Topic A3 Flashcards

1
Q

What are the classifications of Optic Neuropathy

By cause

A

1) Inflammatory - Optic Neuritis + demylinating, parainfectious,infectious, non-infectious & neuroretinitis
2) Glaucomatous - various types of glaucoma
3) Ischaemic
- Anterior non-arteritic
- Anterior arteritic
- Posterior Ischaemic
- Diabetic Papillopathy
4) Hereditary
- Leber hereditary optic neuropathy
- Other hereditary optic neuropathies
5) Nutritional & Toxic
- Ethamnutol
- Vigabatrin
- Amiodarone
6) Papilloedema - secondary to raised ICP
7) Traumatic - Traumatic optic neuropathy
8) Compressive - including secondary to an orbital lesion
9) Infiltrative
- Inflammatory conditions such as sarcodosis
- Tumours
- Infective agents

ICP - Intra-cranial pressure

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2
Q

State cause & what it is to be differentiated from

What is Papilledema?

A

OD oedema which is secondary to elevated ICP
** Differentiate the OD oedema from other causes
Papilledema vs pseudo-papilledema
- ^presence of OD drusen
- usually bilateral

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3
Q

What are the symptoms of papilledema?

A

1) HA early morning + wakes px up from sleep
- more intense w head movement, bending & coughing
2) Transient Vision Loss - due to postural changes
3) No initial vision complaints
4) Sudden nausea & vomiting

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4
Q

What are the symptoms in the EARLY stage of papilledema?

A

1) Blurred disc margins
2) Swollen hyperaemic disc
3) Paton’s lines/folds
4) Dilation of superficial capillaries

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5
Q

VA+Fundus features

What are the symptoms in the ACUTE stage of papilledema?

A

1) Normal/Reduced VA
2) Severe disc hyperaemia
3) Moderate elevation w indistinct margins & absence of physiological cup (OD not in a defined shape)
4) Venous Engorgement
5) CWS
6) Flame-shaped haemorrhages
7) ONH appears enlarged as swelling increases
8) Paton lines (circumferential retinal folds)
9) Enlarged blind spot

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6
Q

What are the symptoms in the CHRONIC stage of papilledema?

A

1) VA is variable
2) Disc elevation w/o CWS or haemorrhages
3) Nerve fibre loss

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7
Q

What are the symptoms in the ATROPHIC stage of papilledema?

A

1) VA severely impaired
2) Prolonged raised ICP
3) Gross nerve fibre loss
4) Lesser disc swelling
5) Optic disc pallor
6) Optic atrophy (6-8wks)
7) Poor visual function

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8
Q

What is Spontaneous Venous Pulsations (SVP)?

**One of the symptoms for Papilledema

A

It is the pulsations caused by variations in the pressure gradient along the retinal vein as it travels through the lamina cribrosa.

**Differences in pulse pressure is because
1) Intraocular space
2) Cerebrospinal fluid

Normally occurs to 80% of the population as well.

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9
Q

What is the management for papilledema?

A

1) Urgent referral to neurologist / neuro-ophthalmologist
- CT scan
- Brain MRI
2) Differentiate from psuedopapilledema

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10
Q

What is Optic Neuritis/Papillae?

A

Swelling of the OD caused by local inflammation - associated w demyelination of axons = multiple sclerosis

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11
Q

What are the causes of optic neuritis/papillae?

A

Children:
- Mumps
- Meningitis
- Chicken Pox
- Upper respiratory tract infections

Adults:
- Viral Infection
- Toxoplasmosis

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12
Q

What are the signs & symptoms of Optic Neuritis/Papillae?

A

1) Mild/severe pain in or behind eye = vision loss in 1-2 days
2) Loss of vision to 6/18-6/60 = lasts 2-4 weeks
3) Usually unilateral
4) Age typically 18-45 years
5) Swollen & hyperemic disc but w lesser haemorrhage & CWS than papilledema
6) May have macular star
7) RAPD
8) Colour desaturation
9) Central Scotoma
10) May have cells in the vitreous

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13
Q

What is the management for Optic Neuritis/papillitis?

A

1) Urgent referral to a neurologist/neuro-ophthalmologist
2) Intravenous steroids

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14
Q

What is NAION?

A

Non-arteritic anterior ischemic optic neuropathy
This disease occurs due to occlusion of the short posterior ciliary arteries which leads to
partial/total infarction of ONH.

Infarction = obstruction of blood supply to an organ or a region of tissue

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15
Q

What conditions make it prone for people to get NAION?

A

1) small physiological cupping
2) Hypertension
3) DM
4) Usually >50 y/o

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16
Q

What are the signs & symptoms of NAION?

A

1) Sudden painless monocular visual loss, frequently on awakening
2) VA normal OR slightly reduced in about 30% of px
3) Moderate to severe visual impairment in the remaining 70% of px
4) VF defects = usually inferior altitudinal
5) CV defect proportional to the level of visual impairment
6) Diffuse/sectoral hyperemic disc swelling = often comes with splinter haemorrhage

17
Q

What is the management for NAION?

