Gradual Loss Of Vision Flashcards

1
Q

List the causes of gradual loss of vision

A

Cataract
Glaucoma
Age related macular degeneration
Trauma
Optic atrophy
Diabetic retinopathy
Corneal opacity
Refractive errors
Drugs and nutritional deficiencies
Ocular tumors
Retinitis pigmentosa

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2
Q

What is cataract?

A

Cataract is opacity of the lens and its capsule

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3
Q

What is the classification of cataract?

A

BASED ON AETIOLOGY
1.Congenital
(a) Heredity
(b) Maternal causes; Infections, Radiation, Drugs
(c) Foetal; Birth trauma, prematurity, Metabolic Diseases (galactosemia, hypoglycaemia), associated with other congenital anomalies (e.g. Lowe syndrome, Trisomy)

  1. Acquired
    (a) Senile cataract
    (b) Traumatic cataract
    (c) Complicated cataract; uveitic, Acute congestive angle closure glaucoma
    (d) Metabolic cataract; diabetes, galactosaemia, ↓Ca
    (e) Electric cataract
    (f) Radiational cataract; infra-red, x or γ-ray, ultraviolet ray
    (g) Toxic cataract e.g. corticosteroid-induced cataract, copper (in chalcosis) and iron (in siderosis) induced cataract.
    (h) Cataract associated with skin diseases – Dermatogenic cataract

BASED ON MORPHOLOGY
•Cortical
•Nuclear
•Capsular – anterior or posterior
•Subcapsular – anterior or posterior
•Polar – anterior or posterior
•Lamella
•Coronary
•Blue dot
•Membranous

BASED ON MATURITY
•Immature
•Mature
•Hypermature
•Morgagnian

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4
Q

What are the clinical features of cataract?

A

•Loss of vision (blurred, cloudy)
•Glare
•Coloured haloes
•Uniocular polyopia (double vision)
•Reduced VA

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5
Q

What are the management options for cataract?

A

•Treat any Underlying cause
•Medical management with eye drops that dilate the eyes
•Surgery
1.intracapsular cataract extraction (uncommon)
2.extracapsular cataract extraction
i) conventional
ii)manual small incision cataract surgery
3.phacoemulsification

NB:- Introduction of intraocular lens; There are 4 places where it can be attached-: Anterior chamber, Posterior chamber, Iris fixation, Sclera fixation.

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6
Q

What are the intraop complications of cataract surgery

A

1.Iris prolapse
2.Suprachoroidal haemorrhage (space between the choroid and sclera)
3.Zonular dehiscence (weakness or rupture of the zonules or suspensory ligament of the lens)
4.Posterior capsule rupture
5.Vitreous loss
6.Nucleus drop (a part of the lens that is cut off in cataract surgery)
7.Hyphaema (presence of blood in the aqueous humor/anterior chamber of the eye)

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7
Q

What are the postop complications of cataract surgery?

A

Early
1) Hyphema
2) Corneal edema
3) Acute endolphthalmitis
4) Shallow anterior chamber
5) Striae keratopathy
6) Iris prolapse

Late
1) Endolphthalmitis (inflammation of the inner coat of the eye from infection)
2) Lens subluxation
3) Bullous keratopathy (blister-like swelling of the cornea) from corneal edema
4) Dislocation of lens
5) Retinal detachment
6) Pseudophakic glaucoma
7) Posterior capsular opacity

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8
Q

What is glaucoma

A

A group of eye disorders that is characterized by progressive and characteristic optic neuropathy.

NB:- IOP may or may not be elevated

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9
Q

What is the classification of glaucoma?

A

Congenital and developmental glaucomas
1. Primary congenital glaucoma (without associated anomalies).
2. Developmental glaucoma (with associated anomalies).

Primary adult glaucomas
1. Primary open angle glaucomas (POAG)
2. Primary angle closure glaucoma (PACG)
3. Primary mixed mechanism glaucoma

Secondary glaucomas

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10
Q

List some glaucomatous changes in optic disc

A
  • Generalized or focalized increase in optic cup size
  • Increase in cup-disc ratio
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11
Q

What are the risk factors for primary open angle glaucoma?

A

Age
Family history
Myopia
Vascular disease - HTN migraine
Race

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12
Q

What are the clinical features of primary open angle glaucoma

A

•May be symptomless initially
•Visual disturbances
•Elevated IOP
•Corneal haziness in very high IOP
•Pupillary light reflex – normal → RAPD → APD

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13
Q

Which investigations are done for suspected POAG

A

•Slit lamp exam. to exclude causes of secondary glaucoma and Optic disc assessment – enlarged cupping
•Pachymetry (measures corneal thickness)
•Gonioscopy - (measures angle between iris and cornea)
•Visual field defects
•Optic disc or peripapillary RNFL imaging - Confocal scanning laser tomography, Scanning laser polarimetry and Optical coherence tomography

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14
Q

What are the treatment options for POAG

A

Medical – Pressure lowering drugs
• beta-blockers e.g. timolol, betaxolol
•Alpha-2 agonist e.g. brimonidine, Apraclonidine
•Miotics e.g. pilocarpine, carbachol
•Prostanglandin analogues e.g. latanoprost, travoprost
•Topical carbonic anhydrase inhibitors CAI e.g. Dorzolamide, brinzolamide
•Systemic CAI e.g acetazolamide, dichlorphenamide
•Osmotic agents e.g. mannitol, glycerol, isosorbide

Surgical
TRABECULECTOMY
Artificial drainage shunts

Laser trabeculoplasty
i) Argon laser trabeculoplasty
ii) Selective laser trabeculoplasty

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15
Q

What is normal variant glaucoma?

