Each study has a usefulness score out of 100 (rubric version 4.0). Tap a score to see what makes it up.
Highest usefulness score first. Studies without a score come last.
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We performed an observational analysis of prospectively collected data on 1,474 adult patients who were hospitalized for community-acquired pneumonia; 1,169 patients were under 80 years of age and 305 (21%) patients were over 80 years ("very elderly").
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Utilization and costs for patients with AD were higher compared to controls and were substantially higher for patients with both AD and co-morbid diseases commonly targeted for disease management.
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In this cohort of hospitalized patients with advanced dementia, risk of receiving a new feeding tube is high, associated with African American ethnicity, and prior residence in a nursing home, and has no measurable influence on survival.
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We investigated the range of behavioral abnormalities in patients with Alzheimer's disease (AD) compared with normal age-matched control subjects.
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Receiving any home health care in the last 3 years of life was associated with a lower probability of inpatient death without hospice (Pr 23.3% vs 31.5%, p < .001), and this effect was stronger when home health care began prior to versus during the last year of life (Pr 22.5% vs 24.3%, p < .001).
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Of 2 684 704 Fee-for-Service patients with Alzheimer dementia, 769 141 met all inclusion criteria; among these, 281 042 (36.5%) had agitation.
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Obesity is a significant health crisis affecting more than 123 million adults and children/adolescents in the US.
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Dementia research lacks appropriate representation of diverse groups who often face substantial adversity and greater risk of dementia.
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Reactions to disclosure did not significantly differ among participant groups based on self-reported race and ethnicity.
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Among 88 African Americans with cognitive impairment (mean = 10 years follow-up), Medicare claims identified dementia <2 years from cohort diagnosis in 55%; 27% were identified 2-9.9 years after cohort diagnosis, and in 18% there was either no claims diagnosis during the study period, or claims identified dementia 10+ years after cohort diagnosis.
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Testing interventions in real-world settings requires fidelity monitoring to ensure implementation integrity.
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Among 4505 respondents aged ≥70 years, 1750 (38.8%) had possible or probable dementia and 2755 (61.2%) had no dementia.
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NPS frequency varied from 18% for appetite and/or eating changes to 42% for delusions.
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Individuals with poor social health were 42 % more likely to develop CVD (p = 0.01) and twice as likely to die from CVD (p = 0.02) over a median 4.5 years follow-up.
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46/100
Both Restriction (HR = 2.22, 95% CI [1.42, 3.47], P < .001) and Isolation (HR = 1.78, 95% CI [1.17, 2.70], P = 0.007) were associated with episodic memory and incident dementia, controlling for age, sex, and education.
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Specialised care services were highly prevalent.
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The timing of palliative care initiation may be more appropriately directed using a needs-based approach, instead of a prognostically driven one.
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3,001,987 Medicare beneficiaries were identified, of which 8.2% had a dementia diagnosis.
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Tele-STAR reduced caregiver burden and retained good program and treatment fidelity to STAR-C. We found Tele-STAR reduced caregiver burden and had good fidelity to the original protocol.
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46/100
Dementia care, both at EOL and not at EOL, was associated with the most caregiver burden relative to regular care.
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Hearing loss is a marker of risk for cognitive decline and dementia.
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The friendship subset of social networks was significantly related to cognition (independent of age, gender, depression, loneliness, and family subset of social network): B = 0.284, P = 0.01.
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The nature and outcome of family caregiving is different for various racial and ethnic groups.
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The relationships between caregiver burden as measured with the Burden Scale for Family Caregivers-short form and 6 characteristics of caregivers caring for patients with dementia were investigated for caregivers from England (n = 36), Finland (n = 42), and Greece (n = 46) using survey data.
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As full citizens, people with dementia are entitled to engage in social and occupational activities in residential care settings.
From across this topic
9 of the 1,022 studies in this topic, picked by a fixed rule (a hash of each study's address), not by score or date; each page of this list shows a different 9. The same 9 appear here every time.
- Home, but Not Homebound: A Prospective Analysis of Persons Living With Dementia
- Care Home Life and Identity: A Qualitative Case Study
- Music therapy in UK palliative and end-of-life care: a service evaluation
- Deaths: preliminary data for 2000
- Models of home care services for persons with dementia: a narrative review
- The aftermath of hip fracture: discharge placement, functional status change, and mortality
- Exploring Memory Care Clinics in Minnesota: A Qualitative Analysis
- Hospitalizations for ambulatory care sensitive conditions and unplanned readmissions among Medicare beneficiaries with Alzheimer's disease
- Digital and Health Literacy Are Associated with Health-Related Quality of Life Across Cognitive Impairment Stages in Older Adults