Ophthalmology (again lol) Flashcards

(90 cards)

1
Q

afferent pupillary defect

A

Features
• No direct response but intact consensual response
• Cannot initiate consensual response in contralateral
eye.
• Dilatation on moving light from normal to abnormal eye
Causes
• Total CN II lesion

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2
Q

RAPD

A
Relative Afferent Pupillary Defect
• = Marcus-Gunn Pupil
Features
• Minor constriction to direct light
• Dilatation on moving light from normal to abnormal eye.
• RAPD = Marcus Gunn Pupil
Causes
• Optic neuritis
• Optic atrophy
• Retinal disease
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3
Q

efferent eye defect

A

Efferent Defect
Feature
• Dilated pupil does not react to light
• Initiates consensual response in contralateral pupil
• Ophthalmoplegia + ptosis
Cause
• 3rd nerve palsy
§ The pupil is often spared in a vascular lesion
(e.g. DM) as pupillary fibres run in the periphery

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4
Q

ddx fixed dilated pupil

A
Differential of a fixed dilated pupil
• Mydriatics: e.g. tropicamide
• Iris trauma
• Acute glaucoma
• CN3 compression: tumour, coning
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5
Q

Holmes Adie pupil

A

Holmes-Adie Pupil
Features
• Young woman ¯c sudden blurring of near vision
• Initially unilateral and then bilateral pupil dilatation
§ Dilated pupil has no response to light and
sluggish response to accommodation.
§ A “tonic” pupil
Ix
• Iris shows spontaneous wormy movements on slit-lamp
examination
§ Iris streaming
Cause
• Damage to postganglionic parasympathetic fibres
• Idiopathic: may have viral origin
Holmes-Adie Syndrome
• Tonic pupil + absent knee/ankle jerks + ↓ BP

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6
Q

Horner’s syndrome and cauess

A
Features: PEAS
• Ptosis: partial (superior tarsal muscle)
• Enophthalmos
• Anhydrosis
• Small pupil
Causes
• Central
§ MS
§ Wallenberg’s Lateral Medullary Syndrome
• Pre-ganglionic (neck)
§ Pancoast’s tumour: T1 nerve root lesion
§ Trauma: CVA insertion or CEA
• Post-ganglionic
§ Cavernous sinus thrombosis
§ Usually 2O to spreading facial infection via the
ophthalmic veins
§ CN 3, 4, 5, 6 palsies
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7
Q

Argyll Robertson pupil

A
Argyll Robertson Pupil
Features
• Small, irregular pupils
• Accommodate but doesn’t react to light
• Atrophied and depigmented iris
Cause
• DM
• Quaternary syphilis
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8
Q

optic neuropathy signs

A
Features
• ↓ acuity
• ↓colour vision (esp. red)
• Central scotoma
• Pale optic disc
• RAPD
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9
Q

optic neuropathy ddx

A
commonest MS glaucoma
congenital
Alcohol and Other Toxins
• Ethambutol
• Lead
• B12 deficiency
Compression
• Neoplasia: optic glioma, pituitary adenoma
• Glaucoma
• Paget’s
Vascular: DM, GCA or thromboembolic
Inflammatory: optic neuritis – MS, Devic’s, DM
Sarcoid / other granulomatous
Infection: herpes zoster, TB, syphilis
Oedema: papilloedema
Neoplastic infiltration: lymphoma, leukaemia
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10
Q

taking a red eye hx

A
Vision
• Blurred
• Distorted
• Diplopia
• Field defect / Scotoma
• Floaters, Flashes
Sensation
• Irritation
• Pain
• Itching
• Photophobia
• FB
Appearance
• Red: ?distribution
• Lump
• Puffy lids
Discharge
• Watering
• Sticky
• Stringy
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11
Q

