Initial Treatment for Lupus Flare
For a lupus flare, initiate treatment with glucocorticoids combined with the patient's baseline immunosuppressive therapy, with the specific regimen intensity determined by flare severity and organ involvement. 1, 2
Treatment Algorithm Based on Flare Severity
Mild to Moderate Flares (Non-Organ Threatening)
- Start with oral prednisone 0.5 mg/kg/day (maximum 40 mg) combined with hydroxychloroquine if not already on it, as hydroxychloroquine reduces flare frequency and should be maintained in all lupus patients unless contraindicated 2
- For rapid symptom control, consider intramuscular triamcinolone 100 mg as a single dose, which may provide faster initial response than oral methylprednisolone 3
- Taper glucocorticoids over 4-6 weeks to ≤7.5 mg/day prednisone equivalent 1, 2
Severe Flares (Organ-Threatening Disease)
Begin with intravenous methylprednisolone pulses 250-750 mg daily for 1-3 days, followed by oral prednisone 1:
Initial oral prednisone dosing depends on severity 1:
- Reduced-dose scheme: 0.5-0.6 mg/kg/day (max 40 mg) for weeks 0-2
- Moderate-dose scheme: 0.6-0.7 mg/kg/day (max 50 mg) for weeks 0-2
- High-dose scheme: 0.8-1.0 mg/kg/day (max 80 mg) for weeks 0-2
Taper systematically over 24+ weeks to ≤5 mg/day 1
Active Lupus Nephritis Flares (Class III/IV)
Combine glucocorticoids with one of the following immunosuppressive regimens 1:
- Mycophenolate mofetil 3 g/day (or mycophenolic acid equivalent) for 6 months 1
- Low-dose intravenous cyclophosphamide (total 3 g over 3 months) 1
- Belimumab plus either mycophenolate or cyclophosphamide for patients with repeated flares 1, 2
- Mycophenolate plus calcineurin inhibitor when eGFR >45 ml/min/1.73 m² 1
Preemptive Treatment for Serologic Flares
- In clinically stable patients with rising anti-dsDNA (≥25% increase) and C3a (≥50% increase), consider short-term prednisone 30 mg/day for 2 weeks, then 20 mg/day for 1 week, then 10 mg/day for 1 week to prevent severe clinical flares 4
- This preemptive approach reduced severe flares from 30% to 0% within 90 days in one controlled trial 5, 4
Critical Monitoring During Flare Treatment
Assess patients every 2-4 weeks during the first 2-4 months 2:
- Blood pressure, serum creatinine, eGFR, serum albumin
- Proteinuria quantification and urinary sediment
- Complement levels (C3, C4) and anti-dsDNA antibodies 1, 2
Common Pitfalls to Avoid
- Do not abruptly discontinue glucocorticoids in patients on chronic therapy, as this may trigger withdrawal symptoms mimicking true flares; the CORTICOLUP trial showed 45% flare rate with abrupt discontinuation versus 20% with continuation 1
- Avoid prolonged high-dose glucocorticoids (>7.5 mg/day prednisone equivalent) beyond 4-6 months, as this significantly increases organ damage accrual and morbidity 1, 6
- Do not delay immunosuppressive therapy in organ-threatening disease; glucocorticoids alone are insufficient for severe lupus nephritis 1
- Maintain hydroxychloroquine throughout flares unless contraindicated, as discontinuation increases flare risk 2