2010
DOI: 10.1017/s104161021000150x
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Clinical progression of moderate-to-severe Alzheimer's disease and caregiver burden: a 12-month multicenter prospective observational study

Abstract: These findings reinforce previous AD knowledge and add data on the clinical course of advanced stages of AD. Caregiver burden depended more on patients' behavioral alterations than on their functional or cognitive declines; and it was diminished by their patients having higher levels of education and being treated with AD-specific medications. Research into unexplored factors that might reduce caregiver burden, ultimately benefiting both patients and caregivers, is encouraged.

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Cited by 42 publications
(43 citation statements)
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“…This yielded an average score of 8.1 points (95% CI 4.1 to 12.3) less for caregivers receiving the intervention compared with those receiving usual care. The SD applied is similar to that observed in an observational study (Agüera‐Ortiz et al ., ) of caregivers of individuals with dementia, which reported an SD of 18.8 on the Zarit Burden Scale.…”
Section: Resultsmentioning
confidence: 99%
“…This yielded an average score of 8.1 points (95% CI 4.1 to 12.3) less for caregivers receiving the intervention compared with those receiving usual care. The SD applied is similar to that observed in an observational study (Agüera‐Ortiz et al ., ) of caregivers of individuals with dementia, which reported an SD of 18.8 on the Zarit Burden Scale.…”
Section: Resultsmentioning
confidence: 99%
“…In addition, levels of education among patients with dementia (Agüera‐Ortiz et al. ; Kim et al. ) were recognized as the patient socio‐demographical factor of caregiver burden.…”
Section: Resultsmentioning
confidence: 99%
“…We did not control for education and gender in the analyses because of the lack of an effect on the cognitive measures in this small sample and lack of a priori hypotheses, even though education may correlate with stress in this population. 59 The small sample size also limited the ability to statistically explore the potential interactions of education, gender, and the relationship of the caregiver to the person with dementia to the cognitive measures. Dementia caregivers are difficult to recruit for extensive physiological and psychological studies since they already have very demanding time pressures.…”
Section: Discussionmentioning
confidence: 99%