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Microbiome in the setting of burn patients: implications for infections and clinical outcomes
Burn damage can lead to a state of immune dysregulation that facilitates the development of infections in patients. The most deleterious impact of this dysfunction is the loss of the skin’s natural protective barrier. Furthermore, the risk of infection is exacerbated by protracted hospitalization, u...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7428410/ https://www.ncbi.nlm.nih.gov/pubmed/32821744 http://dx.doi.org/10.1093/burnst/tkaa033 |
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author | Corcione, Silvia Lupia, Tommaso De Rosa, Francesco G |
author_facet | Corcione, Silvia Lupia, Tommaso De Rosa, Francesco G |
author_sort | Corcione, Silvia |
collection | PubMed |
description | Burn damage can lead to a state of immune dysregulation that facilitates the development of infections in patients. The most deleterious impact of this dysfunction is the loss of the skin’s natural protective barrier. Furthermore, the risk of infection is exacerbated by protracted hospitalization, urinary catheters, endotracheal intubation, inhalation injury, arterial lines and central venous access, among other mainstays of burn care. Currently, infections comprise the leading cause of mortality after major burn injuries, which highlights the improvements observed over the last 50 years in the care provided to burn victims. The need to implement the empirical selection of antibiotic therapy to treat multidrug-resistant bacteria may concomitantly lead to an overall pervasiveness of difficult-to-treat pathogens in burn centres, as well as the propagation of antimicrobial resistance and the ultimate dysregulation of a healthy microbiome. While preliminary studies are examining the variability and evolution of human and mice microbiota, both during the early and late phase burn injury, one must consider that abnormal microbiome conditions could influence the systemic inflammatory response. A better understanding of the changes in the post-burn microbiome might be useful to interpret the provenance and subsequent development of infections, as well as to come up with inferences on the prognosis of burn patients. This review aims to summarise the current findings describing the microbiological changes in different organs and systems of burn patients and how these alterations affect the risks of infections, complications, and, ultimately, healing. |
format | Online Article Text |
id | pubmed-7428410 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-74284102020-08-19 Microbiome in the setting of burn patients: implications for infections and clinical outcomes Corcione, Silvia Lupia, Tommaso De Rosa, Francesco G Burns Trauma Review Burn damage can lead to a state of immune dysregulation that facilitates the development of infections in patients. The most deleterious impact of this dysfunction is the loss of the skin’s natural protective barrier. Furthermore, the risk of infection is exacerbated by protracted hospitalization, urinary catheters, endotracheal intubation, inhalation injury, arterial lines and central venous access, among other mainstays of burn care. Currently, infections comprise the leading cause of mortality after major burn injuries, which highlights the improvements observed over the last 50 years in the care provided to burn victims. The need to implement the empirical selection of antibiotic therapy to treat multidrug-resistant bacteria may concomitantly lead to an overall pervasiveness of difficult-to-treat pathogens in burn centres, as well as the propagation of antimicrobial resistance and the ultimate dysregulation of a healthy microbiome. While preliminary studies are examining the variability and evolution of human and mice microbiota, both during the early and late phase burn injury, one must consider that abnormal microbiome conditions could influence the systemic inflammatory response. A better understanding of the changes in the post-burn microbiome might be useful to interpret the provenance and subsequent development of infections, as well as to come up with inferences on the prognosis of burn patients. This review aims to summarise the current findings describing the microbiological changes in different organs and systems of burn patients and how these alterations affect the risks of infections, complications, and, ultimately, healing. Oxford University Press 2020-08-14 /pmc/articles/PMC7428410/ /pubmed/32821744 http://dx.doi.org/10.1093/burnst/tkaa033 Text en © The Author(s) 2020. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Review Corcione, Silvia Lupia, Tommaso De Rosa, Francesco G Microbiome in the setting of burn patients: implications for infections and clinical outcomes |
title | Microbiome in the setting of burn patients: implications for infections and clinical outcomes |
title_full | Microbiome in the setting of burn patients: implications for infections and clinical outcomes |
title_fullStr | Microbiome in the setting of burn patients: implications for infections and clinical outcomes |
title_full_unstemmed | Microbiome in the setting of burn patients: implications for infections and clinical outcomes |
title_short | Microbiome in the setting of burn patients: implications for infections and clinical outcomes |
title_sort | microbiome in the setting of burn patients: implications for infections and clinical outcomes |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7428410/ https://www.ncbi.nlm.nih.gov/pubmed/32821744 http://dx.doi.org/10.1093/burnst/tkaa033 |
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