Qs to ask o/e for red eye and serious disease signs

A
Key Examination Questions
• Inspect from anterior to posterior
• Is acuity affected?
• Is the globe painful?
• Pupil size and reactivity?
• Cornea: intact, cloudy? Use fluorescein
Signs of Serious Disease
• Photophobia
• Poor vision
• Corneal fluorescein staining
• Abnormal pupil
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12
Q

acute glaucoma vs anterior uveitis vs conjunctivitis

A

acute glaucoma: most painful, no photophobia, reduced acuity, cornea hazy/cloudy, large pupil, raised IOP

anterior uveitis: medium painful, most photophobia, reduced acuity, normal cornea, small pupil, normal IOP

conjunct: may not have pain, photophobic mildly, rest normal

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13
Q

acute glaucoma

A

acute glaucoma: most painful, no photophobia, reduced acuity, cornea hazy/cloudy, large pupil, raised IOP

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14
Q

anterior uveitis

A

anterior uveitis: medium painful, most photophobia, reduced acuity, normal cornea, small pupil, normal IOP

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15
Q

conjuncitviits

A

conjunct: may not have pain, photophobic mildly, rest normal

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16
Q

acute closed angle glaucoma risk factors and presentation

A
Acute Closed Angle Glaucoma
• Blocked drainage of aqueous from anterior chamber
via the canal of Schlemm.
• Pupil dilatation (e.g. @ night) worsens the blockage.
• Intraocular pressure rises from 15-20 → >60mmHg
Risk Factors
• Hypermetropia
• Shallow ant. chamber
• Female
• FH
• ↑age
• Drugs
§ Anti-cholinergics
§ Sympathomimetics
§ TCAs
§ Anti-histamines
Symptoms
• Prodrome: rainbow haloes around lights at night-time.
• Severe pain ¯c n/v
• ↓ acuity and blurred vision
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17
Q

inv and management acute closed angle glaucoma

A

Examination
• Cloudy cornea c¯ circumcorneal injection
• Fixed, dilated, irregular pupil
• ↑ IOP makes eye feel hard
Ix
• Tonometry: ↑↑ IOP (usually >40mmHg)
Acute Mx: Refer to Ophthalmologist
• Pilocarpine 2-4% drops stat: miosis opens blockage
• Topical β-B (e.g. timolol): ↓ aqueous formation
• Acetazolamide 500mg IV stat: ↓ aqueous formation
• Analgesia and antiemetics
Subsequent Mx
• Bilat YAG peripheral iridotomy once IOP ↓ medically

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18
Q

path, symp, o/e anterior uveitis

A
Pathophysiology
• Uvea is pigmented part of eye and included: iris,
ciliary body and choroid.
• Iris + ciliary body = anterior uvea
• Iris inflammation involves ciliary body too.
Symptoms
• Acute pain and photophobia
• Blurred vision (aqueous precipitates)
Examination
• Small pupil initially, irregular later
• Circumcorneal injection
• Hypopyon: pus in anterior chamber
• White (keratic) precipitates on back of cornea
• Talbots test: ↑pain on convergence
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19
Q

anterior uveitis assoc + treat

A

Associations (most have no systemic associations)
• Seronegative arthritis: AS, psoriatic, Reiter’s
• Still’s / JIA
• IBD
• Sarcoidosis
• Behcet’s
• Infections: TB, leprosy, syphilis, HSV, CMV, toxo
Mx
• Refer to ophthalmologist
• Prednisolone drops
• Cyclopentolate drops: dilates pupil and prevents
adhesions between iris and lens (synechiae)

