Method and system for fast patient-specific cardiac electrophysiology simulations for therapy planning and guidance

US10296809B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10296809-B2
Application numberUS-201313780230-A
CountryUS
Kind codeB2
Filing dateFeb 28, 2013
Priority dateFeb 28, 2012
Publication dateMay 21, 2019
Grant dateMay 21, 2019

How to read this patent

A practical reading order for non-experts. Skip the full description unless you need deep technical detail.

  1. Title

    What the patent document calls the invention.

  2. Abstract

    A short plain-language summary of the technical disclosure.

  3. Assignees and inventors

    Who owns or filed the patent and who is credited as inventor.

  4. Key dates

    Filing, priority, publication, and grant dates set the timeline.

  5. First independent claim

    The legal scope of protection — read this for what is actually claimed.

  6. CPC / IPC classifications

    Technology tags used to group this patent with similar filings.

  7. Citations and related patents

    Prior art links and similar publications in this corpus.

Abstract

Official abstract text for this publication.

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.

First claim

Opening claim text (preview).

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

Assignees

Inventors

Classifications

  • Deformable models or variational models, e.g. snakes or active contours · CPC title

  • G06T7/143Primary

    involving probabilistic approaches, e.g. Markov random field [MRF] modelling · CPC title

  • Aspects of pattern recognition specially adapted for signal processing · CPC title

  • Heart; Cardiac · CPC title

  • 4D tomography; Time-sequential 3D tomography · CPC title

Patent family

Related publications grouped by family.

External sources

Frequently asked questions

Answers are generated from the same data shown on this page.

What does patent US10296809B2 cover?
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 …
Who is the assignee on this patent?
Rapaka Saikiran, Mansi Tommaso, Georgescu Bogdan, and 3 more
What technology area does this patent fall under?
Primary CPC classification G06T7/143. Mapped technology areas include Physics.
When was this patent published?
Publication date Tue May 21 2019 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 5 related publications on this page (citations in our corpus or others sharing the same primary CPC).