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Tight Glycemic Control Models for Critically Ill Patients in Intensive Care Units

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Academic year: 2021

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(1)

S. Penning

1

, A. Le Compte

2

, T. Desaive

1

, K. Moorhead

1

and J.G. Chase

2 1Cardiovascular Research Centre, Physics Institute, Liege University

2 Centre for Bio-Engineering, University of Canterbury, Christchurch, New Zealand

Tight glycemic control models for critically ill patients

in intensive care units

Critically ill patients often present stress-induced hyperglycemia and low insulin sensitivity [1]. Recent studies have shown that high blood glucose (BG) levels are linked to worsened patient outcomes and increased mortality [2, 3]. Tight glycemic control (TGC) aims at reducing BG levels taking into account inter-patient variability, evolving physiological patient conditions and minimizing hypoglycemic risks. Clinical protocols are used to specify insulin and nutrition rates and BG measurement frequency during control. This research compares different protocols to determine the best one to use at the CHU of Liege.

Introduction

The STAR-Belgium controller is the best clinical protocol for TGC in this study. We have shown it is highly effective and safe. Pilot trials are currently underway to assess its control performance in real clinical conditions.

Conclusions

sophie.penning@ulg.ac.be tdesaive@ulg.ac.be

geoff.chase@canterbury.ac.nz

Contacts

Initial results : better performance for the Targeted and STAR controllers.

Two main problems with the STAR controller :

1. Aggressiveness, increasing the risk of hypoglycemia (BG < 40 mg/dL)  nutrition rates can be increased & limit the insulin rate changes;

2. Controller differences, harmful to comparison quality  define new BG target of 144 mg/dL and allow 2-hourly measurement

The resulting controller, STAR-Belgium, has the lowest percent of hypoglycemic events and provides the tightest control around its BG target illustrated by the steeper BG cumulative density function (CDF) in Figure 1 and in Table 2.

Results

Table 2 – Virtual trial results: whole cohort statistics

Figure 1 – Comparison of BG CDF for Glucontrol B (blue line) and STAR-Belgium (green line) controllers, for whole cohort

% BG Glucontrol B STAR STAR-Belgium

< 40 mg/dL 0.054 0.062 0.020

> 180 mg/dL 24.1 6.8 12.9

in 140-180 mg/dL 42.4 8.5 50.1

in 120-160 mg/dL 39.33 67.96 58.43

References

1. Lin, J., et al., Comput Methods Programs Biomed, 2008.

89(2): p. 141-52.

2. Egi, M., et al., Anesthesiology, 2006. 105(2): p. 244-52. 3. Krinsley, J.S., Mayo Clin Proc, 2003. 78(12): p. 1471-1478. We compare three protocols described in

Table 1. Glucontrol B is a experimental protocol while Targeted and STAR controllers are model-based. Moreover, STAR controller uses a stochastic model accounting for hour-to-hour patient variability.

Methods

Controller performance was tested in virtual trials using Glucontrol retrospective clinical data and the glucose-insulin model. STAR was adapted to Belgian ICU requirements to create STAR-Belgium.

Table 1 – TGC protocols description

% BG Glucontrol B Targeted/STAR controllers

Origin Belgian protocol Designed for Christchurch, NZ

Features Experimental sliding scale Adaptive, model-based predictive controller

BG target 140 – 180 mg/dL 90 mg/dL

BG measurement

frequency 1 – 4 hours 1 hour

0 50 100 150 200 250 300 350 400 0 0.1 0.2 0.3 0.4 0.5 0.6 0.7 0.8 0.9 1 BG [mg/dL] C u m . fre q . Glucontrol B STAR-Belgium STAR BG target value Glucontrol BG target band

Acknowledgments

Sophie Penning is a FRS-FNRS research fellow. This work was financially supported in part by the University of Liege (post-doctoral fellowship grant) and the University of Canterbury.

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