Session Information
Session Type: Abstract Submissions (ACR)
Background/Purpose: Significant RA worsening or flare may predict poorer outcomes and signal a need for treatment reassessment. However, there is little agreement about how to reliably identify a flare. Candidate domains essential for assessing RA flare were identified by OMERACT patients (pts)and health care providers including pain, function, stiffness, participation, coping, patient global assessment, fatigue and self-management1. We aimed to determine the extent of agreement between pts and treating rheumatologists (MD) in identifying a flare, and concordance of clinical and patient-reported outcomes (PROs) with flare status.
Methods: Pts in the Canadian early ArThritis CoHort (CATCH) completed the OMERACT preliminary flare questionnaire (PFQ). In the PFQ pts were asked if they were in a flare and to rate severity, pain, function, stiffness, participation, coping, patient global assessment and fatigue (0-10 NRS). Pts also identified tender and swollen joints (TJC and SJC)(42 joint homunculus). MDs rated if their patient (pt) was in a flare and performed a joint count. Pt-MD agreement on flare status was assessed using Cohen’s kappa. Wilcoxon rank sum test was used to compare MD and pt reported joint counts. Clinical indices and PROs between flare and non-flare pts were compared using paired t-tests.
Results: 512 pts (75% female) answered PFQ: 13% at baseline, 39% at 3-12 months and 49% at 12 months+ after study entry. Pts had a mean age of 53 ± 14 yrs; 18% were smokers, 63% RF+, 51% CCP+ and 18% had erosions. 149 (29%) reported a flare at study visits. Pts and MDs agreed about flare status 72% of the time (Kappa=0.34). Changes in DAS28 and CDAI from previous visits were higher in flare vs. non flare pts(0.44 vs. -0.14) (1.67 vs. -3.20) (both p<.0001). PROs were significantly different between flare and non-flare pts and were highest when pts and MDs both agreed the pt was in a flare (p<.0001) (see Table). Pts in a flare reported higher TJC/SJCs than MDs. The differences between pt and MD TJC & SJC were 3.74 (p<.0001) and 2.31 (p<.0004). Agreement was modest (Kappa=.32) when pts/MDs agreed on flare status but poor then they didn’t (Kappa=.20)
Table 1: Ratings of flare severity and PROs by Patient/MD concordance
Domain |
Pt Flare /MD Flare(n=86) |
Pt Flare /MD Non-Flare (n=63) |
Pt Non Flare /MD Flare (n=83) |
Pt Non Flare /MD Non Flare (n=280) |
p-values |
Flare severity |
6.2 (2.4) |
5.2 (2.6) |
0.3 (1.5) |
0.2 (0.8) |
<.001 |
Pain |
6.3 (2.4) |
5.1 (2.7) |
3.7 (2.6) |
1.7 (1.9) |
<.001 |
Function |
6.2 (2.6) |
4.1 (3.2) |
3.7 (2.8) |
1.3 (1.8) |
<.001 |
Stiffness |
5.8 (2.8) |
4.3 (2.9) |
3.7 (2.5) |
1.7 (1.9) |
<.001 |
Participation |
5.6 (2.8) |
3.8 (3.0) |
3.4 (2.8) |
1.2 (1.9) |
<.001 |
Fatigue |
5.6 (2.8) |
4.7 (3.1) |
4.1 (3.0) |
2.0 (2.5) |
<.001 |
Coping |
4.8 (2.6) |
3.2 (2.7) |
3.1 (2.6) |
1.1 (1.8) |
<.001 |
Values are mean (SD)
*Domains scored 0-10 on a numerical rating score, ascending by severity.
Conclusion: Pts reporting a flare have clinical indices reflecting worsening disease activity. PROs (pain, function, stiffness, coping, participation, and fatigue) significantly discriminated between pts reporting flare vs. no flare. There is modest agreement between pts and MDs regarding flare status. Flare pts identify more swollen and tender joints than MDs. PROs and pt-joint counts may reliably identify pts in disease flares but some ratings are higher in pts than MDs. More research is needed to identify predictors of concordance and discrepancy between pts and providers in flare assessment.
References: 1Bartlett SJ, et al. ArthRheum 2011;63(suppl):128.
Disclosure:
V. P. Bykerk,
None;
C. O. Bingham III,
Genentech, Roche Pharmaceuticals,
5;
E. Choy,
None;
J. Xiong,
None;
G. Boire,
None;
C. A. Hitchon,
None;
J. E. Pope,
None;
J. C. Thorne,
None;
B. Haraoui,
None;
E. Keystone,
Amgen,
2,
Pfizer Inc,
2,
Hoffmann-La Roche, Inc.,
2,
United Chemicals of Belgium (UCB) Canada Inc.,
2,
Bristol-Myers Squibb,
2,
Abbott Laboratories,
2,
Janssen Inc.,
2;
S. J. Bartlett,
None.
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