Gradual Visual Loss Flashcards

1
Q

cataracts importance/stats

A
#1 cause of blindness
increases with age (100% 100yo)

RF: age, UV, smoking, alcohol, CST, DM, renal, radiation, Down’s, myotonic dystrophy

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2
Q

types of cataracts

A
fibrotic: total; atopy;
age-related/subcapsular
nuclear sclerotic
cortical: radial spokes
blue dot: congenital
snowflake: DM osmotic hydration
traumatic: iris torn
metabolic: galacotsaemia, wilson's
other: uveitis, high myopia, steroids, chlorpromazine (yellow)
systemic: myotonic dystrophy (Xmas tree), Marfan's, NF2
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3
Q

classification/aetiology

A

anatomical:
posterior subcapsular (PSC): vacuolated; DM/steroids
cortocal: radial spokes; UV, DM, drugs
nuclear: yellow/brown, distance > near;

aetiological:
age-related
congenital
traumatic: iris/lens damage
metaolic
toxic
secondary
systemic disease
maternal infection

developmental:
immature
mature: completely opaque cortex
hypermature: small, wrinkled, leaky

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4
Q

phaco detail

A
corneal incision, maintain pressure, anti-scar
peel off anterior capsule
US high frequency probe to fragmaent
aspirate and replace after irrigation
close edges of flap
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5
Q

differentials for GLoV

A

corneal dystrophy, ectasia (detail)
lens: cataract
macula: AMD, dystrophy, DM/CSMO
optic disc: compression, toxins
retina/choroid: RP (spicules, nyctalopia, optic atrophy, ring scotoma)
other: choroidal melanoma, stargardt, tobacco-alcohol amblyopia (CN)

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6
Q

age-related and congenital

A

age: commonest; multifactorial (allergy, BP, LD, UV, infrared, DM)
anterior or posterior, bright lights,
posterior: near > far; DM/steroids

congenital: 33% inherited; present at birth; variable; amblyopia risk

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7
Q

traumatic

A
rosette-shaped lens damage
penetrating eye injury: direct damage
blunt injury: pigment onto lens (Vossius ring)
Glass blower's (infrar red); anterior
shock; ionising radiations
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8
Q

metabolic

A

DM: age-related earlier,; true juvenile (snowflake); true DM (osmotic hydration; snowflake capsules)

galactosaemia: oil-drop
Wilson’s: red/brown sunflower
hypocalcaemia, Fabry’s, mannosidosis

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9
Q

toxic

A

CST: posterior subcapsular, esp with CST

chlorpromazine: fine yellow spots, anterior capsule
chemotherapy (busulphan)

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10
Q

secondary

A
uveitis
hereditary retinal generation e.g. RP
high myopia
glaucomflecken (grey/white specks), anterior sucap, PACG
ciliary malignant melanoma: sectoral
post-op glaucoma: posterior subcapsular
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11
Q

systemic disease

A

cutaneous: atopic eczema (posterior stellate/anterior shield/fibrosis)
CTD: Marfan’s, mm dystrophy (xmas tree)
CNS: NF2
Down’s/Alport’s syndrome

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12
Q

maternal infection

A
rubella: 50% cataracts
toxoplasmosis,
CMV
thalidomide
CMV
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13
Q

clinical features

A

change in vision: VA, contrast, yellow/brown tint, glare, ghosting, monocular/diplopia

change in fundus: diffult view

change in refraction: myopic shift, astigmatism

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14
Q

investigations

A

history + slit lamp
comorbidities

ocular B scan USS: rule out posterior pole pathology/posterior segment

refraction + biometry for IOL:
axial length (A-scan), corneal diopters (keratometry), anterior chamber depth
corneal integrity (post-op risk e.g. oedema)
*leave myopic: near vision
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15
Q

management

A

assessment: disability, experience, VA, ocular pathology, general health, age, development stage, biometry

no medical; can try lenses
surgery:
phacoemulsification
intracapsular cataract extraction (ICCE)
ECCE
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16
Q

phaco complications

A

choroidal detachment, capsule phimosis, pupillary block, hyphaema, cystoid macular degen, retinal detachment, vitreous loss, acute endohpthalmitis

later:
astigmatism, lens dislocation, cornea oedema, capsule opacification (laser capsulotomy, 20%), chronic uveitis/endophthalmitis, wrong IOL power

17
Q

posterior subcapsular (PSC)

A

vacuolated/plaque-like
associated with DM and steroids
reading > distance

18
Q

acute endophthalmitis

pain + redness

A

0.1%; worst complication
staph epi, staph aureus, pseudomonas

pain, LOV, red reflex lost, corneal haze, fibrin exudate, hypopyon

IV ABx