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Critical illness-induced dysglycaemia: diabetes and beyond

Type 2 diabetes has reached epidemic proportions in many parts of the world. The disease is projected to continue to increase and double within the foreseeable future. Dysglycaemia develops in the form of hyperglycaemia, hypoglycaemia and marked glucose variability in critically ill adults whether t...

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Autores principales: Smith, Fang Gao, Sheehy, Ann M, Vincent, Jean-Louis, Coursin, Douglas B
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3220014/
https://www.ncbi.nlm.nih.gov/pubmed/21067560
http://dx.doi.org/10.1186/cc9266
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author Smith, Fang Gao
Sheehy, Ann M
Vincent, Jean-Louis
Coursin, Douglas B
author_facet Smith, Fang Gao
Sheehy, Ann M
Vincent, Jean-Louis
Coursin, Douglas B
author_sort Smith, Fang Gao
collection PubMed
description Type 2 diabetes has reached epidemic proportions in many parts of the world. The disease is projected to continue to increase and double within the foreseeable future. Dysglycaemia develops in the form of hyperglycaemia, hypoglycaemia and marked glucose variability in critically ill adults whether they are known to have premorbid diabetes or not. Patients with such glucose dysregulation have increased morbidity and mortality. Whether this is secondary to cause and effect from dysglycaemia or is just related to critical illness remains under intense investigation. Identification of intensive care unit (ICU) patients with unrecognised diabetes remains a challenge. Further, there are few data regarding the development of type 2 diabetes in survivors after hospital discharge. This commentary introduces the concept of critical illness-induced dysglycaemia as an umbrella term that includes the spectrum of abnormal glucose homeostasis in the ICU. We outline the need for further studies in the area of glucose regulation and for follow-up of the natural history of abnormal glucose control during ICU admission and beyond.
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spelling pubmed-32200142011-11-18 Critical illness-induced dysglycaemia: diabetes and beyond Smith, Fang Gao Sheehy, Ann M Vincent, Jean-Louis Coursin, Douglas B Crit Care Viewpoint Type 2 diabetes has reached epidemic proportions in many parts of the world. The disease is projected to continue to increase and double within the foreseeable future. Dysglycaemia develops in the form of hyperglycaemia, hypoglycaemia and marked glucose variability in critically ill adults whether they are known to have premorbid diabetes or not. Patients with such glucose dysregulation have increased morbidity and mortality. Whether this is secondary to cause and effect from dysglycaemia or is just related to critical illness remains under intense investigation. Identification of intensive care unit (ICU) patients with unrecognised diabetes remains a challenge. Further, there are few data regarding the development of type 2 diabetes in survivors after hospital discharge. This commentary introduces the concept of critical illness-induced dysglycaemia as an umbrella term that includes the spectrum of abnormal glucose homeostasis in the ICU. We outline the need for further studies in the area of glucose regulation and for follow-up of the natural history of abnormal glucose control during ICU admission and beyond. BioMed Central 2010 2010-11-05 /pmc/articles/PMC3220014/ /pubmed/21067560 http://dx.doi.org/10.1186/cc9266 Text en Copyright ©2010 BioMed Central Ltd
spellingShingle Viewpoint
Smith, Fang Gao
Sheehy, Ann M
Vincent, Jean-Louis
Coursin, Douglas B
Critical illness-induced dysglycaemia: diabetes and beyond
title Critical illness-induced dysglycaemia: diabetes and beyond
title_full Critical illness-induced dysglycaemia: diabetes and beyond
title_fullStr Critical illness-induced dysglycaemia: diabetes and beyond
title_full_unstemmed Critical illness-induced dysglycaemia: diabetes and beyond
title_short Critical illness-induced dysglycaemia: diabetes and beyond
title_sort critical illness-induced dysglycaemia: diabetes and beyond
topic Viewpoint
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3220014/
https://www.ncbi.nlm.nih.gov/pubmed/21067560
http://dx.doi.org/10.1186/cc9266
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