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EQ-5D in Patients with Dementia: An Investigation of Inter-Rater Agreement

Background. There are difficulties in obtaining health-related quality of life (HRQL) data from patients with dementia due to variation in their cognitive ability, degree of insight and capacity to make judgments. The use of proxies is one solution. Objectives. To examine the inter-rater agreement o...

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Published in:Medical care 2001-08, Vol.39 (8), p.760-771
Main Authors: Coucill, Wendy, Bryan, Stirling, Bentham, Peter, Buckley, Ann, Laight, Ann
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container_title Medical care
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creator Coucill, Wendy
Bryan, Stirling
Bentham, Peter
Buckley, Ann
Laight, Ann
description Background. There are difficulties in obtaining health-related quality of life (HRQL) data from patients with dementia due to variation in their cognitive ability, degree of insight and capacity to make judgments. The use of proxies is one solution. Objectives. To examine the inter-rater agreement of patient and proxy completion of the EuroQol EQ-5D instrument (EQ-5D). Research Design. The EQ-5D instrument was completed separately by patients, their caregivers and a physician. Assessment of inter-rater agreement involved comparison of self-completed (patient) and proxy-completed (care-giver and physician) responses for each dimension of EQ-5D, using a weighted kappa score. Three key hypotheses were tested. (1) Interrater agreement would be stronger between patient and caregiver than between patient and physician. (2) Interrater agreement would be stronger on the 'observable' and objective dimensions of EQ-5D. (3) Interrater agreement between patient and proxies would be stronger for patients with earlier dementia. Subjects. The sample comprised 64 patients with a range of dementia severity. Measures. The EQ-5D health state classification system and visual analogue scale were used to assess HRQL. Global severity of dementia was determined using the Clinical Dementia Rating Scale. Results. The principal finding of this study was that responses to EQ-5D questions were highly variable across the three raters such that none of the three hypotheses were strongly supported. Conclusions. The data provide some support for the use of EQ-5D when interviewer administered. However, there are serious concerns regarding the validity of patient self-rated HRQL data obtained in this study and uncertainty exists regarding who the appropriate proxy should be, as different groups of proxies provide different results. It was not clear whether caregivers or physicians represent better proxies. Further research should focus on the comparison of caregivers and physicians as proxies.
doi_str_mv 10.1097/00005650-200108000-00003
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There are difficulties in obtaining health-related quality of life (HRQL) data from patients with dementia due to variation in their cognitive ability, degree of insight and capacity to make judgments. The use of proxies is one solution. Objectives. To examine the inter-rater agreement of patient and proxy completion of the EuroQol EQ-5D instrument (EQ-5D). Research Design. The EQ-5D instrument was completed separately by patients, their caregivers and a physician. Assessment of inter-rater agreement involved comparison of self-completed (patient) and proxy-completed (care-giver and physician) responses for each dimension of EQ-5D, using a weighted kappa score. Three key hypotheses were tested. (1) Interrater agreement would be stronger between patient and caregiver than between patient and physician. (2) Interrater agreement would be stronger on the 'observable' and objective dimensions of EQ-5D. (3) Interrater agreement between patient and proxies would be stronger for patients with earlier dementia. Subjects. The sample comprised 64 patients with a range of dementia severity. Measures. The EQ-5D health state classification system and visual analogue scale were used to assess HRQL. Global severity of dementia was determined using the Clinical Dementia Rating Scale. Results. The principal finding of this study was that responses to EQ-5D questions were highly variable across the three raters such that none of the three hypotheses were strongly supported. Conclusions. The data provide some support for the use of EQ-5D when interviewer administered. However, there are serious concerns regarding the validity of patient self-rated HRQL data obtained in this study and uncertainty exists regarding who the appropriate proxy should be, as different groups of proxies provide different results. It was not clear whether caregivers or physicians represent better proxies. 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Lippincott Williams and Wilkins Inc</publisher><subject>Activities of Daily Living ; Aged ; Aged, 80 and over ; Alzheimers disease ; Analysis of Variance ; Caregivers ; Dementia ; Dementia - diagnosis ; Dementia - psychology ; England ; Female ; Humans ; Male ; Middle Aged ; Observer Variation ; Older adults ; Physicians ; Proxy ; Proxy reporting ; Proxy statements ; Psychometrics - methods ; Quality of Life ; Questionnaires ; Reproducibility of Results ; Self Care ; Severity of Illness Index ; Strokes</subject><ispartof>Medical care, 2001-08, Vol.39 (8), p.760-771</ispartof><rights>Copyright 2001 Lippincott Williams &amp; Wilkins</rights><rights>2001 Lippincott Williams &amp; Wilkins, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3773-86ecae9954e251f628055863489f886464c84d334c244cd5544bb0b666b662db3</citedby><cites>FETCH-LOGICAL-c3773-86ecae9954e251f628055863489f886464c84d334c244cd5544bb0b666b662db3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/3767966$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/3767966$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,58238,58471</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11468496$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Coucill, Wendy</creatorcontrib><creatorcontrib>Bryan, Stirling</creatorcontrib><creatorcontrib>Bentham, Peter</creatorcontrib><creatorcontrib>Buckley, Ann</creatorcontrib><creatorcontrib>Laight, Ann</creatorcontrib><title>EQ-5D in Patients with Dementia: