Second pilot trials of the STAR-Liege protocol for tight glycemic control in critically ill patients

<p>Abstract</p> <p>Background</p> <p>Critically ill patients often present increased insulin resistance and stress-induced hyperglycemia. Tight glycemic control aims to reduce blood glucose (BG) levels and variability while ensuring safety from hypoglycemia. This paper...

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Main Authors: Penning Sophie, Le Compte Aaron J, Massion Paul, Moorhead Katherine T, Pretty Christopher G, Preiser Jean-Charles, Shaw Geoffrey M, Suhaimi Fatanah, Desaive Thomas, Chase J
Format: Article
Language:English
Published: BMC 2012-08-01
Series:BioMedical Engineering OnLine
Subjects:
Online Access:http://www.biomedical-engineering-online.com/content/11/1/58
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spelling doaj-85d7a8da443444c1b1e611b5a75d117b2020-11-25T00:16:18ZengBMCBioMedical Engineering OnLine1475-925X2012-08-011115810.1186/1475-925X-11-58Second pilot trials of the STAR-Liege protocol for tight glycemic control in critically ill patientsPenning SophieLe Compte Aaron JMassion PaulMoorhead Katherine TPretty Christopher GPreiser Jean-CharlesShaw Geoffrey MSuhaimi FatanahDesaive ThomasChase J<p>Abstract</p> <p>Background</p> <p>Critically ill patients often present increased insulin resistance and stress-induced hyperglycemia. Tight glycemic control aims to reduce blood glucose (BG) levels and variability while ensuring safety from hypoglycemia. This paper presents the results of the second Belgian clinical trial using the customizable STAR framework in a target-to-range control approach. The main objective is reducing measurement frequency while maintaining performance and safety of the glycemic control.</p> <p>Methods</p> <p>The STAR-Liege 2 (SL2) protocol targeted the 100–140 mg/dL glycemic band and offered 2-hourly and 3-hourly interventions. Only insulin rates were adjusted, and nutrition inputs were left to the attending clinicians. This protocol restricted the forecasted risk of BG < 90 mg/dL to a 5% level using a stochastic model of insulin sensitivity to assess patient-specific responses to insulin and its future likely variability to optimize insulin interventions. The clinical trial was performed at the Centre Hospitalier Universitaire de Liege and included 9 patients. Results are compared to 24-hour pre-trial and 24-hour post-trial, but also to the results of the first pilot trial performed in Liege, STAR-Liege 1 (SL1). This trial was approved by the Ethics Committee of the Medical Faculty of the University of Liege (Liege, Belgium).</p> <p>Results</p> <p>During the SL2 trial, 91 measurements were taken over 194 hours. BG levels were tightly distributed: 54.9% of BG within 100–140 mg/dL, 40.7% were ≥ 140 mg/dL and 4.4% were < 100 mg/dL with no BG < 70 mg/dL. Comparing these results with 24-hour pre-trial and post-trial shows that SL2 reduced high and low BG levels and reduced glycemic variability. Nurses selected 3-hourly measurement only 5 of 16 times and overrode 12% of 91 recommended interventions (35% increased insulin rates and 65% decreased insulin rates). SL1 and SL2 present similar BG levels distribution (p > 0.05) with significantly reduced measurement frequency for SL2 (p < 0.05).</p> <p>Conclusions</p> <p>The SL2 protocol succeeded in reducing clinical workload while maintaining safety and effectiveness of the glycemic control. SL2 was also shown to be safer and tighter than hospital control. Overall results validate the efficacy of significantly customizing the STAR framework.</p> http://www.biomedical-engineering-online.com/content/11/1/58Glycemic controlCritical careIntensive care unitPilot trial
collection DOAJ
language English
format Article
sources DOAJ
author Penning Sophie
Le Compte Aaron J
Massion Paul
Moorhead Katherine T
Pretty Christopher G
Preiser Jean-Charles
Shaw Geoffrey M
Suhaimi Fatanah
