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The Emerging Role of GLP-1 Agonists in Burn Care: What Do We Know?

Authors :
Manasyan A
Cannata B
Ross E
Lasky S
Stanton EW
Malkoff N
Collier Z
Johnson MB
Gillenwater TJ
Source :
Journal of burn care & research : official publication of the American Burn Association [J Burn Care Res] 2024 Oct 15. Date of Electronic Publication: 2024 Oct 15.
Publication Year :
2024
Publisher :
Ahead of Print

Abstract

Glucagon-like peptide-1 (GLP-1) agonists mimic the action of GLP-1, a hormone that regulates blood glucose levels via stimulation of insulin release and inhibition of glucagon secretion. After burn, the current literature suggests that the use of GLP-1 agonists results in less insulin dependence with similar glucose control and hypoglycemic events to patients receiving a basal-bolus insulin regimen. GLP-1 agonists may also promote wound healing through various mechanisms including angiogenesis and improved keratinocyte migration. Despite the potential benefits, GLP-1 agonists reduce gastrointestinal motility which impacts their widespread adoption in burn care. This dysmotility can result in inadequate nutrition delivery, unintentional weight loss, and is a potential aspiration risk. The net impact of these medications on burn patients is unclear. Given their potential to demonstrate the safety, efficacy, and optimal dosing of various GLP-1 agonists in acute burn management.<br /> (© The Author(s) 2024. Published by Oxford University Press on behalf of the American Burn Association. All rights reserved. For commercial re-use, please contact reprints@oup.com for reprints and translation rights for reprints. All other permissions can be obtained through our RightsLink service via the Permissions link on the article page on our siteā€”for further information please contact journals.permissions@oup.com.)

Details

Language :
English
ISSN :
1559-0488
Database :
MEDLINE
Journal :
Journal of burn care & research : official publication of the American Burn Association
Publication Type :
Academic Journal
Accession number :
39405180
Full Text :
https://doi.org/10.1093/jbcr/irae189