Optic neuritis Flashcards

1
Q

What are the signs and symptoms of optic neuritis

A

Symptoms

· Acute vision loss (hours to days)

· Eye pain and worsening of this pain on movement of the eye

Signs

· RAPD

· Often presence of a central scotoma (but can have any pattern of unilateral retinal nerve fibre loss)

· Papillitis with hyperemia and swelling of disk (1/3rd of patients)

· Blurred optic disc margins

· Elevated optic nerve head

· Flashes of light in some patients

· Colour vision defect (or reduced ability to see red)

· Perivenous sheathing (exudation from inflammatory cells around blood vessels)

· Periphlebitis retinae

· Contrast Sensitivity reduced

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2
Q

Why does optic neuritis occur?

A

. Occurs as a result of inflammatory responses destroying the myelin sheath in the optic nerve.
· Immune mediated response which is a result of T-cell activation leading to the release of inflammatory agents including cytokines

· The cause is usually idiopathic but may also be the initial presenting sign of multiple sclerosis

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3
Q

What are the 4 different types of optic neuritis?

A

retrobulbar

Papillitis

Perineuritis

Neuroretinitis

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4
Q

Retrobulbar optic disc appearance? Prevalence stat?

A

With normal optic disc appearance,

2/3 of cases are this type

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5
Q

perineuritis optic disc appearance? what signs to look for?

A

Perineuritis, which involves the optic nerve sheath while the optic disc may or may not be swollen

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6
Q

Signs to look for in neuroretinitis?

A

Neuroretinitis with optic disc oedema and macular star exudates.

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7
Q

DDx’s to consider

A

Anterior Ischaemic Optic Neuropathy

· NAION (pain on motilities in 10% of patients, patients age >40 atleast)

· Scleritis

· Malignant hypertension

· Hypertensive retinopathy

· BRVO/CRVO

· Acute Angle closure

· Compressive optic neuropathy

· Cystoid macular oedema

· Retinal detachment

· Macula hole

· Leber’s Optic Neuropathy - Bilateral vision loss (inherited condition, which mostly occurs in young males)

  • Main symptoms
  • Blurring of vision
  • Clouding of Vision
  • Loss of colour vision
  • Progressive Loss
  • Can start in one eye then develop to the other eye

· Papillodema (normally no pain on motilities, minimal to no decrease in VA)

· Retrobulbar tumour

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8
Q

Risk factors:

A

· Young patients aged 15-45 years

· Females are more frequently affected

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9
Q

targetted history?

A

· Do you experience eye pain on movement?

· Do you experience washed out colour in one eye?

· Do you notice any blurry vision on one eye compared to the other?

· Do you have any headaches? Could be a sign of AION

· Is the pain in both eyes or one eye?

· How is your general health? Most cases of Optic neuritis are associated with Multiple Sclerosis

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10
Q

exam plan?

A

· Vision

· Red Cap test: positive due to optic nerve head involvement

· Pelli-robson contrast sensitivity: usually decrease

· Pupil: Positive for RAPD

· Red Cap test, D-15: looking for acquired colour vision defect

· Ocular Motilities: pain on eye movement

· Tonometry – normal IOPs can rule out angle closure

· Gonioscopy: wide anterior chamber angle can rule out acute angle closure

· Dilated Fundus Examination looking at optic nerve head oedema, myelination, macular oedema, infectious retinopathy

· OCT - macula oedema, optic disc swelling

· Visual fields: often central defect, but can be nay pattern of unilateral retinal nerve fibre loss (particularly important in retrobulbar optic neuritis

· MRI - To investigate the presence of MS

· Lumbar Puncture - To investigate the presence of MS by taking a sample of cerebrospinal fluid

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11
Q

Management of optic neuritis?

A

Immediate Management

· Referral to neuro ophthalmologist

· If visual acuity is <6/12 recommended treatments as per Optic Neuritis Treatment Trial (ONTT) is intravenous methylprednisolone (1g/day x 3), followed by oral prednisolone 1mg/kg for 11 days

· Intravenous steroids (IV methylprednisolone) treatment is recommended when 3 or more signal abnormalities are present on MRI and reduces risk of developing MS by 2 years (Optic Neuritis Treatment Trial)

· Recovery of visual functions in ON is observed spontaneously within 2-3 weeks in more than 80% of patients without treatment

Long-term management

· Most patients regain vision over one month, but often report persisting reduction in the quality of vision

· There is an associated risk of developing demyelinating disease (most commonly multiple sclerosis), especially if other neurologic symptoms and signs are present

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12
Q

Systemic associations?

A
MS or demyelination (ret or pap)
sinus related e.g ethmoiditis (ret) 
Lyme disease (ret or neu)
Viral infections (pap)
syphilis (pap or neu)
cat scratch fever (neu)
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13
Q

What is uhthoff’s sign?

A

worsening of symptoms with exercise or increase in body temperature. A key signs of optic neuritis.

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