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<p>Multi-label chest X-ray classification faces three critical challenges: (i)&#xa0;inadequate modeling of inter-pathology dependencies despite clinical co-occurrence patterns, (ii)&#xa0;severe class imbalance (11.2−47.6%) causing minority-class underperformance, and (iii)&#xa0;limited interpretability hindering clinical trust. Existing methods address these challenges independently; no current framework jointly models pathology dependencies, imbalance-aware training, and interpretable attention. We propose a Hierarchical Pathology-aware Vision Transformer (HP-ViT), which jointly addresses these limitations in a unified architecture by employing: Hierarchical Pathology-Aware Attention (HPAA) for explicit disease co-occurrence modeling through two-stage token refinement, Multi-Scale Feature Aggregation (MSFA) for detecting localized and diffuse abnormalities across four hierarchical scales, and Balanced Adaptive Focal Loss (BAFL) implementing curriculum-scheduled focal modulation that progressively transitions from class-balanced to difficulty-focused training. Evaluated on COVIDx, ChestX-ray14, and BIMCV-COVID19+ (<InlineEquation ID="IEq1"> <EquationSource Format="TEX">\(N{=}36{,}904\)</EquationSource> </InlineEquation> images), HP-ViT achieves macro-F1 of 0.924, exact match ratio of 0.842, and PPV of 0.925, representing 1.76%, 1.32%, and 1.5% improvements over state-of-the-art, with statistical significance (<InlineEquation ID="IEq2"> <EquationSource Format="TEX">\(p&lt;0.001\)</EquationSource> </InlineEquation>, McNemar’s test on per-sample exact-match correctness). HP-ViT requires only 12.6 M parameters (85% reduction vs. ViT-B/16) with 29.8&#xa0;ms inference time, enabling real-time clinical deployment. Interpretability evaluation yields 83.7% mean SSIM between attention maps and radiologist annotations, confirming pathology-aligned localization.</p>

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Pathology aware hierarchical transformers for multi-label thoracic disease classification using chest X-rays

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2026年4月27日

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  • Muneeb A. Khan,
  • Heemin Park,
  • Khurelbaatar Zagarzusem,
  • Seonuck Paek

摘要

Multi-label chest X-ray classification faces three critical challenges: (i) inadequate modeling of inter-pathology dependencies despite clinical co-occurrence patterns, (ii) severe class imbalance (11.2−47.6%) causing minority-class underperformance, and (iii) limited interpretability hindering clinical trust. Existing methods address these challenges independently; no current framework jointly models pathology dependencies, imbalance-aware training, and interpretable attention. We propose a Hierarchical Pathology-aware Vision Transformer (HP-ViT), which jointly addresses these limitations in a unified architecture by employing: Hierarchical Pathology-Aware Attention (HPAA) for explicit disease co-occurrence modeling through two-stage token refinement, Multi-Scale Feature Aggregation (MSFA) for detecting localized and diffuse abnormalities across four hierarchical scales, and Balanced Adaptive Focal Loss (BAFL) implementing curriculum-scheduled focal modulation that progressively transitions from class-balanced to difficulty-focused training. Evaluated on COVIDx, ChestX-ray14, and BIMCV-COVID19+ ( \(N{=}36{,}904\) images), HP-ViT achieves macro-F1 of 0.924, exact match ratio of 0.842, and PPV of 0.925, representing 1.76%, 1.32%, and 1.5% improvements over state-of-the-art, with statistical significance ( \(p<0.001\) , McNemar’s test on per-sample exact-match correctness). HP-ViT requires only 12.6 M parameters (85% reduction vs. ViT-B/16) with 29.8 ms inference time, enabling real-time clinical deployment. Interpretability evaluation yields 83.7% mean SSIM between attention maps and radiologist annotations, confirming pathology-aligned localization.