Self-Reports and Caregivers' Proxy Reports of Unmet Needs of Persons With Dementia: Implications for Both Partners' Health-Related Quality of Life

Autor: Janet MacNeil Vroomen, Terrence D. Jorgensen, Joan K. Monin
Přispěvatelé: Geriatrics, ANS - Neurodegeneration, APH - Methodology, APH - Aging & Later Life, Preventive Youth Care (RICDE, FMG), Methods and Statistics (RICDE, FMG)
Rok vydání: 2019
Předmět:
Zdroj: Am J Geriatr Psychiatry
American journal of geriatric psychiatry, 28(3), 363-367. Lippincott Williams and Wilkins
The American Journal of Geriatric Psychiatry, 28(3), 363-367. Lippincott Williams & Wilkins
ISSN: 1545-7214
1064-7481
Popis: OBJECTIVES: This study examined in a large sample of dementia caregiving dyads the associations between both partners’ reports of unmet needs in persons with dementia (PwDs) and both partners’ health-related quality of life (HRQOL). METHODS: This was a cross-sectional self-report survey of 521 community-dwelling dyads in a pragmatic trial in the Netherlands. The Camberwell Needs Assessment was used to measure PwDs’ unmet needs. Both partners’ self-reported their HRQOL using the EuroQol-5. RESULTS: Controlling for covariates, PwDs’ self-reported greater unmet needs were significantly associated with PwDs’ and caregivers’ lower self-reported HRQOL (actor effect; b = −0.044, β = −0.226, z =−3.588, p < .001 and partner effect; β =−0.021, p = −0.131, z=−2.154, p=0.031). Caregivers’ proxy reports were greater than PwDs’ self-reported unmet needs (Δ = 0. 66,χ(2) (1) = 55.881,p < .0001) . CONCLUSION: Clinicians should use caution in relying on caregiver proxy reports of PwDs’ needs and HQOL alone regarding healthcare decision making.
Databáze: OpenAIRE