Ophthalmology Flashcards

1
Q

Argyll-Robertson pupils?

A

It is sometimes seen in neurosyphilis. A mnemonic used for the Argyll-Robertson Pupil (ARP) is Accommodation Reflex Present (ARP) but Pupillary Reflex Absent (PRA)

Features
small, irregular pupils
no response to light but there is a response to accommodate

Causes
diabetes mellitus
syphilis

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2
Q

Peripheral curtain over vision + spider webs + flashing lights?

A

Retinal detachment

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3
Q

Differentiate between Episcleritis and scleritis?

A

In episcleritis, the injected vessels are mobile when gentle pressure is applied on the sclera. Typically painless

In scleritis, vessels are deeper, hence do not move. Painful

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4
Q

Features of glaucoma?

A

red eye, severe pain, haloes, ‘semi-dilated’ pupil

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5
Q

Features of uveitis?

A

red eye, small, fixed oval pupil, ciliary flush

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6
Q

Summary of Subconjunctival haemorrhage

A

Causes:
Clotting disorders
Systemic HTN
Spontaneous
Strenuous activity, heavy lifting, coughing, WL.
Warfarin, NOACs
1 of BV in conjunctiva ruptures, releases blood in space between sclera + conjunctiva

Sx:
Bright red (due to exposure to ambient O2 levels)
Painless
Doesn’t affect vision

Tx:
Self limiting

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7
Q

Summary of corneal foreign bodies/abrasion?

A

Corneal injury, vasodilation of scleral vessels = limbal/ciliary flush

Causes: contact lenses (infection w pseudomonas), FB, fingernails, eyelashes, entropion (inward turning eyelid)

Sx:
Extreme pain + epiphora (watering) 
Red
FB sensation 
Blurred vision 
Photopia 
Ring of inflam around FB

Complications:
Corneal ulceration + keratitis

Ix:
Fluorescein stain applied. Yellow/ orange colour, collects in abrasions or ulcers
Slit lamp exam

Refer: threat to vision, penetrating eye injury, sig orbital or peri-ocular trauma. FB organic (soils, seeds ↑risk of infection), FB near centre of cornea. Red flags (severe pain, irreg dilated or non-reactive pubils, sig ↓in visual acuity)

Tx:
Removed using needle
Simple analgesia, lubricating eye drops, eg diclofenac ophthalmic, ketorolac ophthalmic, ibuprofen. 
Most abrasions heal within 1-2 days. 
Topical gentamicin in contact wearers
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8
Q

Summary of corneal erosion?

A

Detachment of corneal epithelium from tissue layers below

Spont due to lack of regen capacity of cornea: corneal dystrophy, corneal uclers, DM, contact lens use, dry eye disease. Injury of cornea

Sudden onset of Sx similar to those of corneal abrasion, typically upon waking or without obvious signs of trauma

Artificial tears + nightly lubrication drops

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9
Q

Summary of corneal ulcers

A

Open sore of cornea physical, chemical trauma or infection. Usually due to corneal drying + exposure

RF: contact lens overwear/ misuse, prolonged use of steroid eye drops, dry eye syndrome, eyelid disorders, Bells palsy, herpes zoster/ simplex, corneal burns, injuries.

Sx:
Grey/white opaque or translucent area on normally clear + transparent corena
Pain 
Redness
FB sensation 
Photophobia 
Blurry vision 
Eye watering 

Comps:
Can cause LOV, refer
Most commonly occurs as complication of keratitis

Slit lamp + fluorescein
Focal fluorescein staining in cornea

Scape ulcer, MC+S, wide spectrum Abx eye drops

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10
Q

Summary of conjunctivitis?

