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用于前馈控制的血浆葡萄糖浓度多输入特定受试者建模

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

作者信息

Kotz Kaylee, Cinar Ali, Mei Yong, Roggendorf Amy, Littlejohn Elizabeth, Quinn Laurie, Rollins Derrick K

机构信息

Department of Chemical and Biological Engineering, Iowa State University , Ames, Iowa 50011, United States.

Department of Chemical and Biological Engineering, Illinois Institute of Technology , Chicago, Illinois 60616, United States.

出版信息

Ind Eng Chem Res. 2014 Nov 26;53(47):18216-18225. doi: 10.1021/ie404119b. Epub 2014 Nov 3.

Abstract

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.

摘要

针对大量输入集准确开发血糖浓度(BGC)的特定主题输入因果模型的能力,可能对加强胰岛素依赖型糖尿病的控制产生重大影响。更具体地说,对于1型糖尿病患者(T1D),在关键干扰因素发生极端变化的情况下,它可以促成有效的人工胰腺(即一种输送外源性胰岛素的自动控制系统)。这些干扰因素包括食物摄入、活动变化和生理应激变化。因此,本文提出了一种针对BGC的自由生活、门诊、多输入建模方法,该方法具有很强的因果属性,稳定且能防止过拟合,为前馈控制(FFC)提供了一种有效的建模方法。这种方法是一种面向维纳块的方法,具有满足有效长期FFC关键要求的独特属性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d67c/4299404/3b2c1f6f4945/ie-2013-04119b_0001.jpg

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