Neuro-ophthalmology Flashcards

1
Q

Describe optic neuropathy?

A

-Neuropathy = disease or dysfunction of one or more peripheral nerves
-Damage to the optic nerve due to any cause – encompasses optic atrophy, optic oedema, optic neuritis
-Both swelling and atrophy give signs of optic neuropathy

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2
Q

Describe optic atrophy?

A

-Type of optic neuropathy
-Atrophy = wasting away
-Generally causes pale coloured nerve

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3
Q

Describe optic oedema?

A

-Type of optic neuropathy
-Oedema = swelling

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4
Q

Describe optic neuritis?

A

-Type of optic neuropathy
-‘itis’ = inflammation
-Kanski: inflammation, infection or demyelinating process of the optic nerve
-Retrobulbar neuritis = inflammation of optic nerve just behind the ONH  ONH may look normal but something behind it is causing inflammation
-MS is most common cause of optic neuritis –> demyelinating process of optic nerve

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5
Q

List all the possible symptoms a px with a neuro issue may have?

A
  • Decreased vision:
    o H&S important to find out if refractive problem or neuro
  • Pain
  • Headache:
    o Common symptom of neuro problem
  • Double vision:
    o Common symptom of neuro problem
  • Ocular motility problems:
    o If problem with nerve supply
  • Nystagmus / spontaneous eye movements
  • Pupillary abnormalities
  • Eyelid / facial / head abnormalities
  • Transient visual loss (short period of time)
  • Illusions / hallucinations
  • Higher cortical function:
    o Dyschromatopsia – colour defects – px experiences loss of intensity or saturation or total loss of colour perception
    o Visual agnosia – problem with recognition of visually presented objects
    o Micropsia – objects perceived to be smaller than actually are
    o Macropsia – objects perceived to be bigger than they are
    o Metamorphopsia – if px looks at grid of straight line, lines appear wavy, parts of grid may appear missing
  • Ataxia (loss of bodily movement), hemiparesis (weakness of one entire side of body) / hemisensory weakness (loss of sensation on one half of body)
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6
Q

Describe history of reduced vision in neuro and the symptoms/time course?

A

Associated symptoms
* – do they happen at the same time? w/ the reduced vision?
* Unilateral/bilateral:
o Unilateral: lesion anterior to chisam
 Some pxs may say if affects RE but they actually mean right side of their vision
 Get them to shut each eye to check this
 Homonymous hemianopia: pxs often describe as monocular involvement on side of affected hemifield
o Bilateral: either bilateral optic nerve or retinal, chiasmal or retrochiasmal disease
* Time course:
o Rules of thumb:
 Minutes: ischaemic retinal event
* Blockage of BV can happen v quickly & reduced vision happening v quick
 Hours: most commonly ischaemic, more likely optic nerve
 Days-weeks: more frequently inflammation (may reflect ischaemia)
 Months-years: compressive
o There could be overlap – not everything follows the above
o Pxs can become suddenly aware of chronic problem when fellow eye covered
 Ask px to describe what happened – px may describe that they covered eye

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7
Q

Describe sympathetic innervation of pupil?

A
  • Innervates dilator pupillae muscle
  • Info leaves eye, travels along short ciliary nerve, synapsing in ciliary ganglion
    o Keeps travelling towards brain via 3rd CN, synapsing at Edinger-Westphal nucleus & then hypothalamus
  • Sympathetic innervation going back to dilator pupillae, starts at hypothalamus, travels down spinal cord where it synapses, before travelling within spine to level between C8 & T1.
    o Travel upwards & synapse in superior cervical ganglion.
    o Continue to travel up to level of internal carotid artery (in neck).
    o Travel alongside ophthalmic division of trigeminal ganglion.
    o Fibres pass through ciliary ganglion w/o synapsing & join the short & posterior ciliary nerves back into eye & back to dilator – causing dilation of pupil in dim light
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8
Q

Describe parasympathetic innervation of pupil?

A
  • Innervates sphincter pupillae muscle – causes pupil constriction
  • Afferent pathway – light travels AWAY from eye to brain
    o If light shone into left eye (see left image), at optic chiasm it branches & ½ of info goes to R side of brain & ½ goes to L side & ends up in R & L pretectal nuclei
  • Efferent pathway – light travels from brain to Eye
    o Starts at pretectal nuclei, some info crosses over just as leaving pretectal nuclei – info from one pretectal nucleus goes to both eyes, travels to Edinger-Westphal nuclei, then via CN3, synapsing at ciliary ganglion & travelling into eye via short ciliary nerves, moving forward & innervating sphincter pupillae muscle
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9
Q

What are the four steps in investigating pupils?

A
  1. Observe size, shape & (a)symmetry of pupils
  2. Check for direct & consensual reflexes
  3. Swinging flashlight test (check for RAPD)
  4. Check for near reflex
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10
Q

Describe the first step in testing pupils - 1. observe size, shape & (a)symmetry of pupils

A
  • A distant, non-accommodative target (spot light) in dim light
  • Evaluate if px’s pupil are round, symmetrical, regular
  • Anisocoria:
    o Difference of >0.4mm between 2 eyes
    o 25% of normal have this in dim light, 10% in room light
    o If anisocoria is present, measure pupil sizes in dim & bright light
    o If difference remains constant in all light levels: likely to be normal
    o If difference largest in dim light: could be normal or possibly problem with dilation of smaller pupil
    o If difference largest in bright light: possibly problem with constriction of larger pupil
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11
Q

Describe the second step in testing pupils - 2. check for direct & consensual reflexes

A
  • Shine pen torch onto RE, observe R pupil reaction, remove
    o R direct
  • Shine pen torch onto RE, observe L pupil reaction, remove
    o L consensual
  • Shine pen torch onto LE, observe L pupil reaction, remove
    o L direct
  • Shine pen torch onto LE, observe R pupil reaction, remove
    o R consensual
  • Can get no response, or sluggish responses (or normal)
    o E.g. LE Direct no response
  • Magnitude of response correlated to degree of damage (not necessarily acuity)
  • Direct reflex affected: problem anywhere in nerve pathway
  • Direct reflex reduced but not absent: could be problem anywhere in nerve pathway
  • No direct reflex in one eye & no consensual reflex in other eye: likely to be problem inside eye/affecting nerve of eye where direct response affected
  • Direct but no consensual: problem with efferent (brain –> eye) of consensual eye
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12
Q

Describe the third step in testing pupils - 3. swinging flashlight test (check for RAPD)?