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20
Q

episcleritis

A
Episcleritis
• Inflammation below conjunctiva in the episclera
Presentation
• Localised reddening: can be moved over sclera
• Painless / mild discomfort
• Acuity preserved
Causes
• Usually idiopathic
• May complicate RA or SLE
Rx: Topical or systemic NSAIDs
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21
Q

scleritis

A
Scleritis
• Vasculitis of the sclera
Presentation
• Severe pain: worse on eye movement
• Generalised scleral inflammation
§ Vessels won’t move over sclera
• Conjunctival oedema (chemosis)
Causes
• Wegener’s
• RA
• SLE
• Vasculitis
Mx
• Refer to specialist
• most need or corticosteroids or immunosuppressants
Complications:
• Scleromalacia (thinning) → globe perforation
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22
Q

conjunctivitis

A

Conjunctivitis
Presentation
• Often bilateral ¯c purulent discharge
§ Bacterial: sticky (staph, strep, Haemophilus)
§ Viral: watery
• Discomfort
• Conjunctival injection
§ Vessels may be moved over the sclera
• Acuity, pupil responses and cornea are unaffected.
Causes
• Viral: adenovirus
• Bacterial: staphs, chlamydia, gonococcus
• Allergic
Rx
• Bacterial: chloramphenicol 0.5% ointment
• Allergic: anti-histamine drops: e.g. emedastine

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23
Q

corneal abrasion

A
Corneal Abrasion
• Epithelial breech w/o keratitis
• Cause: trauma
Symptoms
• Pain
• Photophobia
• Blurred vision
Ix
• Slit lamp: fluorescein stains defect green
Rx
• Chloramphenicol ointment for infection prophylaxis
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24
Q

corneal ulcer + keratitis

A

Corneal Ulcer + Keratitis (corneal inflam)
Causes: bacteria, herpes, fungi, protozoa, RA
• Dendritic ulcer = Herpes simplex
• Acanthamoeba: protazoal infection affecting contact
lens wearers swimming in pools.
Presentation
• Pain, photophobia
• Conjunctival hyperaemia
• ↓ acuity
• White corneal opacity
Risk factors: contact lens wearers
Ix: green ¯c fluorescein on slit lamp
Rx: refer immediately to specialist who will
• Take smears and cultures
• Abx drops, oral/topical aciclovir
• Cycloplegics/mydriatics ease photophobia
• Steroids may worsen symptoms: professionals only
Complications
• Scarring and visual loss

