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Identifying dementia cases with routinely collected health data: A systematic review.
Wilkinson, Tim; Ly, Amanda; Schnier, Christian; Rannikmäe, Kristiina; Bush, Kathryn; Brayne, Carol; Quinn, Terence J; Sudlow, Cathie L M.
Afiliação
  • Wilkinson T; Centre for Clinical Brain Sciences, University of Edinburgh, Edinburgh, Scotland; Usher Institute of Population Health Sciences and Informatics, Nine Bioquarter, Edinburgh, Scotland. Electronic address: tim.wilkinson@ed.ac.uk.
  • Ly A; Usher Institute of Population Health Sciences and Informatics, Nine Bioquarter, Edinburgh, Scotland.
  • Schnier C; Usher Institute of Population Health Sciences and Informatics, Nine Bioquarter, Edinburgh, Scotland.
  • Rannikmäe K; Centre for Clinical Brain Sciences, University of Edinburgh, Edinburgh, Scotland; Usher Institute of Population Health Sciences and Informatics, Nine Bioquarter, Edinburgh, Scotland.
  • Bush K; Centre for Clinical Brain Sciences, University of Edinburgh, Edinburgh, Scotland; Usher Institute of Population Health Sciences and Informatics, Nine Bioquarter, Edinburgh, Scotland.
  • Brayne C; Institute of Public Health, Cambridge University, Cambridge, UK.
  • Quinn TJ; Institute of Cardiovascular and Medical Sciences, University of Glasgow, Glasgow, Scotland.
  • Sudlow CLM; Centre for Clinical Brain Sciences, University of Edinburgh, Edinburgh, Scotland; Usher Institute of Population Health Sciences and Informatics, Nine Bioquarter, Edinburgh, Scotland; UK Biobank, Coordinating Centre, Stockport, UK.
Alzheimers Dement ; 14(8): 1038-1051, 2018 08.
Article em En | MEDLINE | ID: mdl-29621480
INTRODUCTION: Prospective, population-based studies can be rich resources for dementia research. Follow-up in many such studies is through linkage to routinely collected, coded health-care data sets. We evaluated the accuracy of these data sets for dementia case identification. METHODS: We systematically reviewed the literature for studies comparing dementia coding in routinely collected data sets to any expert-led reference standard. We recorded study characteristics and two accuracy measures-positive predictive value (PPV) and sensitivity. RESULTS: We identified 27 eligible studies with 25 estimating PPV and eight estimating sensitivity. Study settings and methods varied widely. For all-cause dementia, PPVs ranged from 33%-100%, but 16/27 were >75%. Sensitivities ranged from 21% to 86%. PPVs for Alzheimer's disease (range 57%-100%) were generally higher than those for vascular dementia (range 19%-91%). DISCUSSION: Linkage to routine health-care data can achieve a high PPV and reasonable sensitivity in certain settings. Given the heterogeneity in accuracy estimates, cohorts should ideally conduct their own setting-specific validation.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Coleta de Dados / Atenção à Saúde / Doença de Alzheimer Tipo de estudo: Diagnostic_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Limite: Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Coleta de Dados / Atenção à Saúde / Doença de Alzheimer Tipo de estudo: Diagnostic_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Limite: Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article