Polymyalgia Rheumatica: Workup and Management
The diagnosis and management of polymyalgia rheumatica (PMR) requires a specific laboratory workup, exclusion of mimicking conditions, and treatment with glucocorticoids at an initial dose of 12.5-25 mg prednisone daily with a structured tapering schedule over 1-2 years. 1
Clinical Presentation and Diagnosis
PMR typically presents with:
- Bilateral proximal muscle pain and morning stiffness affecting:
- Neck
- Shoulders and upper arms
- Lower back, hips, and thighs
- Constitutional symptoms (fatigue, low-grade fever, weight loss)
- Acute onset over days to weeks
- Affects patients >50 years (peak incidence 70-75 years)
- More common in women (2-3 times) 2, 3
Diagnostic Workup
Required Laboratory Tests
- Inflammatory markers: ESR and/or CRP (typically markedly elevated)
- Rheumatoid factor and/or anti-CCP antibodies (to exclude RA)
- Complete blood count
- Metabolic panel: glucose, creatinine, liver function tests
- Bone profile: calcium, alkaline phosphatase
- Urinalysis 1
Additional Recommended Tests
- Protein electrophoresis
- Thyroid stimulating hormone (TSH)
- Creatine kinase (to exclude myopathy)
- Vitamin D level 1
Further Testing Based on Clinical Presentation
- ANA, ANCA (if other autoimmune conditions suspected)
- Tuberculosis testing (if relevant)
- Chest radiograph (to exclude malignancy or other conditions)
- Ultrasound of shoulders and hips (can show bursitis, synovitis) 1, 2
Differential Diagnosis
Critical to exclude conditions that mimic PMR:
- Rheumatologic conditions: Elderly-onset rheumatoid arthritis, seronegative spondyloarthropathies
- Malignancies: Solid tumors and hematologic malignancies (particularly concerning if poor response to steroids)
- Endocrine disorders: Thyroid disease
- Infections: Chronic infections
- Neurologic conditions: Parkinson's disease, polymyositis
- Drug-induced myalgia 1, 4
Management
Initial Treatment
- Glucocorticoid therapy:
Tapering Schedule
- Reduce to 10 mg/day within 4-8 weeks
- Then decrease by 1 mg every 4 weeks until discontinuation
- Total treatment duration typically 1-2 years
- Monitor for relapses during tapering 1, 5
Monitoring
- Follow-up visits:
- Every 4-8 weeks in first year
- Every 8-12 weeks in second year
- As needed for relapses or during tapering
- Monitor for:
- Disease activity (symptoms, inflammatory markers)
- Steroid-related side effects
- Comorbidities
- Risk factors for relapse 1
Management of Refractory Cases
- Methotrexate: Consider at 7.5-10 mg/week for patients with:
Special Considerations
Indications for Specialist Referral
- Atypical presentation (peripheral arthritis, systemic symptoms, low inflammatory markers, age <60)
- High risk of or experiencing steroid-related side effects
- PMR refractory to glucocorticoid therapy
- Frequent relapses or need for prolonged therapy
- Suspected giant cell arteritis (GCA) 1
Risk Factors for Relapse/Prolonged Therapy
- Female sex
- High ESR (>40 mm/hr)
- Peripheral inflammatory arthritis 1
Patient Education and Support
- Provide education about PMR and treatment
- Discuss potential steroid side effects and monitoring
- Advise on individually tailored exercise programs
- Ensure rapid access to healthcare providers for flares or adverse events 1
Complications and Comorbidities
- Giant Cell Arteritis: 15-30% of PMR patients may develop GCA
- Glucocorticoid-related adverse effects:
Proper diagnosis, appropriate initial dosing of glucocorticoids, careful monitoring, and structured tapering are essential for optimal management of PMR to reduce morbidity and improve quality of life.