Polymyalgia Rheumatica Flashcards

1
Q

Define PMR

A

Polymyalgia Rheumatica

inflammatory disease causing pain and stiffness in the shoulder, neck and pelvic girdle.

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2
Q

What are the RF for PMR?

A
  • Adults, > 50 yrs
  • Women
  • Caucasian
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3
Q

How does PMR present?

A
  • Features presents for > 2wks:
    o Bilateral shoulder pain that may radiate to the elbow
    o Bilateral pelvic girdle pain
    o Worse with movement
    o Interferes with sleep
    o Stiffness for at least 45 minutes in the morning
  • Other symp:
    o Systemic symp – weight loss, fatigue, fever, low mood.
    o Peripheral arthritis
    o Carpal tunnel syn
    o Pitting oedema – hand, wrists, feet and ankles.
    o Upper arm tenderness
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4
Q

How is PMR diagnosed?

A
  • diagnosis of exclusion.
  • also based on starting trial of steriod and pos response to Tx.
  • ESR and CRP will be raised (but normal does not exclude diagnosis).

order various tests to exclude other diagnoses, e.g:
o FBC – incl U+E, LFT, TFT, RF (rheumatioid arthiritis)
o Creatine kinase for myostisis
o Serum protein electrophoresis for myeloma and other protein disorders
o Ca2+ - raised in hyperparathyroidism and cancer, or low in osteromalacia.
o Urine dip
o Anti-nuclear antibodies (ANA) for systemic lupus erythematosus
o Anti-cyclic citrullinated peptide (anti-CCP) for rheumatoid arthritis
o Urine Bence Jones protein for myeloma
o Chest Xray for lung and mediastinal abnormalities

ALSO RULE OUT GIANT CELL ARTERITIS - MOST IMPORTANT

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5
Q

In someone with suspected PMR why is it important to exclude giant cell arteritis?

A

Giant cell arteritis - need to start steroid straight away.

but not in PMR - allows time for workup before starting steroid tx.

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6
Q

How would you diffn PMR and myositis?

A
  • Myositis causes bilateral proximal muscle weakness, but there is not pain/ mild pain.
  • WHEREAS in PMR – lots of pain and stiffness BUT no muscle weakness on exam (but can be difficult to confirm as movement limited to pain).
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7
Q

How is PMR managed?

A

Initially give trial of oral prednisolone, 15mg OD – follow up after 1 wk.
o If there has been no improvement in symp – mostly likely not PMR – STOP steriods and consider DDx.

o If good respose, re-check again after 3-4 wks – symp should have resolved and inflammatory markers should have come back down to normal.

If 3-4 weeks of steroids has given a good response then start a reducing regime with the aim of getting the patient off steroids:
* 15mg until symptoms are fully controlled then
* 12.5mg for 3 weeks then
* 10mg for 4-6 weeks then
* Reduce by 1mg every 4-8 weeks

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8
Q

What is included in the patient workup before starting steriods?

A
  • Prevent and Tx steroid induced osteoporosis – DEXA scan
  • Screen fr increased risk of side effects of steriods – e.g DM, HTN, PMHx of peptic ulcer, osteoporosis, mental health history.
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9
Q

How often should patients with PMR be reviewed?

A

Ptx should be reviewed 1 wks after every dose change and every 3 months in first yr after diagnosis.

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10
Q

What is done at the review in PMR?

A

every 3 motnhs in first yr of diagnosis.

  • Review symp of giant cell arthritis – and exclude
  • Relapsing symp of PMR – proximal pain, fatigue and morning stiffness – if present increase dose of prednisolone to last dose that controlled symp.
  • Assess side effects of steroids – weight gain, dyspepsia, muscle weakness, skin thinning and easy bruising.
    o BP and glucose checks – affected by long term steroids.
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11
Q

When should someone with PMR be referred?

A

Refer if atypical features of PMR and no other cause of symp:
o < 60 yrs
o Red flags – weight loss, night pain, neuro features
o Don’t have core feature of PMR (bilateral shoulder/ pelvic pain or stiffness).
o features uncommon w/ PMR – normal inflammatory markers and or chronic onset of symp.
o Steroid required for more than 2 yrs.
o Repetitive flares of PMR
o Ptx is experiencing or is at high risk of adverse effects of steroids.

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