Table 3.
RA state | Poor prognostic factors | Presence allows for | Treatment target | |
---|---|---|---|---|
EULAR [3] | RA, first DMARD failure | High disease activity, RF/ACPA positivity, early presence of joint damage | bDMARDs | Low disease activity or remission |
ACR [4] | Early RA <6 months | Moderate disease activity + ≥1 of functional limitation, extraarticular disease, RF/ACPA positivity, erosions | csDMARD combination | |
High disease activity + one or more of functional limitation, extra-articular disease, RF/ACPA positivity, erosions | bDMARD or csDMARD combination | |||
Established RA (≥6 months or 1987 ACR criteria) | LDA + one or more of functional limitation, extraarticular disease, RF/ACPA positivity, erosions or at least moderate disease activity | csDMARD combination, bDMARD at 3 months | ||
Italy [5] | RA, DMARD failure | 1. High disease activity (DAS28 > 5.1 for ≥1 months 2. Moderate disease activity (DAS >3.2) + ACPA/RF positive and elevated CRP or ESR, persistence of one or more swollen joint, bone erosions on X-rays, active synovitis with power Doppler signal 3. New erosions |
bDMARD | |
France [35] | RA, DMARD failure | Existence or progression of structural damage, high clinical and/or laboratory activity, high RF/ACPA titers | bDMARD | |
Germany [34] | RA, 1st DMARD failure | High disease activity, RF/ACPA positivity, early presence of joint damage | bDMARD | |
Canada [36] | RA | Not further specified | Initial csDMARD combination |
ACPA anti-citrullinated protein-peptide antibodies, ACR American College of Rheumatology, CRP C-reactive protein, ESR erythrocyte sedimentation rate, EULAR European League Against Rheumatism, DAS disease activity score, bDMARD biologic disease-modifying antirheumatic drug, csDMARD conventional synthetic disease-modifying antirheumatic drug, RA rheumatoid arthritis, RF rheumatoid factor