2.3- to 2.5-fold) in both treatment groups after 12 weeks compared to the controls. Quantitative determination of bone volume and tissue volume showed superior bone healing after EPO treatment at all follow-up time points, with the highest values after 12 weeks in locally treated animals (3.0- to 3.4-fold). More vascularization was found in both EPO treatment groups. INTERPRETATION: Initial single dosing with EPO was sufficient to increase bone healing substantially after 12 weeks of follow-up. Local application inside the defect was most effective, and it can be administered directly during surgery. Apart from effects on ossification, systemic and local EPO treatment leads to increased callus vascularization. Taylor & Francis 2016-08 2016-06-27 /pmc/articles/PMC4967288/ /pubmed/27348783 http://dx.doi.org/10.1080/17453674.2016.1198200 Text en © 2016 The Author(s). Published by Taylor & Francis on behalf of the Nordic Orthopedic Federation. https://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution-Non-Commercial License (https://creativecommons.org/licenses/by-nc/3.0)
spellingShingle Articles
Omlor, Georg W
Kleinschmidt, Kerstin
Gantz, Simone
Speicher, Anja
Guehring, Thorsten
Richter, Wiltrud
Increased bone formation in a rabbit long-bone defect model after single local and single systemic application of erythropoietin
title Increased bone formation in a rabbit long-bone defect model after single local and single systemic application of erythropoietin
title_full Increased bone formation in a rabbit long-bone defect model after single local and single systemic application of erythropoietin
title_fullStr Increased bone formation in a rabbit long-bone defect model after single local and single systemic application of erythropoietin
title_full_unstemmed Increased bone formation in a rabbit long-bone defect model after single local and single systemic application of erythropoietin
title_short Increased bone formation in a rabbit long-bone defect model after single local and single systemic application of erythropoietin
title_sort increased bone formation in a rabbit long-bone defect model after single local and single systemic application of erythropoietin
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4967288/
https://www.ncbi.nlm.nih.gov/pubmed/27348783
http://dx.doi.org/10.1080/17453674.2016.1198200
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