Evidence map›Paper›PMID 39476551›Full record

ArticleComputer methods and programs in biomedicine2024

Fast interactive simulations of cardiac electrical activity in anatomically accurate heart structures by compressing sparse uniform cartesian grids.

Abouzar Kaboudian, Richard A Gray, Ilija Uzelac, Elizabeth M Cherry, Flavio H Fenton

Abstract read
In one paragraph

Article in Computer methods and programs in biomedicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

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0cells of the map it votes in
4citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Reply to: Stochastic virtual heart model predictions.Nature cardiovascular research · 2025
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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Abouzar KaboudianDivision of Biomedical Physics, Office of Science and Engineering Laboratories, Center for Devices and Radiological Health, US Food and Drug Administration, Silver Spring, MD, USA. Electronic address: abouzar.kaboudian@fda.hhs.gov.
Richard A GrayDivision of Biomedical Physics, Office of Science and Engineering Laboratories, Center for Devices and Radiological Health, US Food and Drug Administration, Silver Spring, MD, USA.
Ilija UzelacSchool of Physics, Georgia Institute of Technology, Atlanta, GA, USA; School of Medicine, Virginia Commonwealth University, Richmond, VA, USA.
Elizabeth M CherrySchool of Computational Science and Engineering, Georgia Institute of Technology, Atlanta, GA, USA.
Flavio H FentonSchool of Physics, Georgia Institute of Technology, Atlanta, GA, USA.

Funding

Integrative High-Resolution Experimental and Multiscale Modeling of Arrhythmias to Optimize Low Energy Anti-fibrillation Pacing (LEAP)R01HL143450 · NHLBI · GEORGIA INSTITUTE OF TECHNOLOGY · PI Flavio H Fenton · 2018 to 2026
$3.2M
Intramural FDA HHS FD999999NHLBI NIH HHS R01 HL143450
6 · The paper itself

Abstract

BACKGROUND AND

objectiveNumerical simulations are valuable tools for studying cardiac arrhythmias. Not only do they complement experimental studies, but there is also an increasing expectation for their use in clinical applications to guide patient-specific procedures. However, numerical studies that solve the reaction-diffusion equations describing cardiac electrical activity remain challenging to set up, are time-consuming, and in many cases, are prohibitively computationally expensive for long studies. The computational cost of cardiac simulations of complex models on anatomically accurate structures necessitates parallel computing. Graphics processing units (GPUs), which have thousands of cores, have been introduced as a viable technology for carrying out fast cardiac simulations, sometimes including real-time interactivity. Our main objective is to increase the performance and accuracy of such GPU implementations while conserving computational resources.

methodsIn this work, we present a compression algorithm that can be used to conserve GPU memory and improve efficiency by managing the sparsity that is inherent in using Cartesian grids to represent cardiac structures directly obtained from high-resolution MRI and mCT scans. Furthermore, we present a discretization scheme that includes the cross-diagonal terms in the computational cell to increase numerical accuracy, which is especially important for simulating thin tissue sections without the need for costly mesh refinement.

resultsInteractive WebGL simulations of atrial/ventricular structures (on PCs, laptops, tablets, and phones) demonstrate the algorithm's ability to reduce memory demand by an order of magnitude and achieve calculations up to 20x faster. We further showcase its superiority in slender tissues and validate results against experiments performed in live explanted human hearts.

conclusionsIn this work, we present a compression algorithm that accelerates electrical activity simulations on realistic anatomies by an order of magnitude (up to 20x), thereby allowing the use of finer grid resolutions while conserving GPU memory. Additionally, improved accuracy is achieved through cross-diagonal terms, which are essential for thin tissues, often found in heart structures such as pectinate muscles and trabeculae, as well as Purkinje fibers. Our method enables interactive simulations with even interactive domain boundary manipulation (unlike finite element/volume methods). Finally, agreement with experiments and ease of mesh import into WebGL paves the way for virtual cohorts and digital twins, aiding arrhythmia analysis and personalized therapies.

Indexed as

AlgorithmsComputer GraphicsComputer SimulationHeartHumansMagnetic Resonance ImagingModels, CardiovascularArrhythmia simulationsDigital twinsInteractive 3D heart computationsWebGL parallel computing

Identifiers

PMID39476551
PMCPMC11581144

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.