A

Inflam of conjunctiva
Bacterial: unilat 1st then bilat
Viral: unilat 1st + bilat due to rubbing + transfer

Types:
Bacterial: discharge, red, sticky in morning, gritty eye
Allergic: red, itchy, swelling, watery discharge. Bilat.
Viral: red, watery, recent URTI, preauricular LN, follicles (bumps on inner part of eyelid

Beware chlamydia infection in eye = refer
Newborns: ophthalmia neonatorum (very severe + dangerous)
Refer if <1mnth as neonatal conjunctivitis can be associated with gonococcal infection + can cause loss of sight/ pneumonia

Ix:
Acuity, pupillary responses unaffected 
May be photophobia 
Advice not to share towels
School exclusion not necessary 
Contact lenses should be avoided 
Normally self-limiting in 1-2 wks 

Tx:
Bacterial: chloramphenicol drops, 2-3hrly. Topical fusidic acid for pregnant
Allergic: antihistamine drops (cetririzine, loratadine). If LT, topical mast cell stabilisers eg sodium cromoglicate + nedocromil. Topical NSAIDs: ketorolac, diclofenac.
If severe: topical steroids/ ciclosporin

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11
Q

Summary of entropion?

A

Inward growing eyelid, lashes rubbing inward too.
Common in elderly

Foreign body sensation
Watery eyes

Ectropion: turning out of eyelids

Lubricant eye drops

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12
Q

Summary of blepharitis?

A

Inflam of eyelids, can be chronic due to build-up of myblobian glands
Seborrheic dermatitis/ staph infection

RF: oily skin, dandruff, pts with rosacea

Sx:
Thick secretions, crust/ inflam of eyelid. Bilat 
Eyelids sticky in morn
Red eye
Grittiness/discomfort
Burning/ itching 
Dry eye 
Conjunctival hyperaemia
Photophobia 
↓vision 
Styes + chalazions 

Topical Abx: topical chloramphenicol oral tetracycline, doxycycline

Clean eyes reg
Soften lid margin using hot compress 2X a day
Mechanical removal of debris from lid margin. Cotton wool dipped in cooled boiled water, baby shampoo
Artificial tears
Topical CS

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13
Q

Summary of pterygium

A

Triangular fold in sclera or conjunctiva.
Common in tropical countries, UV damage. Inflam, chronic irritation of eye

Wing shaped fibrovascular overgrowth from conjunctiva onto corneal surface
Ocular irritation, burning + tearing

Can be loss of vision if covering a lot, blurred/double vision

Sunglasses + lubricating eye drops. Wide brimmed hats
Artificial tears
Surgery if affecting vision

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14
Q

Summary of keratitis

A

Inflam of cornea

Bacterial: most common, s aureus, pseudomonas (contact lens)
Viral, acanthamoeba (eye exposure to soil or contaminated water),
Fungal, non-infectious.
Parasitic: onchocercal keratitis (river blindness)
Photokeratitis: cornea damaged by severe UV light, pain, welder’s

Sx:
Bacterial: purulent discharge, hypopyon, round corneal infiltrate/ ulcer.
Pain + redness
FB sensation
Photophobia
XS tearing
Blurry vision
Corneal clouding
Periumbilical injection
Herpes simplex: dendritic/geographic corneal ulcer.
Herpes zoster: ↓corneal sensation, punctate lesion on corneal surface, vesicular eruption on forehead, nose.
Acanthamoeba: contact lenses, corneal ring infiltrate.

Comps:
Corneal scarring
Perforation 
Endophthalmitis
Visual loss

Ix:
Slit like exam
Emergency, can lead to irreversible vision loss left untreated
Same day referral to eye specialist usually required to rule out microbial keratitis
Stop using contact lenses until Sx resolved

Tx:
Topical broad spec Abx. Quinolones
Oral acyclovir, valacyclovir
Topical steroids
Topical acyclovir
Topical antiseptic eg chlorhexidine with propamidine
Antimycotics: natamycin, nystatin, amphotericin B
Cycloplegic for pain relief e.g. cyclopentolate

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15
Q

Summary of scleritis?

A

Inflam of full thickness of sclera, not usually caused by infection, contents of eye can pop out.

Systemic inflam condition: RA, SLE, gout, granulomatous with polyangiitis + polymyositis.

Sx:
Severe PAIN
Pain w eye movement
Photophobia 
Eye watering 
Gradual ↓ in vision 
Scleral thinning: may appear violet or blue discolouration of eye.

