4.5 Article

Impact of Alzheimer's disease on the family caregiver's long-term quality of life: results from an ALSOVA follow-up study

Journal

QUALITY OF LIFE RESEARCH
Volume 25, Issue 3, Pages 687-697

Publisher

SPRINGER
DOI: 10.1007/s11136-015-1100-x

Keywords

Family caregivers; Alzheimer's disease; Health-related quality of life; 15D; Psychological distress

Funding

  1. Yrjo Jahnsson Foundation
  2. Finnish Brain Research and Rehabilitation Foundation Center Neuron
  3. Social Insurance Institute of Finland (Kela)
  4. Novartis Pharma AG
  5. Kuopio University Hospital (EVO/VTR) [5220/5772728]
  6. Finnish Nurses Association (TV)
  7. Foundation of Municipal Development in Finland (TV)

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To examine caregivers' health-related quality of life (HRQoL) and well-being during the first 3 years after their family member's Alzheimer's disease (AD) diagnosis and assessed the relationship between caregivers' HRQoL, well-being, and the severity of AD. Further, to compare of caregivers' HRQoL to general population. Longitudinal design (36 months) after AD diagnosis of 236 caregiver-patient dyads. Linear regression was used to assess age- and gender-adjusted association between repeated measurements of caregivers' HRQoL and the severity of AD. For comparison with general population, the National Health 2011 Health Examination Survey data was utilized. Caregivers had significantly lower HRQoL than age- and gender-standardized counterparts. Severity of AD was significantly (p < 0.05) associated with the mobility and depression dimensions of caregiver's HRQoL but not with the total HRQoL index score. Caregivers' HRQoL seems to deteriorate earlier than previously noted. The severity of AD has not that great impact on caregiver's HRQoL as assumed.

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