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Establishing a Reproducible Hypertrophic Scar following Thermal Injury: A Porcine Model
BACKGROUND: Our complete understanding of hypertrophic scarring is still deficient, as portrayed by the poor clinical outcomes when treating them. To address the need for alternative treatment strategies, we assess the swine animal burn model as an initial approach for immature scar evaluation and t...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4350315/ https://www.ncbi.nlm.nih.gov/pubmed/25750848 http://dx.doi.org/10.1097/GOX.0000000000000277 |
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author | Rapp, Scott J. Rumberg, Aaron Visscher, Marty Billmire, David A. Schwentker, Ann S. Pan, Brian S. |
author_facet | Rapp, Scott J. Rumberg, Aaron Visscher, Marty Billmire, David A. Schwentker, Ann S. Pan, Brian S. |
author_sort | Rapp, Scott J. |
collection | PubMed |
description | BACKGROUND: Our complete understanding of hypertrophic scarring is still deficient, as portrayed by the poor clinical outcomes when treating them. To address the need for alternative treatment strategies, we assess the swine animal burn model as an initial approach for immature scar evaluation and therapeutic application. METHODS: Thermal contact burns were created on the dorsum of 3 domestic swine with the use of a branding iron at 170°F for 20 seconds. Deep partial-thickness burns were cared for with absorptive dressings over 10 weeks and wounds evaluated with laser and negative pressure transduction, histology, photographic analysis, and RNA isolation. RESULTS: Overall average stiffness (mm Hg/mm) increased and elasticity (mm) decreased in the scars from the initial burn injury to 8 weeks when compared with normal skin (P < 0.01). Scars were thicker, more erythematous, and uniform in the caudal dorsum. The percent change of erythema in wounds increased from weeks 6 to 10. Histology demonstrated loss of dermal papillae, increased myofibroblast presence, vertically oriented vessels, epidermal and dermal hypercellularity, and parallel-layered collagen deposition. Immature scars remained elevated at 10 weeks, and minimal RNA was able to be isolated from the tissue. CONCLUSIONS: Deep partial-thickness thermal injury to the back of domestic swine produces an immature hypertrophic scar by 10 weeks following burn with thickness appearing to coincide with the location along the dorsal axis. With minimal pig to pig variation, we describe our technique to provide a testable immature scar model. |
format | Online Article Text |
id | pubmed-4350315 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-43503152015-03-06 Establishing a Reproducible Hypertrophic Scar following Thermal Injury: A Porcine Model Rapp, Scott J. Rumberg, Aaron Visscher, Marty Billmire, David A. Schwentker, Ann S. Pan, Brian S. Plast Reconstr Surg Glob Open Experimental BACKGROUND: Our complete understanding of hypertrophic scarring is still deficient, as portrayed by the poor clinical outcomes when treating them. To address the need for alternative treatment strategies, we assess the swine animal burn model as an initial approach for immature scar evaluation and therapeutic application. METHODS: Thermal contact burns were created on the dorsum of 3 domestic swine with the use of a branding iron at 170°F for 20 seconds. Deep partial-thickness burns were cared for with absorptive dressings over 10 weeks and wounds evaluated with laser and negative pressure transduction, histology, photographic analysis, and RNA isolation. RESULTS: Overall average stiffness (mm Hg/mm) increased and elasticity (mm) decreased in the scars from the initial burn injury to 8 weeks when compared with normal skin (P < 0.01). Scars were thicker, more erythematous, and uniform in the caudal dorsum. The percent change of erythema in wounds increased from weeks 6 to 10. Histology demonstrated loss of dermal papillae, increased myofibroblast presence, vertically oriented vessels, epidermal and dermal hypercellularity, and parallel-layered collagen deposition. Immature scars remained elevated at 10 weeks, and minimal RNA was able to be isolated from the tissue. CONCLUSIONS: Deep partial-thickness thermal injury to the back of domestic swine produces an immature hypertrophic scar by 10 weeks following burn with thickness appearing to coincide with the location along the dorsal axis. With minimal pig to pig variation, we describe our technique to provide a testable immature scar model. Wolters Kluwer Health 2015-03-06 /pmc/articles/PMC4350315/ /pubmed/25750848 http://dx.doi.org/10.1097/GOX.0000000000000277 Text en Copyright © 2015 The Authors. Published by Wolters Kluwer Health, Inc. on behalf of The American Society of Plastic Surgeons. All rights reserved. This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License, where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially. |
spellingShingle | Experimental Rapp, Scott J. Rumberg, Aaron Visscher, Marty Billmire, David A. Schwentker, Ann S. Pan, Brian S. Establishing a Reproducible Hypertrophic Scar following Thermal Injury: A Porcine Model |
title | Establishing a Reproducible Hypertrophic Scar following Thermal Injury: A Porcine Model |
title_full | Establishing a Reproducible Hypertrophic Scar following Thermal Injury: A Porcine Model |
title_fullStr | Establishing a Reproducible Hypertrophic Scar following Thermal Injury: A Porcine Model |
title_full_unstemmed | Establishing a Reproducible Hypertrophic Scar following Thermal Injury: A Porcine Model |
title_short | Establishing a Reproducible Hypertrophic Scar following Thermal Injury: A Porcine Model |
title_sort | establishing a reproducible hypertrophic scar following thermal injury: a porcine model |
topic | Experimental |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4350315/ https://www.ncbi.nlm.nih.gov/pubmed/25750848 http://dx.doi.org/10.1097/GOX.0000000000000277 |
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