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Abstract Number: 351

Doctor, Will My Fatigue be Better If I’m in Remission? an Exploratory Analysis of 1284 Rheumatoid Arthritis (RA) Patients Indicates Fatigue Is the Only Aspect of Patient-Perceived Impact to Remain Significant in ACR/EULAR Boolean Remission

Laure Gossec1,2,3, Bruno Fautrel2,4, John Kirwan1, Andra Balanescu1, Maarten de Wit3, Ben A.C. Dijkmans1, Matthias Englbrecht1, Philippe Gaudin4, Feride Gogus1, Turid Heiberg3, Tore Kristian Kvien1, Emilio Martín-Mola5, Marco Matucci-Cerinic1, Kati Otsa3, Adeline Ruyssen-Witrand4, Tuulikki Sokka-Isler1, Martin Soubrier4 and Maxime Dougados1,4, 1RAID working group for EULAR, Zurich, Switzerland, 2Rheumatology, UPMC GRC08, Paris 06 University, Pitié Salpétrière Hospital, Paris, France, 3PsAID taskforce, EULAR, Zurich, Switzerland, 4COMEDRA trial group, Paris, France, 5Rheumatology, Hospital Universitario La Paz, Madrid, Spain

Meeting: 2014 ACR/ARHP Annual Meeting

Keywords: Fatigue, remission and rheumatoid arthritis (RA)

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Session Information

Title: Rheumatoid Arthritis - Clinical Aspects: Novel Biomarkers and Other Measurements of Disease Activity

Session Type: Abstract Submissions (ACR)

Background/Purpose

Fatigue is an important issue for patients with rheumatoid arthritis (RA). The ACR/EULAR Boolean definition of remission comprises values <=1/10 for joint counts, CRP and patient global assessment; fatigue is not specifically assessed. Near-remission (defined as remission for joint counts and CRP but with patient global assessment > 1/10) is a status which may, or may not, be an acceptable objective for patients. Fatigue levels in this status are unknown.

Objectives: To assess fatigue levels and other aspects of impact, in patients in ACR/EULAR remission, compared to patients in near-remission and not in remission.

Methods

Ancillary analysis of the RAID database, based on an international multicenter cross-sectional study of consecutive RA patients from 12 European countries, and the baseline data in COMEDRA, a French national study in stable RA patients (refs 1, 2). Remission, near-remission and non-remission were assessed cross-sectionally and patient-reported impact of RA including fatigue was assessed using the RA Impact of Disease (RAID) score (ref 1). The RAID assesses pain, function, fatigue, sleep, coping and well-being; each component of the RAID score ranges from 0 (no impact) to 10 (high impact). Patients in remission were compared to those in near-remission and not in remission for mean levels and the proportion of patients with a score <=1/10, in each of the RAID components. The discriminant capacity of fatigue and of the other RAID components for the status of remission was assessed by Cohen’s effect size.

Results

In total, 1284 patients had complete data for this analysis: mean (±standard deviation) age 57±11 yrs, disease duration 13±10 yrs, 78% women. Mean RAID score was 3.3±2.2. Mean fatigue in this population was 4.1±2.7. With the ACR/EULAR Boolean definition, only 87 (6.8%) were in remission and 84 (6.5%) were in near-remission. In remission patients, all the components of the RAID were very low (mean value below 1), except fatigue (mean value of 1.2±1.8; i.e., fatigue was above 1/10 in 25% of the patients in remission, versus 9-21% for the other aspects of RA impact. Near-remission was characterised by more impact of RA for all components of the RAID but particularly fatigue (mean fatigue 4.0±2.3, similar to patients not in remission: 4.3±2.7). Fatigue levels, psychological well-being and sleep had the lowest discriminant capacity to distinguish patients in remission versus not.

Conclusion

The ACR/EULAR definition of remission is extremely stringent and rarely attained for patients with long-standing RA. Fatigue was the only aspect of the impact of RA to remain at significant levels for many patients in Boolean remission, and was much higher in patients in near-remission. More work is needed to understand the link between fatigue and disease activity.


Disclosure:

L. Gossec,
None;

B. Fautrel,
None;

J. Kirwan,
None;

A. Balanescu,
None;

M. de Wit,
None;

B. A. C. Dijkmans,
None;

M. Englbrecht,
None;

P. Gaudin,
None;

F. Gogus,
None;

T. Heiberg,
None;

T. K. Kvien,
None;

E. Martín-Mola,
None;

M. Matucci-Cerinic,
None;

K. Otsa,
None;

A. Ruyssen-Witrand,
None;

T. Sokka-Isler,
None;

M. Soubrier,
None;

M. Dougados,
None.

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