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Year 1
Rheumatology
Polymyalgia rheumatica
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Megan Vann
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Polymyalgia rheumatica (PMR) is an
inflammatory
condition that causes
pain
and
stiffness
in the
shoulders
, pelvic
girdle
and
neck.
There is a strong association with giant cell
arteritis
, and the two conditions often occur
together.
The cause is not fully understood. There are no relevant
antibodies.
It is more common in
older
white
patients. Associated
autoimmune
disease.
Presentation:
Relatively
rapid
onset of symptoms over days to
weeks
(should be present for
2
weeks before diagnosis is considered)
Pain
and
stiffness
in:
Shoulders
- potentially radiating to the upper
arm
and elbow
Pelvic girdle
- potentially radiating to the
thighs
Neck
Characteristic features of pain and stiffness:
Worse in the
morning
Worse after
rest
of inactivity
Interfere with sleep
Take at least
45
minutes to ease in the
morning
Somewhat
improve
with
activity
Associated features:
Systemic symptoms - weight
loss
,
fatigue
and
low
grade fever
Muscle
tenderness
Carpel
tunnel
syndrome
Peripheral
oedema
Diagnosis is based on
clinical
presentation, response to
steroids
and excluding
differentials.
Inflammatory markers (e.g., ESR and CRP) are usually
raised
(but may be normal).
Investigations before starting steroids:
FBC
Renal
profile U&Es
LFTs
Calcium -
hyperparathyroid
,
cancer
and osteomalacia as differentials
Serum protein
electrophoresis
for
myeloma
TSH -
thyroid
disease as differential
Creatinine
kinase for myositis
Rheumatoid
factor for rheumatoid arthritis
Urine
dipstick
Additional investigations to consider:
Anti-nuclear
antibodies (ANA) for systemic lupus
erythematosus
Anti-cyclic
citrullinated peptide (anti-CCP) for
rheumatoid
arthritis
Urine
Bence
Jones protein for
myeloma
Chest
x-ray
for lung and mediastinal abnormalities (e.g., lung
cancer
or lymphoma)
Treatment of PMR is with
steroids.
The NICE clinical knowledge summaries recommend:
15mg
prednisolone daily initially
Follow up after
1
week
Patients with PMR have a
dramatic
improvement in symptoms within one week on steroids
Inflammatory markers return to
normal
within one month
Poor response to steroids suggests an
alternative
diagnosis
Treatment with steroids typically lasts
1-2
years. NICE suggest the following reducing regime of prednisolone:
15mg
until the symptoms are fully controlled, then
12.5mg for 3 weeks, then
10mg for 4-6 weeks, then
Reducing by 1mg every 4-8 weeks
Additional management for patients on long-term steroids can be remembered with the “Don’t STOP” mnemonic:
Don’t – steroid dependence occurs after 3 weeks of treatment, and abruptly
stopping
risks
adrenal
crisis
S –
Sick
day rules (steroid doses may need to be
increased
if the patient becomes unwell)
T – Treatment
card
– patients should carry a steroid treatment card to alert others that they are
steroid-dependent
O –
Osteoporosis
prevention may be required (e.g.,
bisphosphonates
and
calcium
and vitamin
D
)
P – Proton pump inhibitors are considered for
gastro-protection
(e.g., omeprazole)