Glucose Requirements Following Burn Injury: Parameters of Optimal Glucose Infusion and Possible Hepatic and Respiratory Abnormalities Following Excessive Glucose Intake
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Glucose and leucine metabolism in 18 severely burned patients were studied using the primed constant infusion of U-13C-glucose and 1-13C-leucine, respectively. The leucine data were used to calculate rates of whole-body protein synthesis. In four additional burn patients and seven normal controls, the effects of exogenously infused insulin on the metabolism of infused glucose were evaluated. Also, the effect on leucine metabolism of adding insulin to infused glucose was tested and rates of protein synthesis were calculated. The protein studies were divided into two groups depending on the rate of glucose infusion. Protein synthesis was 4.3 + 0.54 g protein/kg/day during the lower infusion rates (1.4--4.5 mg/kg/min) and 5.17 + 0.19 g protein/kg/day during the higher infusion rates (4.7--9.3 mg/kg/min) (statistically different, p less than 0.05). However, when the high infusion rate group was divided into two subgroups (high, 4.7--6.8 mg/kg/min, and very high, 7.03--9.31 mg/kg/min), there was no difference in the rate of protein synthesis. When U-13C-glucose was infused during varying rates of unlabeled glucose infusion, we found that the per cent of CO2 coming from the direct oxidation of glucose rose rapidly at the lower infusion rates but reached a plateau at approximately 55% as the infusion rates exceeded 5 mg/kg/min. Addition of insulin did not affect the rate of glucose oxidation but did seem to exert a stimulatory effect on protein synthesis. It was concluded that there appears to be a maximal rate of glucose infusion, beyond which physiologically significant increases in protein synthesis and direct oxidation of glucose cannot be expected. Furthermore, there appears to be a physiological cost of exceeding the optimal glucose infusion rate, as indicated by increased rates of CO2 production during infusion as well as large fat deposits in the liver at autopsy in patients infused with large amounts of glucose.
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Hyperglycemia related to PN enriched in dextrose requires higher doses of insulin.
“The hyperglycemia related to PN enriched in dextrose requires higher doses of insulin (193).”
From ESPEN guideline on clinical nutrition in the intensive care unit. (2019) · cites this paper as [193]
A number of physiologic advantages are associated with the use of enteral nutrition, such as preservation of gut integrity and intestinal permeability, down modulation of the inflammatory response and of insulin resistance.
“A number of physiologic advantages are associated with the use of EN, such as the preservation of gut integrity and intestinal permeability, as well as a down modulation of the inflammatory response and of insulin resistance (193).”
From ESPEN guideline on clinical nutrition in the intensive care unit. (2019) · cites this paper as [193]
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ESPEN guideline on clinical nutrition in the intensive care unit.
Singer, P., Blaser, A. R., Berger, M. M., Alhazzani, W., Calder, P. C., Casaer, M. P., Hiesmayr, M., Mayer, K., Montejo, J. C., Pichard, C., et al. (2019) · Clinical Nutrition · doi:10.1016/j.clnu.2018.08.037 · Cited by 2,904 · see citing works
The metabolic effects of thermal injury
Tredget, E. E., & Yu, Y. M. (1992) · World Journal of Surgery · doi:10.1007/bf02067117 · Cited by 149 · see citing works
- Authors
- BURKE, J. F., WOLFE, R. R., MULLANY, C. J., MATHEWS, D. E., & BIER, D. M.
- Affiliations
- Washington University in St. Louis (US)
- Venue
- Annals of Surgery
- Published
- 1979-09
- Volume
- 190
- Issue
- 3
- Pages
- 274-285
- ISSN
- 0003-4932 (ISSN-L)
- PMC
- PMC1344652
- OpenAlex
- W2039217866
- Cited by
- 360
- References
- 0
- Citations by year
- 2026: 2 · 2025: 2 · 2024: 2 · 2023: 6 · 2022: 2 · 2021: 3 · 2020: 1 · 2019: 5 · 2018: 6 · 2017: 2 · 2016: 7 · 2015: 4 · 2014: 10 · 2013: 9 · 2012: 5
- FWCI
- 11.37
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Annals of Surgery (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Epidemiology › Burn Injury Management and Outcomes
- Health Sciences › Nursing › Nutrition and Dietetics › Clinical Nutrition and Gastroenterology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Muscle metabolism and nutrition
- Keywords
- burns, glucose infusion rate, whole-body protein synthesis, leucine metabolism, insulin, glucose oxidation, CO2 emissions, hepatic lipid accumulation, hypermetabolism
- MeSH terms
- Adolescent, Adult, Aged, Burns, Carbon Dioxide, Child, Glucose, Humans, Infusions, Parenteral, Insulin, Leucine, Liver, Middle Aged, Protein Biosynthesis
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