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Multiple-Input Subject-Specific Modeling of Plasma Glucose Concentration for Feedforward Control

The ability to accurately develop subject-specific, input causation models, for blood glucose concentration (BGC) for large input sets can have a significant impact on tightening control for insulin dependent diabetes. More specifically, for Type 1 diabetics (T1Ds), it can lead to an effective artif...

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Detalles Bibliográficos
Autores principales: Kotz, Kaylee, Cinar, Ali, Mei, Yong, Roggendorf, Amy, Littlejohn, Elizabeth, Quinn, Laurie, Rollins, Derrick K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2014
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4299404/
https://www.ncbi.nlm.nih.gov/pubmed/25620845
http://dx.doi.org/10.1021/ie404119b
Descripción
Sumario:The ability to accurately develop subject-specific, input causation models, for blood glucose concentration (BGC) for large input sets can have a significant impact on tightening control for insulin dependent diabetes. More specifically, for Type 1 diabetics (T1Ds), it can lead to an effective artificial pancreas (i.e., an automatic control system that delivers exogenous insulin) under extreme changes in critical disturbances. These disturbances include food consumption, activity variations, and physiological stress changes. Thus, this paper presents a free-living, outpatient, multiple-input, modeling method for BGC with strong causation attributes that is stable and guards against overfitting to provide an effective modeling approach for feedforward control (FFC). This approach is a Wiener block-oriented methodology, which has unique attributes for meeting critical requirements for effective, long-term, FFC.