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Dementia Phenotypes in Primary Care, Hospital, and National Mortality Registries

11 september 2015 uppdaterad av: Harry Hemingway, University College, London

Dementia Phenotypes in Primary Care, Hospital, and National Mortality Registries: a Cohort Study in Linked Electronic Health Records

Most patients with dementia in the UK use their local hospitals and general (family) practices throughout their illness. Linked electronic health records from primary care, hospital and death certificates records therefore provide useful information about the diagnosis and prognosis of patients who develop dementia.

In this study we will assess the validity of dementia diagnoses in linked primary care, hospital and death records, by examining the timing of important health transitions in patients with recorded dementia, and we will estimate the lifetime risk of recorded dementia in different age and sex groups

Studieöversikt

Status

Okänd

Betingelser

Detaljerad beskrivning

Dementia is a clinical syndrome with insidious onset that is difficult to diagnose in its earliest stages. Presentation to healthcare depends not only upon the rates of disease progression, but also on social support, recognition by clinicians, and patients' and carers' fear of diagnosis. Maintaining complete follow up in cohorts of patient with dementia is difficult, because patients with dementia are frequently lost to follow up.

Most patients with dementia in the UK use their local hospitals and general (family) practices throughout their illness. Linked electronic health records from primary care, hospital and death certificates records should therefore provide useful information about the diagnosis and prognosis of patients who develop dementia with minimal loss to follow-up rates and improved completeness of diagnosis.

Demonstrating that patients with recorded dementia have an earlier onset of typical symptoms, functional impairment and death than patients in the general population would support the veracity of diagnosed dementia recorded in electronic health records and its use as an outcome or exposure in cohort studies and for evaluating policy. Previous studies have found that dementia is poorly recorded in routine clinical practice in comparison to face-to-face studies, although this varies by setting and region. However, ascertainment may be improved by examining linked, longitudinal resources. Comparing the lifetime risk of dementia calculated from linked electronic health records with lifetime risks from other sources will also be a useful information to support the use of linked electronic health records in dementia research.

Electronic health records contain information on important health transitions in patients with dementia: from the earliest stage of the illness (depression, anxiety, memory complaints); the development of cognitive impairment that manifest as loss of capacity or missed appointments; and significant functional impairment, with admission to nursing homes or hospital admission. In this study, we will assess the validity of dementia diagnoses in linked primary care, hospital and death records, by examining the timing of important health transitions in patients with recorded dementia, and estimate the lifetime risk of recorded dementia in different age and sex groups.

Studietyp

Observationell

Inskrivning (Förväntat)

51000

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studieorter

      • London, Storbritannien
        • London Farr Institute of Health Informatics

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

18 år och äldre (Vuxen, Äldre vuxen)

Tar emot friska volontärer

Ja

Kön som är behöriga för studier

Allt

Testmetod

Icke-sannolikhetsprov

Studera befolkning

Patients registered in English general practices contributing with data to the CALIBER research platform from 1997 onward.

Beskrivning

Inclusion Criteria:

  • Patients aged 18 years and over
  • Registered with a participating general practice during the study period
  • Minimum one year of records prior to study entry meeting CPRD data quality criteria
  • Followed on or after 1 January 1997

Exclusion Criteria:

  • Patients without recorded gender
  • Less than 1 year of follow-up between study entry and date of administrative censoring

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

Kohorter och interventioner

Grupp / Kohort
Intervention / Behandling
Dementia
Patients with a recorded diagnosis of dementia in primary or secondary care
This study is based on the retrospective analysis of linked electronic health records.
Non-dementia
Patients without a recorded diagnosis of dementia in primary or secondary care
This study is based on the retrospective analysis of linked electronic health records.

Vad mäter studien?

Primära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Proportion of patients with dementia diagnosis (any type) in primary care that also are recorded in secondary care
Tidsram: 10 years
10 years
Factors associated with dementia diagnosis (any type) recording in mortality data only
Tidsram: 10 years
These will be estimated from multivariable logistic regression models
10 years
Symptoms associated with subsequent diagnosis of dementia
Tidsram: 10 years
These will be estimated from multivariable logistic regression models
10 years
Lifetime risk of dementia (any type)
Tidsram: 10 years
10 years
Lifetime risk of mortality associated with dementia (any time)
Tidsram: 10 years
10 years
Factors associated with dementia diagnosis (any type) recording in secondary care only
Tidsram: 10 years
These will be estimated from multivariable logistic regression models
10 years
Factors associated with dementia diagnosis (any type) recording in primary care only
Tidsram: 10 years
These will be estimated from multivariable logistic regression models
10 years
Proportion of patients with dementia diagnosis (any type) in primary care that also are recorded in mortality data
Tidsram: 10 years
10 years
Proportion of patients with dementia diagnosis (any type) in secondary care that also are recorded in mortality data
Tidsram: 10 years
10 years

Sekundära resultatmått

Resultatmått
Tidsram
Proportion of patients with Alzheimer's disease in primary care that are also diagnosed in secondary care
Tidsram: 10 years
10 years
Proportion of patients with vascular dementia in primary care that are also diagnosed in secondary care
Tidsram: 10 years
10 years
Lifetime risk of Alzheimer's disease
Tidsram: 10 years
10 years
Lifetime risk of vascular dementia
Tidsram: 10 years
10 years
Lifetime risk of mortality associated with Alzheimer's disease
Tidsram: 10 years
10 years
Proportion of patients with Alzheimer's disease in primary care that are also diagnosed in mortality data
Tidsram: 10 years
10 years
Proportion of patients with Alzheimer's disease in secondary care that are also recorded in mortality data
Tidsram: 10 years
10 years
Proportion of patients with vascular dementia in primary care that are also recorded in secondary care
Tidsram: 10 years
10 years
Proportion of patients with vascular dementia in secondary care that are also recorded in mortality data
Tidsram: 10 years
10 years

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart

1 september 2015

Primärt slutförande (Förväntat)

1 oktober 2015

Avslutad studie (Förväntat)

1 december 2015

Studieregistreringsdatum

Först inskickad

3 september 2015

Först inskickad som uppfyllde QC-kriterierna

11 september 2015

Första postat (Uppskatta)

15 september 2015

Uppdateringar av studier

Senaste uppdatering publicerad (Uppskatta)

15 september 2015

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

11 september 2015

Senast verifierad

1 september 2015

Mer information

Termer relaterade till denna studie

Denna information hämtades direkt från webbplatsen clinicaltrials.gov utan några ändringar. Om du har några önskemål om att ändra, ta bort eller uppdatera dina studieuppgifter, vänligen kontakta register@clinicaltrials.gov. Så snart en ändring har implementerats på clinicaltrials.gov, kommer denna att uppdateras automatiskt även på vår webbplats .

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