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

11. September 2015 aktualisiert von: 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

Studienübersicht

Status

Unbekannt

Bedingungen

Detaillierte Beschreibung

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.

Studientyp

Beobachtungs

Einschreibung (Voraussichtlich)

51000

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienorte

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

18 Jahre und älter (Erwachsene, Älterer Erwachsener)

Akzeptiert gesunde Freiwillige

Ja

Studienberechtigte Geschlechter

Alle

Probenahmeverfahren

Nicht-Wahrscheinlichkeitsprobe

Studienpopulation

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

Beschreibung

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

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

Kohorten und Interventionen

Gruppe / Kohorte
Intervention / Behandlung
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.

Was misst die Studie?

Primäre Ergebnismessungen

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

Sekundäre Ergebnismessungen

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

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn

1. September 2015

Primärer Abschluss (Voraussichtlich)

1. Oktober 2015

Studienabschluss (Voraussichtlich)

1. Dezember 2015

Studienanmeldedaten

Zuerst eingereicht

3. September 2015

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

11. September 2015

Zuerst gepostet (Schätzen)

15. September 2015

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Schätzen)

15. September 2015

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

11. September 2015

Zuletzt verifiziert

1. September 2015

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

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