Cargando…
Blood Glucose Variability and Outcomes in Critically Ill Children
OBJECTIVES: To find the incidence of hyperglycemia (blood glucose [BG] ≥150 mg/dl), hypoglycemia (BG ≤60 mg/dl), and variability (presence of hypoglycemia and hyperglycemia) in critically ill children in the 1(st) week of Intensive Care Unit (ICU) stay and their association with mortality, length of...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5363099/ https://www.ncbi.nlm.nih.gov/pubmed/28400681 http://dx.doi.org/10.4103/ijccm.IJCCM_364_16 |
_version_ | 1782517105898291200 |
---|---|
author | Naranje, Kirti Mahadeorao Poddar, Banani Bhriguvanshi, Arpita Lal, Richa Azim, Afzal Singh, Ratender K. Gurjar, Mohan Baronia, Arvind K. |
author_facet | Naranje, Kirti Mahadeorao Poddar, Banani Bhriguvanshi, Arpita Lal, Richa Azim, Afzal Singh, Ratender K. Gurjar, Mohan Baronia, Arvind K. |
author_sort | Naranje, Kirti Mahadeorao |
collection | PubMed |
description | OBJECTIVES: To find the incidence of hyperglycemia (blood glucose [BG] ≥150 mg/dl), hypoglycemia (BG ≤60 mg/dl), and variability (presence of hypoglycemia and hyperglycemia) in critically ill children in the 1(st) week of Intensive Care Unit (ICU) stay and their association with mortality, length of ICU stay, and organ dysfunction. MATERIALS AND METHODS: The design was a retrospective observational cohort study. Consecutive children ≤18 years of age admitted from March 2003 to April 2012 in a combined adult and pediatric closed ICU. Relevant data were collected from chart review and hospital database. RESULTS: Out of 258 patients included, isolated hyperglycemia was seen in 139 (53.9%) and was unrelated to mortality and morbidity. Isolated variability in BG was noted in 76 (29.5%) patients and hypoglycemia was seen in 9 (3.5%) patients. BG variability was independently associated with multiorgan dysfunction syndrome on multivariate analysis (adjusted odds ratio [OR]: 7.1; 95% confidence interval [CI]: 1.6–31.1). Those with BG variability had longer ICU stay (11 days vs. 4 days, on log-rank test, P = 0.001). Insulin use was associated with the occurrence of variability (adjusted OR: 3.6; 95% CI: 1.8–7.0). CONCLUSION: Glucose disorders were frequently observed in critically ill children. BG variability was associated with multiorgan dysfunction and increased ICU stay. |
format | Online Article Text |
id | pubmed-5363099 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-53630992017-04-11 Blood Glucose Variability and Outcomes in Critically Ill Children Naranje, Kirti Mahadeorao Poddar, Banani Bhriguvanshi, Arpita Lal, Richa Azim, Afzal Singh, Ratender K. Gurjar, Mohan Baronia, Arvind K. Indian J Crit Care Med Research Article OBJECTIVES: To find the incidence of hyperglycemia (blood glucose [BG] ≥150 mg/dl), hypoglycemia (BG ≤60 mg/dl), and variability (presence of hypoglycemia and hyperglycemia) in critically ill children in the 1(st) week of Intensive Care Unit (ICU) stay and their association with mortality, length of ICU stay, and organ dysfunction. MATERIALS AND METHODS: The design was a retrospective observational cohort study. Consecutive children ≤18 years of age admitted from March 2003 to April 2012 in a combined adult and pediatric closed ICU. Relevant data were collected from chart review and hospital database. RESULTS: Out of 258 patients included, isolated hyperglycemia was seen in 139 (53.9%) and was unrelated to mortality and morbidity. Isolated variability in BG was noted in 76 (29.5%) patients and hypoglycemia was seen in 9 (3.5%) patients. BG variability was independently associated with multiorgan dysfunction syndrome on multivariate analysis (adjusted odds ratio [OR]: 7.1; 95% confidence interval [CI]: 1.6–31.1). Those with BG variability had longer ICU stay (11 days vs. 4 days, on log-rank test, P = 0.001). Insulin use was associated with the occurrence of variability (adjusted OR: 3.6; 95% CI: 1.8–7.0). CONCLUSION: Glucose disorders were frequently observed in critically ill children. BG variability was associated with multiorgan dysfunction and increased ICU stay. Medknow Publications & Media Pvt Ltd 2017-03 /pmc/articles/PMC5363099/ /pubmed/28400681 http://dx.doi.org/10.4103/ijccm.IJCCM_364_16 Text en Copyright: © 2017 Indian Journal of Critical Care Medicine http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Research Article Naranje, Kirti Mahadeorao Poddar, Banani Bhriguvanshi, Arpita Lal, Richa Azim, Afzal Singh, Ratender K. Gurjar, Mohan Baronia, Arvind K. Blood Glucose Variability and Outcomes in Critically Ill Children |
title | Blood Glucose Variability and Outcomes in Critically Ill Children |
title_full | Blood Glucose Variability and Outcomes in Critically Ill Children |
title_fullStr | Blood Glucose Variability and Outcomes in Critically Ill Children |
title_full_unstemmed | Blood Glucose Variability and Outcomes in Critically Ill Children |
title_short | Blood Glucose Variability and Outcomes in Critically Ill Children |
title_sort | blood glucose variability and outcomes in critically ill children |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5363099/ https://www.ncbi.nlm.nih.gov/pubmed/28400681 http://dx.doi.org/10.4103/ijccm.IJCCM_364_16 |
work_keys_str_mv | AT naranjekirtimahadeorao bloodglucosevariabilityandoutcomesincriticallyillchildren AT poddarbanani bloodglucosevariabilityandoutcomesincriticallyillchildren AT bhriguvanshiarpita bloodglucosevariabilityandoutcomesincriticallyillchildren AT lalricha bloodglucosevariabilityandoutcomesincriticallyillchildren AT azimafzal bloodglucosevariabilityandoutcomesincriticallyillchildren AT singhratenderk bloodglucosevariabilityandoutcomesincriticallyillchildren AT gurjarmohan bloodglucosevariabilityandoutcomesincriticallyillchildren AT baroniaarvindk bloodglucosevariabilityandoutcomesincriticallyillchildren |