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2019
DOI: 10.1016/j.jval.2019.07.002
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How Should We Capture Health State Utility in Dementia? Comparisons of DEMQOL-Proxy-U and of Self- and Proxy-Completed EQ-5D-5L

Abstract: Background: Dementia-specific and proxy-completed preference-based measures have been proposed for use in intervention studies involving people living in residential care, in instances where generic, self-reported preference-based measures have been deemed inappropriate. Objective: This study was conducted to investigate the construct validity, criterion validity, and responsiveness of DEMQOL-Proxy-U and of self-and proxy-completed EQ-5D-5L. Methods: The analysis used a 3-wave, individual-level data set of 100… Show more

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Cited by 19 publications
(30 citation statements)
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“…Research published after our study had started indicates that the EQ-5D performs better than the DEMQOL in care homes. 21 30 EQ-5D has been shown to be more responsive to change, 31 which is the justification for our conclusion that the GtACH programme was cost effective. The DEMQOL focuses more on the emotional impact of dementia, whereas in this study the outcome was not dementia specific, and not all residents had dementia.…”
Section: Discussionmentioning
confidence: 62%
“…Research published after our study had started indicates that the EQ-5D performs better than the DEMQOL in care homes. 21 30 EQ-5D has been shown to be more responsive to change, 31 which is the justification for our conclusion that the GtACH programme was cost effective. The DEMQOL focuses more on the emotional impact of dementia, whereas in this study the outcome was not dementia specific, and not all residents had dementia.…”
Section: Discussionmentioning
confidence: 62%
“…There are many controversies regarding the methods of modeling the cost-effectiveness of treatments for AD, 25 including whether disease measures adequately capture benefits to patients, 26 how to link short-term measures of cognition with disease progression and the need for institutional care, 27 how best to capture health-related quality of life, 28 and whether and how to include the health and cost effects of treatment on caregivers and society. 29 It is, however, well established that unpaid and informal care for AD patients by family members and other caregivers is widespread, and caregivers may experience adverse emotional and financial consequences leading to decreased quality of life and increased health care costs.…”
Section: Discussionmentioning
confidence: 99%
“…However, the intervention program on which the cost estimation is based on focused on improvement of physical performance, with quality of life only representing a secondary outcome, leading to restricted effects on quality of life . The estimation of QALYs was based on self-reported quality of life, which is shown to be higher than proxy ratings [41]. This limits the external validity of QALYs reported in this study; however, it does not influence the results of our cost-utility analysis.…”
Section: Discussionmentioning
confidence: 92%