Literature DB >> 16721641

Health status in patients with Alzheimer's disease: an investigation of inter-rater agreement.

J L Novella1, F Boyer, C Jochum, N Jovenin, I Morrone, D Jolly, S Bakchine, F Blanchard.   

Abstract

OBJECTIVE: The purpose of the present study was to examine the level of agreement between health status ratings provided by patients with Alzheimer's disease and by their proxies.
BACKGROUND: Because proxy-completed responses are often necessary in assessing health outcomes for the elderly, it is necessary to determine the feasibility and potential limitations of using proxies as a patient substitutes.
METHODS: To assess the potential utility of proxy responses on health status when subjects present a cognitive impairment, this study compared the responses of 70 subjects with Alzheimer's disease and those of their family and/or care provider proxy using the SF-36. Agreement between proxies and patients was measured by intraclass correlation coefficients (ICCs).
RESULTS: The proportion of exact agreement between patients and proxies on the 36 items ranged from 3.3 to 41.7%. Results reveal poor to moderate agreement between patient and proxy reports. Proxy reliability varied according to the relationship of the proxy to the index subject. Agreement decreased significantly with increasing severity of dementia and with increasing severity of Physical status (Katz ADL). Agreement was better for measures of functions that are directly observable and relatively poor for more subjective measures.
CONCLUSIONS: Our results confirm the importance of the information source used for patient health status.

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Mesh:

Year:  2006        PMID: 16721641     DOI: 10.1007/s11136-005-5434-7

Source DB:  PubMed          Journal:  Qual Life Res        ISSN: 0962-9343            Impact factor:   4.147


  57 in total

1.  Limitations of the SF-36 in a sample of nursing home residents.

Authors:  E M Andresen; G W Gravitt; M E Aydelotte; C A Podgorski
Journal:  Age Ageing       Date:  1999-10       Impact factor: 10.668

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4.  Health-related quality of life of nursing home residents: differences in patient and provider perceptions.

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Journal:  J Am Geriatr Soc       Date:  1995-07       Impact factor: 5.562

Review 5.  Methodological issues in measuring the functional status of cognitively impaired nursing home residents: the use of proxies and performance-based measures.

Authors:  S I Zimmerman; J Magaziner
Journal:  Alzheimer Dis Assoc Disord       Date:  1994       Impact factor: 2.703

6.  Individual quality of life factors distinguishing low-burden and high-burden caregivers of dementia patients.

Authors:  Robert F Coen; Ciaran A O'Boyle; Davis Coakley; Brian A Lawlor
Journal:  Dement Geriatr Cogn Disord       Date:  2002       Impact factor: 2.959

Review 7.  Measuring health-related quality of life.

Authors:  G H Guyatt; D H Feeny; D L Patrick
Journal:  Ann Intern Med       Date:  1993-04-15       Impact factor: 25.391

8.  What explains differences between dementia patients' and their caregivers' ratings of patients' quality of life?

Authors:  Laura P Sands; Patricia Ferreira; Anita L Stewart; Meryl Brod; Kristine Yaffe
Journal:  Am J Geriatr Psychiatry       Date:  2004 May-Jun       Impact factor: 4.105

9.  Dementia and cancer: a comparison of spouse caregivers.

Authors:  E C Clipp; L K George
Journal:  Gerontologist       Date:  1993-08

10.  Physical and functional health assessment in normal aging and in Alzheimer's disease: self-reports vs family reports.

Authors:  H A Kiyak; L Teri; S Borson
Journal:  Gerontologist       Date:  1994-06
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  7 in total

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Authors:  Alasdair Grant Rooney; Shanne McNamara; Mairi Mackinnon; Mary Fraser; Roy Rampling; Alan Carson; Robin Grant
Journal:  J Neurooncol       Date:  2013-02-24       Impact factor: 4.130

2.  Magnitude and causes of bias among family caregivers rating Alzheimer disease patients.

Authors:  Richard Schulz; Thomas B Cook; Scott R Beach; Jennifer H Lingler; Lynn M Martire; Joan K Monin; Sara J Czaja
Journal:  Am J Geriatr Psychiatry       Date:  2013-01-02       Impact factor: 4.105

3.  Mapping utility scores from the Barthel index.

Authors:  Billingsley Kaambwa; Lucinda Billingham; Stirling Bryan
Journal:  Eur J Health Econ       Date:  2011-11-02

Review 4.  Quality of life in glaucoma and three other chronic diseases: a systematic literature review.

Authors:  Tim Mills; Simon K Law; John Walt; Patricia Buchholz; Jan Hansen
Journal:  Drugs Aging       Date:  2009       Impact factor: 3.923

5.  Quality of life in dementia: a study on proxy bias.

Authors:  Alexander M M Arons; Paul F M Krabbe; Carla J M Schölzel-Dorenbos; Gert Jan van der Wilt; Marcel G M Olde Rikkert
Journal:  BMC Med Res Methodol       Date:  2013-09-06       Impact factor: 4.615

6.  Proxy reporting of health-related quality of life for people with dementia: a psychometric solution.

Authors:  S C Smith; A A J Hendriks; S J Cano; N Black
Journal:  Health Qual Life Outcomes       Date:  2020-05-24       Impact factor: 3.186

7.  Healthcare professionals and managers' participation in developing an intervention: a pre-intervention study in the elderly care context.

Authors:  Isabelle Vedel; Matthieu De Stampa; Howard Bergman; Joel Ankri; Bernard Cassou; François Blanchard; Liette Lapointe
Journal:  Implement Sci       Date:  2009-04-21       Impact factor: 7.327

  7 in total

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