Cargando…

Variability of insulin sensitivity during the first 4 days of critical illness: implications for tight glycemic control

BACKGROUND: Effective tight glycemic control (TGC) can improve outcomes in critical care patients, but it is difficult to achieve consistently. Insulin sensitivity defines the metabolic balance between insulin concentration and insulin-mediated glucose disposal. Hence, variability of insulin sensiti...

Descripción completa

Detalles Bibliográficos
Autores principales: Pretty, Christopher G, Le Compte, Aaron J, Chase, J Geoffrey, Shaw, Geoffrey M, Preiser, Jean-Charles, Penning, Sophie, Desaive, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3464183/
https://www.ncbi.nlm.nih.gov/pubmed/22703645
http://dx.doi.org/10.1186/2110-5820-2-17
_version_ 1782245378771386368
author Pretty, Christopher G
Le Compte, Aaron J
Chase, J Geoffrey
Shaw, Geoffrey M
Preiser, Jean-Charles
Penning, Sophie
Desaive, Thomas
author_facet Pretty, Christopher G
Le Compte, Aaron J
Chase, J Geoffrey
Shaw, Geoffrey M
Preiser, Jean-Charles
Penning, Sophie
Desaive, Thomas
author_sort Pretty, Christopher G
collection PubMed
description BACKGROUND: Effective tight glycemic control (TGC) can improve outcomes in critical care patients, but it is difficult to achieve consistently. Insulin sensitivity defines the metabolic balance between insulin concentration and insulin-mediated glucose disposal. Hence, variability of insulin sensitivity can cause variable glycemia. This study quantifies and compares the daily evolution of insulin sensitivity level and variability for critical care patients receiving TGC. METHODS: This is a retrospective analysis of data from the SPRINT TGC study involving patients admitted to a mixed medical-surgical ICU between August 2005 and May 2007. Only patients who commenced TGC within 12 hours of ICU admission and spent at least 24 hours on the SPRINT protocol were included (N = 164). Model-based insulin sensitivity (SI) was identified each hour. Absolute level and hour-to-hour percent changes in SI were assessed on cohort and per-patient bases. Levels and variability of SI were compared over time on 24-hour and 6-hour timescales for the first 4 days of ICU stay. RESULTS: Cohort and per-patient median SI levels increased by 34% and 33% (p < 0.001) between days 1 and 2 of ICU stay. Concomitantly, cohort and per-patient SI variability decreased by 32% and 36% (p < 0.001). For 72% of the cohort, median SI on day 2 was higher than on day 1. The day 1–2 results are the only clear, statistically significant trends across both analyses. Analysis of the first 24 hours using 6-hour blocks of SI data showed that most of the improvement in insulin sensitivity level and variability seen between days 1 and 2 occurred during the first 12–18 hours of day 1. CONCLUSIONS: Critically ill patients have significantly lower and more variable insulin sensitivity on day 1 than later in their ICU stay and particularly during the first 12 hours. This rapid improvement is likely due to the decline of counter-regulatory hormones as the acute phase of critical illness progresses. Clinically, these results suggest that while using TGC protocols with patients during their first few days of ICU stay, extra care should be afforded. Increased measurement frequency, higher target glycemic bands, conservative insulin dosing, and modulation of carbohydrate nutrition should be considered to minimize safely the outcome glycemic variability and reduce the risk of hypoglycemia.
format Online
Article
Text
id pubmed-3464183
institution National Center for Biotechnology Information
language English
publishDate 2012
publisher Springer
record_format MEDLINE/PubMed
