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Etiology of hyperglycemia in critically ill children and the impact of organ dysfunction

OBJECTIVE: This study aimed to study the incidence of stress hyperglycemia in critically ill children and to investigate the etiological basis of the hyperglycemia based on homeostasis model assessment. METHODS: This was a prospective cohort study in one of the pediatric intensive care units of Cair...

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Autores principales: El-Sherbini, Seham Awad, Marzouk, Huda, El-Sayed, Riham, Hosam-ElDin, Sarah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Associação de Medicina Intensiva Brasileira - AMIB 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6180474/
https://www.ncbi.nlm.nih.gov/pubmed/30328985
http://dx.doi.org/10.5935/0103-507X.20180051
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author El-Sherbini, Seham Awad
Marzouk, Huda
El-Sayed, Riham
Hosam-ElDin, Sarah
author_facet El-Sherbini, Seham Awad
Marzouk, Huda
El-Sayed, Riham
Hosam-ElDin, Sarah
author_sort El-Sherbini, Seham Awad
collection PubMed
description OBJECTIVE: This study aimed to study the incidence of stress hyperglycemia in critically ill children and to investigate the etiological basis of the hyperglycemia based on homeostasis model assessment. METHODS: This was a prospective cohort study in one of the pediatric intensive care units of Cairo University, including 60 critically ill children and 21 healthy controls. Serum blood glucose, insulin, and C-peptide levels were measured within 24 hours of admission. Homeostasis model assessment was used to assess β-cell function and insulin sensitivity. RESULTS: Hyperglycemia was estimated in 70% of patients. Blood glucose values ≥ 180mg/dL were associated with a poor outcome. Blood glucose levels were positively correlated with Pediatric Risk for Mortality (PRISM III) score and number of organ dysfunctions (p = 0.019 and p = 0.022, respectively), while insulin levels were negatively correlated with number of organ dysfunctions (r = -0.33, p = 0.01). Homeostasis model assessment revealed that 26 (43.3%) of the critically ill patients had low β-cell function, and 18 (30%) had low insulin sensitivity. Combined pathology was detected in 2 (3.3%) patients only. Low β-cell function was significantly associated with the presence of multi-organ dysfunction; respiratory, cardiovascular, and hematological dysfunctions; and the presence of sepsis. CONCLUSIONS: β-Cell dysfunction appeared to be prevalent in our cohort and was associated with multi-organ dysfunction.
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spelling pubmed-61804742018-10-15 Etiology of hyperglycemia in critically ill children and the impact of organ dysfunction El-Sherbini, Seham Awad Marzouk, Huda El-Sayed, Riham Hosam-ElDin, Sarah Rev Bras Ter Intensiva Original Article OBJECTIVE: This study aimed to study the incidence of stress hyperglycemia in critically ill children and to investigate the etiological basis of the hyperglycemia based on homeostasis model assessment. METHODS: This was a prospective cohort study in one of the pediatric intensive care units of Cairo University, including 60 critically ill children and 21 healthy controls. Serum blood glucose, insulin, and C-peptide levels were measured within 24 hours of admission. Homeostasis model assessment was used to assess β-cell function and insulin sensitivity. RESULTS: Hyperglycemia was estimated in 70% of patients. Blood glucose values ≥ 180mg/dL were associated with a poor outcome. Blood glucose levels were positively correlated with Pediatric Risk for Mortality (PRISM III) score and number of organ dysfunctions (p = 0.019 and p = 0.022, respectively), while insulin levels were negatively correlated with number of organ dysfunctions (r = -0.33, p = 0.01). Homeostasis model assessment revealed that 26 (43.3%) of the critically ill patients had low β-cell function, and 18 (30%) had low insulin sensitivity. Combined pathology was detected in 2 (3.3%) patients only. Low β-cell function was significantly associated with the presence of multi-organ dysfunction; respiratory, cardiovascular, and hematological dysfunctions; and the presence of sepsis. CONCLUSIONS: β-Cell dysfunction appeared to be prevalent in our cohort and was associated with multi-organ dysfunction. Associação de Medicina Intensiva Brasileira - AMIB 2018 /pmc/articles/PMC6180474/ /pubmed/30328985 http://dx.doi.org/10.5935/0103-507X.20180051 Text en http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
El-Sherbini, Seham Awad
Marzouk, Huda
El-Sayed, Riham
Hosam-ElDin, Sarah
Etiology of hyperglycemia in critically ill children and the impact of organ dysfunction
title Etiology of hyperglycemia in critically ill children and the impact of organ dysfunction
title_full Etiology of hyperglycemia in critically ill children and the impact of organ dysfunction
title_fullStr Etiology of hyperglycemia in critically ill children and the impact of organ dysfunction
title_full_unstemmed Etiology of hyperglycemia in critically ill children and the impact of organ dysfunction
title_short Etiology of hyperglycemia in critically ill children and the impact of organ dysfunction
title_sort etiology of hyperglycemia in critically ill children and the impact of organ dysfunction
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6180474/
https://www.ncbi.nlm.nih.gov/pubmed/30328985
http://dx.doi.org/10.5935/0103-507X.20180051
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