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Inflammation Biomarkers and Correlation to Wound Status After Full-Thickness Skin Grafting
Background: A surgical site infection (SSI) is believed to be the result of an exaggerated inflammatory response. Objective: Examine the relationship between clinical status and inflammation biomarkers in full-thickness skin grafting wounds. Methods: Twenty patients planned for facial full-thickness...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6640317/ https://www.ncbi.nlm.nih.gov/pubmed/31355202 http://dx.doi.org/10.3389/fmed.2019.00159 |
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author | Saleh, Karim Strömdahl, Ann-Charlotte Riesbeck, Kristian Schmidtchen, Artur |
author_facet | Saleh, Karim Strömdahl, Ann-Charlotte Riesbeck, Kristian Schmidtchen, Artur |
author_sort | Saleh, Karim |
collection | PubMed |
description | Background: A surgical site infection (SSI) is believed to be the result of an exaggerated inflammatory response. Objective: Examine the relationship between clinical status and inflammation biomarkers in full-thickness skin grafting wounds. Methods: Twenty patients planned for facial full-thickness skin grafting were enrolled. A week after surgery, all graft wounds were clinically assessed using a 3-step scale for inflammation (low, moderate, high). All wounds were swabbed for routine microbiological analysis and assessment of numbers of aerobic bacteria. Tie-over dressings from all patients were collected and used for wound fluid extraction and subsequent analysis of MMPs, cytokines, and NF-κB inducing activity. Results: Wounds with a high degree of inflammation contained increased total MMP activity (P ≤ 0.05) in their corresponding fluids. Likewise, the level of the cytokines IL-1ß, IL-8, IL-6, TNF-α was analyzed, and particularly IL-1ß was discriminatory for highly inflamed wounds (P ≤ 0.01). Moreover, bacterial loads were increased in highly inflamed wounds compared to wounds with a low degree of inflammation (P ≤ 0.01). NF-κB activation in the monocytic cell line THP-1 was significantly higher when these cells were stimulated by wound fluids with a high degree of inflammation (P ≤ 0.01). Growth of S. aureus in wounds did not vary between wounds with different degrees of inflammation (chi-square 3.8, P = 0.144). Conclusion: Biomarkers analyzed from tie-over dressings correlated to clinical wound healing in full-thickness skin grafting. |
format | Online Article Text |
id | pubmed-6640317 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-66403172019-07-26 Inflammation Biomarkers and Correlation to Wound Status After Full-Thickness Skin Grafting Saleh, Karim Strömdahl, Ann-Charlotte Riesbeck, Kristian Schmidtchen, Artur Front Med (Lausanne) Medicine Background: A surgical site infection (SSI) is believed to be the result of an exaggerated inflammatory response. Objective: Examine the relationship between clinical status and inflammation biomarkers in full-thickness skin grafting wounds. Methods: Twenty patients planned for facial full-thickness skin grafting were enrolled. A week after surgery, all graft wounds were clinically assessed using a 3-step scale for inflammation (low, moderate, high). All wounds were swabbed for routine microbiological analysis and assessment of numbers of aerobic bacteria. Tie-over dressings from all patients were collected and used for wound fluid extraction and subsequent analysis of MMPs, cytokines, and NF-κB inducing activity. Results: Wounds with a high degree of inflammation contained increased total MMP activity (P ≤ 0.05) in their corresponding fluids. Likewise, the level of the cytokines IL-1ß, IL-8, IL-6, TNF-α was analyzed, and particularly IL-1ß was discriminatory for highly inflamed wounds (P ≤ 0.01). Moreover, bacterial loads were increased in highly inflamed wounds compared to wounds with a low degree of inflammation (P ≤ 0.01). NF-κB activation in the monocytic cell line THP-1 was significantly higher when these cells were stimulated by wound fluids with a high degree of inflammation (P ≤ 0.01). Growth of S. aureus in wounds did not vary between wounds with different degrees of inflammation (chi-square 3.8, P = 0.144). Conclusion: Biomarkers analyzed from tie-over dressings correlated to clinical wound healing in full-thickness skin grafting. Frontiers Media S.A. 2019-07-12 /pmc/articles/PMC6640317/ /pubmed/31355202 http://dx.doi.org/10.3389/fmed.2019.00159 Text en Copyright © 2019 Saleh, Strömdahl, Riesbeck and Schmidtchen. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Medicine Saleh, Karim Strömdahl, Ann-Charlotte Riesbeck, Kristian Schmidtchen, Artur Inflammation Biomarkers and Correlation to Wound Status After Full-Thickness Skin Grafting |
title | Inflammation Biomarkers and Correlation to Wound Status After Full-Thickness Skin Grafting |
title_full | Inflammation Biomarkers and Correlation to Wound Status After Full-Thickness Skin Grafting |
title_fullStr | Inflammation Biomarkers and Correlation to Wound Status After Full-Thickness Skin Grafting |
title_full_unstemmed | Inflammation Biomarkers and Correlation to Wound Status After Full-Thickness Skin Grafting |
title_short | Inflammation Biomarkers and Correlation to Wound Status After Full-Thickness Skin Grafting |
title_sort | inflammation biomarkers and correlation to wound status after full-thickness skin grafting |
topic | Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6640317/ https://www.ncbi.nlm.nih.gov/pubmed/31355202 http://dx.doi.org/10.3389/fmed.2019.00159 |
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