Most severe, necrotising scleritis (visual impairment but no pain + can lead to perf of sclera).

Ix:
Abnormal pupil reaction to light
Refer, medical emergency

Tx:
NSAIDs + steroids
Immunosuppression appropriate to underlying systemic condition

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16
Q

What is episcleritis?

A

Inflam of episcleral, outermost layer of sclera, just underneath conjunctiva
Nodular: raised area
Not usually caused by infection
Young + middle aged, inflam disorders RA + IBD

Sx:
Localised redness, not diffuse
Classically not painful
Watering + mild photophobia 
FB sensation 
Dilated episcleral vessels.

Ix:
Injected vessels, mobile when gentle pressure is applied to sclera, in scleritis vessels deeper, don’t move
Safety net, benign, self limiting

Tx:
Artificial tears
Phenylephrine drops: blanches conjunctival + episcleral vessels, not scleral. If eye redness improves = episcleritis

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17
Q

Summary of trichiasis?

A

Lashes rubbing against eye, eyelash grow inwards
Can cause blepharitis

Sx:
FB sensation, grittness, discomfort
Sx usually bilat

Ix:
No referral
Regularly come back

Tx:
Remove with forceps
Fine needle, laser to damage hair follicles.

18
Q

Summary of primary open angle glaucoma?

A

↑IOP.
Iris clear of trabecular meshwork. ↑ resistance to outflow. ↑aqueous production/ ↓outflow.
RF: age, genetics, afro Caribbean, myopia, DM, HTN, CS
2° to uveitis, vitreous haem, retinal detachment. Thickening of trabecular lamellae (↓pore size), ↓in no of trabecular cells, ↑ECM in trabecular meshwork.

Sx:
Insidious 
Periph visual loss, nasal scotomas, tunnel vision. 
↓visual acuity
Optic disc cupping 

Ix:
Fundoscopy: optic disc cupping, cup to disc ratio >0.7, optic disc pallor (atrophy), bayonetting of vessels (vessels have breaks as they disappear into deep cup + re-appear at base), cup nitching (usually inf where vessels enter disc), disc haem.
Automated perimetry asses visual field
Slit lamp w pupil dilation, assess optic N + fundus. Optic N head damage.
Measure IOP >24

Tx:
1st: prostaglandin analogue latanoprost.
2nd: BB (timolol), carbonic anhydrase inhib (dorzolamide), sympathomimetic eyedrop (brimonidine, α 2 adrenoceptor agonis).
Miotics: pilocarpine
Laser, periph iridotomy, creates tiny hole in periph iris > aqueous humour flowing to angle.
Surgical trabeculectomy: alternative drainage pathway between ant chamber + subconjunctival space.

19
Q

Summary of angle closure glaucoma?

A

RF: hypermetropia (long sightedness), pupillary dilation, lens growth, age, small eyes
Iris covering, chronic/ acutely. Narrow/ closure of ant chamber angle, inadequate drainage, ↑IOP, optic N damage.
Sometimes response to pupil dilatation (periph iris bunches up in angle), resistance ↑, pressure ↑, iris bow forward, closes drainage angle
2°: trabecular meshwork damage, trauma (blood/direct damage), pigment from iris (pigment dispersion syndrome), ocular surgery, ↑episcleral venous pressure, abnormal iris BVs (prolif diabetic retinopathy), steroid induced, cataract (swell, push iris forward to close drainage angle).

Sx:
Severe pain: ocular or headache 
↓visual acuity 
Hard red eye 
Haloes around light 
Sx worse with mydriasis eg watching TV in dark room
Conjunctival redness,
Corneal oedema,
Cloudy cornea. Photophobia, 
Eye watering. 
Ix:
Semi dilated non reacting pupil 
Fundoscopy 
Tonometry: ↑IOP, 60 
Lie pt back 
Slit lamp: visualise angle (gonioscopy), assess periph ant chamber configuration + depth, optic nerve head damage visible under slit lamp. 

