Burn size determines the inflammatory and hypermetabolic response

Marc G. Jeschke, Ronald P. Mlcak, Celeste Finnerty, William Norbury, Gerd G. Gauglitz, Gabriela A. Kulp, David Herndon

Research output: Contribution to journalArticle

160 Citations (Scopus)

Abstract

Background: Increased burn size leads to increased mortality of burned patients. Whether mortality is due to inflammation, hypermetabolism or other pathophysiologic contributing factors is not entirely determined. The purpose of the present study was to determine in a large prospective clinical trial whether different burn sizes are associated with differences in inflammation, body composition, protein synthesis, or organ function. Methods: Pediatric burned patients were divided into four burn size groups: <40% total body surface area (TBSA) burn, 40-59% TBSA burn, 60-79% TBSA burn, and >80% TBSA burn. Demographic and clinical data, hypermetabolism, the inflammatory response, body composition, the muscle protein net balance, serum and urine hormones and proteins, and cardiac function and changes in liver size were determined. Results: One hundred and eighty-nine pediatric patients of similar age and gender distribution were included in the study (<40% TBSA burn, n = 43; 40-59% TBSA burn, n = 79; 60-79% TBSA burn, n = 46; >80% TBSA burn, n = 21). Patients with larger burns had more operations, a greater incidence of infections and sepsis, and higher mortality rates compared with the other groups (P < 0.05). The percentage predicted resting energy expenditure was highest in the >80% TBSA group, followed by the 60-79% TBSA burn group (P < 0.05). Children with >80% burns lost the most body weight, lean body mass, muscle protein and bone mineral content (P < 0.05). The urine cortisol concentration was highest in the 80-99% and 60-79% TBSA burn groups, associated with significant myocardial depression and increased change in liver size (P < 0.05). The cytokine profile showed distinct differences in expression of IL-8, TNF, IL-6, IL-12p70, monocyte chemoattractant protein-1 and granulocyte-macrophage colony-stimulating factor (P < 0.05). Conclusion: Morbidity and mortality in burned patients is burn size dependent, starts at a 60% TBSA burn and is due to an increased hypermetabolic and inflammatory reaction, along with impaired cardiac function.

Original languageEnglish (US)
Article numberR90
JournalCritical Care
Volume11
Issue number4
DOIs
StatePublished - Aug 23 2007

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Mortality
Muscle Proteins
Body Composition
Burns
Urine
Pediatrics
Inflammation
Chemokine CCL2
Liver
Age Distribution
Granulocyte-Macrophage Colony-Stimulating Factor
Interleukin-8
Bone Density
Hydrocortisone
Interleukin-6
Sepsis
Proteins
Body Weight
Demography
Clinical Trials

ASJC Scopus subject areas

  • Critical Care and Intensive Care Medicine
  • Medicine(all)

Cite this

Jeschke, M. G., Mlcak, R. P., Finnerty, C., Norbury, W., Gauglitz, G. G., Kulp, G. A., & Herndon, D. (2007). Burn size determines the inflammatory and hypermetabolic response. Critical Care, 11(4), [R90]. https://doi.org/10.1186/cc6102

Burn size determines the inflammatory and hypermetabolic response. / Jeschke, Marc G.; Mlcak, Ronald P.; Finnerty, Celeste; Norbury, William; Gauglitz, Gerd G.; Kulp, Gabriela A.; Herndon, David.

In: Critical Care, Vol. 11, No. 4, R90, 23.08.2007.

Research output: Contribution to journalArticle

Jeschke, MG, Mlcak, RP, Finnerty, C, Norbury, W, Gauglitz, GG, Kulp, GA & Herndon, D 2007, 'Burn size determines the inflammatory and hypermetabolic response', Critical Care, vol. 11, no. 4, R90. https://doi.org/10.1186/cc6102
Jeschke, Marc G. ; Mlcak, Ronald P. ; Finnerty, Celeste ; Norbury, William ; Gauglitz, Gerd G. ; Kulp, Gabriela A. ; Herndon, David. / Burn size determines the inflammatory and hypermetabolic response. In: Critical Care. 2007 ; Vol. 11, No. 4.
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abstract = "Background: Increased burn size leads to increased mortality of burned patients. Whether mortality is due to inflammation, hypermetabolism or other pathophysiologic contributing factors is not entirely determined. The purpose of the present study was to determine in a large prospective clinical trial whether different burn sizes are associated with differences in inflammation, body composition, protein synthesis, or organ function. Methods: Pediatric burned patients were divided into four burn size groups: <40{\%} total body surface area (TBSA) burn, 40-59{\%} TBSA burn, 60-79{\%} TBSA burn, and >80{\%} TBSA burn. Demographic and clinical data, hypermetabolism, the inflammatory response, body composition, the muscle protein net balance, serum and urine hormones and proteins, and cardiac function and changes in liver size were determined. Results: One hundred and eighty-nine pediatric patients of similar age and gender distribution were included in the study (<40{\%} TBSA burn, n = 43; 40-59{\%} TBSA burn, n = 79; 60-79{\%} TBSA burn, n = 46; >80{\%} TBSA burn, n = 21). Patients with larger burns had more operations, a greater incidence of infections and sepsis, and higher mortality rates compared with the other groups (P < 0.05). The percentage predicted resting energy expenditure was highest in the >80{\%} TBSA group, followed by the 60-79{\%} TBSA burn group (P < 0.05). Children with >80{\%} burns lost the most body weight, lean body mass, muscle protein and bone mineral content (P < 0.05). The urine cortisol concentration was highest in the 80-99{\%} and 60-79{\%} TBSA burn groups, associated with significant myocardial depression and increased change in liver size (P < 0.05). The cytokine profile showed distinct differences in expression of IL-8, TNF, IL-6, IL-12p70, monocyte chemoattractant protein-1 and granulocyte-macrophage colony-stimulating factor (P < 0.05). Conclusion: Morbidity and mortality in burned patients is burn size dependent, starts at a 60{\%} TBSA burn and is due to an increased hypermetabolic and inflammatory reaction, along with impaired cardiac function.",
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AU - Mlcak, Ronald P.

