Management of Polymyalgia Rheumatica
Start prednisone at 12.5-25 mg daily as first-line therapy, with the specific dose determined by relapse risk factors and comorbidity burden. 1, 2
Initial Dose Selection
The choice between 12.5 mg and 25 mg prednisone daily depends on two competing considerations:
Use higher doses (20-25 mg/day) for patients with: 2
- Female sex
- ESR >40 mm/hr
- Peripheral inflammatory arthritis
- Age ≥60 years with typical presentation
- Absence of significant comorbidities
Use lower doses (12.5-15 mg/day) for patients with: 1, 2
- Diabetes mellitus
- Osteoporosis
- Glaucoma
- Hypertension
- Cardiovascular disease
- Peptic ulcer disease
The European League Against Rheumatism guidelines provide this dose range specifically to allow individualization based on these factors, rather than using a one-size-fits-all approach. 1
Expected Response and Red Flags
Clinical improvement should occur within 7 days of starting therapy. 3 If a patient does not respond adequately to 20 mg/day prednisone within one week, reconsider the diagnosis—this may not be isolated PMR. 3
Tapering Protocol
Initial Taper (First 4-8 Weeks)
Reduce prednisone to 10 mg/day within 4-8 weeks of starting therapy. 1, 2 This relatively rapid initial taper is safe once symptoms are controlled and helps minimize cumulative steroid exposure. 4
Maintenance Taper (After Reaching 10 mg/day)
Decrease by 1 mg every 4 weeks until discontinuation. 1, 5, 2 This slow taper rate (1 mg per month) is critical for minimizing relapse risk, which increases substantially with faster tapering. 4
Alternative dosing schedules (such as alternating 10 mg and 7.5 mg every other day) can be used during this phase. 5, 2
Management of Relapses
Relapses are common, particularly when prednisone is reduced to ≤5 mg/day. 5, 3
For relapse on ≤5 mg/day: 5
- Return to the previous dose that controlled symptoms
- Re-establish remission over 4-8 weeks
- Resume tapering at 1 mg per month (slower than the initial taper)
For persistent nighttime pain when reducing below 5 mg/day: 5
- Consider splitting the daily dose rather than increasing total dose
Glucocorticoid-Sparing Agents
Methotrexate
Add methotrexate 7.5-10 mg weekly for: 2
- Multiple or frequent relapses
- Prolonged therapy requirements (>2 years anticipated)
- Significant glucocorticoid-related adverse effects
- High-risk comorbidities requiring lower steroid exposure
Methotrexate is the most commonly used steroid-sparing agent and has the strongest evidence base among conventional DMARDs. 6, 3
Biologic Agents
Consider tocilizumab or sarilumab for: 6
- Refractory disease despite methotrexate
- Intolerable glucocorticoid toxicity
- Frequent relapses requiring repeated dose escalations
Anti-IL-6 receptor agents (tocilizumab and sarilumab) have demonstrated efficacy in reducing relapse frequency and cumulative glucocorticoid burden. 6 Anti-TNF agents have failed to show benefit in isolated PMR. 6
Monitoring Schedule
- Every 4-8 weeks during the first year
- Every 8-12 weeks in the second year
- As needed for relapses or dose adjustments
- Clinical symptoms (pain, stiffness)
- Inflammatory markers (ESR, CRP)
- Glucocorticoid-related adverse effects
- Comorbidity status
Essential Adjunctive Measures
Initiate bone protection at treatment start. 2 Prednisone causes significant bone loss, and osteoporosis prophylaxis is mandatory, not optional.
Provide patient education on: 1, 2
- Expected disease course and treatment duration (typically 1-4 years)
- Symptoms of relapse
- Steroid side effects to monitor
- Importance of adherence to tapering schedule
Recommend individually tailored exercise programs to maintain function and prevent deconditioning. 1, 2
Specialist Referral Indications
Refer to rheumatology for: 1
- Age <60 years
- Atypical presentations (peripheral inflammatory arthritis, systemic symptoms)
- Low or normal inflammatory markers despite typical symptoms
- Inadequate response to 20 mg prednisone within 7 days
- Refractory disease or frequent relapses
- High risk of therapy-related complications
Common Pitfalls
The most frequent error is tapering too quickly after the initial response, which substantially increases relapse risk. 4 The second common mistake is failing to initiate bone protection at treatment onset. 2 Finally, continuing to escalate steroids without considering alternative diagnoses when response is inadequate represents a critical missed opportunity for correct diagnosis. 3