A 3D insulin sensitivity prediction model enables more patient-specific prediction and model-based glycaemic control

被引:22
|
作者
Uyttendaele, Vincent [1 ,2 ]
Knopp, Jennifer L. [1 ]
Stewart, Kent W. [1 ]
Desaive, Thomas [2 ]
Benyo, Balazs [3 ]
Szabo-Nemedi, Noemi [4 ]
Illyes, Attila [4 ]
Shaw, Geoffrey M. [5 ,6 ]
Chase, J. Geoffrey [1 ]
机构
[1] Univ Canterbury, Dept Mech Engn, Private Bag 4800, Christchurch, New Zealand
[2] Univ Liege, GIGA Sil Med, Allee 6 Aout 19,Bat B5a, B-4000 Liege, Belgium
[3] Budapest Univ Technol & Econ, Dept Control Engn & Informat Technol, Budapest, Hungary
[4] Kalman Pandy Cty Hosp, Dept Intens Care, Gyula, Hungary
[5] Christchurch Hosp, Dept Intens Care, Christchurch, New Zealand
[6] Univ Otago, Sch Med, Christchurch, New Zealand
关键词
Critical care; Insulin sensitivity; Glycaemic control; Blood glucose; Hyperglycaemia; Insulin; CRITICALLY-ILL PATIENTS; GLUCOSE CONTROL; CRITICAL-CARE; PARAMETER-IDENTIFICATION; ADULT PATIENTS; MORTALITY; THERAPY; HYPERGLYCEMIA; HYPOGLYCEMIA; PROTOCOL;
D O I
10.1016/j.bspc.2018.05.032
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Background: Insulin therapy for glycaemic control (GC) in critically ill patients may improve outcomes by reducing hyperglycaemia and glycaemic variability, which are both associated with increased morbidity and mortality. However, initial positive results have proven difficult to repeat or achieve safely. STAR (Stochastic TARgeted) is a model-based glycaemic control protocol using a risk-based dosing approach. STAR uses a 2D stochastic model to predict distributions of likely future changes in model-based insulin sensitivity (SI) based on its current value, and determines the optimal intervention. Objectives: This study investigates the impact of a new 3D stochastic model on the ability to predict more accurate future SI distributions, which would allow more aggressive insulin dosing and improved glycaemic control. Methods: The new 3D stochastic model is built using both current SI and its prior variation to predict future SI distribution from 68,629 h of clinical data (819 GC episodes). The 5th-95th percentile range of predicted SI distribution are calculated and compared with the 2D model. Results: Results show the 2D model is over-conservative compared to the 3D case for more than 77% of the data, predominantly where SI is stable (vertical bar%Delta SI vertical bar <= 25%). These formerly conservative prediction ranges are now similar to 30% narrower with the 3D model, which safely enables more aggressive insulin dosing for these patient hours. In addition, distributions of predicted SI within the 5th-95th percentile range are much closer to the ideal value of 90% for more patients with the 3D model. Conclusions: The new 3D model better characterises patient specific metabolic variability and patient specific response to insulin, allowing more optimal insulin dosing to increase performance and safety. (C) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:192 / 200
页数:9
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