A

It is a variant of POAG. The IOP is usually normal.

Risk factors include female gender, family history, mutations in the OPTN gene.

There is also History of migraine, Raynaud phenomenon, Obstructive sleep apnoea syndrome

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16
Q

What is primary angle closure glaucoma?

A

Angle closure is occlusion of the trabecular meshwork by the peripheral iris leading to obstruction of aqueous humour drainage.

It can be primary or secondary and commonly affects women.

17
Q

List some of the risk factors for angle closure glaucoma

A

•Hypermetropia from short axial length
•Narrow and shallow anterior chamber
•Smaller cornea
•Plateau iris configuration
•Family history

18
Q

What are the ways primary angle closure glaucoma will present

A

➢Latent primary angle-closure glaucoma (primary angle-closure glaucoma suspect)
➢Subacute (intermittent) primary angle-closure
➢Acute primary angle-closure glaucoma
➢Postcongestive angle-closure glaucoma
➢Chronic primary angle-closure glaucoma
➢Absolute glaucoma

19
Q

Primary congenital glaucoma can be classified as

A

•True congenital glaucoma
•Infantile glaucoma
•Juvenile glaucoma

20
Q

Diabetic retinopathy is commoner in Type 1 DM

True or False?

A

True

21
Q

What are the risk factors for diabetic retinopathy?

A

Duration of diabetes
Poor control of diabetes
Pregnancy
Hypertension
Hyperlipidaemia
Smoking
Obesity
Anaemia

22
Q

What is the classification of diabetic retinopathy?

A

•Non proliferative diabetic retinopathy (NPDR)
•Proliferative diabetic retinopathy
•Diabetic maculopathy
•Advanced eye disease

23
Q

Age related macular degeneration is usually unilateral

True or false

A

False
It is usually bilateral
Usually seen in prime aged 65 and above

24
Q

What are the Russo factors for development of ARMD

A

•Age
•Race - caucasians
•Genetic* chromosome 1q32 for complement factor H (CFH)
•Smoking
•Diet - High fat intake, low antioxidants
•Hypertension

25
Q

What are the two clinical types of ARMD and their management

A

Atrophic/Dry/Non exudative ARMD
Associated with gradual loss of vision
TREATMENT
•No effective - Syfovre and Izervay
•Supplements(prophylaxis) – antioxidants : vitamin C, vitamin E, beta-carotene, zinc, copper (cupric oxide) to prevent zinc-induced copper deficiency
•Management of risk factors
•Low vision aid
•Laser photocoagulation

Neovascular/Wet/Exudative ARMD
Associated with severe visual loss
TREATMENT
•Photodynamic therapy (PDT) -
•Transpupillary thermotherapy (TTT)
•Surgical treatment in the form of submacular surgery
•Pharmacologic modulation with antiangiogenic agent

26
Q

List some of the characteristics features of retinitis pigmentosa

A
  • It’s a hereditary condition affecting rods more than cones
  • Affects males more than females
  • Starts in childhood
  • Slow progression
  • Bilateral
  • Rhodopsin gene mutation
27
Q

What are the clinical features of retinitis pigmentosa

A

•Night blindness
•Tunnel vision
•Dark adaptation problem
•Arteriolar attenuation, retinal pigmentary changes (bone spicule like hyperpigmentation)
•Optic disc pallor
•Tessellated fundus appearance
•Cystoid macular oedema
•Choroidal sclerosis, cellophane maculopathy
•Macular atrophy

28
Q

What are the treatment options for retinitis pigmentosa

A

No effective treatment

• Some things that can be done to either prevent it or reduce the rate of progression include;
1) Genetic counselling
2) Regular follow-up
3) Avoid smoking and retinotoxic medications
4) High-dose vitamin A supplementation
5) Low vision aid
6) Rehabilitation

29
Q

What are the possible causes of corneal opacity?

A

Trachoma
Infective corneal ulcers
Trauma
Entropion
Trichiasis
Vitamin A deficiency
Interstitial keratitis (growth of blood vessels into the cornea)
Harmful traditional eye medication
Corneal dystrophy
Onchocerciasis
Congenital corneal opacity (sclerocornea, trauma, ulcer, mucopolysaccharidosis, Peter’s anomaly, congenital hereditary endothelial dystrophy)

30
Q

What are the types of corneal opacity?

A

Nebular
Macular
Leucoma
Adherent leucoma
Kerectasia
Anterior staphyloma

31
Q

What is Xeropthalmia and what are the treatment options?

A

This is one of the ocular manifestations of vitamin A deficiency.

TREATMENT
- Treat cause
- Artificial tears
- Vitamin A supplements

32
Q

What is optic atrophy and what are the management options?

A

This is the degeneration of optic nerves following an insult.

Treatment is aimed at preventing further loss of optic nerves.

33
Q

List the class of drugs that can cause gradual loss of vision.

A

• Antituberculous drugs (ethambutol and isoniazid) - optic neuritis
• Chloroquine & Hydroxychloroquine – maculopathy and Vortex keratopathy
•Amiodarone - Vortex keratopathy which presents with bilateral, fine greyish or golden-brown opacities in the inferior corneal epithelium which may become whorl-like.
•Systemic steroids - cataracts and glaucoma
•Tetracyclines - (benign intracranial hypertension)
•Tamoxifen – retinopathy, maculopathy, optic neuritis
•Alcohol, smoking and nutritional deficiency - Tobacco-alcohol amblyopia, Methanol poisoning, Vitamin A deficiency