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Quantifying variabilities in cardiac digital twin models of the electrocardiogram

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arxiv 2407.17146 v2 pith:NMOPQ3F6 submitted 2024-07-24 physics.med-ph cs.NAmath.NAq-bio.TO

classification physics.med-phcs.NAmath.NAq-bio.TO
keywords electrophysiologycardiacdigitalmodelmorphologyanalyzebeat-to-beatcalibration
verification ladder T0 review T1 audit T2 compute T3 formal
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Cardiac digital twins (CDTs) of human cardiac electrophysiology (EP) are digital replicas of patient hearts that match like-for-like clinical observations. The electrocardiogram (ECG), as the most prevalent non-invasive observation of cardiac electrophysiology, is considered an ideal target for CDT calibration. Recent advanced CDT calibration methods have demonstrated their ability to minimize discrepancies between simulated and measured ECG signals, effectively replicating all key morphological features relevant to diagnostics. However, due to the inherent nature of clinical data acquisition and CDT model generation pipelines, discrepancies inevitably arise between the real physical electrophysiology in a patient and the simulated virtual electrophysiology in a CDT. In this study, we aim to qualitatively and quantitatively analyze the impact of these uncertainties on ECG morphology and diagnostic markers. We analyze residual beat-to-beat variability in ECG recordings obtained from healthy subjects and patients. Using a biophysically detailed and anatomically accurate computational model of whole-heart electrophysiology combined with a detailed torso model calibrated to closely replicate measured ECG signals, we vary anatomical factors (heart location, orientation, size), heterogeneity in electrical conductivities in the heart and torso, and electrode placements across ECG leads to assess their qualitative impact on ECG morphology. Our study demonstrates that diagnostically relevant ECG features and overall morphology appear relatively robust against the investigated uncertainties. This resilience is consistent with the narrow distribution of ECG due to residual beat-to-beat variability observed in both healthy subjects and patients.

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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. 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.

  2. Integrating anatomy and electrophysiology in the healthy human heart: Insights from biventricular statistical shape analysis using universal coordinates

    q-bio.TO 2025-01 conditional novelty 6.0 of 10

    A biventricular statistical shape model from 271 healthy CT scans shows heart size and elongation are the main shape variations and correlate with ECG intervals and amplitudes, and provides 100 synthetic heart meshes ...

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