Dual-Pathway Fusion of EHRs and Knowledge Graphs for Predicting Unseen Drug-Drug Interactions

Franklin Lee, Tengfei Ma

Published: 27 Nov 2025, Last Modified: 09 Dec 2025ML4H 2025 PosterEveryoneRevisionsBibTeXCC BY 4.0
Keywords: Drug–drug interactions, Knowledge graphs, EHRs, Multimodal fusion, Zero-shot generalization, Knowledge distillation, Clinically aligned evaluation
TL;DR: To our knowledge, the first KG+EHR system distilled to an EHR-only zero-shot model, improving mechanism precision, cutting false alerts, and missing fewer significant alerts for pharmacist review.
Track: Findings
Abstract: Drug–drug interactions (DDIs) remain a major source of preventable harm, and many clinically important mechanisms are still unknown. Existing models either rely on pharmacologic knowledge graphs (KGs), which fail on unseen drugs, or on electronic health records (EHRs), which are noisy, temporal, and site-dependent. We introduce, to our knowledge, the first system that conditions KG relation scoring on patient-level EHR context and distills that reasoning into an EHR-only model for zero-shot inference. A fusion “Teacher” learns mechanism-specific relations for drug pairs represented in both sources, while a distilled “Student” generalizes to new or rarely used drugs without KG access at inference. Both operate under a shared ontology (set) of pharmacologic mechanisms (drug relations) to produce interpretable, auditable alerts rather than opaque risk scores. Trained on a multi-institution EHR corpus paired with a curated DrugBank DDI graph, and evaluated using a a clinically aligned, decision-focused protocol with leakage-safe negatives that avoid artificially easy pairs, the system maintains precision across multi-institutuion test data, produces mechanism-specific, clinically consistent predictions, reduces false alerts (higher precision) at comparable overall detection performance (F1), and misses fewer true interactions compared to prior methods. Case studies further show zero-shot identification of clinically recognized CYP-mediated and pharmacodynamic mechanisms for drugs absent from the KG, supporting real-world use in clinical decision support and pharmacovigilance.
General Area: Applications and Practice
Specific Subject Areas: Public & Social Health, Representation Learning
Supplementary Material: zip
Data And Code Availability: Yes
Ethics Board Approval: No
Entered Conflicts: I confirm the above
Anonymity: I confirm the above
Submission Number: 188
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