Tx:
Urgent referral, can damage optic nerve.
Combo of eye drops: eg pilocarpine, BB, α 2 agonist
IV acetazolamide
Laser peripheral iridotomy, tiny hole in peripheral iris once acute attack settled

20
Q

Summary of anterior uveitis/iritis

A

Inflam of ant portion of uvea, iris + ciliary body.
Associated with HLA-B27
Associated conditions: ankylosing spondylitis, reactive arthritis, UC, CD, Behcet’s disease, sarcoidosis (bilat disease may be seen)

Sx:
Red eye 
Acute onset 
Ocular discomfort + pain, ↑with use 
Pupil small, +/- irregular > sphincter muscle contraction 
Photophobia (intense) 
Blurred vision 
Lacrimation 
Ciliary flush: ring of red spread out 
Hypopyon: pus + inflam cells in ant chamber, visible fluid level 
Visual acuity initially normal > impaired 
Floaters/ flashes 

Tx:
Urgent review by ophthalmology
Cycloplegics: dilate pupil which helps relieve pain + photophobia e.g. atropine, cyclopentolate
Steroid eye drop

21
Q

Summary of vitreous haemorrhage?

A

Bleeding into vitreous humour.
Disruption of any vessel in retina, extension through retina from other areas
Once bleeding stops, blood typically cleared from retina at 1% per day
Causes: prolif diabetic retinopathy, post vitreous detachment, ocular trauma, bleeding disorders, anticoag, retinal detachment, macular degen, post vitreous detachment

Sx:
Sudden painless loss of vision or haze
Disruption to vision from floaters to complete vision loss
Numerous dark spots
Red hue in vision
Visual field defect
Vitreous appear black against red reflex

May precede a retinal detachment

Ix:
Dilated fundoscopy: haem in vitreous cavity
Slit lamp exam: RBC in ant vitreous
USS: rule out retinal tear/ detach, find cause
Fluorescein angiography: identify neovascularisation
Orbital CT: used if open globe injury

Tx:
Find source of bleeding + stop

22
Q

Summary of posterior vitreous detachment

A

Separation of vitreous membrane from retina
Due to natural changes to vitreous fluid of eye with ageing. Becomes less viscous, doesn’t hold shape as well, pulls vitreous membrane away from retina to centre of eye.
Highly myopic (near sighted) pts at risk earlier in life, myopic eye has longer axial length
75% of >65, F>M

No pain/loss of vision
Sudden floaters/ flashes of light
Blurred vision
Cobweb across vision

Retinal detachment: dark curtain descending

Weiss ring on opthalmoscopy: detachment of vitreous membrane around optic nerve to form ring shaped floater
Examined by opthalmologist within 24 hrs.

Sx gradually improve over 6mnths. No Tx
If associated retinal tear or detachment, surgery.

23
Q

Causes of gradual vision loss?

A

Cloudy media: cataract, corneal opacity, vitreous haem, chronic glaucoma

Medial clear: ARMD, optic neuropathy, macula dystrophy, CN disease, retinal dystrophy. Optical neuropathy

24
Q

Causes sudden visual loss?

A

Painful: angle closure glaucoma, uveitis, corneal ulcer/ keratitis, endophthalmitis, retrobulbar optic neuritis, orbital cellulitis, giant cell arteritis

Painless fleeting: embolic retinal artery occlusion, migraine, ↑IOP, prodrome in giant cell arteritis

Painless prolonged: ischaemic optic neuropathy, retinal a/v occlusion, retinal detachment, ARMD, vitreous haem, orbital disease affecting optic N, IC disease affecting visual pathway. Amaurosis fugax.

25
Q

Summary of central retinal vein occlusion

A

RF: age, HTN, CVD, glaucoma, polycythaemia.

Sudden, painless, vision loss/↓acuity

Fundoscopy: widespread hyperaemia. Severe retinal haem, stormy sunset.