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25
ophthalmic shingles
``` Ophthalmic Shingles • Zoster of CNV1 • 20% of all Shingles (only commoner in thoracic dermatomes) Presentation • Pain in CNV1 dermatome precedes blistering rash • 40% → keratitis, iritis • Hutchinson’s sign § Nose-tip zoster due to involvement of nasociliary branch. § ↑ chance of globe involvement as nasociliarry nerve also supplies globe • Ophthalmic involvement § Keratitis + corneal ulceration (fluorescein stains) § ± iritis ```
26
sudden vision loss Qs
Key Questions • Headache associated: GCA • Eye movements hurt: optic neuritis • Lights / flashes preceding visual loss: detached retina • Like curtain descending: TIA, GCA • Poorly controlled DM: vitreous bleed from new vessels
27
optic neuritis
``` Optic Neuritis Symptoms • Unilateral loss of acuity over hrs – days • ↓ colour discrimination (dyschromatopsia) • Eye movements may hurt Signs • ↓ acuity • ↓ colour vision • Enlarged blind-spot • Optic disc may be: normal, swollen, blurred • Afferent defect Causes • Multiple sclerosis (45-80% over 15yrs) • DM • Drugs: ethambutol, chloramphenicol • Vitamin deficiency • Infection: zoster, Lyme disease Rx • High-dose methyl-pred IV for 72h • Then oral pred for 11/7 ```
28
vitreous haemmorhage
``` Vitreous Haemorrhage Source • New vessels: DM • Retinal tears / detachment / trauma Presentation • Small bleeds → small black dots / ring floaters • Large bleed can obscure vision → no red reflex, retina can’t be visualised Ix • May use B scan US to identify cause Mx • VH undergoes spontaneous absorption • Vitrectomy may be performed in dense VH ```
29
central retinal artery occlusion
Central Retinal Artery Occlusion Presentation • Dramatic unilateral visual loss in seconds • Afferent pupil defect (may precede retinal changes) • Pale retina ¯c cherry-red macula Causes • GCA • Thromboembolism: clot, infective, tumour Rx • If seen w/i 6h aim is to ↑ retinal blood flow by ↓ IOP § Ocular massage § Surgical removal of aqueous § Anti-hypertensives (local and systemic) I think peripheral would be less dramatic with blurring
30
central retinal vein occlusion
``` Retinal Vein Occlusion Central • Commoner than arterial occlusion • Causes: arteriosclerosis, ↑BP, DM, polycythaemia • Pres: sudden unilat visual loss ¯c RAPD • Fundus: Stormy Sunset Appearance § Tortuous dilated vessels § Haemorrhages § Cotton wool spots • Complications § Glaucoma § Neovascularisation • Prognosis: possible improvement for 6mo-1yr ``` check pics
31
branch retinal vein occlusiono
Branch • Presentation: unilateral visual loss • Fundus: segmental fundal changes • Comps: retinal ischaemia → VEGF release and neovascularisation (Rx: laser photocoagulation) check pics
32
retinal detachement presentation o/e traetment
Retinal Detachment • Holes/tears in retina allow fluid to separate sensory retina from retinal pigmented epithelium • May be 2O to cataract surgery, trauma, DM Presentation: 4 F’s • Floaters: numerous, acute onset, “spiders-web” • Flashes • Field loss • Fall in acuity • Painless Fundus: grey, opalescent retina, ballooning forwards Rx • Urgent surgery • Vitrectomy + gas tamponade ¯c laser coagulation to secure the retina
33
causes transient visual loss
``` Causes of transient visual loss • Vascular: TIA, migraine • MS • Subacute glaucoma • Papilloedema ```
34
causes gradual vision loss
``` Causes Common • Diabetic retinopathy • ARMD • Cataracts • Open-angle Glaucoma Rarer • Genetic retinal disease: retinitis pigmentosa • Hypertension • Optic atrophy` ```
35
age related macular degeneration
``` Age-Related Macular Degeneration (ARMD) • Commonest cause of blindness >60yrs • 30% of >75yrs will have dry AMD Risk Factors • Smoking • ↑ age • Genetic factors Presentation • Elderly pts. • Central visual loss ```
36
dry age related mac degen
