TL;DR
This paper introduces a novel action-conditioned world model for cardiac time-series analysis that captures disease progression dynamics, outperforming static models especially in low-resource settings.
Contribution
It adapts the LeJEPA framework to physiological data, modeling pathology as dynamic state transitions rather than static labels, improving robustness and sample efficiency.
Findings
Outperforms supervised baselines on triage tasks.
Demonstrates over 0.05 AUROC improvement in low-resource regimes.
Effectively disentangles anatomical features from pathological dynamics.
Abstract
Self-supervised learning in healthcare has largely relied on invariance-based objectives, which maximize similarity between different views of the same patient. While effective for static anatomy, this paradigm is fundamentally misaligned with clinical diagnosis, as it mathematically compels the model to suppress the transient pathological changes it is intended to detect. We propose a shift towards Action-Conditioned World Models that learn to simulate the dynamics of disease progression, or Event-Conditioned. Adapting the LeJEPA framework to physiological time-series, we define pathology not as a static label, but as a transition vector acting on a patient's latent state. By predicting the future electrophysiological state of the heart given a disease onset, our model explicitly disentangles stable anatomical features from dynamic pathological forces. Evaluated on the MIMIC-IV-ECG…
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