Conservative
Tx indications: macular oedema (anti-VEGF), retinal neovascularisation (laser)

26
Q

Summary of Central retinal a occlusion

A

Causes:
Thromboembolism, arteritis

Sx:
Sudden unilat visual loss

Ix:
Cherry red spot on pale retina
Affterent pupil defect

27
Q

Summary of retinal detachment

A

RF: age, prev cataract surgery, myopia, eye trauma, FHx, PMH of retinal break/ detachment
Rhegmatogenous: post vitreous detachment creates traction by vitreous humour on specific part of retina, causing tear
Non-rhegmatogenous: pulled off by contracting fibrous tissue on retinal surface eg prolif DR, retinopathy of prem. Fluid can accumulate in sub retinal space due to exudative process, due to tumours or toxaemia of preg

Sx:
Floaters or flashes: pigment cells entering vitreous space or traction on retina
When rdetaches: sudden onset progressive visual loss, shadow or curtain, starts periph, progresses centrally. Progression rapid
If macula detaches: marked fall in visual acuity with central visual loss
Straight lines appear curved
Infants: squint or white pupillary reflex

Ix:
Opthalmic emergency, untreated, permanent vision loss due to ischaemia of retinal layer. Reversible if Tx before macula affected
Fundoscopy: waxy, changes with eye movement, changes in vessel direction, tear in retina appears pink/ reddish because of underlying choroidal vessels. May be debris in vitreous comprising blood + pigment. Red reflex lost. Retinal folds pale, opaqe or wrinkled.

Tx:
Close break in retina ↑strength of attachment between retina + RPE by inducing inflam, cryoprobe or laser.
External (conventional): indent sclera with externally located silicone band, relieving vitreous traction + apposing RPE to retina. May require drainage 1st.
Internal (vitreoretinal): virectomy, relieving traction, fluid drained through causative break, laser or cryotherapy to surrounding retina.

28
Q

Summary of macular holes

A

Holes centre of macular region, destroy fovea, major loss of visual acuity. Due to vitreous traction on thin macular retina, idiopathic

29
Q

Summary of central serous retinopathy

A

Localised accumulation of fluid between neuro retina + RPE separates 2 layers causing photoreceptor disturbance

Due to breakdown of barrier function of RPE, usually unilat, affects young/middle ages males

Visual distortion + blurring, visual acuity may fall markedly

Exam: dome shaped elevation of retina

Usually self remitting

30
Q

Summary of macular oedema

A

EC accumulation of fluid within retina
Associated with: intra-ocular surgery, uveitis, retinal vascular disease, retinitis peigmentosa, DM, ARMD

Sx
Distorted + blurred vision

Ix
Loss of normal foveal reflex
Fovea have cystic apperance
Optical coherence tomogram or fluorescein angiogram

Tx:
Anti-VEGF
Laser
Vitrectomy

31
Q

Summary of toxic maculopathies

A

Accumulation in drugs in RPE can cause macular damage
Anti-malarial chloroquine + hydroxychloroquine
Phenothiazines, tamoxifen

If detected early reversible

If target lesion seen metamorphopsia + irreversible central visual loss

32
Q

Summary of retinas pigmentosa

A

In isolation or systemic disease
Inheritance: Usher syndrome, Abetalipoproteinaemia, Lawrence-Moon Biedl syndrome, Kearns-Sayre syndrome, Alport’s, Refusum disease (cerebellar ataxia, periph neuropathy, deafness, ichthyosis),
Affects both types of photoreceptors, particularly rods

Poor night vision 1st
Primarily periph retina > tunnel vision. Central ultimately lost
Impaired dark adaptation, difficult entering cinema/ going outside
Photopsia: flashes of light
Early development of cataracts common
Glare from bright light

Cone dystrophy: less common than rods. AD. Pt presents 1st decade of life with poor vision. Abnormal banded macula appearance > bulls eye target.

