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Biomedical implications from a morphoelastic continuum model for the simulation of contracture formation in skin grafts that cover excised burns
A continuum hypothesis-based model is developed for the simulation of the (long term) contraction of skin grafts that cover excised burns in order to obtain suggestions regarding the ideal length of splinting therapy and when to start with this therapy such that the therapy is effective optimally. T...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5511621/ https://www.ncbi.nlm.nih.gov/pubmed/28181018 http://dx.doi.org/10.1007/s10237-017-0881-y |
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author | Koppenol, Daniël C. Vermolen, Fred J. |
author_facet | Koppenol, Daniël C. Vermolen, Fred J. |
author_sort | Koppenol, Daniël C. |
collection | PubMed |
description | A continuum hypothesis-based model is developed for the simulation of the (long term) contraction of skin grafts that cover excised burns in order to obtain suggestions regarding the ideal length of splinting therapy and when to start with this therapy such that the therapy is effective optimally. Tissue is modeled as an isotropic, heterogeneous, morphoelastic solid. With respect to the constituents of the tissue, we selected the following constituents as primary model components: fibroblasts, myofibroblasts, collagen molecules, and a generic signaling molecule. Good agreement is demonstrated with respect to the evolution over time of the surface area of unmeshed skin grafts that cover excised burns between outcomes of computer simulations obtained in this study and scar assessment data gathered previously in a clinical study. Based on the simulation results, we suggest that the optimal point in time to start with splinting therapy is directly after placement of the skin graft on its recipient bed. Furthermore, we suggest that it is desirable to continue with splinting therapy until the concentration of the signaling molecules in the grafted area has become negligible such that the formation of contractures can be prevented. We conclude this study with a presentation of some alternative ideas on how to diminish the degree of contracture formation that are not based on a mechanical intervention, and a discussion about how the presented model can be adjusted. |
format | Online Article Text |
id | pubmed-5511621 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-55116212017-07-31 Biomedical implications from a morphoelastic continuum model for the simulation of contracture formation in skin grafts that cover excised burns Koppenol, Daniël C. Vermolen, Fred J. Biomech Model Mechanobiol Original Paper A continuum hypothesis-based model is developed for the simulation of the (long term) contraction of skin grafts that cover excised burns in order to obtain suggestions regarding the ideal length of splinting therapy and when to start with this therapy such that the therapy is effective optimally. Tissue is modeled as an isotropic, heterogeneous, morphoelastic solid. With respect to the constituents of the tissue, we selected the following constituents as primary model components: fibroblasts, myofibroblasts, collagen molecules, and a generic signaling molecule. Good agreement is demonstrated with respect to the evolution over time of the surface area of unmeshed skin grafts that cover excised burns between outcomes of computer simulations obtained in this study and scar assessment data gathered previously in a clinical study. Based on the simulation results, we suggest that the optimal point in time to start with splinting therapy is directly after placement of the skin graft on its recipient bed. Furthermore, we suggest that it is desirable to continue with splinting therapy until the concentration of the signaling molecules in the grafted area has become negligible such that the formation of contractures can be prevented. We conclude this study with a presentation of some alternative ideas on how to diminish the degree of contracture formation that are not based on a mechanical intervention, and a discussion about how the presented model can be adjusted. Springer Berlin Heidelberg 2017-02-08 2017 /pmc/articles/PMC5511621/ /pubmed/28181018 http://dx.doi.org/10.1007/s10237-017-0881-y Text en © The Author(s) 2017 Open AccessThis 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 | Original Paper Koppenol, Daniël C. Vermolen, Fred J. Biomedical implications from a morphoelastic continuum model for the simulation of contracture formation in skin grafts that cover excised burns |
title | Biomedical implications from a morphoelastic continuum model for the simulation of contracture formation in skin grafts that cover excised burns |
title_full | Biomedical implications from a morphoelastic continuum model for the simulation of contracture formation in skin grafts that cover excised burns |
title_fullStr | Biomedical implications from a morphoelastic continuum model for the simulation of contracture formation in skin grafts that cover excised burns |
title_full_unstemmed | Biomedical implications from a morphoelastic continuum model for the simulation of contracture formation in skin grafts that cover excised burns |
title_short | Biomedical implications from a morphoelastic continuum model for the simulation of contracture formation in skin grafts that cover excised burns |
title_sort | biomedical implications from a morphoelastic continuum model for the simulation of contracture formation in skin grafts that cover excised burns |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5511621/ https://www.ncbi.nlm.nih.gov/pubmed/28181018 http://dx.doi.org/10.1007/s10237-017-0881-y |
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