In Silico Diabetes Simulation Environment for Control Algorithm Validation

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Solution Overview

Problem

Current diabetes management systems, particularly for type 1 diabetes, face challenges in accurately simulating individual glucose-insulin dynamics and sensor errors, limiting the effectiveness of closed-loop control algorithms for outpatient use.

Innovation Solution

A computer simulation environment is developed, incorporating a Glucose Insulin Model (GIM) with individualized parameters for 300 subjects, simulating subcutaneous continuous glucose monitoring and insulin delivery, and accounting for sensor errors to test treatment strategies and control algorithms in a realistic manner.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Productivity

If population-based diabetes models are used for simulation, then computational efficiency is improved, but individual glucose-insulin dynamics accuracy deteriorates

Engineering Contradiction:
Improvecomputational efficiencyVSAvoidindividual glucose-insulin dynamics accuracy
Core Design Contradiction:
ProductivityVSMeasurement precision

Solution Approach 1:

The patent creates virtual copies (avatars) of real diabetic patients by transferring their actual physiological parameters, sensor characteristics, and insulin pump settings into simulation models. This allows individualized testing of control algorithms on multiple patient-specific virtual models simultaneously, maintaining both computational efficiency and individual accuracy.

Inventive Principle:
Principle #26Copying

Solution Approach 2:

The simulation system segments the diabetes management system into distinct modular components: glucose dynamics models, sensor error models, insulin pump models, and control algorithms. This modular segmentation enables efficient computational processing while allowing precise individualization of each component's parameters for different patient avatars.

Inventive Principle:
Principle #1Segmentation

2Device complexity

If simplified sensor and pump models are used, then model complexity is reduced, but realism of simulation deteriorates

Engineering Contradiction:
Improvemodel complexityVSAvoidrealism of simulation
Core Design Contradiction:
Device complexityVSReliability

Solution Approach 1:

The patent changes the parameters of existing sensor and pump models to match actual device characteristics. Sensor models incorporate specific error patterns, delays, and measurement ranges observed in real continuous glucose monitors. Insulin pump models include actual delivery rates, absorption dynamics, and operational constraints from real devices, enhancing simulation realism without requiring completely new complex models.

Inventive Principle:
Principle #35Parameter changes

3Measurement precision

If individualized patient parameters are implemented, then simulation accuracy for specific patients is improved, but data requirements and model setup complexity increase

Engineering Contradiction:
Improvesimulation accuracy for specific patientsVSAvoidmodel setup complexity
Core Design Contradiction:
Measurement precisionVSDevice complexity

Solution Approach 1:

The patent performs preliminary actions by pre-processing real patient data during avatar creation, organizing physiological parameters, sensor characteristics, and pump settings into structured formats ready for simulation. This preliminary data preparation and parameter extraction work is done once per patient, reducing the complexity of setting up individualized simulations for each new patient avatar.

Inventive Principle:
Principle #10Preliminary action

Data Source

PatentEP2203112B1Method, system and computer simulation environment for testing of monitoring and control strategies in diabetes
Publication Date: 2020.03.11 UNIV OF VIRGINIA PATENT FOUND
  • EP2203112B1 patent drawingFigure 1
  • EP2203112B1 patent drawingFigure 2
  • EP2203112B1 patent drawingFigure 3A~3B

AI summary

A simulation environment for in silico testing of monitoring methods, open-loop and closed-loop treatment strategies in type 1 diabetes. Some exemplary principal components of the simulation environment comprise, but not limited thereto, the following: 1) a "population" of in silico "subjects" with type 1 diabetes in three age groups; 2) a simulator of CGM sensor errors; 3) a simulator of insulin pumps and discrete insulin delivery; 4) an interface allowing the input of user-specified treatment scenarios; and 5) a set of standardized outcome measures and graphs evaluating the quality of the tested treatment strategies. These components can be used separately or in combination for the preclinical evaluation of open-loop or closed-loop control treatments of diabetes.