Essential Practices for Managing Polymyalgia Rheumatica
Glucocorticoid therapy is the cornerstone of polymyalgia rheumatica (PMR) management, with an initial recommended dose of 12.5-25 mg prednisone equivalent daily, individualized based on patient risk factors for relapse and adverse effects. 1, 2
Initial Assessment and Diagnosis
- Consider specialist referral for atypical presentations (peripheral inflammatory arthritis, systemic symptoms, low inflammatory markers, age <60 years), high risk of therapy-related side effects, or PMR refractory to glucocorticoid therapy 1
- Determine comorbidities that may affect treatment decisions, particularly hypertension, diabetes, osteoporosis, glaucoma, cardiovascular disease, and peptic ulcer 1
- Assess risk factors for relapse/prolonged therapy, including female sex, high ESR (>40 mm/hr), and peripheral inflammatory arthritis 1
Glucocorticoid Treatment Protocol
- Use glucocorticoids as first-line therapy rather than NSAIDs for PMR treatment 1, 2
- Select initial prednisone dose within 12.5-25 mg/day range:
- Consider intramuscular methylprednisolone as an alternative to oral glucocorticoids 1, 2
Tapering Schedule
- Initial tapering: Reduce dose to 10 mg/day prednisone equivalent within 4-8 weeks 1, 2
- Once remission is achieved: Taper daily prednisone by 1 mg every 4 weeks (or using alternate-day schedules) until discontinuation 1, 2
- Slow tapering (<1 mg/month) is associated with fewer relapses and more frequent treatment cessation 3
Management of Relapses
- For relapse: Increase prednisone to the pre-relapse dose and decrease gradually (within 4-8 weeks) to the dose at which relapse occurred 4, 2
- After re-establishing control, reduce more slowly than initially, not exceeding 1 mg per month 4
- For persistent nighttime pain when tapering below 5 mg/day, consider splitting the daily dose 4, 2
Steroid-Sparing Agents
- Consider methotrexate (7.5-10 mg weekly) as adjunctive therapy for:
- Methotrexate has demonstrated efficacy at doses of 10 mg/week or higher 3, 5
- Avoid TNFα blocking agents (such as infliximab) for PMR treatment 2, 6
Monitoring and Follow-up
- Schedule follow-up visits every 4-8 weeks in the first year, every 8-12 weeks in the second year, and as indicated for relapses or during tapering 1, 2
- Monitor for:
- Steroid-related side effects
- Disease activity and inflammatory markers (ESR, CRP)
- Comorbidities and risk factors for relapse 1
- Ensure patients have rapid access to healthcare providers to report flares and adverse events 1
Patient Education and Support
- Provide education about PMR impact, treatment effects, comorbidities, and disease predictors 1
- Advise on individually tailored exercise programs 1
- Create an individualized PMR management plan with shared decision-making between patient and physician 1