Dry ARMD: Geographic Atrophy • Drusen: fluffy white spots around macula • Degeneration of macula • Slow visual decline over 1-2yrs
37
wet age related mac degen
Wet ARMD: Subretinal Neovascularisation • Aberrant vessels grow into retina from choroid and → haemorrhage • Rapid visual decline (sudden / days / wks) ¯c distortion • Fundoscopy shows macular haemorrhage → scarring • Amsler grid detects distortion
38
treat age mac degen
``` Ix • OCT: optical coherence tomography § Gives high resolution images of the retina Mx for Wet AMRD • Photodynamic therapy • Intravitreal VEGF inhibitors § Bevacizumab (Avastin) § Ranibizumab (Lucentis) • Antioxidant vitamins (C,E) + zinc may help early ARMD ``` can't treat dry
39
FYITobacco-Alcohol Amblyopia
• Due to toxic effects of cyanide radicals when combined with thiamine deficiency. • Pres: Optic atrophy, loss of red/green discrimination, scotomata • Rx: vitamins may help
40
chronic open angle glaucoma presentatin
Chronic Simple (Open-Angle) Glaucoma Pathogenesis • Depends on susceptibility of pt’s. retina and optic nerve to ↑ IOP damage. • IOP >21mmHg → ↓blood flow and damage to optic nerve → optic disc atrophy (pale) + cupping Presentation • Peripheral visual field defect: superior nasal first • Central field is intact \ acuity maintained until late § Presentation delayed until optic N. damage is irreversible
41
screening and inv open angle glaucoma
``` Screen if High Risk • >35yrs • Afro-Caribbean • FH • Drugs: steroids • Co-morbidities: DM, HTN, migraines • Myopia Ix • Tonometry: IOP ≥21mmHg • Fundoscopy: cupping of optic disc • Visual field assessment: peripheral loss ```
42
management chronic open angle glaucoma
``` Mx • Life-long f/up Eye-drops to ↓ IOP to baseline • 1st line: β-blockers § Timolol, betaxolol § ↓ aqueous production § Caution in asthma, heart failure • Prostaglandin analogues § Latanoprost, travoprost § ↑ uveoscleral outflow • α-agonists § Brimonidine, apraclonidine § ↓ aqueous production and ↑ uveoscleral outflow • Carbonic anhydrase inhibitors § Dorzolamide drops, acetazolamide PO • Miotics § Pilocarpine Non-medical Options • Laser trabeculoplasty • Surgery (trabeculectomy) is used if drugs fail § New channel allows aqueous to flow into conjunctival bleb ```
43
commonest worldwide causes of blindness
``` Commonest Causes of Blindness Worldwide • Trachoma • Cataracts • Glaucoma • Keratomalacia: vitamin A deficiency • Onchocerciasis • Diabetic Retinopathy ```
44
diabetes and eye trouble
Cataract • DM accelerates cataract formation • Lens absorbs glucose which is converted to sorbitol by aldose reductase. Retinopathy • Microangiopathy → occlusion • Occlusion → ischaemia → new vessel formation in retina § Bleed → vitreous haemorrhage § Carry fibrous tissue ¯c them → retinal detachment • Occlusion also → cotton wool spots (ischaemia) • Vascular leakage → oedema and lipid exudates • Rupture of microaneurysms → blot haemorrhage Screening • All diabetics should be screened annually • Fundus photography • Refer those ¯c maculopathy, NPDR and PDR to ophthalmologist § 30% NPDR develop PDR in 1y
45
inv and management diabetic eye diseas
``` Ix • Fluorescein angiography Mx • Good BP and glycaemic control • Rx concurrent disease: HTN, dyslipidaemia, renal disease, smoking, anaemia • Laser photocoagulation § Maculopathy: focal or grid § Proliferative disease: pan-retinal (macula spared) ```
46
background diabetic retionopathy
Background Retinopathy: Leakage • Dots: microaneurysms • Blot haemorrhages • Hard exudates: yellow lipid patches
47
pre proliferative diabetic retinopathy
``` Pre-proliferative Retinopathy: Ischaemia • Cotton-wool spots (infarcts) • Venous beading • Dark Haemorrhages • Intra-retinal microvascular abnormalities ```
48
diabetic proliferative retinopathy
Proliferative Retinopathy • New vessels • Pre-retinal or vitreous haemorrhage • Retinal detachment
49
diabetic maculopathy