A
  • Shine light into one eye, observe direct and consensual response
  • After 2-3 seconds, QUICKLY swap the light to the other eye, looking for any change in pupil size of this eye
  • After 2-3 seconds, QUICKLY swap the light to the first eye, looking for any change in pupil size of this eye
  • RAPD:
    o Gross retinal abnormality (VA 6/60 or worse), in one eye or asymmetric
    o Impaired optic nerve function – unilateral – before optic chiasm
    o Asymmetric chiasmal compression – affecting optic chiasm but location affecting one eye more than other
    o Everything from optic chiasm backwards  NOT likely to get RAPD because nerve fibres have crossed over
  • 3 types of response:
    o Pupil stays constricted (normal) = no RAPD
    o Pupils dilate fully = total RAPD
    o Pupils dilate a little bit and slowly; sluggish response = partial RAPD
    o Magnitude correlated to degree of damage to nerve (not necessarily acuity)
    o Partial Left RAPD = LE has dilated a little when moved light onto it
  • RAPD: extra tips:
    o May be detected even if pupillary response in 1 eye cannot be evaluated – trauma, pharmacologic
    o RAPD does not result in anisocoria – RAPD & anisocoria are independent findings
    o Which 2 pathways are affected in a L RAPD? The afferent pathway from LE to left side of brain and the afferent pathway from LE to right side of brain
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13
Q

Describe the fourth step in testing pupils - 4. near reflex

A

o No condition where near reflex is solely affected – so in general, this is only needed if one of above 3 steps is abnormal  narrows down where problem is
o Look at distant, non-accommodative target – in dim light illumination
o Look at near, accommodative target - ~30cm – budge stick – look from spotlight to letter on stick – binocularly – should be constriction at near & dilation at distance

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14
Q

Which tests should be involved in fundus examination of neuro cases?

A
  • Volk lens to get 3D view
  • OCT
  • Pictures
    Plus: colour vision, contrast sensitivity, visual fields
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15
Q

Describe Visual Field Testing and lesions/what would you expect to see (neuro)?

A
  • Supplements acuity in assessing visual loss
  • Helps localise lesion along afferent visual pathway
  • Quantifies defect and assesses change over time – do it repeatedly on different visits
  • Choice of field testing
    o Degree of detail required
    o Patient’s ability to co-operate
  • Confrontational, Amsler, Perimetry
  • Post-chiasmal defects affect both eyes & respect vertical midline
    o Further back the defects are more congruous (similar between the two eyes)
    o Keep going back, defects are more homonymous (same part of VF in both eyes)
    o Further back in optic radiations towards cortex, macula is interpreted in different place to peripheral fibres so get macular sparing or just macula affected
  • Lesion at Retina:
    o If lesion affect RNFL, in general it would follow the RNFL pattern & respects horizontal midline due to anatomy of RNFL
    o Affects one eye only or would be difference/asymmetry between the 2 eyes
  • Lesion affecting Optic Nerve:
    o Large defect/lesion affecting optic nerve  no visual field in that eye but other eye unaffected
  • Lesion affecting nasal part of left optic nerve:
    o Produces temporal visual field defect in LE  one eye only
  • Lesion affecting centre of optic chiasm (where fibres cross):
    o Likely to cause bitemporal hemianopia
    o At optic chiasm –> macular fibres go through centre, inferior fibres cross anteriorly looping into contralateral optic radiations, superior fibres cross posteriorly looping into ipsilateral optic radiations before crossing over
    o Lesion on one side of optic chiasm just pressing –> nasal part of one eye affected
    o Lesion on one side of optic chiasm but pressing hard & compressing fibres on other side too –> binasal hemianopia
  • Lesion affecting optic radiations:
    o Both eyes affected – inferior right VFs
  • Lesion affecting further back in optic radiations:
    o Affects right VFs of both eyes with macular sparing
  • Lesion affecting primary visual cortex:
    o Affects right side of macula in both eyes
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16
Q

Describe colour vision in neuro?

A
  • Can help narrow down the location
  • Optic neuropathies manifest as red-green defects
    o Red desaturation –> bright red looks “maroon”
  • Problem w/ Optic nerve: dyschromatopsia > visual acuity loss
  • Problem w/ Macula: dyschromatopsia = visual acuity loss
  • Persisting defect even after visual recovery
17
Q

Describe contrast sensitivity in neuro?

A
  • Visual acuity tested at a high level of contrast
  • Contrast sensitivity is a more sensitive
  • Grating tests – Vistech:
    o Difficulty to administer and hard to reliably reproduce – results can vary
  • Pelli-Robson:
    o Single size optotype with gradually diminishing contrast level
    o Letters grouped in 3s
    o Px reads chart from top down until they can’t see anymore
    o VA at high contrast may be fine but then contrast sensitivity may be reduced if px is complaining of reduced vision
  • Useful in detection and quantitation of visual loss in presence of normal visual acuity