Ix
Fundoscopy: periph clumps of black retinal pigmentation ‘bone spicule’, attenuation of retinal arterioles, disc pallor (optic atrophy), mottling of retinal pigment epithelium.
Full field electroretinogram

Tx:
Nothing can be done to prevent progression of disease
Visual aids
Vit A retinol supplementation

33
Q

Summary of albinism

A

Congen condition, skin, eyes, hair, partially/ completely devoid of pigment
Oculocutaneous: eyes, skin, hair. AR. 7 types OCA1, OCA2 most common
Ocular: only eyes, OA1 most common, X-linked recessive. Nettleship-Falls syndrome. Lack of pigment in retinal epithelium

Complete/ partial absence of skin pigmentation
Light yellow/ white hair
Light eye colour, light blue (parital pigment production), pink (complete absence)

Complications
↑sunburn + skin ca
Visual development in fetus dependent on melanin production. Abnormal arrangement in optic N fibres (abnormal optic chiasm), severe sensitivity to light, poor visual acuity due to foveal hypoplasia. Amblyopia/nystagmus

Ix
Marked transillumination: red reflex seen through iris because of lack of pigmentation

34
Q

Summary of retinoblastoma

A

Malig tumour of eye, embryonal tumour of retinal cells
5% visual impairment in children
Inherited AD or sporadic.
Retinoblastoma gene tumour suppressor on Chr13, incomplete penetrance.

Sx
Mean age 8 mnth if inherited, 25mnth if sporadic, rare >5.
Inherited bilat
Absent red reflex, instead white pupillary reflex (leukocoria), light scatter from pale tumour at post pole of eye.
Squint due to ↓vision
If advanced painful red eye

Complications
Pseudo-orbital cellulitis

Ix:
CSF + BM for mets
MRI, biopsy not taken
Fundoscopy + exam: whitish-pink mass, retinal detachment, retinal vessels visible behind lens, vitreous +/or subretinal seeding
Ophthalmic A + B scan US: A scan: variable or ↑ internal reflectivity, B: mass filling globe with calcification + shadowing.

Tx:
Enucleation not only option = removal of eye
External beam radiation, chemo, photocoagulation
Genetic counselling
>90% survive into adulthood, some 50% of children develop 2° tumour, esp sarcoma. Many have permanent visual impairment

35
Q

Summary of age related macular degeneration

A

Most common cause of blindness in UK. Degen of central retina (macula), usually bilat.
RF: ↑age, smoking, FH, HTN, DM.
Retinal pigment epithelium removes + processes used discs of photoreceptor outer segments. Over time, undigested lipid products (age pigment lipofuscin) accumulate in REP + XS material transferred to Bruch’s membrane (between RPE + choroid layer) impairing its diffusion properties
Dry: 90% atrophic. Drusen.
Wet: 10%, exudative or neurovascular. New vessels from choroid stimulated by angiogenic factors eg VEGF, grow through Bruch’s membrane + RPE into sub- retinal space. Leakage of serous fluid + blood > rapid vision loss. Worst prognosis.

Sx:
Subacute visual loss
↓visual acuity, particularly near objects
Difficult dark adaptation, ↓night vision.
Fluctuations in visual disturbance, may vary day to day.
Photopsia (flickering or flashing lights) glare around objects
Distortion of line perception on Amsler grid testing.
Metamorphosia

Ix
Slit lamp microscopyy pigmentary, exudative or haem changes affecting retina. Drusen (yellow round spots, dry). Wet (well demarcated red patches, haem)
Fluorescein angiography: if wet, guide intervention with anti-VEGF
Ocular coherence tomography: visualise retina in 3D, reveal damage not visible on microscopy alone.
Foveal reflex absent, grey discolouration of retina > neovascularisation

Tx
Zinc with anti-oxidant A/C/E: ↓ progression. Dry.
Anti-vascular VEGF wet, limit progression, stabilise/ reverse vision loss. Within 2 mnths vision of diagnosis. Ranibizumab, bevacizumab, pegaptanib. 4wkly injection.
Laser photocoag: slow progress when new vessel. Risk of acute vision loss after Tx
Betacarotene: ↑risk of lung Ca. CI in smokers.