spelling pubmed-34641832012-10-05 Variability of insulin sensitivity during the first 4 days of critical illness: implications for tight glycemic control Pretty, Christopher G Le Compte, Aaron J Chase, J Geoffrey Shaw, Geoffrey M Preiser, Jean-Charles Penning, Sophie Desaive, Thomas Ann Intensive Care Research BACKGROUND: Effective tight glycemic control (TGC) can improve outcomes in critical care patients, but it is difficult to achieve consistently. Insulin sensitivity defines the metabolic balance between insulin concentration and insulin-mediated glucose disposal. Hence, variability of insulin sensitivity can cause variable glycemia. This study quantifies and compares the daily evolution of insulin sensitivity level and variability for critical care patients receiving TGC. METHODS: This is a retrospective analysis of data from the SPRINT TGC study involving patients admitted to a mixed medical-surgical ICU between August 2005 and May 2007. Only patients who commenced TGC within 12 hours of ICU admission and spent at least 24 hours on the SPRINT protocol were included (N = 164). Model-based insulin sensitivity (SI) was identified each hour. Absolute level and hour-to-hour percent changes in SI were assessed on cohort and per-patient bases. Levels and variability of SI were compared over time on 24-hour and 6-hour timescales for the first 4 days of ICU stay. RESULTS: Cohort and per-patient median SI levels increased by 34% and 33% (p < 0.001) between days 1 and 2 of ICU stay. Concomitantly, cohort and per-patient SI variability decreased by 32% and 36% (p < 0.001). For 72% of the cohort, median SI on day 2 was higher than on day 1. The day 1–2 results are the only clear, statistically significant trends across both analyses. Analysis of the first 24 hours using 6-hour blocks of SI data showed that most of the improvement in insulin sensitivity level and variability seen between days 1 and 2 occurred during the first 12–18 hours of day 1. CONCLUSIONS: Critically ill patients have significantly lower and more variable insulin sensitivity on day 1 than later in their ICU stay and particularly during the first 12 hours. This rapid improvement is likely due to the decline of counter-regulatory hormones as the acute phase of critical illness progresses. Clinically, these results suggest that while using TGC protocols with patients during their first few days of ICU stay, extra care should be afforded. Increased measurement frequency, higher target glycemic bands, conservative insulin dosing, and modulation of carbohydrate nutrition should be considered to minimize safely the outcome glycemic variability and reduce the risk of hypoglycemia. Springer 2012-06-15 /pmc/articles/PMC3464183/ /pubmed/22703645 http://dx.doi.org/10.1186/2110-5820-2-17 Text en Copyright ©2012 Pretty et al.; licensee Springer. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Pretty, Christopher G
Le Compte, Aaron J
Chase, J Geoffrey
Shaw, Geoffrey M
Preiser, Jean-Charles
Penning, Sophie
Desaive, Thomas
Variability of insulin sensitivity during the first 4 days of critical illness: implications for tight glycemic control
title Variability of insulin sensitivity during the first 4 days of critical illness: implications for tight glycemic control
title_full Variability of insulin sensitivity during the first 4 days of critical illness: implications for tight glycemic control
title_fullStr Variability of insulin sensitivity during the first 4 days of critical illness: implications for tight glycemic control
title_full_unstemmed Variability of insulin sensitivity during the first 4 days of critical illness: implications for tight glycemic control
title_short Variability of insulin sensitivity during the first 4 days of critical illness: implications for tight glycemic control
title_sort variability of insulin sensitivity during the first 4 days of critical illness: implications for tight glycemic control
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3464183/
https://www.ncbi.nlm.nih.gov/pubmed/22703645
http://dx.doi.org/10.1186/2110-5820-2-17
work_keys_str_mv AT prettychristopherg variabilityofinsulinsensitivityduringthefirst4daysofcriticalillnessimplicationsfortightglycemiccontrol
AT lecompteaaronj variabilityofinsulinsensitivityduringthefirst4daysofcriticalillnessimplicationsfortightglycemiccontrol
AT chasejgeoffrey variabilityofinsulinsensitivityduringthefirst4daysofcriticalillnessimplicationsfortightglycemiccontrol
AT shawgeoffreym variabilityofinsulinsensitivityduringthefirst4daysofcriticalillnessimplicationsfortightglycemiccontrol
AT preiserjeancharles variabilityofinsulinsensitivityduringthefirst4daysofcriticalillnessimplicationsfortightglycemiccontrol
AT penningsophie variabilityofinsulinsensitivityduringthefirst4daysofcriticalillnessimplicationsfortightglycemiccontrol
AT desaivethomas variabilityofinsulinsensitivityduringthefirst4daysofcriticalillnessimplicationsfortightglycemiccontrol