Emergency Management of Suspected New Onset Rheumatoid Arthritis
Immediately refer the patient to a rheumatologist for evaluation within 6 weeks of symptom onset while initiating symptomatic treatment in the emergency department, as early DMARD therapy (ideally within 3 months) prevents irreversible joint damage in up to 90% of patients. 1, 2
Immediate ED Assessment and Documentation
Perform a focused clinical examination to identify definite synovitis (joint swelling), as this is the cornerstone of RA diagnosis and the method of choice for detecting arthritis. 1, 3
Key examination findings to document:
- 28-joint count assessment examining metacarpophalangeal joints (MCPs), proximal interphalangeal joints (PIPs), wrists, elbows, shoulders, and knees for tenderness and swelling 4
- Morning stiffness duration (>30 minutes suggests inflammatory arthritis; >1 hour is typical for RA) 1, 5
- Symmetric small joint involvement pattern (MCPs, PIPs, wrists, metatarsophalangeal joints are characteristic) 4, 5
- Squeeze test of MCPs and metatarsophalangeal joints to assess for clinical synovitis 4
- Skin examination for psoriatic plaques or nail changes to exclude psoriatic arthritis 4
Critical pitfall: Distal interphalangeal joints are typically spared in RA—if these are prominently involved, consider alternative diagnoses like psoriatic arthritis or osteoarthritis. 4
Essential Laboratory Testing from the ED
Order the following tests immediately to facilitate rheumatology evaluation:
Autoimmune serology panel:
- Rheumatoid factor (RF) - sensitivity 60%, specificity 70% 4, 3
- Anti-citrullinated protein antibodies (ACPA/anti-CCP) - sensitivity 60%, specificity 90% 4, 3
Inflammatory markers:
- C-reactive protein (CRP) - preferred over ESR as it is more reliable and not age-dependent 4, 3
- Erythrocyte sedimentation rate (ESR) 1
Baseline laboratory assessment:
- Complete blood count with differential (assess for cytopenias before treatment) 4, 3
- Comprehensive metabolic panel including liver function tests, renal function, glucose 4
- Urinalysis 1, 4
Conditional testing based on presentation:
- Antinuclear antibodies (ANA) if diagnosis uncertain to screen for lupus or other connective tissue diseases 4, 3
- HLA-B27 if axial or entheseal involvement suggests spondyloarthropathy 4
- Hepatitis B, Hepatitis C, and tuberculosis screening (required before any biologic therapy) 4
Critical pitfall: Never dismiss RA diagnosis based on negative RF or normal inflammatory markers—20-30% of RA cases are seronegative, and acute phase reactants can be normal even in active disease. 4
Imaging Studies to Order
Baseline radiographs:
- Bilateral hand, wrist, and foot X-rays to assess for erosions, which predict RA diagnosis and disease persistence 4, 3
- Radiographic findings in early disease: soft tissue swelling, juxtaarticular osteoporosis, and potentially early erosions 5
Advanced imaging if diagnosis uncertain:
- Ultrasound with Power Doppler detects synovitis 2.18-fold more frequently than clinical examination and can identify subclinical inflammation 3
- MRI with IV contrast is more sensitive than ultrasound in early stages and detects bone marrow edema (osteitis), the best single predictor of future disease progression 4, 3
Symptomatic Treatment Initiated from the ED
NSAIDs for symptomatic relief:
- Naproxen 500 mg twice daily (or equivalent NSAID) at the minimum effective dose for the shortest time possible 1, 6
- Assess gastrointestinal, renal, and cardiovascular risks before prescribing 1
- Onset of pain relief begins within 1 hour for naproxen, with analgesic effect lasting up to 12 hours 6
Short-term glucocorticoids as bridge therapy:
- Prednisone 5-10 mg daily for temporary relief (<6 months) while awaiting DMARD effect 1, 7, 8
- Systemic glucocorticoids reduce pain, swelling, and structural progression but must be used at the lowest dose necessary due to cumulative side effects 1
- Intra-articular glucocorticoid injections can be considered for localized joint inflammation 1, 7
Critical pitfall: Never use corticosteroid monotherapy long-term—steroids must be combined with DMARDs for disease modification, as they do not prevent joint damage when used alone. 7
Urgent Rheumatology Referral Criteria
Refer within 6 weeks if:
- Any joint swelling associated with pain or stiffness 1, 3
- Small joints of hands/feet affected 3
- More than one joint involved 3
- Delay of 3 months or longer between symptom onset and seeking medical advice 3
The 3-month window is critical: Patients at risk of persistent arthritis should be started on DMARDs as early as possible (ideally within 3 months), even if they do not fulfill classification criteria for RA, as this is the "window of opportunity" to prevent irreversible joint damage. 1, 7, 9
Risk Stratification for Persistent/Erosive Disease
Document the following prognostic factors to guide rheumatology management decisions:
- Number of swollen and tender joints 1
- Elevated acute phase reactants (CRP/ESR) 1
- Positive rheumatoid factor 1
- Positive ACPA antibodies 1
- Presence of erosions on baseline radiographs 1, 4
Patients with multiple poor prognostic factors require aggressive early treatment with methotrexate 15-25 mg weekly, with rapid escalation to biologic DMARDs if remission is not achieved within 3 months. 7, 2
ED Discharge Instructions and Follow-up
Provide patient education on:
- The importance of urgent rheumatology follow-up within 6 weeks 1, 3
- Expected morning stiffness and joint symptoms 5
- Smoking cessation (smoking is a modifiable predictor of adverse outcomes) 1, 7
- Return precautions for worsening symptoms, fever, or inability to perform activities of daily living 5
Ensure rheumatology appointment is scheduled before discharge with all laboratory results and imaging studies forwarded to the specialist. 1
Critical pitfall: Never delay DMARD initiation waiting for definitive classification criteria to be met—early treatment within 3 months prevents irreversible joint damage and improves long-term outcomes in up to 90% of patients. 7, 2