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Abstract Number: 2639

Residual Disease Activity in Patients with Early Rheumatoid Arthritis Who Were Classified As Being in Remission According to 8 Different Descriptions: Post Hoc Analysis of the Etude Et Suivi Des Polyarthrites Indifférenciées Récentes (ESPOIR) Cohort

Isabel Castrejón1, Maxime Dougados2, Bernard Combe3, Francis Guillemin4, Bruno Fautrel5 and Theodore Pincus1, 1Rheumatology, Rush University Medical Center, Chicago, IL, 2Rheumatology B Department, Paris-Descartes University, APHP, Cochin Hospital, Paris, France, 3Rheumatology, Hopital Lapeyronie, Montpellier, France, 4Hopitaux de Brabois, Nancy, France, 5Rheumatology / GRC08-EEMOIS, APHP-Pitie Salpetriere Hospital / UPMC, Paris, France

Meeting: ACR/ARHP Annual Meeting 2012

Keywords: Assessment, remission and rheumatoid arthritis (RA)

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Session Information

Title: Epidemiology and Health Services Research V: Rheumatoid Arthritis Management in the Treat-to-Target Era

Session Type: Abstract Submissions (ACR)

Background/Purpose: No single gold standard for remission is available for rheumatoid arthritis (RA). All available descriptions, including 2 proposed by an ACR/EULAR committee, allow residual joint abnormalities and RA symptoms. Relatively little information is reported concerning these abnormalities in patients who meet various descriptions of remission.

Methods: The ESPOIR cohort of 734 patients with complete 6-month data was analyzed to identify those in remission according to 8 descriptions, 4 requiring a formal joint count: disease activity score (DAS28) ≤2.6, clinical disease activity index (CDAI) ≤2.8, and the 2 proposed by ACR/EULAR – Boolean dichotomy with tender joint count (TJC28), swollen joint count (SJC28), C-reactive protein (CRP) and patient global estimate (PATGL) all ≤1, and simplified disease activity index (SDAI) ≤3.3. Four additional descriptions are based on routine assessment of patient index data (RAPID3), an index of patient-reported function, pain and PATGL with remission (RAPID3R) described by a score ≤3 (0-30 scale), and 3 more stringent definitions that add a careful joint examination and physician global estimate (DOCGL): RAPID3R+J1 (RAPID3 ≤3 and £1 swollen joint); RAPID3R+J1D1 (RAPID3 ≤3, £1 swollen joint and DOCGL ≤1); and RAPID3R+J0D1 (RAPID3 ≤3, no swollen joint and DOCGL ≤1). Proportions of patients with TJC28, SJC28, CRP, DOCGL, PATGL, pain or fatigue >1, or HAQ function (FN) >0.5, and specific swollen joints (n=28) were computed for each remission description.

Results: Boolean dichotomy and RAPID3R+J0D1 indicated 13% of all patients in remission vs 16–19% by SDAI, CDAI, RAPID3R+J1 and RAPID3R+J1D1. RAPID3R (26%) and DAS28 (32%) were least stringent. TJC28 >1 was seen in 0% by Boolean criteria (by definition) vs 3–11% by SDAI, CDAI, DAS28; 13–16% by RAPID3R+J1, RAPID3R+J1D1, RAPID3R+J0D1; and 24% by RAPID3R. SJC28 >1 was seen in 0% by Boolean criteria, RAPID3R+J1, RAPID3R+J1D1 and RAPID3R+J0D1 (by definition); 2% by CDAI and SDAI; 16% by DAS28; and 27% by RAPID3R. CRP >1 was seen in <8%, and HAQ-FN >0.5 in 2–12% by all 8 descriptions. PATGL >1 was seen in 10–21% by all but Boolean (0% by definition) and DAS28 (49%); pain >1 in 9–23% by all but DAS28 (46%); and fatigue >1 in 47–65% by all 8 descriptions. Knees, shoulders and elbows were involved in <5% of patients by all 8 descriptions; wrists in <6%, MCPs in <9% and PIPs in <5%, except by DAS28 and RAPID3R. Most residual joint involvement was of MCPs or PIPs.

 

Conclusion: At least 9% of patients in remission by any description had pain, and at least 47% fatigue. RAPID3R and DAS28 had the largest proportions of patients with residual abnormalities, while CDAI and stringent RAPID3-based remission descriptions are similar to the 2 proposed by ACR/EULAR. RAPID3-based descriptions do not require formal joint counts or laboratory data, but do require DOCGL and careful joint examination, and could be feasible in usual care.


Disclosure:

I. Castrejón,
None;

M. Dougados,
None;

B. Combe,
None;

F. Guillemin,
None;

B. Fautrel,
None;

T. Pincus,
None.

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