Initial Treatment for Polymyalgia Rheumatica and Polymyositis
For polymyalgia rheumatica (PMR), glucocorticoids at a dose of 12.5-25 mg prednisone equivalent daily are the initial treatment of choice, while polymyositis typically requires higher doses of 60 mg/day prednisone. 1, 2
Polymyalgia Rheumatica (PMR) Treatment
Initial Glucocorticoid Therapy
- Starting dose: 12.5-25 mg prednisone equivalent daily 1
- Higher initial doses within this range for patients with high risk of relapse and low risk of adverse events
- Lower initial doses for patients with comorbidities (diabetes, osteoporosis, glaucoma)
- Doses ≤7.5 mg/day are discouraged and doses >30 mg/day are strongly discouraged 1
- Administration: Single daily dose rather than divided doses 1
- Alternative option: Intramuscular methylprednisolone (120 mg injection every 3 weeks) can be considered as an alternative to oral glucocorticoids 1
Tapering Schedule
- Initial tapering: Reduce dose to 10 mg/day within 4-8 weeks
- Maintenance tapering: Once remission is achieved, taper by 1 mg every 4 weeks (or by 1.25 mg using alternate day schedules) until discontinuation 1
- Relapse management: If relapse occurs, increase to pre-relapse dose and decrease gradually (within 4-8 weeks) to the dose at which relapse occurred 1
Glucocorticoid-Sparing Agents
- Methotrexate: Consider early introduction (7.5-10 mg/week) in addition to glucocorticoids for:
- Anti-IL-6 agents: Tocilizumab and sarilumab have shown efficacy in reducing relapses and glucocorticoid burden in recent studies 3
- Not recommended: TNFα blocking agents are strongly discouraged 1
Monitoring and Follow-up
- Follow-up visits every 4-8 weeks in the first year, every 8-12 weeks in the second year 1
- Monitor for:
- Disease activity (symptoms, inflammatory markers)
- Glucocorticoid-related side effects
- Comorbidities and risk factors for relapse 1
Polymyositis Treatment
Initial Therapy
- Starting dose: Prednisone 60 mg/day 2
- Severe cases: Consider IV methylprednisolone pulse therapy 1
- Tapering: Based on clinical response, taper slowly to prevent recurrence 2
Additional Therapies
- For severe or refractory cases:
- Consider immunosuppressants (methotrexate, azathioprine)
- IVIG may be indicated in some cases
- Plasmapheresis for cases with poor response to glucocorticoids or life-threatening situations 1
Important Considerations
Diagnostic Confirmation
- Ensure correct diagnosis before initiating treatment:
Treatment Pitfalls to Avoid
- Underdosing: Starting with doses <12.5 mg for PMR may lead to inadequate symptom control
- Overdosing: Starting with doses >30 mg for PMR increases risk of adverse effects without additional benefit
- Rapid tapering: Tapering faster than recommended (>1 mg/month below 10 mg/day) increases relapse risk 1, 6
- Inadequate monitoring: Failure to regularly assess disease activity and glucocorticoid-related adverse effects
- Delayed use of steroid-sparing agents: Consider early introduction in high-risk patients 1
Special Populations
- Elderly patients: Carefully monitor for glucocorticoid side effects
- Patients with comorbidities: Consider lower initial doses and earlier introduction of steroid-sparing agents
- Patients with atypical presentation: Consider specialist referral, particularly for cases with peripheral inflammatory arthritis, systemic symptoms, or low inflammatory markers 1
By following these evidence-based recommendations, clinicians can effectively manage both PMR and polymyositis while minimizing disease activity and treatment-related complications.