EULAR 2019 Guidelines for Rheumatoid Arthritis Management
The 2019 EULAR recommendations for rheumatoid arthritis management emphasize early DMARD therapy immediately upon diagnosis, with methotrexate as the first-line treatment, aiming for sustained remission or low disease activity in all patients. 1
Overarching Principles
- Shared Decision Making: Treatment should aim at best care based on shared decision between patient and rheumatologist
- Treatment Considerations: Decisions based on disease activity, safety issues, and patient factors including comorbidities
- Specialist Care: Rheumatologists should primarily care for RA patients
- Multiple Treatment Options: Patients require access to multiple drugs with different modes of action
- Cost Considerations: Individual, medical, and societal costs should be considered in management
Treatment Algorithm
Initial Treatment
- Start DMARDs immediately upon diagnosis (Level of Evidence 1a, Strength of Recommendation A) 1
- Methotrexate (MTX) should be first-line therapy (LoE 1a, SoR A) 1
- Optimal dosing: 7.5-25mg weekly 2
- Consider subcutaneous administration for better bioavailability
- If MTX contraindicated or early intolerance: Use leflunomide or sulfasalazine (LoE 1a, SoR A) 1
- Add short-term glucocorticoids when initiating/changing csDMARDs
- Various dose regimens and routes possible
- Taper as rapidly as clinically feasible (LoE 1a, SoR A) 1
Monitoring and Treatment Adjustment
- Monitor frequently in active disease (every 1-3 months)
- Adjust therapy if:
- No improvement within 3 months
- Target not reached by 6 months (LoE 2b, SoR B) 1
Treatment Escalation
If target not achieved with first csDMARD:
bDMARDs and tsDMARDs should be combined with csDMARDs (LoE 1a, SoR A) 1
- If csDMARDs cannot be used, IL-6 pathway inhibitors and JAK inhibitors may have advantages over other bDMARDs
If first bDMARD/tsDMARD fails:
- Consider another bDMARD or tsDMARD
- After TNF inhibitor failure, can use another TNF inhibitor or agent with different mode of action (LoE 1b, SoR A) 1
Treatment Tapering
If in persistent remission after tapering glucocorticoids:
- Consider tapering bDMARDs or tsDMARDs (especially if combined with csDMARD) (LoE 1b, SoR A) 1
If in persistent remission:
- Consider tapering csDMARD (LoE 2b, SoR B) 1
Important Clinical Considerations
Biologic DMARDs Options
- TNF inhibitors: Adalimumab, certolizumab pegol, etanercept, golimumab, infliximab
- T-cell costimulation modulator: Abatacept
- IL-6 pathway inhibitors: Tocilizumab, sarilumab
- B-cell depleting agent: Rituximab
Targeted Synthetic DMARDs
- JAK inhibitors: Tofacitinib, baricitinib, filgotinib, upadacitinib 3
Common Pitfalls to Avoid
- Delayed DMARD initiation: Start immediately upon diagnosis to prevent irreversible joint damage
- Inadequate MTX dosing: Ensure proper dosing and consider subcutaneous administration if oral not effective
- Prolonged glucocorticoid use: Taper as rapidly as clinically feasible to minimize adverse effects
- Infrequent monitoring: Regular assessment is crucial for timely treatment adjustments
- Failure to adjust therapy promptly: Change treatment if no improvement by 3 months or target not reached by 6 months
- Not considering tapering in sustained remission: Consider tapering to minimize exposure to potential side effects
Special Considerations
- Monotherapy: In patients who cannot use csDMARDs, IL-6 inhibitors and JAK inhibitors may have advantages 1
- Comorbidities: Always consider patient-specific factors when selecting therapy
- Persistent disease: Multiple successive drug options are often needed to reach therapeutic goals 1
The 2019 EULAR recommendations provide a comprehensive, evidence-based approach to RA management with the goal of achieving sustained remission or low disease activity in all patients through early intervention and strategic treatment escalation.