Why Specialist Models Still Matter: A Heterogeneous Multi-Agent Paradigm for Medical Artificial Intelligence

The impressive performance of generalist large language models (LLMs) such as GPT and Claude in healthcare raises a critical question: will domain-specific medical specialist models become obsolete? We argue that the future of medical artificial intelligence (AI) lies not in building monolithic medical foundation models, nor in replacing human expertise, but in orchestrating collaboration among generalist LLMs, domain-specific specialist models, and clinicians. We propose HetMedAgent, a heterogeneous medical multi-agent framework that enables conflict-aware evidence fusion, uncertainty-based clinician intervention triggering, and adaptive threshold calibration. Experiments on three real-world clinical decision-making tasks demonstrate that the synergy between generalist LLMs and domain-specific specialist models significantly outperforms using either type of model alone, validating the irreplaceable value of specialist models in modality-specific analysis. HetMedAgent represents a shift from building medical LLMs or foundation models to multi-agent collaboration, achieving a balance between general reasoning capabilities and domain-specific precision.

Amplitude-Phase Fusion for Enhanced Electrocardiogram Morphological Analysis

Considering the variability of amplitude and phase patterns in electrocardiogram (ECG) signals due to cardiac activity and individual differences, existing entropy-based studies have not fully utilized these two patterns and lack integration. To address this gap, this paper proposes a novel fusion entropy metric, morphological ECG entropy (MEE) for the first time, specifically designed for ECG morphology, to comprehensively describe the fusion of amplitude and phase patterns. MEE is computed based on beat-level samples, enabling detailed analysis of each cardiac cycle. Experimental results demonstrate that MEE achieves rapid, accurate, and label-free localization of abnormal ECG arrhythmia regions. Furthermore, MEE provides a method for assessing sample diversity, facilitating compression of imbalanced training sets (via representative sample selection), and outperforms random pruning. Additionally, MEE exhibits the ability to describe areas of poor quality. By discussing, it proves the robustness of MEE value calculation to noise interference and its low computational complexity. Finally, we integrate this method into a clinical interactive interface to provide a more convenient and intuitive user experience. These findings indicate that MEE serves as a valuable clinical descriptor for ECG characterization. The implementation code can be referenced at the following link: https://github.com/fdu-harry/ECG-MEE-metric.