Posterior eye/retinal pathology Flashcards

1
Q

What is the vitreous body?

A

Gel inside eye ball that maintains structure of the eyeball and keeps retina pressed onto choroid.

Made of collagen and water and in age becomes less able to maintain its shape.

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2
Q

What is posterior vitreal detatchment?

A

Where the vitreous body comes away from the retina, common in older patients.

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3
Q

Clinical presentation of posterior virtual detachment?

A

Completely painless and asymptomatic.

Can present with spots of vision loss/floaters and flashing lights.

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4
Q

Management of posterior vitreous detachment?

A

No treatment required vision will improve as brain adjusts.

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5
Q

What conditions are patients with posterior vitreous detachment predisposed to?

A

Retinal tears

Retinal detachment

Both present in a similar way

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6
Q

What is retinal detachment?

A

The retina of the eye separates from the underlying choroid. This is usually due to an underlying retinal tear.

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7
Q

Why is retinal detachment sight threatening?

A

The retina relies on the blood vessels from the choroid for its blood supply and detachment can therefore lead to retinal ischaemia.

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8
Q

Risk factors for retinal detachment?

A

posterior virtual detachment

Diabetic retinopathy

Trauma to the eye

Retinal malignancy

Older age

Family history

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9
Q

Clinical presentation of retinal deatchment?

A

Acute onset peripheral vision loss

Blurred or distorted vision

Flashes/floaters in vision

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10
Q

Management of retinal detachment?

A

Slit lamp examination

Immediate referral to ophthalmology

Surgical intervention to create adhesions - e.g. Laser therapy or cryotherapy.

OR

Vitrectomy (vitreous body removed and replaced with oil or gas), scleral buckling or pneumatic retinopexy

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11
Q

Clinical presentation of retinal vein occlusion?

A

Blood clot or thrombus forms in the retinal veins at the back of the eye and blocks the drainage of blood away from the retina.

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12
Q

Course of the retinal vein and overall role?

A

Runs through the optic nerve and is responsible for draining blood from the retina.

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13
Q

Clinical presentation of central retinal vein occlusion?

A

Sudden loss of vision.

VEGF release leading to neovascularisation

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14
Q

Appearance of central retinal vein occlusion on fundoscopy?

A

Flame and blot haemorrhages
Optic disc oedema
Macula oedema
Neovascularisation

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15
Q

Risk factors for central retinal vein occlusion?

A
Hypertension 
Diabetes
Smoking
Glaucoma 
Sytemic inflammatory conditions 
SLE
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16
Q

Investigations for central retinal vein occlusion?

A

Fundoscopy and slit lamp examination

Full medical history 
Full blood count 
ESR (inflammatory disorders)
BP for HTN 
Serum glucose/Hba1c - diabetes?
17
Q

Management of central retinal vein occlusion?

A

Immediate referral

Laser photocoagulation
Intravitreal steroids (e.g. dexamethasone intravitreal implant)
anti-VEGF therapies e.g. Ranibizumab

18
Q

Clinical presentation of central retinal artery occlusion?

A

RAPD

Pale retina with CHERRY RED SPOT.

19
Q

Course of central retinal artery to the orbit?

A

Internal carotid artery branches into the ophthalmic artery which branches off to form the central retinal artery.

20
Q

Most common cause of central retinal artery occlusion?

A

Atherosclerosis

21
Q

What are the causes of central retinal artery occlusion?

A

Atherosclerosis

Temporal arteritis - vasculitis affecting the ophthalmic or central retinal artery reduces the blood flow.

22
Q

Risk factors for retinal artery occlusion?

A
Older age 
Family history 
Smoking
Hypertension 
Alcohol 
Diabetes
Poor diet
Inactivity
Obesity
23
Q

Typical patient of central retinal artery occlusion?

A

White female over the age of 50.

Already affected by RA/polymyalgia rheumatica/giant cell arteritis

24
Q

How are patients managed with central retinal artery occlusion?

A

Immediate referral

ESR blood test and temporal artery biopsy

If GCA - manage with high dose steroids.

If patients present acutely after vision changes - ocular massage, anterior chamber fluid aspiration and inhaling carbogen and sublingual isosorbide dinatrate can be tried.

25
Q

Long term management of central retinal artery occlusion?

A

Treat underlying risk factors

26
Q

What is retinitis pigmentosa?

A

Congenital condition - degeneration of rods and cones of retina in the back of the eye

27
Q

What are the causes of retinitis pigmentosa?

A

Isolated or associated with conditions.

Rods degenerate more than the cones - often present with night blindness.

Decrease in central and peripheral vision.

28
Q

Clinical presentation of retinitis pigmentosa?

A

Most symptoms start in childhood.

Night blindness - due to degeneration in rods

Peripheral vision lost before central vision

29
Q

Fundoscopy findings in retinitis pigmentosa?

A

Pigmentation is most concentrated around mid peripheral area of retina.

Narrowing of arterioles

Pale optic disc.

30
Q

Associated disease with retinitis pigmentosa?

A

Ushers syndrome (hearing loss + retinitis pigmentosa)

31
Q

Management of retinitis pigmentosa?

A

Referral

Vision aids

Sunglasses to protect retina against accelerated damage

Driving limitations/informing DVLA

Oral acetazolamide, anti-VEGF treatments are some specialist options that can be considered.

Regular follow up