Treatment for Temporal Arteritis
The treatment for temporal arteritis requires immediate initiation of high-dose glucocorticoids (prednisone 40-60 mg/day or 1 mg/kg/day up to 80 mg) upon clinical suspicion to prevent permanent vision loss and treat symptoms. 1
Initial Treatment Approach
Immediate Glucocorticoid Therapy
- Start prednisone 40-60 mg/day orally as soon as temporal arteritis is suspected
- For patients with visual symptoms, consider IV methylprednisolone 500-1000 mg/day for 3-5 days before transitioning to oral therapy 1
- Do not delay treatment while awaiting biopsy results, as this can lead to irreversible vision loss 1
Adjunctive Therapy
- Add aspirin (75-150 mg/day) for patients with critical or flow-limiting involvement of vertebral or carotid arteries 1
- Consider tocilizumab (162 mg subcutaneously weekly) in combination with glucocorticoids for:
- Patients at high risk for glucocorticoid-related adverse events
- Refractory or relapsing disease
- Active extracranial large vessel involvement 1
- Methotrexate is an alternative when tocilizumab is contraindicated 1
Diagnostic Confirmation
- Perform temporal artery biopsy within 2 weeks of starting glucocorticoids (specimen length >1 cm) 1
- Temporal artery ultrasound may be used in centers with appropriate expertise (sensitivity 88%, specificity 97%) 1, 2
- Consider noninvasive vascular imaging with clinical assessment for patients with negative biopsy results 1
Treatment Duration and Tapering
- Initial phase (2-4 weeks): Maintain high-dose glucocorticoids until symptoms resolve and inflammatory markers normalize 1
- Early tapering phase: Reduce dose to 15-20 mg/day within 2-3 months 1
- Intermediate tapering phase: Target dose of ≤10 mg/day by 6 months 1
- Long-term tapering: Aim for ≤5 mg/day after one year, with complete tapering based on clinical response and laboratory parameters 1
Monitoring and Follow-up
- Monitor for clinical response (headache typically responds dramatically within a short period) 1
- Regular assessment of symptoms, physical examination, and inflammatory markers (ESR, CRP) 1
- Watch for steroid-related adverse effects and provide bone protection therapy 1
Management of Relapse
- Increase glucocorticoid dose (5-15 mg/day above the last effective dose) 1
- Add tocilizumab (preferred) or methotrexate if not already on immunosuppressive therapy 1
Common Pitfalls to Avoid
- Inadequate initial dosing: Starting with doses below 40 mg/day may be insufficient to control disease activity and prevent complications 1
- Delayed treatment: Waiting for biopsy results before starting treatment can result in permanent vision loss 1, 3
- Rapid steroid tapering: Can lead to disease relapse 1
- Assuming negative biopsy rules out GCA: False negatives can occur 1
- Failure to recognize the emergency: Temporal arteritis is a medical emergency due to the risk of permanent vision loss 1, 4, 3
Remember that temporal arteritis is an ophthalmological emergency requiring prompt treatment to prevent irreversible vision loss. Up to 60% of patients may experience one or more relapses during glucocorticoid tapering, necessitating vigilant monitoring and appropriate adjustments to therapy 1.