Fibromyalgia; PMR; Giant Cell Arthritis Flashcards

1
Q

Define fibromyalgia

A

Chronic widespread pain associated with mechanical hypersensitivity

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2
Q

Describe the clinical presentation of fibromyalgia [6]

A
  • chronic pain: at multiple site, sometimes ‘pain all over’
  • lethargy
  • cognitive impairment: ‘fibro fog’
  • sleep disturbance, headaches, dizziness are common
  • allodynia, a type of neuropathic pain, making
    them extremely sensitive to touch
  • headaches
  • numbness/tingling sensations
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3
Q

Describe how you dx fibromyalgia [3]

A

Clinical:
- presence of chronic (>3 months), widespread body pain and associated symptoms such as fatigue and sleep disturbance

Bloods:
- Should have normal ESR; ANA: RF: thyroid; anti-CCP, vitamin D, ferritin

If a patient is tender in at least 11 of 18 points it makes a diagnosis of fibromyalgia more likely

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4
Q

What are risk factors for fibromyalgia? [5]

A
  • FH
  • Hx of rheumatoid conditions
  • Female; 20-60
  • stressful events
  • sleep problems
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5
Q

Describe how you manage fibromyalgia

A

Education; graded excerise programme

Psychological support
- CBT

Aerobic exercise - strong evidence

Analgesia
- amitriptyline; duloxetine; pregabalin

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6
Q

Describe conversation might have with a patient about how to manage their fibromyalgia [2]

A
  • FM is a chronic illness, akin to that of diabetes mellitus and congestive heart failure, selfmanagement of day-to-day symptoms is key and has been associated with decreased pain,
    depression, catastrophic thinking, and improved quality of life
  • Identify specific goals regarding health status and quality of life, that is encouraging exercise
    and sleep hygiene.
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7
Q

Define polymyalgia rheumatica [1]

Which condition does PMR have a strong association with? [1]

A

Polymyalgia rheumatica (PMR) is an inflammatory condition that causes pain and stiffness in the shoulder and pelvic girdles. It rarely occurs in those under 50 years of age and is more common in women (3:1 female to male ratio).

. There is a strong association with giant cell arteritis, and the two conditions often occur together.

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8
Q

Describe the clinical features of PMR [+]

A

Patients may have a relatively rapid onset of symptoms over days to weeks:

Stiffness and pain in the
* Shoulders, potentially radiating to the upper arm and elbow
* Pelvic girdle (around the hips), potentially radiating to the thighs
* Neck

Systemic symptoms (40-50%).
* Includes low grade fever
* fatigue
* anorexia
* weight loss
* depression.

Peripheral oligoarticular arthritis (50%).

The characteristic features of the pain and stiffness are:
* Worse in the morning
* Worse after rest or inactivity
* Interfere with sleep
* Take at least 45 minutes to ease in the morning
* Somewhat improve with activity

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9
Q

If the patient is younger than [], an alternative explanation should be sought as PMR is very rare in this age group.

A

If the patient is younger than 50, an alternative explanation for the above symptoms should be sought as PMR is very rare in this age group.

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10
Q

RA presents similiarly in the early stages of the disease to PMR.
What specifically should you look for give a ddx? [2]

A

Rheumatoid arthritis can have an initial phase that presents similarly to PMR and so the presence of synovitis or clinical features suggestive of rheumatoid arthritis should prompt consideration of this as a potential diagnosis and referral to secondary care for confirmation.

RA patients also do not respond well to corticosteroids, unlike PMR

RA antibodies (anti-CCP; RF)

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11
Q

How would you investigate for PMR?

A

Baseline blood tests
- Elevated ESR/CRP
- Normal other blood tests

All these would be normal

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12
Q

Which type of bursitis is associated with PMR? [1]

A

subacromial bursitis is associated with PMR.

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13
Q

What are the key clinical features of GCA? [4]

A

unilateral headache
jaw claudication
visual disturbance
tender or thickened temporal artery on palpation

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14
Q

How do you distinguish PMR and fibromyalgia? [2]

A

Differences:
- The pain of fibromyalgia tends to be more widespread and would not have the prolonged stiffness that is associated with PMR
- Inflammatory markers would also be normal.

