An interpretable and interactive clinical AI agent for personalized anti-infective decision support in carbapenem-resistant Gram-negative bacterial infection
Cao, X.; Shi, D.; Du, Z.; Zhou, J.; Wang, Z.; Liu, Z.; Wang, Q.
Show abstract
Carbapenem-resistant Gram-negative bacteria (CRGNB) infections remain difficult to manage because treatment decisions must balance heterogeneous patient risk, limited antibiotic options, potential toxicity and emerging resistance. Clinical care in this setting requires not only single-endpoint risk prediction, but also decision-support frameworks that can jointly enable prognosis assessment, result interpretation, and individualized treatment comparison. Here we present Dr.BUG, an interactive clinical AI agent for personalized decision support in CRGNB infection. Dr.BUG integrates stable feature-set selection, multi-task prognostic modelling, interpretability analysis and model-based simulation of antibiotic regimen recommendation into a unified workflow. Using a development cohort, a temporally independent validation cohort, and external cohorts from the MIMIC-IV dataset, we developed and validated models for four clinically relevant tasks: clinical efficacy, survival outcome, polymyxin resistance and treatment duration. Model inputs were derived primarily from routinely available and relatively low-cost clinical variables, supporting translational feasibility. Across the major tasks, selected-feature models matched or exceeded the performance of their full-feature counterparts while using fewer variables, as reflected in 82.0% of optimized-metric comparisons in the development cohort, and remained robust in both temporal and external validation. Dr.BUG further provided both population-level and patient-level interpretability and generated individualized rankings of candidate antibiotic regimens. In the retrospective analysis of non-survivors, clinician review suggested that regimens recommended by Dr.BUG might be associated with higher predicted survival probabilities. These findings support a broader role for clinical AI in complex drug-resistant infections, extending its utility from offline risk prediction to interpretable, deployable, and personalized decision support.
Matching journals
The top 5 journals account for 50% of the predicted probability mass.
Similar papers in this journal
- FedWeight: Mitigating Covariate Shift of Federated Learning on Electronic Health Records Data through Patients Re-weighting 95%
- Zero Shot Health Trajectory Prediction Using Transformer 94%
- Clinical Knowledge Extraction via Sparse Embedding Regression (KESER) with Multi-Center Large Scale Electronic Health Record Data 94%
Similar papers in this journal
- Deep representation learning for clustering longitudinal survival data from electronic health records 94%
- Convolutional neural networks quantify antibiotic resistance in Mycobacterium tuberculosis with diagnostic grade accuracy and predict treatment response 94%
- Integration of clinical, pathological, radiological, and transcriptomic data improves the prediction of first-line immunotherapy outcome in metastatic non-small cell lung cancer 93%
Similar papers in this journal
Similar papers in this journal
- Interpretable Machine Learning-based Decision Support for Prediction of Antibiotic Resistance for Complicated Urinary Tract Infections 92%
- resLens: genomic language models to enhance antibiotic resistance gene detection 92%
- Genome wide analyses reveal the role of mutator phenotypes in the emergence of drug resistance in Mycobacterium tuberculosis 89%
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.