Desaive Thomas
Chase J
spellingShingle Penning Sophie
Le Compte Aaron J
Massion Paul
Moorhead Katherine T
Pretty Christopher G
Preiser Jean-Charles
Shaw Geoffrey M
Suhaimi Fatanah
Desaive Thomas
Chase J
Second pilot trials of the STAR-Liege protocol for tight glycemic control in critically ill patients
BioMedical Engineering OnLine
Glycemic control
Critical care
Intensive care unit
Pilot trial
author_facet Penning Sophie
Le Compte Aaron J
Massion Paul
Moorhead Katherine T
Pretty Christopher G
Preiser Jean-Charles
Shaw Geoffrey M
Suhaimi Fatanah
Desaive Thomas
Chase J
author_sort Penning Sophie
title Second pilot trials of the STAR-Liege protocol for tight glycemic control in critically ill patients
title_short Second pilot trials of the STAR-Liege protocol for tight glycemic control in critically ill patients
title_full Second pilot trials of the STAR-Liege protocol for tight glycemic control in critically ill patients
title_fullStr Second pilot trials of the STAR-Liege protocol for tight glycemic control in critically ill patients
title_full_unstemmed Second pilot trials of the STAR-Liege protocol for tight glycemic control in critically ill patients
title_sort second pilot trials of the star-liege protocol for tight glycemic control in critically ill patients
publisher BMC
series BioMedical Engineering OnLine
issn 1475-925X
publishDate 2012-08-01
description <p>Abstract</p> <p>Background</p> <p>Critically ill patients often present increased insulin resistance and stress-induced hyperglycemia. Tight glycemic control aims to reduce blood glucose (BG) levels and variability while ensuring safety from hypoglycemia. This paper presents the results of the second Belgian clinical trial using the customizable STAR framework in a target-to-range control approach. The main objective is reducing measurement frequency while maintaining performance and safety of the glycemic control.</p> <p>Methods</p> <p>The STAR-Liege 2 (SL2) protocol targeted the 100–140 mg/dL glycemic band and offered 2-hourly and 3-hourly interventions. Only insulin rates were adjusted, and nutrition inputs were left to the attending clinicians. This protocol restricted the forecasted risk of BG < 90 mg/dL to a 5% level using a stochastic model of insulin sensitivity to assess patient-specific responses to insulin and its future likely variability to optimize insulin interventions. The clinical trial was performed at the Centre Hospitalier Universitaire de Liege and included 9 patients. Results are compared to 24-hour pre-trial and 24-hour post-trial, but also to the results of the first pilot trial performed in Liege, STAR-Liege 1 (SL1). This trial was approved by the Ethics Committee of the Medical Faculty of the University of Liege (Liege, Belgium).</p> <p>Results</p> <p>During the SL2 trial, 91 measurements were taken over 194 hours. BG levels were tightly distributed: 54.9% of BG within 100–140 mg/dL, 40.7% were ≥ 140 mg/dL and 4.4% were < 100 mg/dL with no BG < 70 mg/dL. Comparing these results with 24-hour pre-trial and post-trial shows that SL2 reduced high and low BG levels and reduced glycemic variability. Nurses selected 3-hourly measurement only 5 of 16 times and overrode 12% of 91 recommended interventions (35% increased insulin rates and 65% decreased insulin rates). SL1 and SL2 present similar BG levels distribution (p > 0.05) with significantly reduced measurement frequency for SL2 (p < 0.05).</p> <p>Conclusions</p> <p>The SL2 protocol succeeded in reducing clinical workload while maintaining safety and effectiveness of the glycemic control. SL2 was also shown to be safer and tighter than hospital control. Overall results validate the efficacy of significantly customizing the STAR framework.</p>
topic Glycemic control
Critical care
Intensive care unit
Pilot trial
url http://www.biomedical-engineering-online.com/content/11/1/58
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