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Objective: Previous research using the National Health and Aging Trends Study showed that a claims-based frailty index (CFI) could be useful for identifying moderate-to-severe dementia in Medicare claims data. This study aims to validate the findings in an independent cohort.
Design: Retrospective cohort study.
Setting And Participants: The study included 658 fee-for-service beneficiaries with dementia who participated in the 2016-2020 Medicare Current Beneficiary Survey in the community-dwelling.
Methods: We operationalized the Functional Assessment Staging Test (FAST) scale (range: 1-7, stages 5-7 indicate moderate-to-severe dementia) using survey information. CFI (range: 0-1, higher scores indicate greater frailty) was calculated using Medicare claims 12 months before the participants' interview date. Using the previously proposed cut point of 0.280, we calculated sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV) for identifying moderate-to-severe dementia. Survey procedures were used to account for survey design and weighted to reflect national estimates.
Results: The population had a mean age (SD) of 80.7 (8.9) years, 58.5% female, and 101 beneficiaries (14.8%) had moderate-to-severe dementia. The CFI cut point of 0.280 demonstrated sensitivity 0.49 (95% CI, 0.38-0.59), specificity 0.80 (0.77-0.84), PPV 0.30 (0.23-0.38), and NPV 0.90 (0.87-0.93). Compared with those with a CFI <0.280, beneficiaries with a CFI ≥0.280 had an elevated risk of mortality (2.9% vs 4.1%) over 1 year.
Conclusions And Implications: These results confirm our previous findings that CFI among beneficiaries with a dementia diagnosis is a useful measure of moderate-to-severe dementia for Medicare claims data.
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http://dx.doi.org/10.1016/j.jamda.2024.105176 | DOI Listing |
Alzheimers Dement
September 2025
Laboratory of Alzheimer's Neuroimaging and Epidemiology, IRCCS Istituto Centro San Giovanni di Dio Fatebenefratelli, Brescia, Italy.
Introduction: Receiving an Alzheimer's disease (AD) diagnosis can be a distressing experience, for both the individual with the condition and the family. This cross-sectional study explored whether the disclosure of AD diagnosis generated post-traumatic stress symptoms (PTSSs) in caregivers and how this affected their psychological well-being.
Methods: Seventy-nine caregivers completed the Impact of Event Scale to assess any PTSSs related to the memory of AD disclosure and clinical scales to assess current psychological distress.
J Palliat Med
September 2025
Section of Palliative Care and Medical Ethics, Department of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Despite caring for patients with serious illnesses, gastroenterology (GI) fellows rarely receive training in serious illness conversations (SIC). To describe the development, implementation, and assessment of GITalk, a novel SIC training for GI fellows. GITalk was based on the REMAP framework and involved two simulated encounters.
View Article and Find Full Text PDFNeurology
September 2025
Department of Psychiatry, The University of Texas Southwestern Medical Center, Dallas.
Background And Objectives: This retrospective study used data from the National Alzheimer's Coordinating Center (NACC) database and compared neuropathologic, neuropsychiatric, motor, and neuropsychological features between those with and without chronic traumatic encephalopathy neuropathologic change (CTE-NC).
Methods: Data were obtained from the NACC database from 2014 to December 2024, with the only inclusion criterion being evaluation for CTE-NC. Participants with CTE-NC were identified and matched approximately 1:4 to those without CTE-NC on demographics (age, education, sex) and staging of Alzheimer and Lewy body neuropathology.
Geriatr Nurs
August 2025
The Cheryl Spencer Department of Nursing Faculty of Social Welfare and Health Science, University of Haifa, Israel; Center of Research & Study of Aging, University of Haifa, Israel.
Family caregivers of individuals with advanced dementia face significant emotional and physical burdens, highlighting the need for tools to assess their well-being. This study translated and validated the Self-Transcendence Scale (STS) into Hebrew for family caregivers of nursing home residents with moderate-to-severe dementia, focusing on cultural adaptation and psychometric evaluation. A sample of 175 Hebrew-speaking caregivers completed the scale.
View Article and Find Full Text PDFBMC Geriatr
August 2025
Department of Business Administration, National Changhua University of Education, Changhua, Taiwan.
Background: Caregivers caring for patients with dementia could experience depressive symptoms, distress from patients' behavioral symptoms, and physical morbidities. Factors associated with a caregiving burden are complex and vary with time because burden is a subjective measure influenced by physical, economic, and psychosocial strain and has an interaction among caregiver resources, vulnerabilities, and care demands. The purpose of this study was to elucidate the association of patients' and caregivers' factors especially the severity of behavior and psychiatric symptoms of dementia (BPSD) and specific activities of daily living items impairment with a moderate or even severe caregiving burden.
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