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Accurate and Efficient Cardiac Digital Twin from surface ECGs: Insights into Identifiability of Ventricular Conduction System

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arxiv 2411.00165 v3 pith:GPQ67FKN submitted 2024-10-31 math.OC physics.med-ph

classification math.OCphysics.med-ph
keywords cardiacdigitalactivationecgstwinsaccurateaddressclinical
verification ladder T0 review T1 audit T2 compute T3 formal
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Digital twins for cardiac electrophysiology are an enabling technology for precision cardiology. Current forward models are advanced enough to simulate the cardiac electric activity under different pathophysiological conditions and accurately replicate clinical signals like torso electrocardiograms (ECGs). In this work, we address the challenge of matching subject-specific QRS complexes using anatomically accurate, physiologically grounded cardiac digital twins. By fitting the initial conditions of a cardiac propagation model, our non-invasive method predicts activation patterns during sinus rhythm. For the first time, we demonstrate that distinct activation maps can generate identical surface ECGs. To address this non-uniqueness, we introduce a physiological prior based on the distribution of Purkinje-muscle junctions. Additionally, we develop a digital twin ensemble for probabilistic inference of cardiac activation. Our approach marks a significant advancement in the calibration of cardiac digital twins and enhances their credibility for clinical application.

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Cited by 2 Pith papers

Reviewed papers in the Pith corpus that reference this work. Sorted by Pith novelty score. Full citation record

  1. An efficient end-to-end computational framework for the generation of ECG calibrated volumetric models of human atrial electrophysiology

    math.NA 2025-02 conditional novelty 7.0 of 10

    An end-to-end workflow automatically generates volumetric biatrial models and fast ECG P-wave simulations from patient CT scans, demonstrated on 50 AF patients.

  2. Sensitivity of ECG QRS Complexes to His-Purkinje Structure in Computational Heart Models

    q-bio.QM 2025-05 conditional novelty 6.0 of 10

    Variations in His-Purkinje structure have little individual effect on simulated QRS morphology, but parameter interactions can produce abnormal and premature QRS complexes.

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