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Characteristics of people with dementia lost to follow-up from a dementia care center.
Boyd, Nicole D; Naasan, Georges; Harrison, Krista L; Garrett, Sarah B; D'Aguiar Rosa, Talita; Pérez-Cerpa, Brenda; McFarlane, Shamiel; Miller, Bruce L; Ritchie, Christine S.
Afiliação
  • Boyd ND; Division of Geriatrics, Department of Medicine, University of California San Francisco, San Francisco, California, USA.
  • Naasan G; University of California San Francisco / Global Brain Health Institute, San Francisco, California, USA.
  • Harrison KL; Department of Neurology, Department of Medicine, University of California San Francisco, San Francisco, California, USA.
  • Garrett SB; Department of Neurology, Mount Sinai Hospitals, Ichan School of Medicine, New York City, New York, USA.
  • D'Aguiar Rosa T; Division of Geriatrics, Department of Medicine, University of California San Francisco, San Francisco, California, USA.
  • Pérez-Cerpa B; University of California San Francisco / Global Brain Health Institute, San Francisco, California, USA.
  • McFarlane S; Philip R. Lee Institute for Health Policy Studies, University of California, San Francisco, California, USA.
  • Miller BL; University of California San Francisco / Global Brain Health Institute, San Francisco, California, USA.
  • Ritchie CS; Philip R. Lee Institute for Health Policy Studies, University of California, San Francisco, California, USA.
Article em En | MEDLINE | ID: mdl-34590336
ABSTRACT

OBJECTIVE:

To identify the prevalence and characteristics of people living with dementia (PLWD) lost to follow-up (LTFU) from a specialized dementia care clinic and to understand factors influencing patient follow-up status.

METHODS:

We conducted a retrospective chart review of PLWD seen at a dementia care clinic 2012-2017 who were deceased as of 2018 (n = 746). Participants were evaluated for follow-up status at the time of death. Generalized linear regression was used to analyze demographic and diagnostic characteristics by follow-up status. Text extracted from participant medical records was analyzed using qualitative content analysis to identify reasons patients became LTFU.

RESULTS:

Among PLWD seen at a dementia care clinic, 42% became LTFU before death, 39% of whom had chart documentation describing reasons for loss to follow-up. Increased rates of LTFU were associated with female sex (risk ratio 1.27, [95% confidence interval 1.09-1.49]; p = 0.003), educational attainment of high school or less (1.34, [1.13-1.61]; p = 0.001), and death in a long-term care facility (1.46, [1.19-1.80]; p = 0.003). Commonly documented reasons for not returning for care at the clinic included switching care to another provider (42%), logistical difficulty accessing care (26%), patient-family decision to discontinue care (24%), and functional challenges in accessing care (23%).

CONCLUSIONS:

PLWD are LTFU from specialized memory care at high rates. Attention to care coordination, patient-provider communication, and integrated use of alternative care models such as telehealth are potential strategies to improve care.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Infecções por HIV / Demência Tipo de estudo: Observational_studies / Prognostic_studies / Qualitative_research / Risk_factors_studies Limite: Female / Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Infecções por HIV / Demência Tipo de estudo: Observational_studies / Prognostic_studies / Qualitative_research / Risk_factors_studies Limite: Female / Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article