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Current understanding of the chronic stress response to burn injury from human studies
There is a marked inflammatory and hypermetabolic response following a burn injury. The interlinked responses are more pronounced than for other forms of trauma and can persist for ≥3 years post-injury in burned patients. After a burn, patients have an increased risk of diseases of ageing including...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10013650/ https://www.ncbi.nlm.nih.gov/pubmed/36926636 http://dx.doi.org/10.1093/burnst/tkad007 |
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author | Osborne, Tyler Wall, Bradley Edgar, Dale W Fairchild, Timothy Wood, Fiona |
author_facet | Osborne, Tyler Wall, Bradley Edgar, Dale W Fairchild, Timothy Wood, Fiona |
author_sort | Osborne, Tyler |
collection | PubMed |
description | There is a marked inflammatory and hypermetabolic response following a burn injury. The interlinked responses are more pronounced than for other forms of trauma and can persist for ≥3 years post-injury in burned patients. After a burn, patients have an increased risk of diseases of ageing including cancer, diabetes and cardiovascular disease, highlighting the need for effective long-term strategies to ameliorate the stress response post-burn. Current therapeutic strategies for post-burn recovery include removal of damaged tissue with surgical excision and wound repair, nutritional supplementation and rehabilitative exercise. These strategies aim to minimize the hypermetabolic and inflammatory responses, as well as reducing the loss of lean body mass. This review briefly summarises the inflammatory and hypermetabolic responses and provides an update on the current therapeutic strategies for burned patients. The review examines the persistent nutritional challenge of ensuring sufficient energy intake of each macronutrient to fuel the hypermetabolic and counteract the catabolic response of burn injury, whilst reducing periods of hyperglycaemia and hypertriglyceridemia. Patients require individualized treatment options tailored to unique systemic responses following a burn, facilitated by a precision medicine approach to improve clinical and physiological outcomes in burned patients. Thus, this review discusses the utility of metabolic flexibility assessment to aid clinical decision making and prescription relating to nutritional supplementation and rehabilitative exercise in the burned patient. |
format | Online Article Text |
id | pubmed-10013650 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-100136502023-03-15 Current understanding of the chronic stress response to burn injury from human studies Osborne, Tyler Wall, Bradley Edgar, Dale W Fairchild, Timothy Wood, Fiona Burns Trauma Review There is a marked inflammatory and hypermetabolic response following a burn injury. The interlinked responses are more pronounced than for other forms of trauma and can persist for ≥3 years post-injury in burned patients. After a burn, patients have an increased risk of diseases of ageing including cancer, diabetes and cardiovascular disease, highlighting the need for effective long-term strategies to ameliorate the stress response post-burn. Current therapeutic strategies for post-burn recovery include removal of damaged tissue with surgical excision and wound repair, nutritional supplementation and rehabilitative exercise. These strategies aim to minimize the hypermetabolic and inflammatory responses, as well as reducing the loss of lean body mass. This review briefly summarises the inflammatory and hypermetabolic responses and provides an update on the current therapeutic strategies for burned patients. The review examines the persistent nutritional challenge of ensuring sufficient energy intake of each macronutrient to fuel the hypermetabolic and counteract the catabolic response of burn injury, whilst reducing periods of hyperglycaemia and hypertriglyceridemia. Patients require individualized treatment options tailored to unique systemic responses following a burn, facilitated by a precision medicine approach to improve clinical and physiological outcomes in burned patients. Thus, this review discusses the utility of metabolic flexibility assessment to aid clinical decision making and prescription relating to nutritional supplementation and rehabilitative exercise in the burned patient. Oxford University Press 2023-03-14 /pmc/articles/PMC10013650/ /pubmed/36926636 http://dx.doi.org/10.1093/burnst/tkad007 Text en © The Author(s) 2023. Published by Oxford University Press. https://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 (https://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 Osborne, Tyler Wall, Bradley Edgar, Dale W Fairchild, Timothy Wood, Fiona Current understanding of the chronic stress response to burn injury from human studies |
title | Current understanding of the chronic stress response to burn injury from human studies |
title_full | Current understanding of the chronic stress response to burn injury from human studies |
title_fullStr | Current understanding of the chronic stress response to burn injury from human studies |
title_full_unstemmed | Current understanding of the chronic stress response to burn injury from human studies |
title_short | Current understanding of the chronic stress response to burn injury from human studies |
title_sort | current understanding of the chronic stress response to burn injury from human studies |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10013650/ https://www.ncbi.nlm.nih.gov/pubmed/36926636 http://dx.doi.org/10.1093/burnst/tkad007 |
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