Dynamic Blood Glucose Reference Timing

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Solution Overview

Problem

Current methods for determining blood glucose reference sample times in insulin infusion therapy often follow a fixed schedule, which is not dynamically responsive to individual patient conditions, leading to inefficient glucose monitoring and potential glycemic excursions.

Innovation Solution

A processor-implemented method and system that dynamically determines the timing of blood glucose reference sample measurements based on continuous glucose sensor readings, considering factors like current glucose levels, rate of change, predicted values, and sensor reliability to tailor the frequency of metered blood glucose sample measurements to the patient's specific state.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Productivity

If fixed schedule blood glucose monitoring is used, then monitoring consistency is maintained, but monitoring efficiency decreases and unnecessary measurements increase

Engineering Contradiction:
Improvemonitoring efficiencyVSAvoidtime for unnecessary measurements
Core Design Contradiction:
ProductivityVSLoss of time

Solution Approach 1:

The patent implements dynamic adjustment of blood glucose monitoring frequency based on real-time sensor data and patient state. The system transitions from fixed-schedule monitoring to adaptive monitoring where the frequency of reference sample measurements is continuously adjusted according to glycemic stability, sensor reliability metrics, and rate of change indicators, thereby eliminating unnecessary measurements while maintaining safety.

Inventive Principle:
Principle #15Dynamics

Solution Approach 2:

The system changes the parameter of monitoring frequency from a static fixed value to a dynamic variable that adjusts based on multiple factors including sensor glucose readings, rate of change, predicted glucose values, and sensor reliability metrics. This parameter change enables the system to optimize monitoring efficiency by increasing frequency only when clinically necessary.

Inventive Principle:
Principle #35Parameter changes

2Reliability

If frequent blood glucose sample measurements are taken, then glycemic control safety is improved, but patient burden and resource utilization worsen

Engineering Contradiction:
Improveglycemic control safetyVSAvoidpatient burden
Core Design Contradiction:
ReliabilityVSEase of operation

Solution Approach 1:

The patent applies local quality by differentiating monitoring intensity based on specific patient states and risk factors. Rather than applying uniform frequent monitoring to all patients, the system identifies local conditions (such as rapid glucose changes, hypoglycemia risk, sensor malfunction indicators) and increases monitoring frequency only in those specific contexts, thereby maintaining safety while reducing overall patient burden.

Inventive Principle:
Principle #3Local quality

Solution Approach 2:

The system implements feedback mechanisms where sensor glucose data, sensor reliability metrics, and patient responses to previous measurements are continuously fed back into the monitoring frequency determination algorithm. This feedback loop enables the system to maintain glycemic control safety by detecting when increased monitoring is needed while automatically reducing frequency when conditions are stable, thereby minimizing patient burden.

Inventive Principle:
Principle #23Feedback

3Speed

If continuous glucose sensor monitoring is used, then real-time glucose tracking is improved, but measurement accuracy compared to metered samples decreases

Engineering Contradiction:
Improvereal-time tracking speedVSAvoidglucose measurement accuracy
Core Design Contradiction:
SpeedVSMeasurement precision

Solution Approach 1:

The patent uses metered blood glucose samples as an intermediary reference standard to validate and calibrate continuous sensor measurements. The system strategically determines when reference samples are needed based on sensor reliability metrics, using these intermediary measurements to maintain accuracy while leveraging the speed advantage of continuous monitoring for real-time tracking between reference points.

Inventive Principle:
Principle #24Intermediary (Mediator)

Solution Approach 2:

The system applies partial action by using metered blood glucose samples only when necessary rather than continuously. The patent determines optimal timing for reference samples based on sensor performance indicators, applying the more accurate but invasive measurement method selectively rather than excessively, thereby maintaining overall measurement precision while preserving the benefits of continuous monitoring.

Inventive Principle:
Principle #16Partial or excessive action

4Productivity

If adaptive monitoring frequency is implemented, then resource utilization is improved, but system complexity increases

Engineering Contradiction:
Improveresource utilizationVSAvoidmonitoring system complexity
Core Design Contradiction:
ProductivityVSDevice complexity

Solution Approach 1:

The patent segments the monitoring system into distinct functional modules: sensor glucose measurement module, sensor reliability metric calculation module, reference sample timing determination module, and insulin infusion control module. This segmentation allows the complex adaptive algorithm to be implemented as coordinated subsystems, improving resource utilization while managing system complexity through modular design.

Inventive Principle:
Principle #1Segmentation

Data Source

PatentUS20240197212A1Method and/or system for determining blood glucose reference sample times
Publication Date: 2024.06.20 MEDTRONIC MINIMED INC
  • US20240197212A1 patent drawing
  • US20240197212A1 patent drawing
  • US20240197212A1 patent drawing

AI summary

Techniques disclose herein relate to determining glucose reference sample times. The techniques may involve determining a first glucose reference sample measurement for a patient. The techniques may further involve determining timing information for obtaining a second glucose reference sample measurement based at least in part on readings from a continuous glucose sensor.