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Bone Fracture Acute Phase Response—A Unifying Theory of Fracture Repair: Clinical and Scientific Implications
Bone fractures create five problems that must be resolved: bleeding, risk of infection, hypoxia, disproportionate strain, and inability to bear weight. There have been enormous advancements in our understanding of the molecular mechanisms that resolve these problems after fractures, and in best clin...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6404386/ https://www.ncbi.nlm.nih.gov/pubmed/30930699 http://dx.doi.org/10.1007/s12018-018-9256-x |
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author | Baker, Courtney E. Moore-Lotridge, Stephanie N. Hysong, Alexander A. Posey, Samuel L. Robinette, J. Patton Blum, Deke M. Benvenuti, Michael A. Cole, Heather A. Egawa, Satoru Okawa, Atsushi Saito, Masanori McCarthy, Jason R. Nyman, Jeffry S. Yuasa, Masato Schoenecker, Jonathan G. |
author_facet | Baker, Courtney E. Moore-Lotridge, Stephanie N. Hysong, Alexander A. Posey, Samuel L. Robinette, J. Patton Blum, Deke M. Benvenuti, Michael A. Cole, Heather A. Egawa, Satoru Okawa, Atsushi Saito, Masanori McCarthy, Jason R. Nyman, Jeffry S. Yuasa, Masato Schoenecker, Jonathan G. |
author_sort | Baker, Courtney E. |
collection | PubMed |
description | Bone fractures create five problems that must be resolved: bleeding, risk of infection, hypoxia, disproportionate strain, and inability to bear weight. There have been enormous advancements in our understanding of the molecular mechanisms that resolve these problems after fractures, and in best clinical practices of repairing fractures. We put forth a modern, comprehensive model of fracture repair that synthesizes the literature on the biology and biomechanics of fracture repair to address the primary problems of fractures. This updated model is a framework for both fracture management and future studies aimed at understanding and treating this complex process. This model is based upon the fracture acute phase response (APR), which encompasses the molecular mechanisms that respond to injury. The APR is divided into sequential stages of “survival” and “repair.” Early in convalescence, during “survival,” bleeding and infection are resolved by collaborative efforts of the hemostatic and inflammatory pathways. Later, in “repair,” avascular and biomechanically insufficient bone is replaced by a variable combination of intramembranous and endochondral ossification. Progression to repair cannot occur until survival has been ensured. A disproportionate APR—either insufficient or exuberant—leads to complications of survival (hemorrhage, thrombosis, systemic inflammatory response syndrome, infection, death) and/or repair (delayed- or non-union). The type of ossification utilized for fracture repair is dependent on the relative amounts of strain and vascularity in the fracture microenvironment, but any failure along this process can disrupt or delay fracture healing and result in a similar non-union. Therefore, incomplete understanding of the principles herein can result in mismanagement of fracture care or application of hardware that interferes with fracture repair. This unifying model of fracture repair not only informs clinicians how their interventions fit within the framework of normal biological healing but also instructs investigators about the critical variables and outputs to assess during a study of fracture repair. |
format | Online Article Text |
id | pubmed-6404386 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-64043862019-03-27 Bone Fracture Acute Phase Response—A Unifying Theory of Fracture Repair: Clinical and Scientific Implications Baker, Courtney E. Moore-Lotridge, Stephanie N. Hysong, Alexander A. Posey, Samuel L. Robinette, J. Patton Blum, Deke M. Benvenuti, Michael A. Cole, Heather A. Egawa, Satoru Okawa, Atsushi Saito, Masanori McCarthy, Jason R. Nyman, Jeffry S. Yuasa, Masato Schoenecker, Jonathan G. Clin Rev Bone Miner Metab Fracture Bone fractures create five problems that must be resolved: bleeding, risk of infection, hypoxia, disproportionate strain, and inability to bear weight. There have been enormous advancements in our understanding of the molecular mechanisms that resolve these problems after fractures, and in best clinical practices of repairing fractures. We put forth a modern, comprehensive model of fracture repair that synthesizes the literature on the biology and biomechanics of fracture repair to address the primary problems of fractures. This updated model is a framework for both fracture management and future studies aimed at understanding and treating this complex process. This model is based upon the fracture acute phase response (APR), which encompasses the molecular mechanisms that respond to injury. The APR is divided into sequential stages of “survival” and “repair.” Early in convalescence, during “survival,” bleeding and infection are resolved by collaborative efforts of the hemostatic and inflammatory pathways. Later, in “repair,” avascular and biomechanically insufficient bone is replaced by a variable combination of intramembranous and endochondral ossification. Progression to repair cannot occur until survival has been ensured. A disproportionate APR—either insufficient or exuberant—leads to complications of survival (hemorrhage, thrombosis, systemic inflammatory response syndrome, infection, death) and/or repair (delayed- or non-union). The type of ossification utilized for fracture repair is dependent on the relative amounts of strain and vascularity in the fracture microenvironment, but any failure along this process can disrupt or delay fracture healing and result in a similar non-union. Therefore, incomplete understanding of the principles herein can result in mismanagement of fracture care or application of hardware that interferes with fracture repair. This unifying model of fracture repair not only informs clinicians how their interventions fit within the framework of normal biological healing but also instructs investigators about the critical variables and outputs to assess during a study of fracture repair. Springer US 2018-12-29 2018 /pmc/articles/PMC6404386/ /pubmed/30930699 http://dx.doi.org/10.1007/s12018-018-9256-x Text en © The Author(s) 2018 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Fracture Baker, Courtney E. Moore-Lotridge, Stephanie N. Hysong, Alexander A. Posey, Samuel L. Robinette, J. Patton Blum, Deke M. Benvenuti, Michael A. Cole, Heather A. Egawa, Satoru Okawa, Atsushi Saito, Masanori McCarthy, Jason R. Nyman, Jeffry S. Yuasa, Masato Schoenecker, Jonathan G. Bone Fracture Acute Phase Response—A Unifying Theory of Fracture Repair: Clinical and Scientific Implications |
title | Bone Fracture Acute Phase Response—A Unifying Theory of Fracture Repair: Clinical and Scientific Implications |
title_full | Bone Fracture Acute Phase Response—A Unifying Theory of Fracture Repair: Clinical and Scientific Implications |
title_fullStr | Bone Fracture Acute Phase Response—A Unifying Theory of Fracture Repair: Clinical and Scientific Implications |
title_full_unstemmed | Bone Fracture Acute Phase Response—A Unifying Theory of Fracture Repair: Clinical and Scientific Implications |
title_short | Bone Fracture Acute Phase Response—A Unifying Theory of Fracture Repair: Clinical and Scientific Implications |
title_sort | bone fracture acute phase response—a unifying theory of fracture repair: clinical and scientific implications |
topic | Fracture |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6404386/ https://www.ncbi.nlm.nih.gov/pubmed/30930699 http://dx.doi.org/10.1007/s12018-018-9256-x |
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