What are the diagnostic criteria and initial treatment for Polymyalgia Rheumatica (PMR) in an older adult with chronic pain and stiffness?

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Diagnosis of Polymyalgia Rheumatica

Diagnose PMR based on age ≥50 years, bilateral shoulder pain with morning stiffness, elevated inflammatory markers (ESR and/or CRP), and exclusion of mimicking conditions, followed by confirmation with dramatic response to glucocorticoids within 2 weeks. 1, 2

Clinical Diagnostic Criteria

Essential Features

  • Age ≥50 years at symptom onset 1, 3
  • Bilateral shoulder pain with severe morning stiffness lasting >1 month 1, 3
  • Neck and/or pelvic girdle involvement may be present but is not mandatory 2, 3
  • Functional impairment from pain and stiffness 4

Laboratory Markers

  • Elevated ESR and/or CRP in >90% of cases 4, 5
  • ESR >40 mm/1st hour is typical and associated with higher relapse risk 1, 6
  • Normal inflammatory markers represent an atypical presentation requiring specialist referral 1, 2

Important caveat: ESR is preferred over CRP for long-term monitoring and predicting relapse risk, as high ESR (>40 mm/1st hour) independently predicts need for prolonged therapy 6

Mandatory Exclusion Testing

Rheumatologic Conditions

  • Rheumatoid factor and/or anti-CCP antibodies to exclude elderly-onset rheumatoid arthritis (EORA), which is the most common PMR mimic 1, 2, 7
  • Complete peripheral joint examination to identify inflammatory arthritis 2

Other Mimicking Conditions

  • Thyroid function tests to exclude thyroid disorders 1
  • Serum protein electrophoresis to exclude myeloma 1
  • Consider ANCA testing if vasculitis suspected 1
  • Chest radiograph at physician discretion to exclude malignancy 1

Critical pitfall: Malignancies and seronegative symmetrical polyarthritis are common PMR mimics. Patients with solid malignancies show poor response to low-dose prednisone, while those with hematologic malignancies may have atypical continuous aching rather than movement-related pain 7

Imaging for Diagnostic Support

Ultrasound Findings

  • Bilateral subdeltoid bursitis detected in 69% of PMR patients 4
  • Ultrasound improves diagnostic accuracy when clinical features are present 4

When to Use Imaging

  • Atypical presentations 1, 2
  • Diagnostic uncertainty 4
  • To exclude alternative diagnoses 4

Diagnostic Confirmation Through Treatment Response

Dramatic clinical improvement within 2 weeks of starting glucocorticoids at 12.5-25 mg prednisone equivalent daily confirms the diagnosis 1, 2, 3

  • Almost complete response expected within 4 weeks 1
  • Lack of response within 2 weeks should prompt dose increase to 25 mg or reconsideration of diagnosis 1

Atypical Presentations Requiring Specialist Referral

Refer immediately if any of the following are present 1, 2:

  • Age <60 years 1, 2
  • Peripheral inflammatory arthritis 1, 2
  • Systemic symptoms (fever, weight loss) 1, 2
  • Low or normal inflammatory markers 1, 2
  • Poor response to appropriate glucocorticoid therapy 1

Assessment of Comorbidities Before Treatment

Document the following risk factors for glucocorticoid-related adverse events 1:

  • Hypertension, diabetes, glucose intolerance 1, 2
  • Cardiovascular disease, dyslipidemia 1, 2
  • Osteoporosis (particularly recent fractures) 1, 2
  • Cataract or glaucoma risk factors 1, 2
  • Peptic ulcer disease 1, 2
  • Chronic or recurrent infections 1
  • Concomitant NSAID use 1

Female sex is associated with higher risk of glucocorticoid side effects and higher relapse rates 1, 2

Initial Treatment Algorithm

Starting Dose Selection

Use 12.5-25 mg prednisone equivalent daily as initial therapy 1, 2

Choose higher dose (20-25 mg) when:

  • High ESR (>40 mm/1st hour) 1, 6
  • Peripheral inflammatory arthritis present 1, 2
  • Female sex 1, 2
  • Low risk of adverse events 1

Choose lower dose (12.5-15 mg) when:

  • Diabetes, osteoporosis, or glaucoma present 1
  • Multiple risk factors for glucocorticoid side effects 1
  • Elderly with frailty 1

Strongly avoid initial doses ≤7.5 mg/day (ineffective) or >30 mg/day (excessive toxicity risk) 1

Monitoring Schedule

  • Every 4-8 weeks during first year 1, 2
  • Every 8-12 weeks during second year 1
  • As indicated for relapses or during tapering 1

Document at each visit: disease activity, inflammatory markers, glucocorticoid-related side effects, and relapse risk factors 1

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Polymyalgia Rheumatica Diagnosis and Treatment

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Polymyalgia rheumatica--diagnosis and classification.

Journal of autoimmunity, 2014

Research

Polymyalgia Rheumatica: a Common Disease in Seniors.

Current rheumatology reports, 2020

Guideline

ESR as a Preferred Marker for Polymyalgia Rheumatica

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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