Myocardial Mass Normalization for Nuclear Medicine Ischemia Detection

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Solution Overview

Problem

Existing methods for detecting myocardial ischemia using nuclear medicine imaging underestimate conditions with diffusely lowered myocardial blood flow, particularly in patients with multivessel ischemic cardiomyopathy, due to inappropriate assumptions about tracer distribution.

Innovation Solution

A method that normalizes myocardial nuclear medicine image data using a value related to the size of the heart, such as heart weight, to accurately reflect cardiac function and correct for tracer accumulation, allowing for more precise evaluation of blood flow changes under stress and at rest.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Measurement precision

If existing SUV normalization using body mass is used, then general quantitative evaluation is enabled, but tracer accumulation in myocardia is not accurately reflected

Engineering Contradiction:
Improvetracer accumulation evaluation accuracyVSAvoidischemia detection reliability
Core Design Contradiction:
Measurement precisionVSReliability

Solution Approach 1:

The patent changes the normalization parameter from body mass to myocardial mass. This is achieved by calculating myocardial volume from segmented myocardial images and converting it to myocardial mass using a density coefficient (1.05 g/cm³). The SUV is then recalculated using myocardial mass instead of body mass, which accurately reflects the actual tracer distribution in myocardial tissue and improves both measurement precision and detection reliability.

Inventive Principle:
Principle #35Parameter changes

2Ease of manufacture

If simple body mass normalization is applied, then calculation is simplified, but patients with diffusely lowered myocardial blood flow are underestimated

Engineering Contradiction:
Improvenormalization calculation simplicityVSAvoidischemic condition evaluation accuracy
Core Design Contradiction:
Ease of manufactureVSMeasurement precision

Solution Approach 1:

The patent replaces the simple body mass parameter with a more accurate myocardial mass parameter. The myocardial mass is obtained by segmenting the myocardium from the image, calculating its volume, and multiplying by the density coefficient. This parameter change maintains computational feasibility while significantly improving the accuracy of ischemic condition evaluation, particularly for patients with diffuse blood flow reduction.

Inventive Principle:
Principle #35Parameter changes

3Adaptability or versatility

If existing normalization methods are used, then general applicability is maintained, but multivessel ischemic cardiomyopathy is not properly detected

Engineering Contradiction:
Improvenormalization method applicabilityVSAvoidmultivessel ischemia detection reliability
Core Design Contradiction:
Adaptability or versatilityVSReliability

Solution Approach 1:

The patent modifies the normalization parameter from body mass to myocardial mass, which is calculated by segmenting the myocardium and applying density conversion. This parameter change maintains the SUV framework's versatility while specifically improving detection reliability for multivessel ischemic cardiomyopathy, as the myocardial-specific normalization accurately captures regional perfusion deficits characteristic of this condition.

Inventive Principle:
Principle #35Parameter changes

Data Source

PatentEP3254625B1Method and apparatus for analyzing nuclear medicine image of myocardia
Publication Date: 2019.07.03 NIHON MEDI PHYSICS CO LTD
  • EP3254625B1 patent drawingFigure 1
  • EP3254625B1 patent drawingFigure 2
  • EP3254625B1 patent drawingFigure 3

AI summary

Provided is a highly reliable technique for the evaluation of ischemic conditions. A preferred embodiment is a nuclear medicine measurement protocol in which the administration of a radiopharmaceutical agent and radiation measurement are performed twice at rest and under stress. In the nuclear medicine measurement protocol, radiation collection is performed without radiopharmaceutical agent administration before the second radiopharmaceutical agent administration, and the result is used to correct the nuclear medicine measurement result after the second radiopharmaceutical agent administration.