Maculopathy • Caused by macular oedema • ↓ acuity may be only sign • Hard exudates w/i one disc width of macula
50
cataracts presentation and cause
``` Cataracts Presentation • Increasing myopia • Blurred vision → gradual visual loss • Dazzling in sunshine / bright lights • Monocular diplopia Causes • ↑Age: 75% of >65s • DM • Steroids • Congenital § Idiopathic § Infection: rubella § Metabolic: Wilson’s, galactosaemia § Myotonic dystrophy ```
51
cataracts inv and manage
``` Ix • Visual acuity • Dilated Fundoscopy • Tonometry • Blood glucose to exclude DM Mx Conservative • Glasses • Mydriatic drops and sunglasses may give some relief Surgery • Consider if symptoms affect lifestyle or driving (<6/10) • Day-case surgery under LA § Phacoemulsion + lens implant • 1% risk of serious complications § Anterior uveitis / iritis § VH § Retinal detachment § Secondary glaucoma § Endophthalmitis (→ blindness in 0.1%) • Post-op capsule thickening is common § Easily Rx ¯c laser capsulotomy. • Post-op eye irritation is common and requires drops ```
52
normal optic disc features and key abnormalities
``` Optic Disc Colour • Should be pale pink • Paler in optic atrophy Contour • Margins blurred in papilloedema and optic neuritis Cup • Physiological cup lies centrally and should occupy 1/3 of disc diameter • Cup widening and deepening in glaucoma ```
53
retinitis pigmentosa
Most prevalent inherited degeneration of the macula Presentation • Night blindness • ↓↓ visual fields → tunnel vision • Most are registrable blind (<3/60) by mid 30s Fundoscopy • Pale optic disc: optic atrophy • Peripheral retina pigmentation: spares the macula
54
retinoblastoma
Retinoblastoma • Commonest intraocular tumour in children strabismus and loss of red reflex; white pupil mx: enucleation, C/Rtherapy
55
stye
Stye or hordeolum externum • An abscess / infection in a lash follicle which points outwards. • Rx: local Abx – e.g. fusidic acid
56
chalazion
Chalazion or hordeolum internum • Abscess of the Meibomian glands which points inwards onto conjunctiva. § Sebaceous glands of eyelid
57
blepharitis
``` Blepharitis • Chronic inflammation of eyelid • Causes: seborrhoeic dermatitis, staphs • Features § Red eyes § Gritty / itchy sensation § Scales on lashes. § Often assoc. ¯c rosacea • Rx § Clean crusts of lashes ¯c warm soaks § May need fusidic acid drops ```
58
entropion and ectropion
``` Entropion • Lid inversion → corneal irritation • Degeneration of lower lid fascia Ectropion • Low lid eversion → watering and exposure keratitis • Assoc. ¯c ageing and facial N. palsy ```
59
ptosis causes
``` Ptosis • True ptosis is intrinsic LPS weakness • Bilateral § Congenital § Senile § MG § Myotonic dystrophy • Unilateral § 3rd Nerve palsy § Horner’s syndrome (partial) § Mechanical: xanthelasma, trauma ```
60
orbital cellullitis presentation
``` Orbital Cellulitis Pathophysiology • Infection spreads locally: e.g. from paranasal sinuses, eyelid or external eye. • Staphs, pneumococcus, GAS Presentation • Usually a child ¯c inflammation of the orbit + lid swelling • Pain and ↓ range of eye movement • Exophthalmos • Systemic signs: e.g. fever • ± tenderness over the sinuses ```
61
orbital cellulitis manage / complic
``` Rx • IV Abx: Cefuroxime (20mg/kg/8h IV) Complications • Local extension → meningitis and cavernous sinus thrombosis. • Blindness due to optic N. pressure. ```
62
carotid cavernous fistula
``` Carotid-cavernous fistula • May follow carotid aneurysm rupture ¯c reflux of blood into cavernous sinus. • Causes: spontaneous, trauma • Presentation § Engorgement of eye vessels § Lid and conjunctival oedema, § Pulsatile exophthalmos § Eye bruit • Rx: endovascular treatmen ```
63
Exophthalmos / Proptosis
``` • Protrusion of one or both eyes Common Causes • Graves’ Disease § 25-50% § ↑ risk in smoker’s § Anti-TSH Abs → retro-orbital inflammation and lymphocyte infiltration → swelling • Orbital cellulitis • Trauma Other Causes • Idiopathic orbital inflammatory disease • Vasculitis: Wegener’s • Neoplasm § Lymphoma § Optic glioma: assoc. ¯c NF-1 § Capillary haemangioma § Mets • Carotid-cavernous fistula ```