36
Q

Summary of cataracts

A

Protein deposits on lens, ↓light transmission to retina. Often bilat but asymmetrical
Nuclear: opacification of lens nucleus, slow progression. Change lens refractive index. Age.
Polar: localised, inherited, lie in visual access.
Cortical: opacification of lens fibres surrounding nucleus. Mild degradation of vision.
Post subcapsular: opacification in post cortical layer under lens capsule, rapid progression. Steroids
Dot opacities: common in normal lenses, DM + myotonic dystrophy
RF: age, smoking, XS alcohol, LT CS, UV light, eye trauma, rubella, trisomy 13, 18, 21. Radiation intraocular tumour, DM, WD, galactosemia, myotonic dystrophy, ↓Ca, congen. F. DM

Painless gradual ↓vision
Myopic shift: near sight improved before ↓vision, lens sclerosis ↑refractive power
Blurry vision, poor night vision, dullness of colours
Glare: lights appear brighter than usual.
Halos around bright lights, cortical
Infants: amblyopia, failure in visual maturation by depriving retina of formed image at critical age of development + squint. If bilat > nystagmus.

complications:
Blindness
2° post subscapular cataract due to migration of lens epithelium
Retinal detachment
2° glaucoma: phacolytic (lysed lens proteins clog trabecular meshwork, AI reaction to proteins, swollen lens, ↑pressure.
Surgery: residual lens epithelial cells migrate over capsule, iris prolapse, post capsule rupture.
Toxic ant segment synd: inflam of ant segment due to noninfectious comtaminants of surgical equiptment

Ix
Slit lamp: loss of lens transparency
Indirect/direct fundoscopy: lens opacity, obscuration of fundus details, darkening of normal red reflex from fundus

Endopthalmitis: inflam of aqueous or vitreous humour, few days post surgery, painful red eye, ↓visual acuity, collection of white cells in ant chamber, emergency + requires immediate intravitreal injection of broad spectrum Abx.

Tx:
Infants: therapy within 1st wks of life to save vision.
Non-surgical: early, stronger glasses, contact lenses, brighter lighting
Surgery: removing most of lens fibres, insertion of plastic lens implant. 85- 90% achieving 6/12 corrected vision.
Optical power of lens calculated prior to surgery to match other eye
Post op: short-course of steroids + Abx drops
Referral for surgery dependent whether visual impairment present, impact on QoL + pt choice

37
Q

Summary of Argyll-Robertson pupil

A

Causes
Neurosyphilis, DM

Sx
Small irreg pupils
No response to light
Accommodation sresponse present

38
Q

Summary of eyelid problems?

A

Blepharitis
Stye: infection of glands of eyelid.
Entropion: in turning of eyelid
Ectropion: out turning of eyelid.

Styes
External: staph, glands of Zeis or glands of Moll
Internal: meibomian glands. May leave chalazion.

Chalazion: Meibomian retention cyst. Firm painless lump on eyelid. Majority spont resolve. may need surgery.

Stye: hot compress + analgesia. Abx if conjunctivitis.

39
Q

Summary of herpes zoster opthalmicus

A

Reactivation of VZV in ophthalmic division of trigeminal N.

Vesicular rash around eye.
Hutinson’s sign: rash on nose.

Conjunctivitis, keratitis episcleritis, uveitiss
Ptosis
Post-herpetic neuraligia

Urget opthalmology review

Tx:
Oral acyclovir 7-10 days. IV if severe or IC.
Topical CS

40
Q

Summary of mydriasis

A

Large pupil
3rd N palsy, Holmes-Adie pupil, traumatic iridoplegia, phaeochromocytoma, congen

Drugs: tropicamide, atropine, cocaine amphetamines, TCA.

41
Q

Summary of ocular trauma

A

↑IOP due to blockage of angle + trabecular meshwork with erythrocytes.

Compartment synd: eye pain/swelling, proptosis, rock hard eye, relevant afferent pupillary defect.

Hypema: blood in ant chamber > urgent referrral to opthamology

Strict bed rest.
Compartment synd: urgent lat canthotomy

42
Q

Summary of optic neuritis

A

MS, DM, syphilis

Unilat ↓ in visual acuity over hrs/days
Poor colour discrim > red desat
Pain worse on eye movement

Relevent afferent pupillary defect
Central scotoma
MRI

High dose steroids
Recover 4-6 wks