Rheumatoid Arthritis Clinical Diagnosis and Treatment
The diagnosis of rheumatoid arthritis requires at least one joint with definite clinical synovitis (swelling) not better explained by another disease, with a score of ≥6/10 on the 2010 ACR/EULAR Classification Criteria, and treatment should begin with methotrexate as first-line therapy at 7.5-15mg weekly, escalating to 20-25mg as needed. 1
Diagnostic Criteria for Rheumatoid Arthritis
The 2010 American College of Rheumatology (ACR)/European League Against Rheumatism (EULAR) Classification Criteria are the current standard for diagnosing RA, replacing the older 1987 criteria 2, 1:
Joint involvement (0-5 points):
- 1 large joint (0 points)
- 2-10 large joints (1 point)
- 1-3 small joints (2 points)
- 4-10 small joints (3 points)
10 joints including at least 1 small joint (5 points)
Serology (0-3 points):
- Negative RF and negative ACPA (0 points)
- Low positive RF or low positive ACPA (2 points)
- High positive RF or high positive ACPA (3 points)
Acute phase reactants (0-1 points):
- Normal CRP and normal ESR (0 points)
- Abnormal CRP or abnormal ESR (1 point)
Duration of symptoms (0-1 points):
- <6 weeks (0 points)
- ≥6 weeks (1 point)
A score of ≥6/10 indicates definite RA diagnosis 2, 1.
Key Clinical Assessment Components
Complete examination of all peripheral joints, assessing:
- Joint tenderness
- Swelling
- Temperature
- Erythema
- Morning stiffness duration (≥1 hour is significant)
- Pattern of joint involvement (symmetric involvement is characteristic)
Laboratory tests:
- Anti-CCP antibodies (67-78.5% sensitivity, 95-98% specificity)
- Rheumatoid factor (69-84% sensitivity, 78-85% specificity)
- Inflammatory markers (ESR, CRP)
- Complete blood count with differential
- Renal and hepatic function tests
Imaging:
- Plain radiographs of hands and feet (baseline and every 6-12 months)
- Ultrasound or MRI for early detection of synovitis and erosions 1
Treatment Approach
First-Line Therapy
Methotrexate is the first-line disease-modifying antirheumatic drug (DMARD) for RA 1:
- Starting dose: 7.5-15mg weekly
- Target dose: 20-25mg weekly
- Administered orally or subcutaneously
- Often combined with short-term glucocorticoids initially
Treatment Targets and Monitoring
- Target: Remission or low disease activity within 6 months
- Monitoring: Regular assessment using validated composite measures:
Second-Line and Combination Therapy
If methotrexate monotherapy fails to achieve target within 3-6 months, consider:
Biologic DMARDs:
Janus Kinase (JAK) Inhibitors
Combination therapy:
- Methotrexate plus biologic agent
- Triple therapy (methotrexate, sulfasalazine, hydroxychloroquine)
Special Considerations
- Pre-biologic screening: Test for hepatitis B, hepatitis C, and tuberculosis 1
- Poor prognostic factors: Presence of RF/anti-CCP antibodies, early joint damage, high disease activity
- Extra-articular manifestations: Monitor for lung, eye, and skin involvement
- Comorbidities: Assess cardiovascular risk, bone health, and infection risk
Clinical Pitfalls to Avoid
Delayed diagnosis and treatment: Early diagnosis and treatment (within 12 weeks of symptom onset) significantly improves outcomes and prevents irreversible joint damage 1
Inadequate dosing of methotrexate: Many patients require 20-25mg weekly for optimal effect
Failure to adjust therapy: If treatment targets aren't met within 3-6 months, therapy should be adjusted
Overlooking extra-articular manifestations: RA can affect multiple organ systems beyond joints
Neglecting to monitor disease activity objectively: Regular use of validated composite measures is essential for guiding treatment decisions
Early diagnosis and aggressive treatment using a treat-to-target approach can prevent joint damage in up to 90% of patients with RA, significantly improving long-term outcomes and quality of life 1.