Peer-Reviewed Publication
J Biomed Inform2026;105112.October 16, 2026Journal Article

Augmenting electronic health records for adverse event detection.

Gün Kaynar1, Zhaoyi You1, Richard D Boyce2, Takahiro Yakoh3, Carl Kingsford4
1Ray and Stephanie Lane Computational Biology Department, School of Computer Science, Carnegie Mellon University, Pittsburgh, PA, USA.
2Department of Biomedical Informatics, University of Pittsburgh, Pittsburgh, PA, USA.
3Department of System Design Engineering, Keio University, Yokohama, Japan.
4Ray and Stephanie Lane Computational Biology Department, School of Computer Science, Carnegie Mellon University, Pittsburgh, PA, USA. Electronic address: carlk@cs.cmu.edu.

Abstract

OBJECTIVE: Adverse events (AEs) resulting from medical interventions are significant contributors to patient morbidity, mortality, and healthcare costs. Detection of these events using electronic health records (EHRs) can facilitate timely clinical interventions. However, effective detection remains challenging due to severe class imbalance, missing labels, and the complexity of EHR records. Class…

Create a free account to keep reading

Free members get 10 full research views every month across publications, clinical trials, FDA clearances, adverse events, and NIH grants. No credit card required.

Want unlimited research access? See Pro plans

Data Accuracy Notice: Research intelligence on Health AI Central is aggregated from public sources (PubMed, ClinicalTrials.gov, FDA, NIH, CMS, and others) and refreshed nightly. Classifications and derived metrics are produced by automated methods described in our Methodology. We recommend verifying critical data points against the primary sources before making decisions.