Polymyalgia Rheumatica: Initial Treatment Recommendations
Start prednisone at 12.5-25 mg daily as the initial treatment for polymyalgia rheumatica, with the specific dose within this range determined by relapse risk and comorbidity profile. 1
Immediate Treatment Initiation
- Glucocorticoids are strongly recommended over NSAIDs for disease control in PMR, as they reduce both symptoms and structural progression, whereas NSAIDs provide only symptomatic relief 1
- Clinical improvement should be noted within 2 weeks, with almost complete response expected by 4 weeks 1
- If inadequate response occurs within 2 weeks, increase the oral dose up to 25 mg prednisone equivalent 1
Dose Selection Algorithm
Higher initial dose (20-25 mg/day): 1
- Female sex (associated with higher relapse risk) 1
- High ESR (>40 mm/1st hour) 1
- Peripheral inflammatory arthritis 1
- Low risk of glucocorticoid adverse events 1
Lower initial dose (12.5-15 mg/day): 1
- Diabetes or glucose intolerance 1
- Osteoporosis or recent fractures 1
- Glaucoma or cataracts 1
- Hypertension or cardiovascular disease 1
- Peptic ulcer disease 1
- Female sex (higher risk of glucocorticoid side effects) 1
Strongly discouraged: Initial doses ≤7.5 mg/day (insufficient anti-inflammatory effect) 1
Strongly contraindicated: Initial doses >30 mg/day (no evidence of benefit, high risk of harm) 1
Critical Pre-Treatment Assessment
Before prescribing glucocorticoids, document: 1
Laboratory baseline: 1
- Rheumatoid factor and/or anti-CCP antibodies (exclude rheumatoid arthritis)
- CRP and/or ESR (typically elevated in PMR)
- Complete blood count
- Glucose and HbA1c
- Creatinine and liver function tests
- Calcium, alkaline phosphatase, vitamin D
- Urinalysis
Comorbidity screening: 1
- Hypertension, diabetes, cardiovascular disease
- Dyslipidemia, peptic ulcer disease
- Osteoporosis (consider DEXA scan)
- Glaucoma risk factors, cataracts
- Chronic or recurrent infections
- Current NSAID use
Glucocorticoid Tapering Protocol
Initial tapering (weeks 0-8): 1
- Reduce dose gradually to 10 mg/day prednisone equivalent within 4-8 weeks
- Use single daily dosing (morning preferred) rather than divided doses 1
Maintenance tapering (after week 8): 1
- Once remission is achieved, taper by 1 mg every 4 weeks until discontinuation
- Alternative schedules (e.g., 10/7.5 mg alternate days) are acceptable if 1 mg tablets unavailable 1
Relapse management: 1
- Increase dose to the pre-relapse effective dose
- Decrease gradually within 4-8 weeks back to the dose at which relapse occurred
- Then resume slow taper by 1 mg every 4 weeks 1
Alternative Glucocorticoid Formulation
Intramuscular methylprednisolone may be considered as an alternative to oral prednisone: 1
- Starting dose: 120 mg IM every 3 weeks for first 9 weeks 1
- Consider in patients with difficult-to-control hypertension, diabetes, osteoporosis, or glaucoma where lower cumulative glucocorticoid exposure is desirable 1
- Evidence is limited to a single randomized trial; long-term benefit unclear 1
Adjunctive Methotrexate Therapy
Consider early introduction of methotrexate (7.5-10 mg/week orally) in addition to glucocorticoids for: 1
- High risk of relapse (female sex, high ESR, peripheral arthritis) 1
- Risk factors for glucocorticoid-related adverse events 1
- Patients experiencing relapse during glucocorticoid taper 1
- Methotrexate may reduce cumulative glucocorticoid dosage by 20-44% and relapses by 36-54% 2
Monitoring Schedule
First year: Every 4-8 weeks 1
Second year: Every 8-12 weeks 1
At each visit, assess: 1
- Disease activity (pain, stiffness, functional impairment)
- Inflammatory markers (CRP/ESR)
- Glucocorticoid-related side effects (weight, blood pressure, glucose, bone health)
- Evidence of relapse
Giant Cell Arteritis Screening
Refer immediately for specialist evaluation if: 1
- New-onset headache, particularly temporal headache 3, 4
- Visual disturbances or vision loss 3, 4
- Jaw claudication 3, 4
- Scalp tenderness 3, 4
- Temporal artery abnormalities (tenderness, decreased pulse) 3, 4
Giant cell arteritis occurs in approximately 20% of PMR patients and requires higher glucocorticoid doses (40-60 mg/day prednisone) to prevent irreversible vision loss 5, 4
Specialist Referral Indications
Consider rheumatology referral for: 1
- Age <60 years 1
- Peripheral inflammatory arthritis 1
- Low or normal inflammatory markers 1
- Systemic symptoms beyond typical PMR 1
- High risk of glucocorticoid-related side effects 1
- Inadequate response to initial therapy within 2 weeks 1
- Frequent relapses or prolonged therapy requirement 1
Glucocorticoid-Related Prophylaxis
Mandatory for all patients: 1