Scleritis (OP) Flashcards

1
Q

Define scleritis.

A

Transmural inflammation of the sclera - inflammation of deep scleral vessels

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2
Q

Which demographics is scleritis common in?

A
  • F>M
  • 40-60 years
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3
Q

What other conditions are commonly found along with scleritis? (6)

A

Underlying systemic disorder or infection:

  • commonly RA
  • SLE
  • IBD
  • gout
  • (granulomatosis with polyangiitis)
  • (relapsing polychondritis)
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4
Q

What are the two types of scleritis?

A
  • anterior scleritis (90%) - non-necrotising (75%) vs necrotising (15%)
  • posterior scleritis
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5
Q

What is non-necrotising anterior scleritis (75%)?

A
  • usually unilateral
  • hyperaemia of superficial and deep episcleral vessels
  • does not blanch with vasoconstrictors
  • anterior uveitis may be present
  • tenderness of globe
  • when inflammation resolved, choroidal pigment may show through thinned sclera as a blue/black colouration
  • approximately 60% are diffuse and 40% nodular (nodule cannot be moved over underlying tissue)
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6
Q

What is necrotising anterior scleritis (15%)?

A
  • most severe form may be painless
  • 75% eventually have visual impairment
  • avascular patches –> scleral melting with ectasia and choroidal herniation
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7
Q

What is posterior scleritis (10%)?

A
  • involves sclera posterior to ora serrata
  • eye may be white
  • ophthalmoscopy - exudative retinal detachment, macular oedema, optic disc oedema, may also be normal
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8
Q

What are the clinical features of scleritis? (5)

A
  • pain - deep, aching, boring eye pain exacerbated by eye movement and palpation, may radiate to rest of face
  • red eye
  • photophobia
  • lacrimation
  • no discharge
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9
Q

When is eye pain in scleritis worse?

A

Worse at night, exacerbated by eye movement and palpation

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10
Q

How does scleritis present differently to episcleritis?

A

Episcleritis = painless red eye (inflammation more superficial)

Scleritis = painful red eye

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11
Q

What should you review in PMH in scleritis?

A

Systemic associations - connective tissue disorders etc:

  • RA
  • SLE
  • IBD
  • gout
  • granulomatosis with polyangiitis
  • relapsing polychondritis
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12
Q

What might you find on examination in scleritis? (3)

A
  • deep scleral vessel engorgement and pain on ocular palpation
  • no fluorescein stain
  • visual acuity and pupillary reactions may be abnormal (depending on position of scleritis on globe)
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13
Q

What do we give to distinguish between scleritis and episcleritis?

A

Phenylephrine eye drops - if eye redness improves after –> episcleritis

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14
Q

What scans can we do in scleritis? (2)

A
  • US - to see posterior scleritis
  • orbital CT/MRI - to differentiate between orbital lesions
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15
Q

What else do we need to investigate in scleritis?

A

Systemic diseases e.g. RA, ANA (CRP/ESR)

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16
Q

What are some differentials for scleritis?

A

Acute red eye:

  • episcleritis - usually self-limiting, managed with reassurance
  • anterior uveitis - associated with ankylosing spondylitis, HLA-B27, Crohn’s, psoriatic arthritis
17
Q

What are three major factors that distinguish scleritis vs episcleritis?

A
  1. severity of pain (no pain = episcleritis)
  2. pain on ocular movement
  3. non-blanching vessels
18
Q

What do we need to do urgently if scleritis?

A

Urgent referral to ophthalmologist (threat to sight)

19
Q

What analgesia do we give for scleritis?

A

Fluriprofen PO 100mg TDS generally improves Sx after 2 days

20
Q

What is the management plan for scleritis?

A
  • mild-mod disease: NSAIDs
  • if they do not work: systemic glucocorticoids
  • if unresponsive to steroids: systemic immunosuppressive therapy (azathioprine, methotrexate, biologics e.g. TNF-a)
21
Q

How do we manage acute scleritis?

A

Oral steroids

22
Q

What is a complication of scleritis?

A

Perforation of globe