Neeraja Kambham

Mohammad Daouk, Jan Ulrich Becker, Neeraja Kambham et al.

Adaptive medical AI models often face performance drops in dynamic clinical environments due to data drift. We propose an autonomous continuous monitoring and data integration framework that maintains robust performance over time. Focusing on glomerular pathology image classification (proliferative vs. non-proliferative lupus nephritis), our three-stage method uses multi-metric feature analysis and Monte Carlo dropout-based uncertainty gating to decide when to retrain on new data. Only images statistically similar to the training distribution (via Euclidean, cosine, Mahalanobis metrics) and with low predictive entropy are integrated. The model is then incrementally retrained with these images under strict performance safeguards (no metric degradation >5%). In experiments with a ResNet18 ensemble on a multi-center dataset, the framework prevents performance degradation: new images were added without significant change in AUC (~0.92) or accuracy (~89%). This approach addresses data shift and avoids catastrophic forgetting, enabling sustained learning in medical imaging AI.

Mohammad Daouk, Jan Ulrich Becker, Neeraja Kambham et al.

Stain variability is a pervasive source of distribution shift and potential shortcut learning in renal pathology AI. We ask whether lupus nephritis glomerular lesion classifiers exploit stain as a shortcut, and how to mitigate such bias without stain or site labels. We curate a multi-center, multi-stain dataset of 9{,}674 glomerular patches (224$\times$224) from 365 WSIs across three centers and four stains (PAS, H\&E, Jones, Trichrome), labeled as proliferative vs.\ non-proliferative. We evaluate Bayesian CNN and ViT backbones with Monte Carlo dropout in three settings: (1) stain-only classification; (2) a dual-head model jointly predicting lesion and stain with supervised stain loss; and (3) a dual-head model with label-free stain regularization via entropy maximization on the stain head. In (1), stain identity is trivially learnable, confirming a strong candidate shortcut. In (2), varying the strength and sign of stain supervision strongly modulates stain performance but leaves lesion metrics essentially unchanged, indicating no measurable stain-driven shortcut learning on this multi-stain, multi-center dataset, while overly adversarial stain penalties inflate predictive uncertainty. In (3), entropy-based regularization holds stain predictions near chance without degrading lesion accuracy or calibration. Overall, a carefully curated multi-stain dataset can be inherently robust to stain shortcuts, and a Bayesian dual-head architecture with label-free entropy regularization offers a simple, deployment-friendly safeguard against potential stain-related drift in glomerular AI.