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The effect of obesity on adverse outcomes and metabolism in pediatric burn patients

HYPOTHESIS: Obesity influences metabolism and increases the incidence of clinical complications and worsens outcomes in pediatric burn patients. DESIGN: Retrospective, single-center study. SUBJECTS: Five hundred ninety-two severely burned pediatric patients who had burns covering more than 30% of th...

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Autores principales: Kraft, Robert, Herndon, David N., Williams, Felicia N., Al-Mousawi, Ahmed M, Finnerty, Celeste C., Jeschke, Marc G
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3299841/
https://www.ncbi.nlm.nih.gov/pubmed/22143622
http://dx.doi.org/10.1038/ijo.2011.224
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author Kraft, Robert
Herndon, David N.
Williams, Felicia N.
Al-Mousawi, Ahmed M
Finnerty, Celeste C.
Jeschke, Marc G
author_facet Kraft, Robert
Herndon, David N.
Williams, Felicia N.
Al-Mousawi, Ahmed M
Finnerty, Celeste C.
Jeschke, Marc G
author_sort Kraft, Robert
collection PubMed
description HYPOTHESIS: Obesity influences metabolism and increases the incidence of clinical complications and worsens outcomes in pediatric burn patients. DESIGN: Retrospective, single-center study. SUBJECTS: Five hundred ninety-two severely burned pediatric patients who had burns covering more than 30% of the total body surface area and who were treated between 2001 and 2008 were enrolled in this study. Patients were divided into ≥ 85th percentile (n = 277) and normal (n = 315) weight groups based on body mass index percentiles. RESULTS: Patients stratified below (normal) and ≥ 85(th) percentile had similar age, gender distribution, and total burn size. No significant differences were detected in the incidence of sepsis (11% for obese vs. 10% for normal), the incidence of multiple organ failure (21% for obese and 16% for normal), or mortality (11% for obese vs. 8% for normal). Compared to the normal group, the ≥ 85(th) percentile group had low levels of constitutive proteins (α2macroglobulin and Apolipoprotein A-1) (p < 0.05 for both) as well as high levels of triglycerides and the acute-phase protein, C-reactive protein (p < 0.05 for both) up to 60 days after injury. Patients ≥ 85(th) percentile showed a significant higher loss of bone mineral density and lipolysis compared to normal individuals. Stepwise logistic regression analysis revealed that body mass index had a positive predictive value towards the maximum DENVER2 score, an index of organ failure (p < 0.001). CONCLUSIONS: BMI ≥ 85(th) percentile altered the post-burn acute phase and catabolic response but did not increase the incidence of sepsis, multiple organ failure, or mortality in pediatric burn patients. Our results suggest that impaired metabolism and an altered inflammatory response occurs already in patients starting at the 85th percentile BMI.
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spelling pubmed-32998412012-10-01 The effect of obesity on adverse outcomes and metabolism in pediatric burn patients Kraft, Robert Herndon, David N. Williams, Felicia N. Al-Mousawi, Ahmed M Finnerty, Celeste C. Jeschke, Marc G Int J Obes (Lond) Article HYPOTHESIS: Obesity influences metabolism and increases the incidence of clinical complications and worsens outcomes in pediatric burn patients. DESIGN: Retrospective, single-center study. SUBJECTS: Five hundred ninety-two severely burned pediatric patients who had burns covering more than 30% of the total body surface area and who were treated between 2001 and 2008 were enrolled in this study. Patients were divided into ≥ 85th percentile (n = 277) and normal (n = 315) weight groups based on body mass index percentiles. RESULTS: Patients stratified below (normal) and ≥ 85(th) percentile had similar age, gender distribution, and total burn size. No significant differences were detected in the incidence of sepsis (11% for obese vs. 10% for normal), the incidence of multiple organ failure (21% for obese and 16% for normal), or mortality (11% for obese vs. 8% for normal). Compared to the normal group, the ≥ 85(th) percentile group had low levels of constitutive proteins (α2macroglobulin and Apolipoprotein A-1) (p < 0.05 for both) as well as high levels of triglycerides and the acute-phase protein, C-reactive protein (p < 0.05 for both) up to 60 days after injury. Patients ≥ 85(th) percentile showed a significant higher loss of bone mineral density and lipolysis compared to normal individuals. Stepwise logistic regression analysis revealed that body mass index had a positive predictive value towards the maximum DENVER2 score, an index of organ failure (p < 0.001). CONCLUSIONS: BMI ≥ 85(th) percentile altered the post-burn acute phase and catabolic response but did not increase the incidence of sepsis, multiple organ failure, or mortality in pediatric burn patients. Our results suggest that impaired metabolism and an altered inflammatory response occurs already in patients starting at the 85th percentile BMI. 2011-12-06 2012-04 /pmc/articles/PMC3299841/ /pubmed/22143622 http://dx.doi.org/10.1038/ijo.2011.224 Text en Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Kraft, Robert
Herndon, David N.
Williams, Felicia N.
Al-Mousawi, Ahmed M
Finnerty, Celeste C.
Jeschke, Marc G
The effect of obesity on adverse outcomes and metabolism in pediatric burn patients
title The effect of obesity on adverse outcomes and metabolism in pediatric burn patients
title_full The effect of obesity on adverse outcomes and metabolism in pediatric burn patients
title_fullStr The effect of obesity on adverse outcomes and metabolism in pediatric burn patients
title_full_unstemmed The effect of obesity on adverse outcomes and metabolism in pediatric burn patients
title_short The effect of obesity on adverse outcomes and metabolism in pediatric burn patients
title_sort effect of obesity on adverse outcomes and metabolism in pediatric burn patients
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3299841/
https://www.ncbi.nlm.nih.gov/pubmed/22143622
http://dx.doi.org/10.1038/ijo.2011.224
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