ArticleNPJ digital medicine2026
Prediction of antibiotic-associated cutaneous adverse drug reactions using electronic health record foundation models.
Article in NPJ digital medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
1 citing paper in PubMed.
- Skin on Drugs: Psychotropic Compounds in Cutaneous Biology.International journal of molecular sciences · 2026Review
Corrections and comments
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Authors and funding
11 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Cutaneous adverse drug reactions (CADRs) are the most common form of adverse drug reactions, ranging from mild rashes to life-threatening diseases, such as Stevens-Johnson syndrome and toxic epidermal necrolysis. However, there is no effective tool to predict antibiotic-associated CADRs. In this study, we propose an antibiotic-associated CADR prediction model using electronic health record (EHR) foundation models (FMs). EHR FMs are based on the pretraining-finetuning paradigms of language models, corresponding medical codes and their sequences to words and sentences. We included 802,131 inpatients across three tertiary hospitals in Korea, combining EHR data with nursing statements and reports to extract skin rash records. Our approach achieved the best predictive performance compared to all the other baseline models across all datasets. To enhance clinical relevance, we classified CADRs into immediate and delayed types and conducted a detailed sub-analysis. Finally, we found that properly configured EHR FMs can effectively predict the risk of developing antibiotics-associated CADRs, particularly for delayed-type reactions where predictive testing options are limited.
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Registered trials
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.