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

11 de setembro de 2015 atualizado por: 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

Visão geral do estudo

Status

Desconhecido

Condições

Intervenção / Tratamento

Descrição detalhada

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.

Tipo de estudo

Observacional

Inscrição (Antecipado)

51000

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Locais de estudo

      • London, Reino Unido
        • London Farr Institute of Health Informatics

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

18 anos e mais velhos (Adulto, Adulto mais velho)

Aceita Voluntários Saudáveis

Sim

Gêneros Elegíveis para o Estudo

Tudo

Método de amostragem

Amostra Não Probabilística

População do estudo

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

Descrição

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

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

Coortes e Intervenções

Grupo / Coorte
Intervenção / Tratamento
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.

O que o estudo está medindo?

Medidas de resultados primários

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

Medidas de resultados secundários

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

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Patrocinador

Colaboradores

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo

1 de setembro de 2015

Conclusão Primária (Antecipado)

1 de outubro de 2015

Conclusão do estudo (Antecipado)

1 de dezembro de 2015

Datas de inscrição no estudo

Enviado pela primeira vez

3 de setembro de 2015

Enviado pela primeira vez que atendeu aos critérios de CQ

11 de setembro de 2015

Primeira postagem (Estimativa)

15 de setembro de 2015

Atualizações de registro de estudo

Última Atualização Postada (Estimativa)

15 de setembro de 2015

Última atualização enviada que atendeu aos critérios de controle de qualidade

11 de setembro de 2015

Última verificação

1 de setembro de 2015

Mais Informações

Termos relacionados a este estudo

Outros números de identificação do estudo

  • 15_138

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