Barriers and Best Practices in Disclosing a Dementia Diagnosis: A Clinician Interview Study

Author:

Wollney Easton N1ORCID,Armstrong Melissa J2ORCID,Bedenfield Noheli2,Rosselli Monica3ORCID,Curiel-Cid Rosie E4,Kitaigorodsky Marcela4,Levy Ximena5,Bylund Carma L1

Affiliation:

1. Department of Health Outcomes and Biomedical Informatics, University of Florida College of Medicine, Gainesville, FL, USA

2. Department of Neurology, University of Florida College of Medicine, Gainesville, FL, USA

3. Department of Psychology, Florida Atlantic University, Davie, FL, USA

4. Center for Cognitive Neuroscience and Aging, Department of Psychiatry & Behavioral Sciences, University of Miami Miller School of Medicine, Miami, FL, USA

5. Clinical Research Unit, Division of Research, Florida Atlantic University, Boca Raton, FL, USA

Abstract

The vast majority of individuals with dementia want to receive a diagnosis. Research suggests, however, that only a fraction of individuals with dementia receive a diagnosis and patients and families often feel the information is poorly explained. We thus aimed to assess clinician-reported barriers to dementia disclosure and recommendations for giving a dementia diagnosis. To accomplish this, we performed telephone interviews with 15 clinicians from different specialties using a semi-structured interview guide. Transcripts were analyzed thematically. Clinician-reported barriers fit 3 categories: patient and caregiver-related barriers, clinician-related barriers, and barriers related to the triadic interaction. Patient and caregiver-related barriers included lack of social support, misunderstanding the diagnosis, and denial. Clinician barriers included difficulty giving bad news, difficulty communicating uncertainty, and lack of time. Triadic interaction barriers included c hallenges meeting multiple goals or needs and family requests for non-disclosure. Recommendations for best practice included for clinicians to foster relationships, educate patients and family, and take a family-centered approach. Clinicians described recommendations for fostering relationships such as using empathic communication and developing and maintaining connection. Educating patients and families included tailoring communication, explaining how the diagnosis was reached, and following up. Family approaches included meeting with family members prior to delivering the diagnosis and involving the caregiver in the discussion. Findings may inform updated recommendations for best practices when communicating a dementia diagnosis.

Funder

Florida Department of Health

Publisher

SAGE Publications

Subject

Public Health, Environmental and Occupational Health,Health Policy

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