Treatment of Polymyalgia Rheumatica
Start prednisone at 12.5-25 mg daily based on body weight and comorbidity profile, with higher doses (20-25 mg/day) for patients at high relapse risk and lower doses (12.5-15 mg/day) for those with diabetes, osteoporosis, or glaucoma. 1
Initial Diagnosis Confirmation
Before initiating treatment, confirm the diagnosis by verifying:
- Age ≥60 years (younger patients require specialist referral for atypical presentation) 1
- Bilateral shoulder and hip girdle pain with morning stiffness >45 minutes 1
- Elevated inflammatory markers (ESR >40 mm/hr or elevated CRP) 1
- Dramatic response to glucocorticoids within 7 days (lack of response should prompt reconsideration of diagnosis) 2
Starting Dose Selection Algorithm
For patients with high relapse risk and low adverse event risk:
- Use prednisone 20-25 mg/day 1
- High-risk features include female sex, ESR >40, and peripheral arthritis 1
For patients with relevant comorbidities:
Weight-based dosing consideration:
- The optimal dose correlates with body weight at approximately 0.19 mg/kg 3
- Lower-weight patients (particularly women) may respond adequately to 12.5 mg daily 3
The evidence strongly supports that starting doses of 15 mg/day achieve remission in most patients while minimizing cumulative glucocorticoid exposure 4. Starting doses >15 mg/day are associated with more glucocorticoid-related adverse effects without additional benefit 4.
Glucocorticoid Tapering Protocol
Initial taper (first 4-8 weeks):
- Reduce prednisone to 10 mg/day within 4-8 weeks 1
Maintenance taper:
- Decrease by 1 mg every 4 weeks until discontinuation, provided remission is maintained 1
- Slow tapering (<1 mg/month) is associated with fewer relapses and more frequent treatment cessation compared to faster regimens 4
Common pitfall: Tapering faster than 1 mg/month below 10 mg/day significantly increases relapse risk 4. If persistent nighttime pain occurs when reducing below 5 mg/day, consider splitting the daily dose 5.
Management of Relapses
For relapse during tapering:
- Increase prednisone back to the pre-relapse dose 1, 5
- Taper more slowly over 4-8 weeks back to the dose at which relapse occurred 1, 5
- Then reduce by 1 mg per month 1, 5
For patients relapsing on ≤5 mg prednisone:
- Return to the previous dose that effectively controlled symptoms 5
- Subsequent reduction should not exceed 1 mg per month 5
Glucocorticoid-Sparing Agents
Add methotrexate 7.5-10 mg weekly for:
- Multiple or frequent relapses 1, 5
- Prolonged therapy requirements 1
- Significant glucocorticoid-related adverse effects 1
- High-risk factors for relapse 1
Methotrexate demonstrates glucocorticoid-sparing properties at doses ≥10 mg/week 4. This is the most commonly used corticosteroid-sparing agent in PMR 2.
Emerging biologic options:
- Anti-IL-6 receptor agents (tocilizumab and sarilumab) have demonstrated efficacy in reducing relapse frequency and cumulative glucocorticoid burden 6
- These should be considered for refractory cases, though cost and availability may limit use 6
- Anti-TNF agents have failed to show benefit in isolated PMR 6
Monitoring Schedule
First year:
Second year:
- Schedule visits every 8-12 weeks 1
At each visit, assess:
- Clinical symptoms and inflammatory markers (ESR, CRP) 1, 5
- Glucocorticoid-related adverse effects 1, 5
- Risk factors for relapse 1, 5
Essential Adjunctive Measures
Bone protection:
- Initiate at treatment start, as prednisone causes significant bone loss 1
- Osteoporosis prophylaxis is recommended for all patients 2
Patient education:
- Provide education on disease impact, treatment expectations, and comorbidity management 1
- Recommend individually tailored exercise programs 1
Critical Pitfalls to Avoid
- Starting doses >15 mg/day increase adverse effects without improving outcomes 4
- Tapering faster than 1 mg/month below 10 mg/day dramatically increases relapse risk 4
- Failure to respond to 20 mg/day prednisone within 7 days should prompt reconsideration of the diagnosis 2
- Relapses are most common when prednisone dose is ≤5 mg/day, requiring vigilant monitoring during this phase 2