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sEHR-CE: Language modelling of structured EHR data for efficient and generalizable patient cohort expansion

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arxiv 2211.17121 v1 pith:HHQXMLQD submitted 2022-11-30 cs.CL cs.LGstat.AP

classification cs.CLcs.LGstat.AP
keywords clinicaldatasehr-ceapproachcombiningdiseaseindividualslanguage
verification ladder T0 review T1 audit T2 compute T3 formal
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Electronic health records (EHR) offer unprecedented opportunities for in-depth clinical phenotyping and prediction of clinical outcomes. Combining multiple data sources is crucial to generate a complete picture of disease prevalence, incidence and trajectories. The standard approach to combining clinical data involves collating clinical terms across different terminology systems using curated maps, which are often inaccurate and/or incomplete. Here, we propose sEHR-CE, a novel framework based on transformers to enable integrated phenotyping and analyses of heterogeneous clinical datasets without relying on these mappings. We unify clinical terminologies using textual descriptors of concepts, and represent individuals' EHR as sections of text. We then fine-tune pre-trained language models to predict disease phenotypes more accurately than non-text and single terminology approaches. We validate our approach using primary and secondary care data from the UK Biobank, a large-scale research study. Finally, we illustrate in a type 2 diabetes use case how sEHR-CE identifies individuals without diagnosis that share clinical characteristics with patients.

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  1. Exploring Long-Term Prediction of Type 2 Diabetes Microvascular Complications

    cs.LG 2024-12 conditional novelty 5.0 of 10

    A code-agnostic text representation of EHRs outperformed code-based input for predicting retinopathy, nephropathy and neuropathy at 1, 5, and 10 years in 133,784 UK type 2 diabetes patients.

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