Visual Loss Flashcards

1
Q

Acute visual loss - common and rare causes?

A

Common - AACG, CRAO, vitreous haemorrhage, CVA/TIA

Rarer - temporal arteritis, retinal detachment, CRVO, optic neuritis, anterior ischaemic optic neuropathy

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2
Q

What is optic neuritis

Ix / Tx?

A

Demyelination of the optic nerve, often the first presentation of MS

Headache, painful eye movements, flashes, visual loss in one eye over a few days

Previous episodes, symptoms of MS, young female, positive MS family history

Exam: reduced visual acuity, visual fields and colour vision, RAPD, swollen/blurred disc (OPTIC DISC SWELLING)

Refer to neuro for MRI and give analgesia

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3
Q

What is vitreous haemorrhage?

Ix / Tx?

A

Bleed from retina into vitreous

Sudden loss of vision in one eye

Preceding flashes / floaters, CV disease risk factors, head trauma

Absent red reflex, unable to visualise fundus

Ix: USS. Tx: usually spontaneously reabsorbed but consider vitrectomy in large bleeds

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4
Q

What is anterior ischaemic optic neuropathy (AION)?

Ix / Tx?

A

Visual loss secondary to optic nerve ischaemia, can be arteritic (AAION) or non-arteritic (NA-AION).

AAION is ischaemic due to temporal arteritis, a medium-vessel vasculitis affecting those >50 years of age

NA-AION more common, usually slightly younger (60s > 70s), more likely if CV disease risk factors, male, clotting disorders.
Symptoms: sudden onset painless blurred vision in one eye, usually upper or lower visual field affected.
Exam: RAPD, reduced acuity, visual field loss, swollen disc

Ix: exclude temporal arteritis, screen clotting disorders and CV risk factors.

Mgmt: control risk factors, refer to ophth.

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5
Q

Causes of gradual visual loss?

A

Usually progressive and irreversible

Refractive errors
Cataracts
Age-related macular degeneration
Primary open angle glaucoma
Diabetic maculopathy
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6
Q

Refractive errors

A

Add in

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7
Q

What are cataracts?

Ix / Tx?

A

Gradual opacity of lens, most common cause reversible blindness. Gradual-onset blurred vision, reduce colour vision, glare (lights appear brighter) and halos around light

Most commonly caused by increased age. Also associated with: sunlight (UV) exposure, smoking, alcohol, trauma, diabetes, LONG-TERM CORTICOSTEROIDS, radiation, myotonic dystrophy, HYPOCALCAEMIA,

Exam: reduced red reflex, difficult to visualise fundus.

Ix: opthlamoscopy after pupil dilation - normal fundus and optic nerve, slit lamp - visible cataracts

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8
Q

How are cataracts classified?

A

Nuclear: change lens refractive index, common in old age

Polar: localized, commonly inherited, lie in the visual axis

Subcapsular: due to steroid use, just deep to the lens capsule, in the visual axis

Dot opacities: common in normal lenses, also seen in diabetes and myotonic dystrophy

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9
Q

Management of cataracts?

And its complications?

A

In early stages, age-related cataracts can be managed conservatively (stronger glasses/contacts, using brighter lighting. Optimises vision but does not slow progression, therefore surgery eventually needed).

Surgical extraction - only effective Tx, phacoemulsification - US to fragment lens, then suctioning it out, before inserting an artificial replacement

NICE suggests that referral for surgery should be dependent upon whether a visual impairment is present, impact on QoL and patient choice. Whether bilateral, possible risks and benefits. Prior to surgery, patients provide info on refractive implications of various types of intraocular lenses. After surgery, advise on use of drops and eyewear, what to do if vision changes and mgmt of other ocular problems.

High success rate: 85-90% of pts achieving 6/12 corrected vision (on a Snellen chart) postoperatively.

Complications following surgery
Posterior capsule opacification: thickening of the lens capsule
Retinal detachment
Posterior capsule rupture
Endophthalmitis: inflammation of aqueous and/or vitreous humour

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10
Q

What is age-related macular degeneration?

A

Commonest cause of blind registration in UK, progressive loss of central vision, currently affects 1% of population but rising

Wet or dry

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11
Q

What is DRY AMD?

A

Retinal pigment epithelium atrophy, degeneration of photoreceptors

Gradual distortion and loss of central vision

Risk factors: Smoking, >50, female, Caucasian

Exam: well define deposits on macula (drusen), central scotoma, distorted lines on Amsler grid

Slow progression, currently no Tx to halt visual deterioration - managed with low vision aids, lifestyle changes

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12
Q

What is WET AMD?

A

Neovascularisation of choroidal vessels into retina, RAPID distortion and loss of central vision.

Risk factors: Smoking, >50, female, Caucasian

Exam: distorted macula, haemorrhages, central scotoma, distorted lines on Amsler

Ix: Amsler grid, fluorescein angiography, retinal OCT

Fast progression, new vessels haemorrhage into viterous and obstruct vision

Intravitreal anti-VEGF (ranibizumab) to reduce neovascularisation

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13
Q

What is primary open angle glaucoma?

Risk factors / examination?

A

Progressive optic neuropathy - characteristic ‘cupping’ of optic disc and visual field defect. Often asymptomatic, usually detected by opticians

Loss of nerve fibres running from retina to optic nerve –> thinner ‘cup’ surrounding vessels at the disc

Risk: age, family history, Afro-Caribbean

Exam; visual field defects, optic disc cupping, increased IOP (usually)

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14
Q

Treatment of primary open angle glaucoma?

A

Lowering IOP only way to slow progression.

Medical: Latanoprost (prostaglandin analogue) Timolol (B-blocker), Brimonidine (a-agonist), Pilocarpine (muscarinic agonist), Acetazolamide (carbonic anhydrase inhibitors)

Surgical: trabeculectomy (surgical drainage channel out of anterior chamber)

Laser: trabeculoplasty (enhances aqueous drainage), ciliary body destruction (reduces aqueous production)

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15
Q

What is secondary glaucoma?

A

Angle open but trabecular meshwork blocked by:

  • inflammatory cells e.g. uveitis
  • blood vessels (iris neovascularisation secondary to retinal ischaemia in proliferative diabetic retinopathy)
  • iris pigment (e.g. pigment dispersion syndrome)

Long-term topical steroids can increase IOP and cause irreversible disc damage

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16
Q

What can cause flashes and floaters?

A

Flashes usually when retina displaced inappropriately (tractional pull or retinal tear) but Migraine with aura unrelated to retina

e.g. posterior vitreous detachment, retinal detachment, proliferative diabetic retinopathy

Floaters = opacities in vitreous gel - vitreous haemorrhage, posterior vitreous detachment, vitreous condensations (physiological changes due to age)

17
Q

What is posterior vitreous detachment?

A

Liquefying and shrinking of vitreous leading to separation from the retina

Symptoms: flashes of light, cobwebs in visual field (floaters)

History: myopia, trauma

Exam: occasional retinal detachments, vitreous haemorrhages

Tx: reassurance will resolve, look for signs of retinal detachment - if present emergency Oph review