Evidence map›Paper›PMID 40514403›Full record

ArticleCommunications medicine2025

Pretrained patient trajectories for adverse drug event prediction using common data model-based electronic health records.

Junmo Kim, Joo Seong Kim, Ji-Hyang Lee, Min-Gyu Kim, Taehyun Kim, Chaeeun Cho, Rae Woong Park, Kwangsoo Kim

Abstract read
In one paragraph

Article in Communications medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Junmo KimInterdisciplinary Program in Bioengineering, Seoul National University, Seoul, Republic of Korea.ORCID http://orcid.org/0000-0002-3908-0488
Joo Seong KimDivision of Gastroenterology, Department of Internal Medicine, Dongguk University Ilsan Hospital, Dongguk University College of Medicine, Goyang, Republic of Korea.
Ji-Hyang LeeDrug Safety Center, Seoul National University Hospital, Seoul, Republic of Korea.
Min-Gyu KimDepartment of Biomedical Informatics, Ajou University School of Medicine, Suwon, Republic of Korea.
Taehyun KimCollege of Medicine, Hanyang University, Seoul, Republic of Korea.
Chaeeun ChoDepartment of Medicine, Korea University College of Medicine, Seoul, Republic of Korea.
Rae Woong ParkDepartment of Biomedical Informatics, Ajou University School of Medicine, Suwon, Republic of Korea. veritas@ajou.ac.kr.ORCID http://orcid.org/0000-0003-4989-3287
Kwangsoo KimDepartment of Transdisciplinary Medicine, Institute of Convergence Medicine with Innovative Technology, Seoul National University Hospital, Seoul, Republic of Korea. kksoo716@gmail.com.ORCID http://orcid.org/0000-0002-4586-5062

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPretraining electronic health record (EHR) data using language models has enhanced performance across various medical tasks. Despite the potential of EHR pretraining models, predicting adverse drug events (ADEs) using EHR pretraining models has not been explored.

methodsWe used observational medical outcomes partnership common data model (CDM)-based EHR data from Seoul National University Hospital (SNUH) between January 2001 and December 2023 and Ajou University Medical Center (AUMC) between January 2004 and December 2023. In total 510,879 and 419,505 adult inpatients from SNUH and AUMC are included in internal and external datasets. For pretraining, the model was trained to infer randomly masked tokens using preceding and following history. In this process, we introduced domain embedding (DE) to provide information about the domain of masked tokens, preventing the model from finding codes from irrelevant domains. For qualitative analysis, we identified important features using the attention matrix from each finetuned model.

resultsHere we show that EHR pretraining models with DE outperform the models without pretraining and DE in predicting various ADEs, with the average area under the receiver operating characteristic curve (AUROC) of 0.958 and 0.964 in internal and external validations, respectively. For feature importance analysis, we demonstrate that the results are consistent with priorly reported background clinical knowledge. In addition to cohort-level interpretation, patient-level interpretation is also available.

conclusionsThe CDM-based EHR pretraining model with DE can improve prediction performance for various ADEs and can provide proper explanation at cohort and patient level. Our model has the potential to serve as a foundation model due to its strong prediction performance, interpretability, and compatibility.

Identifiers

PMID40514403
PMCPMC12166071

What Socratic holds

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LicenceCC BY-NC-ND
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.