Abstract

BackgroundElectronic linkage of UK cohorts to routinely collected National Health Service (NHS) records provides virtually complete follow-up for cause-specific hospital admissions and deaths. The reliability of dementia diagnoses recorded in NHS hospital data is not well documented.MethodsFor a sample of Million Women Study participants in England we compared dementia recorded in routinely collected NHS hospital data (Hospital Episode Statistics: HES) with dementia recorded in two separate sources of primary care information: a primary care database [Clinical Practice Research Datalink (CPRD), n = 340] and a survey of study participants’ General Practitioners (GPs, n = 244).ResultsDementia recorded in HES fully agreed both with CPRD and with GP survey data for 85% of women; it did not agree for 1 and 4%, respectively. Agreement was uncertain for the remaining 14 and 11%, respectively; and among those classified as having uncertain agreement in CPRD, non-specific terms compatible with dementia, such as ‘memory loss’, were recorded in the CPRD database for 79% of the women. Agreement was significantly better (p < 0.05 for all comparisons) for women with HES diagnoses for Alzheimer’s disease (95 and 94% agreement with any dementia for CPRD and GP survey, respectively) and for vascular dementia (88 and 88%, respectively) than for women with a record only of dementia not otherwise specified (70 and 72%, respectively). Dementia in the same woman was first mentioned an average 1.6 (SD 2.6) years earlier in primary care (CPRD) than in hospital (HES) data. Age-specific rates for dementia based on the hospital admission data were lower than the rates based on the primary care data, but were similar if the delay in recording in HES was taken into account.ConclusionsDementia recorded in routinely collected NHS hospital admission data for women in England agrees well with primary care records of dementia assessed separately from two different sources, and is sufficiently reliable for epidemiological research.Electronic supplementary materialThe online version of this article (doi:10.1186/s12982-016-0053-z) contains supplementary material, which is available to authorized users.

Highlights

  • Electronic linkage of UK cohorts to routinely collected National Health Service (NHS) records provides virtually complete follow-up for cause-specific hospital admissions and deaths

  • For a sample of Million Women Study participants in England, we aimed to compare information on dementia recorded in hospital admission data (HES) with information on dementia obtained from two different sources of primary care data: (1) through linkage to coded Clinical Practice Research Datalink (CPRD) records; and (2) postal survey information from a sample of study participants’ general pracƟƟoner (GP)

  • Hospital Episode Statistics (HES) diagnoses of dementia fully agreed for 288 (85%, 95% CI 80–88%) women (278 agreed with the CPRD codes listed in Additional file 1: Code list 1 and another ten had dementia coded as cause of death)

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Summary

Introduction

Electronic linkage of UK cohorts to routinely collected National Health Service (NHS) records provides virtually complete follow-up for cause-specific hospital admissions and deaths. The reliability of dementia diagnoses recorded in NHS hospital data is not well documented. Large prospective cohort studies with long-term follow-up through linkage to routinely-collected hospital admissions records provide important opportunities for epidemiological investigations of dementia. In the Million Women Study cohort, virtually complete follow-up for hospital admissions has been established by record linkage to routinely collected National Health Service (NHS) databases in England (Hospital Episode Statistics, HES) and Scotland (Scottish Morbidity Records). The Clinical Practice Research Datalink (CPRD) has for many years collected coded information from GPs on diagnoses, prescriptions and other factors in primary care, with active coverage of around 7% of the UK population [5, 6]

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