Prednisone Dosing for Polymyalgia Rheumatica (PMR)
The recommended initial prednisone dose for PMR is 12.5-25 mg daily, with subsequent tapering to 10 mg/day within 4-8 weeks, followed by a gradual reduction of 1 mg every 4 weeks until discontinuation, as long as remission is maintained. 1, 2
Initial Dosing Considerations
Starting dose range: 12.5-25 mg prednisone equivalent daily 1, 2
- Higher doses within this range (closer to 25 mg) for patients with high relapse risk and low adverse event risk
- Lower doses within this range (closer to 12.5 mg) for patients with comorbidities (diabetes, osteoporosis, glaucoma)
- Doses ≤7.5 mg/day are discouraged (insufficient symptom control)
- Doses >30 mg/day are strongly discouraged (increased adverse effects)
Administration: Single daily oral dose in the morning (before 9 am) is preferred over divided doses 1, 2, 3
Body weight consideration: Response to prednisone is related to body weight, with a target dose of approximately 0.19 mg/kg being effective for most patients 4
Tapering Schedule
Initial tapering phase:
Maintenance tapering phase:
Duration of therapy:
Relapse Management
If relapse occurs during tapering:
- Increase prednisone to the pre-relapse dose
- Gradually decrease (within 4-8 weeks) to the dose at which relapse occurred
- Resume slower tapering when symptoms are controlled 1, 2
Monitoring Schedule
- Every 4-8 weeks during the first year
- Every 8-12 weeks during the second year
- More frequently during relapses or when tapering 1, 2
Steroid-Sparing Strategies
- Methotrexate: Consider early introduction (7.5-10 mg/week) for:
Common Pitfalls and Caveats
Inadequate initial dose: Starting with doses below 12.5 mg may lead to insufficient symptom control and potentially more relapses 1, 2
Too rapid tapering: Reducing prednisone faster than recommended increases relapse risk; slow tapering (<1 mg/month) is associated with better outcomes 5
Failure to adjust for body weight: Lower-weight patients may respond to lower doses; non-response in heavier patients may require dose adjustment based on weight (target ~0.19 mg/kg) 4
Inadequate monitoring: Regular assessment of disease activity, laboratory markers (ESR, CRP), and steroid-related side effects is essential 1, 2
Failure to consider steroid-sparing agents: Early introduction of methotrexate should be considered for patients at high risk of relapse or steroid-related complications 1, 2, 7