An Investigation of Inter-Rater Agreement</title><title>Medical care</title><addtitle>Med Care</addtitle><description>Background. There are difficulties in obtaining health-related quality of life (HRQL) data from patients with dementia due to variation in their cognitive ability, degree of insight and capacity to make judgments. The use of proxies is one solution. Objectives. To examine the inter-rater agreement of patient and proxy completion of the EuroQol EQ-5D instrument (EQ-5D). Research Design. The EQ-5D instrument was completed separately by patients, their caregivers and a physician. Assessment of inter-rater agreement involved comparison of self-completed (patient) and proxy-completed (care-giver and physician) responses for each dimension of EQ-5D, using a weighted kappa score. Three key hypotheses were tested. (1) Interrater agreement would be stronger between patient and caregiver than between patient and physician. (2) Interrater agreement would be stronger on the 'observable' and objective dimensions of EQ-5D. (3) Interrater agreement between patient and proxies would be stronger for patients with earlier dementia. Subjects. The sample comprised 64 patients with a range of dementia severity. Measures. The EQ-5D health state classification system and visual analogue scale were used to assess HRQL. Global severity of dementia was determined using the Clinical Dementia Rating Scale. Results. The principal finding of this study was that responses to EQ-5D questions were highly variable across the three raters such that none of the three hypotheses were strongly supported. Conclusions. The data provide some support for the use of EQ-5D when interviewer administered. However, there are serious concerns regarding the validity of patient self-rated HRQL data obtained in this study and uncertainty exists regarding who the appropriate proxy should be, as different groups of proxies provide different results. It was not clear whether caregivers or physicians represent better proxies. Further research should focus on the comparison of caregivers and physicians as proxies.</description><subject>Activities of Daily Living</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Alzheimers disease</subject><subject>Analysis of Variance</subject><subject>Caregivers</subject><subject>Dementia</subject><subject>Dementia - diagnosis</subject><subject>Dementia - psychology</subject><subject>England</subject><subject>Female</subject><subject>Humans</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Observer Variation</subject><subject>Older adults</subject><subject>Physicians</subject><subject>Proxy</subject><subject>Proxy reporting</subject><subject>Proxy statements</subject><subject>Psychometrics - methods</subject><subject>Quality of Life</subject><subject>Questionnaires</subject><subject>Reproducibility of Results</subject><subject>Self Care</subject><subject>Severity of Illness Index</subject><subject>Strokes</subject><issn>0025-7079</issn><issn>1537-1948</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><recordid>eNp1kUtPAjEUhRujEXz8A2O6cldtp293BFAxJD6i62YeHRgcZrCdkfjvLQziyibtzT35zm1zCgAk-JpgLW9wWFxwjCKMCVahQxuJHoA-4VQiopk6BH2MI44klroHTrxfBFZSHh2DHiFMKKZFHzyOXxAfwaKCz3FT2KrxcF00cziyy9AU8S0cVHBSfVnfFLNA1BWs8yA01qHXOJxwMHN2C5-BozwuvT3f1VPwfjd-Gz6g6dP9ZDiYopRKSZESNo2t1pzZiJNcRApzrgRlSudKCSZYqlhGKUsjxtKMc8aSBCdCiLCjLKGn4Kqbu3L1ZxseZpaFT21ZxpWtW28kwZGSRAdQdWDqau-dzc3KFcvYfRuCzSZH85uj2ee4lWiwXu7uaJOlzf6Mu-ACwDpgXZchBf9RtmvrzNzGZTM3__1PsF10toVvarcfS6WQWgj6A3fKg7I</recordid><startdate>20010801</startdate><enddate>20010801</enddate><creator>Coucill, Wendy</creator><creator>Bryan, Stirling</creator><creator>Bentham, Peter</creator><creator>Buckley, Ann</creator><creator>Laight, Ann</creator><general>J. 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There are difficulties in obtaining health-related quality of life (HRQL) data from patients with dementia due to variation in their cognitive ability, degree of insight and capacity to make judgments. The use of proxies is one solution. Objectives. To examine the inter-rater agreement of patient and proxy completion of the EuroQol EQ-5D instrument (EQ-5D). Research Design. The EQ-5D instrument was completed separately by patients, their caregivers and a physician. Assessment of inter-rater agreement involved comparison of self-completed (patient) and proxy-completed (care-giver and physician) responses for each dimension of EQ-5D, using a weighted kappa score. Three key hypotheses were tested. (1) Interrater agreement would be stronger between patient and caregiver than between patient and physician. (2) Interrater agreement would be stronger on the 'observable' and objective dimensions of EQ-5D. (3) Interrater agreement between patient and proxies would be stronger for patients with earlier dementia. Subjects. The sample comprised 64 patients with a range of dementia severity. Measures. The EQ-5D health state classification system and visual analogue scale were used to assess HRQL. Global severity of dementia was determined using the Clinical Dementia Rating Scale. Results. The principal finding of this study was that responses to EQ-5D questions were highly variable across the three raters such that none of the three hypotheses were strongly supported. Conclusions. The data provide some support for the use of EQ-5D when interviewer administered. However, there are serious concerns regarding the validity of patient self-rated HRQL data obtained in this study and uncertainty exists regarding who the appropriate proxy should be, as different groups of proxies provide different results. It was not clear whether caregivers or physicians represent better proxies. 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source JSTOR Archival Journals and Primary Sources Collection
subjects Activities of Daily Living
Aged
Aged, 80 and over
Alzheimers disease
Analysis of Variance
Caregivers
Dementia
Dementia - diagnosis
Dementia - psychology
England
Female
Humans
Male
Middle Aged
Observer Variation
Older adults
Physicians
Proxy
Proxy reporting
Proxy statements
Psychometrics - methods
Quality of Life
Questionnaires
Reproducibility of Results
Self Care
Severity of Illness Index
Strokes
title EQ-5D in Patients with Dementia: An Investigation of Inter-Rater Agreement
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