Literature DB >> 17472993

Changes in priorities for improvement in patients with rheumatoid arthritis during 1 year of anti-tumour necrosis factor treatment.

Peter M ten Klooster1, Martine M Veehof, Erik Taal, Piet L C M van Riel, Mart A F J van de Laar.   

Abstract

OBJECTIVES: To examine priorities for health status improvement in patients with active rheumatoid arthritis (RA) during anti-tumour necrosis factor (TNF) treatment.
METHODS: Data were used from 173 patients with RA starting treatment with TNF-blocking agents. Outcome measures included assessment of health status with the Arthritis Impact Measurement Scales 2 (AIMS2) at baseline and after 3 and 12 months. The AIMS2 contains a priority list from which patients are asked to select from 12 areas of health the 3 in which they would most like to see improvement.
RESULTS: After 1 year of treatment, 10 out of 12 areas of health on the AIMS2 were significantly improved. The most commonly selected priorities for improvement at baseline were pain (88%), hand and finger function (57%), walking and bending (42%), mobility (33%), and work (29%). At group level, this priority ranking remained largely unchanged during treatment. After adjustment for multiple comparisons, only pain was selected significantly less often at 3 and 12 months (71% at both assessments). Within individual patients, however, priorities often changed. Changes in the priority of pain were related to the achieved level of patient-perceived pain and disease activity.
CONCLUSIONS: This study shows that, at the group level, patients' priorities for improvement are fairly stable during 12 months of anti-TNF therapy, despite major improvements in health status. Although pain reduction becomes somewhat less important, it remains the most commonly selected priority. In contrast, individual patient priorities are not stable over the course of treatment and appear to be associated with differences in disease state.

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Year:  2007        PMID: 17472993      PMCID: PMC2111636          DOI: 10.1136/ard.2007.069765

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


  34 in total

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Review 5.  Outcomes from the Patient Perspective Workshop at OMERACT 6.

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6.  Modified disease activity scores that include twenty-eight-joint counts. Development and validation in a prospective longitudinal study of patients with rheumatoid arthritis.

Authors:  M L Prevoo; M A van 't Hof; H H Kuper; M A van Leeuwen; L B van de Putte; P L van Riel
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7.  Preferences for improved health examined in 1,024 patients with rheumatoid arthritis: pain has highest priority.

Authors:  Turid Heiberg; Tore K Kvien
Journal:  Arthritis Rheum       Date:  2002-08

8.  The impact of rheumatoid arthritis and osteoarthritis: the activities of patients with rheumatoid arthritis and osteoarthritis compared to controls.

Authors:  E Yelin; D Lubeck; H Holman; W Epstein
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9.  Individual quality of life in patients undergoing hip replacement.

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Journal:  Lancet       Date:  1992-05-02       Impact factor: 79.321

10.  The impact of chronic disease: a sociomedical profile of rheumatoid arthritis.

Authors:  R F Meenan; E H Yelin; M Nevitt; W V Epstein
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Review 2.  [Rheumatic diseases and neuropathic pain : Diagnosis and treatment].

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Review 4.  Effect and treatment of chronic pain in inflammatory arthritis.

Authors:  Yvonne C Lee
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Review 7.  [Treat-to-target from the patient perspective].

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Authors:  Yvonne C Lee
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9.  The relationship between disease activity, sleep, psychiatric distress and pain sensitivity in rheumatoid arthritis: a cross-sectional study.

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10.  Neuropathic-like pain features and cross-sectional associations in rheumatoid arthritis.

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