Polymyalgia Rheumatica
General Overview
💡PMR is the most common inflammatory rheumatologic condition in the elderly (peak incidence at 70-80yo) and typically affects women (3 female:1 male).
Manifests with:
Age >50 yo
Musculoskeletal symptoms (lasting > 2 weeks):
Symmetric pain/aching and morning stiffness > 45 mins affecting shoulders/neck/hip
Stiffness relieved with activity
Systemic symptoms (fatigue, malaise, night sweats, depressed mood)
Fever should prompt to rule out inflammatory (GCA) or infectious pathology
Elevated ESR (more prognostic) and/or CRP (more sensitive)
Rapid improvement with low-dose systemic steroids (eg. 15-25mg/day prednisone)
Exclude non-inflammatory, inflammatory (such as giant cell arteritis or rheumatoid arthritis), drug, endocrine, infectious and malignancy
Red Flags (Features of Giant Cell Arteritis)
~20% associated with giant cell (temporal) arteritis
New sudden-onset headache
New sudden-onset visual changes
Upper cranial nerve palsies
Jaw/tongue claudication
Limb claudication or suggestion of large vessel involvement
Prominence, beading or diminished pulse of temporal artery
Temporal tenderness
Fever, anemia, constitutional symptoms/signs
Physical examination
Cardio
Assess bilateral BP discrepancy, temporal arteries swelling/tenderness/bruits (to detect GCA)
MSK
Decreased ROM of shoulders, neck, hips but preserved muscle strength
Muscle tenderness surrounding affected joints
Neuro
Normal muscle strength in PMR (despite subjective weakness or pain)
Investigations
↑ ESR, ↑ CRP
ESR elevation better correlated to severity but CRP more sensitive (99% Sn)
Rule out mimics:
ANA, RF, anti-CCP (SLE, rheumatoid arthritis)
CK (polymyositis/dermatomyositis)
CBC, SPEP/FLC, Calcium, ALP, Vitamin D (bony disease, eg. multiple myeloma)
TSH (hypothyroidism)
Other: LFT, UA
Treatment
💡 Given risks of long-term corticosteroid use, consider baseline BMD and consider osteoporosis prophylaxis
Prednisone 15mg PO daily (can also be divided BID)
Response usually observed within three days
If no response after one week, consider increase to 20mg PO daily
If still no response, consider alternative diagnosis (most commonly RA)
Maintain effective steroid dose for 2-4 weeks until after symptoms resolve, then gradually taper every 2-4 weeks (example regimen:15mg x 2-4w → 12.5mg x 2-4w → 10mg x 2-4w → 9mg x 4-8w → 8mg x 4-8w → 7mg x 4-8w → etc.)
Can often take 1-2 years to fully taper off steroids!
Relapse is common (treat with previously effective dose), monitor for giant cell arteritis (temporal arteritis)
Refer to Rheumatology if atypical (e.g., age < 50, systemic symptoms, peripheral or asymmetric joint involvement, systemic symptoms, low ESR/CR, relapse or prolonged therapy)
Last edited 2021-08-04
B. Paul, K. Chan
References:
ACR 2015. https://www.rheumatology.org/Portals/0/Files/2015%20PMR%20guidelines.pdf
AAFP 2013. http://www.aafp.org/afp/2013/1115/p676.html
BMJ Best Practice. https://bestpractice.bmj.com/topics/en-gb/153
UptoDate.