Literature DB >> 12379521

Measuring the meaning of disability in rheumatoid arthritis: the Personal Impact Health Assessment Questionnaire (PI HAQ).

S Hewlett1, A P Smith, J R Kirwan.   

Abstract

BACKGROUND: Measurement of disability in rheumatoid arthritis is often used to support treatment decisions and outcome assessments, but is used without reference to the impact of disability on individual patients.
OBJECTIVE: To develop and validate a scale to measure individual values for functions, which is used to weight the level of an individual patient's functional loss and thus calculate the personal impact of disability.
METHODS: In four linked studies, first the phraseology for values was explored to develop a stem question for the value scale couched in terms patients understand (face validity). Then short and long versions of the value scale were compared (content validity) and tests of internal consistency and short term reliability undertaken (criterion validity). Finally, the value scale was examined for long term reliability and agreement with expected variables (criterion and construct validity), after which personal impact scores were calculated and their construct validity examined.
RESULTS: Patients understand the concept of values, and a positively phrased stem question was developed for the value scale, for which a short version was reasonably equivalent to a long version. The value scale was reliable over one week (96% changed by <1 point) with positive interitem correlation. Reasonable six and 12 month reliability was shown (52% changed by <0.5 points), and the value scale was independent of disability and clinical, psychological, personality, and social support variables. Personal impact scores were then calculated by using the value scores to weight disability scores. Impact scores varied widely between patients of similar disability. Personal impact for disability showed convergent validity with dissatisfaction with disability, perceived increase in disability, increased disease activity, worse psychological status, low social support, and time trade off for disability. It discriminated between patients with low and high dissatisfaction with disability, life satisfaction, depression, pain, and helplessness.
CONCLUSION: This individualised personal impact scale should lend meaning to disability scores, improving the interpretation of clinical and research data.

Entities:  

Mesh:

Year:  2002        PMID: 12379521      PMCID: PMC1753935          DOI: 10.1136/ard.61.11.986

Source DB:  PubMed          Journal:  Ann Rheum Dis        ISSN: 0003-4967            Impact factor:   19.103


  28 in total

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Journal:  J Rheumatol       Date:  1982 Sep-Oct       Impact factor: 4.666

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Journal:  J Rheumatol       Date:  1987-08       Impact factor: 4.666

8.  Concordance between clinician and patient assessment of physical and mental health status.

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Authors:  E Berkanovic; M L Hurwicz; P A Lachenbruch
Journal:  Arthritis Care Res       Date:  1995-06

10.  Which outcome measures should be used in rheumatoid arthritis clinical trials? Clinical and quality-of-life measures' responsiveness to treatment in a randomized controlled trial.

Authors:  R Buchbinder; C Bombardier; M Yeung; P Tugwell
Journal:  Arthritis Rheum       Date:  1995-11
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  11 in total

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Authors:  T Sanderson; M Morris; M Calnan; P Richards; S Hewlett
Journal:  Arthritis Care Res (Hoboken)       Date:  2010-05       Impact factor: 4.794

Review 3.  Quality-of-life assessment in rheumatoid arthritis.

Authors:  Anthony S Russell
Journal:  Pharmacoeconomics       Date:  2008       Impact factor: 4.981

4.  Measure of function in rheumatoid arthritis: individualised or classical scales?

Authors:  R Seror; F Tubach; G Baron; F Guillemin; P Ravaud
Journal:  Ann Rheum Dis       Date:  2010-01       Impact factor: 19.103

5.  Self-management of fatigue in rheumatoid arthritis: a randomised controlled trial of group cognitive-behavioural therapy.

Authors:  Sarah Hewlett; Nick Ambler; Celia Almeida; Alena Cliss; Alison Hammond; Karen Kitchen; Bev Knops; Denise Pope; Melissa Spears; Annette Swinkels; Jon Pollock
Journal:  Ann Rheum Dis       Date:  2011-06       Impact factor: 19.103

6.  Measuring the impact and distress of health problems from the individual's perspective: development of the Perceived Impact of Problem Profile (PIPP).

Authors:  Julie F Pallant; RoseAnne Misajon; Elizabeth Bennett; Lenore Manderson
Journal:  Health Qual Life Outcomes       Date:  2006-06-29       Impact factor: 3.186

7.  Do patient-reported outcome measures cover personal factors important to people with rheumatoid arthritis? A mixed methods design using the International Classification of Functioning, Disability and Health as frame of reference.

Authors:  Mona Dür; Michaela Coenen; Michaela Alexandra Stoffer; Veronika Fialka-Moser; Alexandra Kautzky-Willer; Ingvild Kjeken; Răzvan Gabriel Drăgoi; Malin Mattsson; Carina Boström; Josef Smolen; Tanja Alexandra Stamm
Journal:  Health Qual Life Outcomes       Date:  2015-02-25       Impact factor: 3.186

8.  Developing Smartphone-Based Objective Assessments of Physical Function in Rheumatoid Arthritis Patients: The PARADE Study.

Authors:  Valentin Hamy; Luis Garcia-Gancedo; Andrew Pollard; Anniek Myatt; Jingshu Liu; Andrew Howland; Philip Beineke; Emilia Quattrocchi; Rachel Williams; Michelle Crouthamel
Journal:  Digit Biomark       Date:  2020-04-30

9.  Purpose in life in patients with rheumatoid arthritis.

Authors:  Pieter J M Verduin; Geertruida H de Bock; Theodora P M Vliet Vlieland; Andreas J Peeters; John Verhoef; Wilma Otten
Journal:  Clin Rheumatol       Date:  2008-01-24       Impact factor: 2.980

10.  Impairment in the activities of daily living in older adults with and without osteoporosis, osteoarthritis and chronic back pain: a secondary analysis of population-based health survey data.

Authors:  Tanja Alexandra Stamm; Karin Pieber; Richard Crevenna; Thomas Ernst Dorner
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