64
myopia
``` Myopia: Short-sightedness The Problem • The eye is too long • Distant objects are focussed too far forward. Causes • Genetic • Excessive close work in the early decades The Solution • Concave lenses ```
65
astigmatism
Astigmatism The Problem • Cornea or lens doesn’t have same degree of curvature in horizontal and vertical planes. • Image of object is distorted longitudinally or vertically The Solution • Correcting lenses
66
hypermetropia
The Problem • Eye is too short • When eye is relaxed and not accommodating, objects are focussed behind the retina. • Contraction of ciliary muscles to focus image → tiredness of gaze and possibly a convergent squint in children. The Solution • Convex lenses
67
presbyopia
Presbyopia • With age, lens becomes stiff and less easy to deform. • Start at about 40yrs and is complete by 60yrs. • Use convex lenses.
68
non paralytic squint / lazy eye
Diagnosis • Corneal reflection: should fall centrally and symmetrically on each cornea. • Cover test: movement of uncovered eye to take up fixation demonstrates manifest squint. Management: 3 O’s • Optical: correct refractive errors • Orthoptic: patching good eye encourages use of squinting eye. • Operations: e.g. resection and recession of rectus muscles – help alignment and cosmesis.
69
third nerve palsy
``` CNIII • Ptosis (LPS) • Fixed dilated pupil (no parasympathetic) • Eye looking down and out • Causes § Medical: DM, MS, infarction § Surgical: ↑ ICP, cavernous sinus thrombosis, posterior communicating artery aneurysm ```
70
fourth nerve palsy
``` CNIV • Diplopia especially on going down stairs • Head tilt • Test: can’t depress in adduction • Causes § Peripheral: DM (30%), trauma (30%), compression § Central: MS, vascular, SOL ```
71
sixth nerve palsy
CNVI • Eye is medially deviated and cannot abduct • Diplopia in the horizontal plane. • Causes § Peripheral: DM, compression, trauma § Central: MS, vascular, SOL • Rx: botulinum toxin can eliminate need for surgery
72
eye trauma and foreign bodies
``` Eye Trauma • Record acuity of both eyes • Take detailed Hx of event • If unable to open injured eye, instil LA (e.g. tetracaine 1%) Foreign Bodies • X-ray orbit if metal FB suspected • Fluorescein may show corneal abrasions Mx • Chloramphenicol drops 0.5% prevent infection § Usually coagulase-negative Staphylococcus • Eye patch • Cycloplegic drops may ↓ pain § Tropicamide, cyclopentolate ```
73
intra ocular haemorrhage
Intra-ocular Haemorrhage • Blood in anterior chamber = hyphaema • Small amounts clear spontaneously, but some may need evacuation. • Complicated by corneal staining and glaucoma (pain) • Keep IOP↓ and monitor
74
orbital blowout fracture
Orbital Blowout Fracture • Blunt injury → sudden ↑ in orbital pressure ¯c herniation of orbital contents into maxillary sinus. Presentation • Ophthalmoplegia + Diplopia § Tethering of inferior rectus and inferior oblique • Loss of sensation to lower lid skin § Infraorbital nerve injury • Ipsilateral epistaxis § Damage to anterior ethmoidal artery • ↓ acuity • Irregular pupil that reacts slowly to light Mx • Fracture reduction and muscle release necessary
75
eye chemical injury
``` Chemical Injury • Alkaline solutions are particularly damaging • Mx § Copious irrigation § Specialist referral ```
76
floaters, causes etc
``` Floaters • Small dark spots in the visual field • Sudden showers of floaters in one eye may be due to blood or retinal detachment Causes • Retinal detachment • VH • Diabetic retinopathy / Hypertension • Old retinal branch vein occlusion • Syneresis (degenerative opacities in the vitreous) ```
77
flashes in eye, causes etdc
