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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Associação de Medicina Intensiva Brasileira -
AMIB
2018
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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. |
format | Online Article Text |
id | pubmed-6180474 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Associação de Medicina Intensiva Brasileira -
AMIB |
record_format | MEDLINE/PubMed |
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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