Indicators of dementia disease progression in primary care: An electronic health record cohort study.


Journal

European journal of neurology
ISSN: 1468-1331
Titre abrégé: Eur J Neurol
Pays: England
ID NLM: 9506311

Informations de publication

Date de publication:
05 2021
Historique:
revised: 17 12 2020
received: 23 07 2020
accepted: 20 12 2020
pubmed: 31 12 2020
medline: 13 8 2021
entrez: 30 12 2020
Statut: ppublish

Résumé

The objectives were to assess the feasibility and validity of using markers of dementia-related health as indicators of dementia progression in primary care, by assessing the frequency with which they are recorded and by testing the hypothesis that they are associated with recognised outcomes of dementia. The markers, in 13 domains, were derived previously through literature review, expert consensus, and analysis of regional primary care records. The study population consisted of patients with a recorded dementia diagnosis in the Clinical Practice Research Datalink, a UK primary care database linked to secondary care records. Incidence of recorded domains in the 36 months after diagnosis was determined. Associations of recording of domains with future hospital admission, palliative care, and mortality were derived. There were 30,463 people with diagnosed dementia. Incidence of domains ranged from 469/1000 person-years (Increased Multimorbidity) to 11/1000 (Home Pressures). An increasing number of domains in which a new marker was recorded in the first year after diagnosis was associated with hospital admission (hazard ratio for ≥4 domains vs. no domains = 1.24; 95% confidence interval = 1.15-1.33), palliative care (1.87; 1.62-2.15), and mortality (1.57; 1.47-1.67). Individual domains were associated with outcomes with varying strengths of association. Feasibility and validity of potential indicators of progression of dementia derived from primary care records are supported by their frequency of recording and associations with recognised outcomes. Further research should assess whether these markers can help identify patients with poorer prognosis to improve outcomes through stratified care and targeted support.

Sections du résumé

BACKGROUND AND PURPOSE
The objectives were to assess the feasibility and validity of using markers of dementia-related health as indicators of dementia progression in primary care, by assessing the frequency with which they are recorded and by testing the hypothesis that they are associated with recognised outcomes of dementia. The markers, in 13 domains, were derived previously through literature review, expert consensus, and analysis of regional primary care records.
METHODS
The study population consisted of patients with a recorded dementia diagnosis in the Clinical Practice Research Datalink, a UK primary care database linked to secondary care records. Incidence of recorded domains in the 36 months after diagnosis was determined. Associations of recording of domains with future hospital admission, palliative care, and mortality were derived.
RESULTS
There were 30,463 people with diagnosed dementia. Incidence of domains ranged from 469/1000 person-years (Increased Multimorbidity) to 11/1000 (Home Pressures). An increasing number of domains in which a new marker was recorded in the first year after diagnosis was associated with hospital admission (hazard ratio for ≥4 domains vs. no domains = 1.24; 95% confidence interval = 1.15-1.33), palliative care (1.87; 1.62-2.15), and mortality (1.57; 1.47-1.67). Individual domains were associated with outcomes with varying strengths of association.
CONCLUSIONS
Feasibility and validity of potential indicators of progression of dementia derived from primary care records are supported by their frequency of recording and associations with recognised outcomes. Further research should assess whether these markers can help identify patients with poorer prognosis to improve outcomes through stratified care and targeted support.

Identifiants

pubmed: 33378599
doi: 10.1111/ene.14710
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1499-1510

Subventions

Organisme : The Dunhill Medical Trust
ID : RPGF 1711/11
Pays : United Kingdom
Organisme : Department of Health
Pays : United Kingdom

Informations de copyright

© 2021 The Authors. European Journal of Neurology published by John Wiley & Sons Ltd on behalf of European Academy of Neurology.

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Auteurs

Trishna Rathod-Mistry (T)

School of Medicine, Keele University, Keele, UK.

Michelle Marshall (M)

School of Medicine, Keele University, Keele, UK.

Paul Campbell (P)

School of Medicine, Keele University, Keele, UK.
Midlands Partnership NHS Foundation Trust, Stafford, UK.

James Bailey (J)

School of Medicine, Keele University, Keele, UK.

Carolyn A Chew-Graham (CA)

School of Medicine, Keele University, Keele, UK.
Midlands Partnership NHS Foundation Trust, Stafford, UK.

Peter Croft (P)

School of Medicine, Keele University, Keele, UK.

Martin Frisher (M)

School of Pharmacy and Bioengineering, Keele University, Keele, UK.

Richard Hayward (R)

School of Medicine, Keele University, Keele, UK.

Rashi Negi (R)

Midlands Partnership NHS Foundation Trust, Stafford, UK.

Louise Robinson (L)

Institute of Health and Society and Newcastle University Institute for Ageing, Newcastle Upon Tyne, UK.

Swaran Singh (S)

Division of Mental Health and Wellbeing, Warwick Medical School, University of Warwick, Coventry, UK.

Athula Sumathipala (A)

School of Medicine, Keele University, Keele, UK.
Midlands Partnership NHS Foundation Trust, Stafford, UK.

Nwe Thein (N)

Midlands Partnership NHS Foundation Trust, Stafford, UK.

Kate Walters (K)

Research Department of Primary Care & Population Health, University College London, London, UK.

Scott Weich (S)

Mental Health Research Unit, School of Health and Related Research, University of Sheffield, Sheffield, UK.

Kelvin P Jordan (KP)

School of Medicine, Keele University, Keele, UK.
Centre for Prognosis Research, Keele University, Keele, UK.

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