Flashes (Photopsia) • Either from intraocular or intracerebral pathology • Headache, n/v: migraine • Flashes and floater: retinal detachment
78
halos in eye
Usually just diffractive phenomena • May be caused by hazy ocular media – cataract, corneal oedema, acute glaucoma • Haloes + eye pain = acute glaucoma • Jagged haloes which change shape are usually migrainous.
79
types of allergic eye disease
Seasonal Allergic Conjunctivitis (SAC) • 50% of allergic eye disease • Small papillae on tarsal conjunctivae • Rx § Antazoline: antihistamine drops: § Cromoglycate: inhibits mast cell degranulation Perennial Allergic Conjunctivitis (PAC) • Symptoms all year ¯c seasonal exacerbations • Small papillae on tarsal conjunctivae • Rx: olopatadine (antihistamine and mast-cell stabiliser) Giant Papillary Conjunctivitis • Iatrogenic FBs: contact lenses, prostheses, sutures • Giant papillae on tarsal conjunctivae • Rx: removal of FB, mast cell stabilisers
80
manage allergic eye diseae
``` Management of Allergic Eye Disorders 1. Remove the allergen responsible where possible 2. General measures § Cold compress § Artificial tears 3. Oral antihistamines: loratadine 10mg/d PO 4. Eye drops § Antihistamines: antazoline, azelastine § Mast cell stabilizers: cromoglycate, lodoxamide § Steroids: dexamethasone - Beware of inducing glaucoma § NSAIDs: diclofenac ```
81
trachoma FYI
``` Trachoma Pathophysiology • Caused by Chlamydia trachomatis (A,B,C) • Spread by flies • Inflammatory reaction under lids → scarring → lid distortion → entropion → eyelashes scratch cornea → ulceration → blindness Rx • Tetracycline 1% ointment ± PO Prevention • Good sanitation • Face washing ```
82
Xerophthalmia and Keratomalacia FYI
• Manifestations of vitamin A deficiency Presentation • Night blindness and dry conjunctivae (xerosis) • Corneal ulceration and perforation Rx • Vitamin A / palmitate reverses early corneal changes
83
hypertensive retinopathy
Hypertensive Retinopathy • Keith-Wagener Classification • Tortuosity and silver wiring • AV nipping • Flame haemorrhages and soft / cotton wool spots • Papilloedema • Grades 3 and 4 = malignant hypertension know the stages+look
84
inflammatory disease and eye signs
Systemic Inflammatory Disease • Conjunctivitis: SLE, reactive arthritis, IBD • Scleritis / episcleritis: RA, vasculitis, SLE, IBD • Iritis : ank spond, IBD, sarcoid • Retinopathy: dermatomyositis
85
HIV eye signs
CMV retinitis: pizza-pie fundus + flames | • HIV retinopathy: cotton wool spots
86
anti muscarinic eye drugs
``` Anti-Muscarinics • Tropicamide § Duration: 3h • Cyclopentolate § Duration: 24h § Preferred for paediatric use • Pupil dilatation + loss of light reflex • Cycloplegia (ciliary paralysis) → blurred vision ```
87
sympthamomimetic eye drugs
Sympathomimetics • Para-hydroxyamphetamine, phenylephrine • May be used ¯c tropicamide • Don’t affect the light reflex or accommodation Indications • Eye examination • Prevention of synechiae in ant. uveitis / iritis Caution • May → acute glaucoma if shallow anterior chamber
88
miotic eye drugs
``` Miotics Effect • Constrict the pupil Pilocarpine • Muscarinic agonist Use • Acute closed-angle glaucoma ```
89
chronic open angle glaucoma treatment summary
``` Chronic Open-Angle Glaucoma • 1st line: β-blockers § Timolol, betaxolol § ↓ aqueous production § Caution in asthma, heart failure • Prostaglandin Analogues § Latanoprost, travoprost § ↑ uveoscleral outflow • α-agonists § Brimonidine, apraclonidine § ↓ aqueous production and ↑ uveoscleral outflow • Carbonic anhydrase inhibitors § Dorzolamide drops, acetazolamide PO • Miotics: Pilocarpine ```
90
vascular occlusion and eye, metabolic syndromes and eye
``` Vascular Occlusion • Emboli → amaurosis fugax: GCA, carotid atheroemboli • Microemboli → Roth spots: infective endocarditis § Boat-shaped haemorrhage ¯c pale centre Metabolic • Kayser-Fleischer Rings: Wilson’s • Exophthalmos: Graves’ • Corneal calcification: HPT ```