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

<h4>Background</h4>National 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, reproducib...

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Main Authors: 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
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-01-01
Series:PLoS ONE
Online Access:https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0110900&type=printable
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author 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
author_facet 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
author_sort Katherine I Morley
collection DOAJ
description <h4>Background</h4>National 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.<h4>Methods</h4>Potentially 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.<h4>Results</h4>The 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.<h4>Conclusions</h4>A 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.
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spelling doaj-art-408ec15445ed489da86a70127f4fdc7a2025-08-20T03:10:06ZengPublic Library of Science (PLoS)PLoS ONE1932-62032014-01-01911e11090010.1371/journal.pone.0110900Defining disease phenotypes using national linked electronic health records: a case study of atrial fibrillation.Katherine I MorleyJoshua WallaceSpiros C DenaxasRoss J HunterRiyaz S PatelPablo PerelAnoop D ShahAdam D TimmisRichard J SchillingHarry Hemingway<h4>Background</h4>National 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.<h4>Methods</h4>Potentially 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.<h4>Results</h4>The 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.<h4>Conclusions</h4>A 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.https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0110900&type=printable
spellingShingle 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
Defining disease phenotypes using national linked electronic health records: a case study of atrial fibrillation.
PLoS ONE
title Defining disease phenotypes using national linked electronic health records: a case study of atrial fibrillation.
title_full Defining disease phenotypes using national linked electronic health records: a case study of atrial fibrillation.
title_fullStr Defining disease phenotypes using national linked electronic health records: a case study of atrial fibrillation.
title_full_unstemmed Defining disease phenotypes using national linked electronic health records: a case study of atrial fibrillation.
title_short Defining disease phenotypes using national linked electronic health records: a case study of atrial fibrillation.
title_sort defining disease phenotypes using national linked electronic health records a case study of atrial fibrillation
url https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0110900&type=printable
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