AU - Finnerty, Celeste

AU - Norbury, William

AU - Gauglitz, Gerd G.

AU - Kulp, Gabriela A.

AU - Herndon, David

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N2 - Background: Increased burn size leads to increased mortality of burned patients. Whether mortality is due to inflammation, hypermetabolism or other pathophysiologic contributing factors is not entirely determined. The purpose of the present study was to determine in a large prospective clinical trial whether different burn sizes are associated with differences in inflammation, body composition, protein synthesis, or organ function. Methods: Pediatric burned patients were divided into four burn size groups: <40% total body surface area (TBSA) burn, 40-59% TBSA burn, 60-79% TBSA burn, and >80% TBSA burn. Demographic and clinical data, hypermetabolism, the inflammatory response, body composition, the muscle protein net balance, serum and urine hormones and proteins, and cardiac function and changes in liver size were determined. Results: One hundred and eighty-nine pediatric patients of similar age and gender distribution were included in the study (<40% TBSA burn, n = 43; 40-59% TBSA burn, n = 79; 60-79% TBSA burn, n = 46; >80% TBSA burn, n = 21). Patients with larger burns had more operations, a greater incidence of infections and sepsis, and higher mortality rates compared with the other groups (P < 0.05). The percentage predicted resting energy expenditure was highest in the >80% TBSA group, followed by the 60-79% TBSA burn group (P < 0.05). Children with >80% burns lost the most body weight, lean body mass, muscle protein and bone mineral content (P < 0.05). The urine cortisol concentration was highest in the 80-99% and 60-79% TBSA burn groups, associated with significant myocardial depression and increased change in liver size (P < 0.05). The cytokine profile showed distinct differences in expression of IL-8, TNF, IL-6, IL-12p70, monocyte chemoattractant protein-1 and granulocyte-macrophage colony-stimulating factor (P < 0.05). Conclusion: Morbidity and mortality in burned patients is burn size dependent, starts at a 60% TBSA burn and is due to an increased hypermetabolic and inflammatory reaction, along with impaired cardiac function.

AB - Background: Increased burn size leads to increased mortality of burned patients. Whether mortality is due to inflammation, hypermetabolism or other pathophysiologic contributing factors is not entirely determined. The purpose of the present study was to determine in a large prospective clinical trial whether different burn sizes are associated with differences in inflammation, body composition, protein synthesis, or organ function. Methods: Pediatric burned patients were divided into four burn size groups: <40% total body surface area (TBSA) burn, 40-59% TBSA burn, 60-79% TBSA burn, and >80% TBSA burn. Demographic and clinical data, hypermetabolism, the inflammatory response, body composition, the muscle protein net balance, serum and urine hormones and proteins, and cardiac function and changes in liver size were determined. Results: One hundred and eighty-nine pediatric patients of similar age and gender distribution were included in the study (<40% TBSA burn, n = 43; 40-59% TBSA burn, n = 79; 60-79% TBSA burn, n = 46; >80% TBSA burn, n = 21). Patients with larger burns had more operations, a greater incidence of infections and sepsis, and higher mortality rates compared with the other groups (P < 0.05). The percentage predicted resting energy expenditure was highest in the >80% TBSA group, followed by the 60-79% TBSA burn group (P < 0.05). Children with >80% burns lost the most body weight, lean body mass, muscle protein and bone mineral content (P < 0.05). The urine cortisol concentration was highest in the 80-99% and 60-79% TBSA burn groups, associated with significant myocardial depression and increased change in liver size (P < 0.05). The cytokine profile showed distinct differences in expression of IL-8, TNF, IL-6, IL-12p70, monocyte chemoattractant protein-1 and granulocyte-macrophage colony-stimulating factor (P < 0.05). Conclusion: Morbidity and mortality in burned patients is burn size dependent, starts at a 60% TBSA burn and is due to an increased hypermetabolic and inflammatory reaction, along with impaired cardiac function.

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