System and method for deep learning based cardiac electrophysiology model personalization
US-2017330075-A1 · Nov 16, 2017 · US
US10296809B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10296809-B2 |
| Application number | US-201313780230-A |
| Country | US |
| Kind code | B2 |
| Filing date | Feb 28, 2013 |
| Priority date | Feb 28, 2012 |
| Publication date | May 21, 2019 |
| Grant date | May 21, 2019 |
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A method and system for patient-specific cardiac electrophysiology is disclosed. Particularly, a patient-specific anatomical model of a heart is generated from medical image data of a patient, a level-set representation of the patient-specific anatomical model is generated of the heart on a Cartesian grid; and a transmembrane action potential at each node of the level-set representation of the of the patient-specific anatomical model of the heart is computed on a Cartesian grid.
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The invention claimed is: 1. A method for patient-specific cardiac electrophysiology computations, comprising: generating a patient-specific anatomical model of a heart from medical image data of a patient; identifying at least one key electrophysiological structures of interest from the patient-specific anatomical model and medical image data; generating a level-set representation of the patient-specific anatomical model of the heart on a Cartesian grid; and computing a transmembrane action potential on at least one node of the level-set representation of the patient-specific anatomical model of the heart, wherein computing the transmembrane action potential is based at least in part on a stimulus current input as an initial condition. 2. The method of claim 1 , wherein the step of generating a patient-specific anatomical model of a heart from medical image data of a patient comprises: detecting a patient-specific left ventricle endocardium model, a patient-specific right ventricle endocardium model, and a patient-specific epicardium model in the medical image data; and fusing the left ventricle endocardium model, the right ventricle endocardium model and the epicardium model into a single bi-ventricular volumetric mesh. 3. The method of claim 2 , wherein the step of generating a patient-specific anatomical model of a heart from medical image data of a patient further comprises: mapping spatial information corresponding to at least one of scars, grey zones, or fibrosis identified from medical-image data and other clinical measurements onto the bi-ventricular volumetric mesh. 4. The method of claim 2 , wherein the step of generating a patient-specific anatomical model of a heart from medical image data of a patient further comprises: registering a tensor field of an in-vivo diffusion tensor magnetic resonance image of cardiac fibers to the bi-ventricular volumetric mesh. 5. The method of claim 2 , wherein the step of generating a patient-specific anatomical model of a heart from medical image data of a patient further comprises: generating a global model of fiber architecture based on the bi-ventricular volumetric mesh and nominal values for fiber elevation angle distribution. 6. The method of claim 1 , wherein the step of computing the transmembrane action potential on at least one node of the level-set representation of the patient-specific anatomical model of the heart further comprising: solving at least one monodomain electrophysiology model using a Lattice-Boltzmann method on at least one node of the level-set representation on a Cartesian grid. 7. The method of claim 1 , wherein the step of generating a level-set representation of the patient-specific anatomical model of the heart on a Cartesian grid comprises: discretizing a domain of the patient-specific model of the heart using a Cartesian lattice in which each node is connected via edges to a predetermined number of neighboring nodes. 8. The method of claim 1 , wherein the step of computing the transmembrane action potential on at least one node of the level-set representation of the patient-specific anatomical model of the heart further comprises: at each of a plurality of time steps: for at least one node of the level-set representation of the patient-specific anatomical model of the heart on a Cartesian grid, calculating collisions of particles for each edge connected to the node based on a distribution function calculated for each edge; calculating the transmembrane action potential at the node based on the collisions of particles calculated at the node; updating all cellular model-dependent internal variables at the node; updating the distribution function for each edge of the node to represent streaming of a particle traveling along each of the edges to a neighboring node; and applying optional Dirichlet boundary conditions. 9. The method of claim 8 , wherein the step of calculating collisions of particles for each edge connected to the node based on a distribution function calculated for each edge comprises: calculating collisions on each edge connected to the node as: f i =f i −A ij ( f j −ω j υ)+δ tω i R (υ, { h }) where f i is the distribution function that represents a probability of finding a particle traveling along the i th edge e i connected to the node, A=(A ij ) i,j ∈ is a collision matrix that relaxes the distribution function f i towards a local potential value, υ, R(v, {h}) is a model-dependent term for electrophysiological currents, which depends on a model-dependent set of internal variables {h}, and ω i and ω j are weighting factors for edges e i and e j , respectively. 10. The method of claim 9 , wherein the collision matrix A is defined as A=M −1 SM, where M is a matrix designed to transform the distribution functions into a vector of moments and S −1 is a matrix of relaxation times corresponding to the moments, and M and S −1 are respectively defined as: M = ( 1 1 1 1 1 1 1 0 - 1 0 0 0 0 0 0 0 1 - 1 0 0 0 0 0 0 0
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