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1.
J Diabetes Sci Technol ; 1(3): 348-56, 2007 May.
Article in English | MEDLINE | ID: mdl-19885089

ABSTRACT

BACKGROUND: Strict blood glucose control by applying nurse-driven protocols is common nowadays in intensive care units (ICUs). Implementation of a predictive control system can potentially reduce the workload for medical staff but requires a model for accurately predicting the glycemia signal within a certain time horizon. METHODS: GlucoDay (A. Menarini Diagnostics, Italy) data coming from 19 critically ill patients (from a surgical ICU) are used to estimate the initial ICU "minimal" model (based on data of the first 24 hours) and to reestimate the model as new measurements are obtained. The reestimation is performed every hour or every 4 hours. For both approaches the optimal size of the data set for each reestimation is determined. RESULTS: The prediction error that is obtained when applying the 1-hour reestimation strategy is significantly smaller than when the model is reestimated only every 4 hours (p < 0.001). The optimal size of the data set to be considered in each reestimation process of the ICU minimal model is found to be 4 hours. The obtained average "mean percentage error" is 7.6% (SD 3.1%) and 14.6% (SD 7.0%) when the model is reestimated every hour and 4 hours, respectively. CONCLUSIONS: Implementation of the ICU minimal model in the appropriate reestimation process results in clinically acceptable prediction errors. Therefore, the model is able to predict glycemia trends of patients admitted to the surgical ICU and can potentially be used in a predictive control system.

5.
Conf Proc IEEE Eng Med Biol Soc ; 2006: 5432-5, 2006.
Article in English | MEDLINE | ID: mdl-17946700

ABSTRACT

In this paper we propose a modified minimal model to be used for glycemia control in critically ill patients. For various reasons the Bergman minimal model is widely used to describe glucose and insulin dynamics. However, since this model is mostly valid in a rather restrictive setting, it might not be suitable to be used in a model predictive controller. Simulations show that the new model exhibits a similar glycemia behaviour but clinically more realistic insulin kinetics. Therefore it is potentially more suitable for glycemia control. The designed model is also estimated on a set of critically ill patients giving promising results.


Subject(s)
Blood Glucose/analysis , Glucose Tolerance Test/instrumentation , Insulin/metabolism , Aged , Biosensing Techniques , Computer Simulation , Critical Illness , Diabetes Mellitus, Type 1/diagnosis , Diabetes Mellitus, Type 1/therapy , Female , Humans , Kinetics , Male , Middle Aged , Models, Statistical , Reproducibility of Results
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