Literature DB >> 3702504

Classifying function for health outcome and quality-of-life evaluation. Self- versus interviewer modes.

J P Anderson, J W Bush, C C Berry.   

Abstract

Validity assessment and the underreporting of dysfunction have been major problems in health-related quality-of-life measurement, including collecting data for analysis by the General Health Policy Model, using the Quality of Well-being scale (QWB). This analysis compares the results of self- versus interviewer modes of measurement and short, direct-answer questions versus probing algorithms in the QWB. The comparisons are made in terms of 1) correlations; 2) aggregate frequencies; 3) individual subject classifications; and 4) the actual state, established using evidence from multiple sources. Despite extremely high correlations between QWB scores from the two modes (greater than 0.98), the lowest interviewer mode sensitivity (0.86) and predictive value dysfunctional (0.91) were substantially superior to the highest self-classification characteristics (0.66 and 0.73). In the populations studied, specificities and predictive values functional were equivalent (greater than 0.94) for the two modes. The probe pattern of the interviewer mode was also less susceptible to false reports of dysfunction. These results are consistent with the underreporting of dysfunction noted by several major investigations of health status measurement. The authors conclude that interviewer-administered instruments using question algorithms are necessary if health-related quality of life is to be measured with sufficient reliability and validity to evaluate major clinical trials and follow-up studies.

Mesh:

Year:  1986        PMID: 3702504     DOI: 10.1097/00005650-198605000-00008

Source DB:  PubMed          Journal:  Med Care        ISSN: 0025-7079            Impact factor:   2.983


  9 in total

1.  Comparing survey data on functional disability: the impact of some methodological differences.

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2.  Comparison of Duke Activity Status Index with cardiopulmonary exercise testing in cancer patients.

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Review 3.  Assessment of quality of life in rheumatoid arthritis: methods and implications.

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4.  Interviewing cancer patients in a research setting: the role of effective communication.

Authors:  A Montazeri; R Milroy; C R Gillis; J McEwen
Journal:  Support Care Cancer       Date:  1996-11       Impact factor: 3.603

5.  Evidence for decline in disability and improved health among persons aged 55 to 70 years: the Framingham Heart Study.

Authors:  S H Allaire; M P LaValley; S R Evans; G T O'Connor; M Kelly-Hayes; R F Meenan; D Levy; D T Felson
Journal:  Am J Public Health       Date:  1999-11       Impact factor: 9.308

Review 6.  Measuring the effects of medication use on health-related quality of life in patients with rheumatoid arthritis. A review.

Authors:  M B Nichol; A S Harada
Journal:  Pharmacoeconomics       Date:  1999-11       Impact factor: 4.981

7.  The Quality of Well-Being scale in asymptomatic HIV-infected patients. HNRC Group. HIV Neural Behavioral Research Center.

Authors:  R M Kaplan; T L Patterson; D N Kerner; J H Atkinson; R K Heaton; I Grant
Journal:  Qual Life Res       Date:  1997-08       Impact factor: 4.147

8.  Cost-effectiveness of SHINE: A Telephone Translation of the Diabetes Prevention Program.

Authors:  Christopher S Hollenbeak; Ruth S Weinstock; Donald Cibula; Linda M Delahanty; Paula M Trief
Journal:  Health Serv Insights       Date:  2016-07-06

9.  Assessing the convergence of self-report and informant measures for adults with autism spectrum disorder.

Authors:  Rachel K Sandercock; Elena M Lamarche; Mark R Klinger; Laura G Klinger
Journal:  Autism       Date:  2020-08-02
  9 in total

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