Opthalmology Cases Flashcards

(22 cards)

1
Q

What are some risk facctcorts for age related macular degeneration

A

Increasing age >75
Smoking
Family history
HTN, diabetes etc

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2
Q

Features and signs of age related macular degeneration

A

Reduction of visual acuity (gradual in dy) (subacute in wet)

Reduced vision at night
Fluctuation in visual disturbance
Glare around objects/ flickering or flashing lights
Hallucinations -Charles bonnet syndrome

Amsler grid: Distortion of line perception
Fundoscopy: drusen

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3
Q

What investigations are done in age related macular degeneration.

A

Amsler grid: distortion of line perception

Fundoscopy: drusen

Slit lamp- identify pigmentary, exudative or haemorrhagic changes

Fluoresce in angiography - if neovascularisation is suspected (in wet)

Optical coherence tomography- used to visualise retina in 3 dimensions

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4
Q

How is age related macular degeneration managed

A

Dry- Zinc with anti-oxidant vitimans - A,C,E

WET: anti-VEGF agents - 4 weekly injections
Laser photocoagulation - risk of acute vision loss

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5
Q

What are the stages of hypertensive retinopathy

A

1: arteriolar narrowing and tortuosit, increased light reflex- silver wiring

2: ateriovenous nipping

3: cotton- wool exudates, flame and blot haemorrhages (may collect around fovea giving a macular star)

4: papiloedema

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6
Q

What are the stages of non proliferative diabetic retinopathy

A

Mild: 1 microaneurys

Moderate: microanurysms, bot haemorrhages, hard exudates (lipid deposits that leak out of damaged vessels), cotton wool spots (areas of retinal infarction)

Severe: blot haemorrhages and microanuerysms in 4 quadrants, venous beading (wall as of veins are no longer straight)

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7
Q

What are the key features of proliferative diabetic retinopathy (more common in type II)

A

Retinal neovascularisation- may lead to vitreous haemorrhage ( stormy sunset)

Fibrous tissue forming in front of retinal disc

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8
Q

What is the management for divetic retinopathy

A

Optimise glyceamic control, blood pressure, hyperlipideamia
Regular review by ophthalmology

Non-proliferative:
regular observation, panretinal laser photocoagulation if severe

Proliferative:
If change in visual acuity- anti vegf injections
Consider panretinal laser photocoagulation in proliferative or severe non-proliferative
If severe or vitreous haemorrhage- consider viteoetinal surgery

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9
Q

Features of acute angle-closure glaucoma

A

Features include:
Severe pain : ocular or headache
Decrease visual acuity
Symptoms worsen in dark
Hard, red eye
Haloes around lights
Semi dilated non-reacting pupil
Corneal oedema (dull or hazy cornea)

Systemic upset- nausea , vomiting even abdo pain

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10
Q

What are some factors predisposing to acute angle-closure glaucoma

A

Long sightedness- hypermetropia
Pupillary dilation
Lens growth associated with age

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11
Q

Investigations for AACG

A

Tonomotry- asses IOP
Goinoscopy- looks at angle

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12
Q

What is the manamagement for AACG

A

Combination of eye drops: direct parasympthetic (pilocarpine), beta blocker (timolol), alpha 2 agonist

IV acetazolamide - reduces aqueous secretions

Diffinitive: laser peripheral iridotomy - hole in peripheral iris

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13
Q

Open angle glaucoma features

A

Peripheral visual field loss - NASA’s scotoms (tunnel vision)
Decreased visual acuity
Optic cupping

Fundoscopy: optic disc cupping (optic disc widens and deepens),
Optic disc pallor (indicating optic atrophy)
Bayoneting of vessels (vessels have breaks as they disappear into deep cupping and reappear at the base)

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14
Q

Investigations for AOAG

A

Visual field testing
Slit lamp:
Tonomotry
Gonioscopy

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15
Q

What is the management for AOAG

A

360 selective laser trabeculoplasty if IOP >24 mmHg may need another at later date

Prostaglandin analogue eye drops - 2nd line

3rd line: beta blocker eye drops, carbonic anhydrase inhibitor eye drops, sympathomimetic eyedrops

In refractory cases:
Surgery- trabeculotomy

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16
Q

What are some common causes of vitreous haemorrhage

A

Proliferative diabetic retinopathy
Posterior vitreous detachment
Ocular trauma - most common cause in children and young adults

17
Q

What are the features of vitreous haemorrhage

A

Painless sudden vision r haze
Red hue in vision
Floaters or shadows/dark spots in vision

Signs: decreased visual acuity depending on size of haemorrhage
Visual field defect if severe haemorrhage

18
Q

Investigations for vitreous haemorrhage

A

Fundoscopy : haemorrhage
Slit-lamp: red blood cells in anterior vitreous
USS: rule out retinal tear/detachment
Fluorescein angiography- identify neovascularisation
Orbital CT- if open globe injury

19
Q

Management of vitreous haemorrhage

A

Urgert Opthalmoscopy referral
Manage underlying causes e,g, glycaemic control
Consider viteroretineal surgery if haemorrhage does not clear spontaneously

20
Q

What are some causes of optic neuritis

A

MS
Syphillis
Diabetes

21
Q

Features and investigation of optic neuritis

A

Unilateral decrease in visual acuity over hours or days
Poor discrimination of colours- red desaturation
Pain on eye movement
Relative afferent pupillary defect
Central scotoma

MRI of brain and orbits with gandalonium contrast is diagnostic

22
Q

What is the management of optic neuritis

A

High dose steroids

4-6 weeks recover