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Evaluation of the Electronic Clinical Dementia Rating for Dementia Screening.
Nosheny, Rachel L; Yen, Daniel; Howell, Taylor; Camacho, Monica; Moulder, Krista; Gummadi, Shilpa; Bui, Chau; Kannan, Sandhya; Ashford, Miriam T; Knight, Kristen; Mayo, Connie; McMillan, Maureen; Petersen, Ronald C; Stricker, Nikki H; Roberson, Erik D; Chambless, Carol; Gersteneker, Adam; Martin, Roy; Kennedy, Richard; Zhang, Yue; Kukull, Walter; Flenniken, Derek; Fockler, Juliet; Truran, Diana; Mackin, R Scott; Weiner, Michael W; Morris, John C; Li, Yan.
Afiliação
  • Nosheny RL; Department of Psychiatry and Behavioral Sciences, University of California, San Francisco.
  • Yen D; Department of Radiology and Biomedical Imaging, University of California, San Francisco.
  • Howell T; Northern California Institute for Research and Education, Department of Veterans Affairs Medical Center, San Francisco.
  • Camacho M; Knight Alzheimer's Disease Research Center, Department of Neurology, Washington University School of Medicine, St Louis, Missouri.
  • Moulder K; Department of Radiology and Biomedical Imaging, University of California, San Francisco.
  • Gummadi S; Department of Radiology and Biomedical Imaging, University of California, San Francisco.
  • Bui C; Knight Alzheimer's Disease Research Center, Department of Neurology, Washington University School of Medicine, St Louis, Missouri.
  • Kannan S; Department of Radiology and Biomedical Imaging, University of California, San Francisco.
  • Ashford MT; Department of Radiology and Biomedical Imaging, University of California, San Francisco.
  • Knight K; Department of Radiology and Biomedical Imaging, University of California, San Francisco.
  • Mayo C; Northern California Institute for Research and Education, Department of Veterans Affairs Medical Center, San Francisco.
  • McMillan M; Department of Radiology and Biomedical Imaging, University of California, San Francisco.
  • Petersen RC; Knight Alzheimer's Disease Research Center, Department of Neurology, Washington University School of Medicine, St Louis, Missouri.
  • Stricker NH; Knight Alzheimer's Disease Research Center, Department of Neurology, Washington University School of Medicine, St Louis, Missouri.
  • Roberson ED; Department of Neurology, Mayo Clinic, Rochester, Minnesota.
  • Chambless C; Division of Neurocognitive Disorders, Department of Psychiatry and Psychology, Mayo Clinic, Rochester, Minnesota.
  • Gersteneker A; Alzheimer's Disease Center, Center for Neurodegeneration and Experimental Therapeutics, Department of Neurology, University of Alabama at Birmingham, Birmingham.
  • Martin R; Alzheimer's Disease Center, Center for Neurodegeneration and Experimental Therapeutics, Department of Neurology, University of Alabama at Birmingham, Birmingham.
  • Kennedy R; Division of Neuropsychology, Department of Neurology, The University of Alabama at Birmingham, Birmingham.
  • Zhang Y; Division of Neuropsychology, Department of Neurology, The University of Alabama at Birmingham, Birmingham.
  • Kukull W; Division of Gerontology, Geriatrics, and Palliative Care, Department of Medicine, University of Alabama at Birmingham, Birmingham.
  • Flenniken D; Alzheimer's Disease Center, Center for Neurodegeneration and Experimental Therapeutics, Department of Neurology, University of Alabama at Birmingham, Birmingham.
  • Fockler J; Department of Epidemiology, University of Washington, Seattle.
  • Truran D; National Alzheimer's Coordinating Center, Seattle, Washington.
  • Mackin RS; Northern California Institute for Research and Education, Department of Veterans Affairs Medical Center, San Francisco.
  • Weiner MW; Department of Radiology and Biomedical Imaging, University of California, San Francisco.
  • Morris JC; Northern California Institute for Research and Education, Department of Veterans Affairs Medical Center, San Francisco.
  • Li Y; Department of Psychiatry and Behavioral Sciences, University of California, San Francisco.
JAMA Netw Open ; 6(9): e2333786, 2023 09 05.
Article em En | MEDLINE | ID: mdl-37707812
ABSTRACT
Importance The Clinical Dementia Rating (CDR) is a well-validated instrument widely used to detect and stage dementia due to Alzheimer disease. The digital Electronic Clinical Dementia Rating (eCDR) can be remotely self-administered and automatically scored, with potential to facilitate efficient dementia screening and staging.

Objective:

To evaluate the association of the eCDR with the CDR and other in-clinic assessments for screening older adults for cognitive impairment. Design, Setting, and

Participants:

This multisite, cross-sectional study used baseline data from a longitudinal, observational study from 2020 to 2023, including up to 3 years of follow-up. Participants were enrolled from 3 Alzheimer Disease Research Centers and the Brain Health Registry. Participants (aged ≥55 years, with a study partner, and no acute or unstable major medical conditions) were recruited during in-clinic visits or by automated emails. Exposures Participants completed the Uniform Data Set Version 3 (UDS; including the CDR) in supervised clinical research settings, and then completed the eCDR remotely, online and unsupervised, using their own device. Main Outcomes and

Measures:

The primary outcomes were eCDR scores (item; categorical box and global; continuous box and global), CDR scores (item; categorical box and global), and UDS assessment scores. Associations were evaluated using linear and logistic regressions.

Results:

A total of 3565 participants were contacted, and 288 were enrolled. Among 173 participants with item-level data (mean [SD] age, 70.84 [7.65] years; 76 women [43.9%]), eCDR to CDR concordance was 90% or higher for 33 items (63%) and 70% to 89% for 13 items (25%). Box (domain) level concordance ranged from 80% (memory) to 99% (personal care). The global score concordance rate was 81%. κ statistics were fair to moderate. Among 206 participants with box and global scores (mean [SD] age, 71.34 [7.68] years; 95 women [46.1%]), eCDR continuous global score was associated with CDR global (categorical) score with an area under the receiver operating characteristic curve of 0.79 (95% CI, 0.70-0.87). Correlations between eCDR and in-clinic UDS assessments were similar to those between CDR sum of box scores and the same in-clinic assessments. Conclusions and Relevance These findings suggest that the eCDR is valid and has potential use for screening and assessment of older adults for cognitive and functional decline related to Alzheimer disease. Instrument optimization and validation in diverse cohorts in remote settings are crucial for evaluating scalability and eCDR utility in clinical research, trials, and health care settings.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Alzheimer Tipo de estudo: Diagnostic_studies / Observational_studies / Prevalence_studies / Risk_factors_studies / Screening_studies Limite: Aged / Female / Humans Idioma: En Revista: JAMA Netw Open Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Alzheimer Tipo de estudo: Diagnostic_studies / Observational_studies / Prevalence_studies / Risk_factors_studies / Screening_studies Limite: Aged / Female / Humans Idioma: En Revista: JAMA Netw Open Ano de publicação: 2023 Tipo de documento: Article