Outcomes generated by patients with rheumatoid arthritis: how important are they?
- 1 September 2005
- journal article
- research article
- Published by Wiley in Musculoskeletal Care
- Vol. 3 (3) , 131-142
- https://doi.org/10.1002/msc.3
Abstract
Background: It has been shown previously that patients with rheumatoid arthritis (RA) can generate a wide range of outcomes that they consider important in treatment. It is not known if these outcomes are generally important in the wider RA patient community. Objectives: (1) To examine whether recent patient-generated outcomes are generalizable within a wider RA population; (2) to assess the relative importance of each outcome; and(3) to explore whether any important outcomes have been omitted. Methods: A questionnaire, listing 23 outcomes previously generated by RA patients, was distributed through three rheumatology centres in the UK. Patients gave an importance score to each outcome (0–3), selected their top three most important outcomes, and then listed any outcomes of personal importance that were missing. Results: 323 questionnaires were returned (65%). All outcomes were deemed important. Independence, pain, and mobility were most frequently selected by patients in their top three outcomes but were not chosen by 61–66% of patients. The next most commonly chosen outcomes related to feeling well and fatigue. Factor analysis revealed six reasonably distinct groupings: general well-being (11.9% explained variance), day-to-day functioning(10.6%), emotional and psychological well-being (10.6%), social role and confidence (10%), physical symptoms (9.5%) and medication issues (7.9%). Conclusion: Outcomes generated by patients as important in RA, are generalizable and inclusive. The most important (independence, pain and mobility) are routinely treated and measured. The next most important (feeling well, fatigue) are infrequently addressed and deserve urgent consideration for measurement, treatment and research. Copyright © 2005 John Wiley & Sons, Ltd.Keywords
This publication has 13 references indexed in Scilit:
- Quality of life, social support, and knowledge of disease in women with rheumatoid arthritisArthritis Care & Research, 2003
- Measuring the meaning of disability in rheumatoid arthritis: the Personal Impact Health Assessment Questionnaire (PI HAQ)Annals of the Rheumatic Diseases, 2002
- Preferences for improved health examined in 1,024 patients with rheumatoid arthritis: Pain has highest priorityArthritis Care & Research, 2002
- Values for function in rheumatoid arthritis: patients, professionals, and publicAnnals of the Rheumatic Diseases, 2001
- Rheumatology patient and physician concordance with respect to important health and symptom status outcomesArthritis & Rheumatism, 2001
- Margaret Holroyd Prize Essay. A patient-centred approach to evaluation and treatment in rheumatoid arthritis: the development of a clinical tool to measure patient-perceived handicapRheumatology, 1996
- Concordant and discrepant views of patients' physical functioningArthritis & Rheumatism, 1995
- The development of depressive symptoms among women with rheumatoid arthritis the role of functionArthritis & Rheumatism, 1995
- The American college of rheumatology preliminary core set of disease activity measures for rheumatoid arthritis clinical trialsArthritis & Rheumatism, 1993
- Fatigue in rheumatoid arthritis: Conditions, strategies, and consequencesArthritis & Rheumatism, 1990