Evidence map›Paper›PMID 25369203›Full record

ArticlePloS one2014

Defining disease phenotypes using national linked electronic health records: a case study of atrial fibrillation.

Katherine I Morley, Joshua Wallace, Spiros C Denaxas, Ross J Hunter, Riyaz S Patel, Pablo Perel, Anoop D Shah, Adam D Timmis, Richard J Schilling, Harry Hemingway

Abstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

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.

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

52 citing papers in PubMed.

  1. Trial
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  5. Role of primary and secondary care data in atrial fibrillation ascertainment: impact on risk factor associations, patient management, and mortality in UK Biobank.Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology · 2025
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  7. Review
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  9. Review
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  11. Prognostic model for atrial fibrillation after cardiac surgery: a UK cohort study.Clinical research in cardiology : official journal of the German Cardiac Society · 2023
    Article
  12. Translating and evaluating historic phenotyping algorithms using SNOMED CT.Journal of the American Medical Informatics Association : JAMIA · 2023
    Article
  13. Article
  14. Article
  15. Transforming and evaluating the UK Biobank to the OMOP Common Data Model for COVID-19 research and beyond.Journal of the American Medical Informatics Association : JAMIA · 2022
    Observational
  16. Article
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  18. Phenotyping in distributed data networks: selecting the right codes for the right patients.AMIA ... Annual Symposium proceedings. AMIA Symposium · 2022
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  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Katherine I MorleyFarr Institute of Health Informatics Research, University College London, London, United Kingdom, and Clinical Epidemiology, Department of Epidemiology and Public Health, University College London, London, United Kingdom; Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, United Kingdom; Melbourne School of Global and Population Health, The University of Melbourne, Melbourne, Australia.
Joshua WallaceFarr Institute of Health Informatics Research, University College London, London, United Kingdom, and Clinical Epidemiology, Department of Epidemiology and Public Health, University College London, London, United Kingdom.
Spiros C DenaxasFarr Institute of Health Informatics Research, University College London, London, United Kingdom, and Clinical Epidemiology, Department of Epidemiology and Public Health, University College London, London, United Kingdom.
Ross J HunterBarts NIHR Biomedical Research Unit, Queen Mary University London, London, United Kingdom.
Riyaz S PatelFarr Institute of Health Informatics Research, University College London, London, United Kingdom, and Clinical Epidemiology, Department of Epidemiology and Public Health, University College London, London, United Kingdom; The Heart Hospital, University College London NHS Trust, London, United Kingdom.
Pablo PerelFarr Institute of Health Informatics Research, University College London, London, United Kingdom, and Clinical Epidemiology, Department of Epidemiology and Public Health, University College London, London, United Kingdom; London School of Hygiene and Tropical Medicine, London, United Kingdom.
Anoop D ShahFarr Institute of Health Informatics Research, University College London, London, United Kingdom, and Clinical Epidemiology, Department of Epidemiology and Public Health, University College London, London, United Kingdom.
Adam D TimmisBarts NIHR Biomedical Research Unit, Queen Mary University London, London, United Kingdom.
Richard J SchillingBarts NIHR Biomedical Research Unit, Queen Mary University London, London, United Kingdom.
Harry HemingwayFarr Institute of Health Informatics Research, University College London, London, United Kingdom, and Clinical Epidemiology, Department of Epidemiology and Public Health, University College London, London, United Kingdom.

Funding

British Heart FoundationCancer Research UKChief Scientist OfficeDepartment of Health RP-PG-0407-10314Medical Research Council G0902393Medical Research Council G0902393/99558Medical Research Council MR/K006584/1Wellcome Trust 093830Wellcome Trust 0938/30/Z/10/ZWellcome Trust MR/K006584
6 · The paper itself

Abstract

backgroundNational electronic health records (EHR) are increasingly used for research but identifying disease cases is challenging due to differences in information captured between sources (e.g. primary and secondary care). Our objective was to provide a transparent, reproducible model for integrating these data using atrial fibrillation (AF), a chronic condition diagnosed and managed in multiple ways in different healthcare settings, as a case study.

methodsPotentially relevant codes for AF screening, diagnosis, and management were identified in four coding systems: Read (primary care diagnoses and procedures), British National Formulary (BNF; primary care prescriptions), ICD-10 (secondary care diagnoses) and OPCS-4 (secondary care procedures). From these we developed a phenotype algorithm via expert review and analysis of linked EHR data from 1998 to 2010 for a cohort of 2.14 million UK patients aged ≥ 30 years. The cohort was also used to evaluate the phenotype by examining associations between incident AF and known risk factors.

resultsThe phenotype algorithm incorporated 286 codes: 201 Read, 63 BNF, 18 ICD-10, and four OPCS-4. Incident AF diagnoses were recorded for 72,793 patients, but only 39.6% (N = 28,795) were recorded in primary care and secondary care. An additional 7,468 potential cases were inferred from data on treatment and pre-existing conditions. The proportion of cases identified from each source differed by diagnosis age; inferred diagnoses contributed a greater proportion of younger cases (≤ 60 years), while older patients (≥ 80 years) were mainly diagnosed in SC. Associations of risk factors (hypertension, myocardial infarction, heart failure) with incident AF defined using different EHR sources were comparable in magnitude to those from traditional consented cohorts.

conclusionsA single EHR source is not sufficient to identify all patients, nor will it provide a representative sample. Combining multiple data sources and integrating information on treatment and comorbid conditions can substantially improve case identification.

Indexed as

Electronic Health RecordsAdultAgedAged, 80 and overAlgorithmsAtrial FibrillationCohort StudiesHospitalsHumansIncidenceMiddle AgedPhenotypeProportional Hazards ModelsRisk Factors

Identifiers

PMID25369203
PMCPMC4219705

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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 OpenQuestion graph.