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15
Q

Describe the treatment regime for PMR

A

Oral corticosteroids 15mg prednisolone daily, initially and gradually weaned off them with dose adjustments typically being every 4-8 weeks and reviews (telephone or face to face) scheduled for one week after each dose adjustment.

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

In secondary care, patients may be considered for DMARD treatment as 2nd line therapy (e.g. methotrexate) or tocilizumab as 3rd line.

NB: Patients with PMR have a dramatic improvement in symptoms (at least 70%) within one week. Inflammatory markers return to normal within one month. A poor response to steroids suggests an alternative diagnosis.

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16
Q

PMR has an overlap with which vasculitis [1]
Why is this clinically significant

A

temporal arthritis / giant cell arthritis

  • Can lead to blindness / acute onset visual loss
17
Q

Features of giant cell arteritis?

A
18
Q

Tx for PMR? [1]

Tx for TA? [1]

A

PMR:
- Prednisolone 15-20mg/day

TA:
- Prednisolone 60 mg/day

19
Q

3 S of PMR?

A

Stiffness
ESR
Steroids

and overlap with TA

20
Q
A

PMR

21
Q

In patients with PMR and suspected GCA, treatment should follow that of GCA with prompt initiation of high-dose corticosteroids to prevent complications such as [].

Patients should be advised about GCA symptoms and told to seek urgent medical attention if they develop.

A

In patients with PMR and suspected GCA, treatment should follow that of GCA with prompt initiation of high-dose corticosteroids to prevent complications such as sight loss. Patients should be advised about GCA symptoms and told to seek urgent medical attention if they develop.

22
Q

Temporal arteritis, also known as giant cell arteritis, is a vasculitis predominantly affecting medium and large arteries, particularly the branches of the [] artery

A

Temporal arteritis, also known as giant cell arteritis, is a vasculitis predominantly affecting medium and large arteries, particularly the branches of the carotid artery.

23
Q

Describe the presentation of temporal arteritis [5]

A

Unilateral headache is the primary presenting feature, typically severe and around the temple and forehead. It may be associated with:
* Scalp tenderness (e.g., noticed when brushing the hair)
* Jaw claudication
* Blurred or double vision
* Loss of vision if untreated

Anterior ischemic optic neuropathy accounts for the majority of ocular complications

Lethargy, depression, low-grade fever, anorexia, night sweats

NB patients are typically > 60; rapid onset (< 1month)

24
Q

Describe why vision testing is key in CGA [1]

A

Anterior ischemic optic neuropathy:
- occlusion of the posterior ciliary artery (a branch of the ophthalmic artery)
- causing ischaemia of the optic nerve head
- may result in temporary visual loss - amaurosis fugax
- permanent visual loss is the most feared complication of temporal arteritis and may develop suddenly

25
Q

Describe investigations would conduct for CGA

A

raised inflammatory markers

temporal artery biopsy
- skip lesions may be present
- multinucleated giant cells present

Duplex ultrasound
- showing the hypoechoic “halosign and stenosis of the temporal artery

26
Q

Management of CGA? [

A

Steroids are the mainstay of treatment. They are started immediately, before confirming the diagnosis, to reduce the risk of vision loss. There is usually a rapid and significant response to steroid treatment. Initial treatment is:

  • 40-60mg prednisolone daily with no visual symptoms or jaw claudication
  • 500mg-1000mg methylprednisolone daily with visual symptoms or jaw claudication

Once the diagnosis is confirmed and the condition is controlled, the steroid dose is slowly weaned over 1-2 years.

low-dose aspirin should be considered to reduce the risk of ischemic complications
Proton pump inhibitor (e.g., omeprazole) for gastroprotection while on steroids
Bisphosphonates and calcium and vitamin D for bone protection while on steroids

27
Q

How do you differentiate CGA to central retinal artery occlusion? [2]

A

Similarities: sudden onset, loss of vision

Differences: fundoscopy may reveal presence of cherry red spot with retinal whitening, no muscle stiffness