A

1) Immediate referral
2) Treatment
- No definitive treatment
- Some advocate short-term systemic steroid treatment

18
Q

What is AANION?

A

Arteritic Anterior Ischemic Optic Neuropathy

  • It is the ocular manifestion due to Giant Cell Arteritis (GCA).
  • Usually occurs in px >55 y/o
  • HA
  • Jaw claudication = pain with chewing
  • Scalp tenderness esp over superficial temporal arteries (tenderness while combing hair)
  • Proximal muscle & joint aches
  • aneroxia, weight loss
  • fever
19
Q

What are the signs & symptoms of AAION?

A

1) Sudden painless loss of vision usually to CF (severe loss)
2) Unilateral first & then progresses to bilateral within days
3) Optic disc pallor & oedema w surrounding flame-shaped haemorrhage
4) VF defect
5) RAPD
6) Colour desaturation
7) Optic atrophy within 4-8 weeks
8) Prognosis is poor where vision loss is usually permanent

20
Q

** What is GCA?

A

Giant Cell Arteritis
It is the swelling & thickening of the small artery under the skin around temporal artery

  • caused by inflammation in the arteries
  • affects px >50 y/o
  • this causes head pain, jaw pain & vision problems
  • closely linked w polymyalgia rheumatica
    **polymyalgia rheumatica = causes muscle pain & stiffness esp around the shoulders
21
Q

What is the management for AAION?

A

1) Immediate referral
2) Medical emergency in ophthal. in order to prevent further vision loss
- Erythrocyte Sedimentation Rate (ESR) - to test for inflammation & rule out GCA
- Temporal artery biopsy
- Cortiocosteroids
- Treatment done to prevent progression to fellow eye

22
Q

What is RAPD?

A

Relative Afferent Pupillary Defect

1) Marcus Gunn Response
2) Determined by “swinging flashlight test”
3) Causes: (Any optic nerve disease)
- Optic Neuritis/Papillitis
- Unilateral optic neuropathies
- Severe glaucoma
- Optic Nerve damage due to trauma, tumour & infections
4) any large/severe retinal lesions
such as;
- large RD
- CRVO
- CRAO

23
Q

Give a brief explanation on what is done during the swinging flashlight test and what is observed in a px w (+) RAPD

A

1) Light is shone in the RE first & both eyes CONSTRICT
2) Light is then shone in the LE & both eyes DILATE
3) Light is shone back to the RE & both eyes CONSTRICT

24
Q

What are the signs & symptoms of Adie’s (tonic) pupil?

A

1) Unilateral & dilated pupil w low response to light
2) Sluggish near response
3) Dilated pupil becomes miotic over time
4) usually occurs in women b/w the age of 20-40 y/o
5) Photophobia
6) Asthenopia (Eyestrain)

25
What happens during the pharmacological testing for Adie's pupil?
Diluted 0.125% pilocarpine eye drops in administered A rapid miotic response will be seen in the affected eye
26
What are the causes of Adie's pupil?
1) Denervation of postganglionic supply to the sphincter pupillae & the ciliary muscle due to viral illness 2) Mostly idiopathic although rarely there can be local disorders within order including tumour, inflammation & trauma **Idiopathic - unknown
27
What is the management for Adie's pupil?
1) Most px don't need treatment if diagnosis is confirmed 2) Unequal near additions 3) Tinted lenses
28
What is the management for Adie's pupil?
1) Most px don't need treatment if diagnosis is confirmed 2) Unequal near additions 3) Tinted lenses
29
What are the signs & symptoms of Horner's Syndrome?
1) Usually unilateral 2) Mild ptosis 3) Miosis resulting from unopposed action of sphincter pupillae - anisocoria is hence greatest in dim illumination as Horner's pupil does not dilate well 4) Reduced sweating in one side of the head in some cases 5) Hypochromic heterochromia = congenital/long-standing 6) Normal reaction to light to near reflexes
30
What happens during the pharmacological testing for Horner's Syndrome?
1) One drop of 0.5%/1.0% apraclonidine instilled in both eyes - Horner's pupil = Dilates - Normal pupil = Not affected 2) One drop of 4% of cocaine instilled in both eyes - Horner's pupil = Not affected - Normal pupil = Dilates
31
What are the causes for Horner's Syndrome?
Lesion in sympathetic pathway to the eye 1) Central (1st order neuron) - Stroke - Tumour 2) Pre-ganglionic (2nd order neuron) - Tumour - Neuroblastoma in children 3) Post-ganglionic (3rd order neuron) - Migraine - Trauma - Carotid disease - Cavernous sinus tumour
32
What is the management for Horner's Syndrome?
Refer IMMEDIATELY to rule out any major causes