What is the recommended treatment for Polymyalgia Rheumatica (PMR)?

Medical Advisory BoardAll articles are reviewed for accuracy by our Medical Advisory Board
Educational purpose only • Exercise caution as content is pending human review
Article Review Status
Submitted
Under Review
Approved

Last updated: November 10, 2025View editorial policy

Personalize

Help us tailor your experience

Which best describes you? Your choice helps us use language that's most understandable for you.

Diagnosis and Treatment of Polymyalgia Rheumatica

Diagnosis

PMR should be suspected in patients over 60 years old presenting with bilateral shoulder and hip girdle pain and morning stiffness lasting more than 45 minutes, accompanied by elevated inflammatory markers (ESR >40 mm/hr or elevated CRP). 1

Key Diagnostic Features:

  • Age ≥60 years is a critical criterion; younger patients warrant specialist referral for atypical presentation 1
  • Bilateral shoulder and hip girdle pain with morning stiffness is the hallmark symptom 1
  • Elevated ESR (>40 mm/1st hour) or CRP supports the diagnosis, though low inflammatory markers should prompt consideration of alternative diagnoses 1
  • Rapid response to glucocorticoids (within 7 days) is highly characteristic; lack of response to 20 mg/day prednisone suggests an alternative diagnosis 2

When to Refer to Specialist:

Refer patients with any of the following 1:

  • Peripheral inflammatory arthritis
  • Systemic symptoms beyond typical PMR
  • Low or normal inflammatory markers
  • Age <60 years
  • Poor response to appropriate glucocorticoid therapy
  • Frequent relapses or need for prolonged therapy
  • High risk of or existing glucocorticoid-related adverse effects

Initial Treatment

Start prednisone at 12.5-25 mg daily as first-line therapy, with the specific dose individualized based on body weight, relapse risk, and comorbidity profile. 3

Dose Selection Algorithm:

  • Use 20-25 mg/day for patients with 3:

    • High risk of relapse (female sex, ESR >40, peripheral arthritis) 1
    • Low risk of adverse events
    • Higher body weight (>0.19 mg/kg appears optimal) 4
  • Use 12.5-15 mg/day for patients with 3:

    • Relevant comorbidities (diabetes, osteoporosis, glaucoma)
    • Lower body weight 4
    • Risk factors for glucocorticoid-related side effects
  • Avoid doses ≤7.5 mg/day (insufficient anti-inflammatory effect) 1, 3

  • Never use doses >30 mg/day (excessive adverse effect risk without added benefit) 1, 3

Alternative Route:

  • Intramuscular methylprednisolone (120 mg every 3 weeks) can be considered as an alternative to oral glucocorticoids 3

Expected Response:

  • Clinical improvement should occur within 7 days 2
  • If no response to 20 mg/day within this timeframe, reconsider the diagnosis 2

Glucocorticoid Tapering Schedule

Taper prednisone to 10 mg/day within 4-8 weeks, then reduce by 1 mg every 4 weeks until discontinuation, provided remission is maintained. 1, 3

Initial Tapering Phase (First 4-8 weeks):

  • Reduce from starting dose to 10 mg/day prednisone 1, 3
  • Monitor clinical symptoms and inflammatory markers (ESR, CRP) at each adjustment 3

Maintenance Tapering Phase (After reaching 10 mg/day):

  • Decrease by 1 mg every 4 weeks 1, 3
  • Alternative: Use alternating schedules (e.g., 10/7.5 mg every other day) for smoother transitions 3
  • Aim for 7.5 mg maintenance dose by 6-9 months 5

Duration of Therapy:

  • Most patients require 2 years of treatment, though some need 4 years or longer 5
  • Relapses are common when dose reaches ≤5 mg/day 2

Management of Relapses

For relapse, increase prednisone to the pre-relapse dose, then taper more slowly (over 4-8 weeks) back to the dose at which relapse occurred, followed by reduction of 1 mg per month. 6, 3

Relapse Management Algorithm:

  1. Increase dose immediately to the pre-relapse dose that controlled symptoms 6, 3
  2. Maintain this dose until symptoms resolve and inflammatory markers normalize 6
  3. Taper over 4-8 weeks back down to the dose at which relapse occurred 6, 3
  4. Resume tapering at 1 mg per month (slower than initial taper) 6

Special Consideration for Low-Dose Relapses:

  • For patients relapsing on ≤5 mg/day with persistent nighttime pain, consider splitting the daily dose rather than increasing total dose 3

Glucocorticoid-Sparing Agents

Add methotrexate 7.5-10 mg weekly for patients with frequent relapses, prolonged therapy requirements, or significant glucocorticoid-related adverse effects. 3

Indications for Methotrexate:

  • Multiple or frequent relapses 6, 3
  • High risk factors for relapse (female sex, ESR >40, peripheral arthritis) 1, 3
  • Risk factors for glucocorticoid adverse events (diabetes, osteoporosis, glaucoma) 3
  • Existing glucocorticoid-related complications 3
  • Inadequate response to glucocorticoids alone 3

Agents to Avoid:

  • TNF-α blocking agents (infliximab, etanercept) are strongly contraindicated—they are ineffective in isolated PMR 3, 7
  • Chinese herbal preparations (Yanghe, Biqi capsules) should not be used 3

Emerging Therapies:

  • Tocilizumab and sarilumab (anti-IL-6 receptor agents) show promise for reducing relapse frequency and cumulative glucocorticoid burden, though they are not yet standard therapy 7

Monitoring and Follow-Up

Schedule visits every 4-8 weeks during the first year, every 8-12 weeks in the second year, and as needed for relapses or dose adjustments. 1, 3

At Each Visit, Assess:

  • Clinical symptoms (pain scores, morning stiffness duration) 1
  • Inflammatory markers (ESR, CRP) 6, 3
  • Glucocorticoid-related adverse effects 1, 3:
    • Bone mineral density (osteoporosis screening)
    • Blood glucose (diabetes screening)
    • Blood pressure (hypertension)
    • Ocular examination (cataracts, glaucoma)
  • Risk factors for relapse (female sex, high ESR, peripheral arthritis) 1
  • Comorbidities and concurrent medications 1

Patient Access:

  • Ensure rapid access to medical advice for reporting flares or adverse events between scheduled visits 1

Adjunctive Measures

Osteoporosis Prophylaxis:

  • Initiate bone protection at treatment start, as prednisone causes significant bone loss 3, 2

Patient Education:

  • Provide education on disease impact, treatment expectations, and comorbidity management 1
  • Recommend individually tailored exercise programs 1

NSAIDs and Analgesics:

  • Use glucocorticoids instead of NSAIDs for disease control 1
  • NSAIDs may be used short-term only for pain from other conditions (e.g., osteoarthritis), not for PMR itself 1
  • NSAIDs provide only symptomatic relief without modifying disease progression 1

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Medical management of polymyalgia rheumatica.

Expert opinion on pharmacotherapy, 2010

Guideline

Polymyalgia Rheumatica Treatment Guidelines

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Treatment of polymyalgia rheumatica/giant cell arteritis.

Bailliere's clinical rheumatology, 1991

Guideline

Management of Relapsing Polymyalgia Rheumatica

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

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.

Have a follow-up question?

Our Medical A.I. is used by practicing medical doctors at top research institutions around the world. Ask any follow up question and get world-class guideline-backed answers instantly.