Ophthalmology Flashcards

1
Q

What are the causes of Red Eye ??

A

Acute Angle closure Glaucoma
Anterior Uveitis
Scleritis
Conjunctivitis (Viral: Clear discharge, Bacterial: Purulent discharge
Subconjunctival Haemorrhage (H/o trauma or Coughing bouts)
Endophthalmitis (Pain+ Vision loss following Intraocular Sx.)

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2
Q

Causes of Sudden Vision loss ??

A

Transient Monocular Vision Loss (TMVL) is a sudden, transient loss of vision lasting < 24hrs
- Ischaemic/ Vascular: Thrombosis, Embolism, Temporal arteritis; CRVO, CRAO
- Vitreous Haemorrhage
- Retinal detachment
- Retinal Migraine

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2
Q

What is Amaurosis fugax ??

A

Ischaemic/ Vascular diseases cause TMVL, ‘Curtain coming down’
- Large artery disease (Athero-thrombosis, Embolus, Dissection)
- Small artery occlusive disease (AION ,vasculitis-eg. Temporal Arteritis), Venous disease & Hypoperfusion
- May represent a form of TIA, therefore Rx.- Aspirin 300mg

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2
Q

What causes Ischaemic Optic Neuropathy ??

A

Occlusion of Short Posterior Ciliary Arteries => damages Optic nerve

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3
Q

Causes of Tunnel Vision ??

A

Concentric diminution of Visual field
- Papilloedema
- Glaucoma
- Retinitis pigmentosa
- Choroidoretinitis
- Optic atrophy secondary to Tabes dorsalis
- Hysteria

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4
Q

Causes of Mydriasis ??

A
  • 3 rd nerve palsy
  • Holmes-Adie Pupil
  • Traumatic Iridoplegia
  • Phaeochromocytoma
  • Congenital
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5
Q

Drugs causing Mydriasis ??

A
  • Tropicamide, Atropine
  • Sympathomimetics: Amphetamines, Cocaine
  • Anticholinergica: TCAs
    Anisocoria can occur in apparent mydriasis, due to the difference with other pupil
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6
Q

What is CRAO ??

A

Due to Thromboembolism (from atherosclerosis) or Arteritis
- Sudden, Painless U/L vision loss
- Relative Afferent Pupil Defect
- ‘CHERRY Red’ spot on Macula

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7
Q

Rx. of CRAO ??

A
  • Treat the underlying cause (eg. IV Steroids for Temporal Arteritis)
  • Acute presentation: Intra-arterial Thrombolysis
  • Generally Poor prognosis
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8
Q

RF & Features of CRVO ??

A
  • Increasing age, HTN, CVS diseases
  • Glaucoma, Polycythaemia
    C/F-
  • Sudden, Painless reduction or loss of visual acuity, usually U/L
  • Severe Retinal Hemorrhage: ‘Stormy sunset’
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9
Q

Rx. of CRVO ??

A

Conservative Rx.
Rx. indication: Macular edema:- Intra-vitreal anti- VEGF agents
Retinal Neovascularization: Laser Photocoagulation

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9
Q

What is BRVO ??

A

Occurs when a vein in the Distal Retinal Venous System is occluded
- Due to blockage of Retinal veins at AV crossings
- LIMITED area of fundus is affected

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10
Q

What is the MCC of blindness in adults aged 35 to 65 yrs old ??

A

Diabetic Retinopathy
- Hyperglycaemia => increase Retinal blood flow & Abnormal metabolism in Retinal Vessel wall => ppt. damage to Endothelial cells & Pericytes
- Endothelial dysfunction => increase vascular permeability => EXUDATE
- Pericyte dysfunc. => Microaneurysm formation
- Retinal ischaemia => GFs production => NEOVASCULARIZATION

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11
Q

Diabetic Retinopathy Classification ??

A

NON-PROLIFERATIVE D R
PROLIFERATIVE D R
- Retinal Neovascularisation- can cause Vitrous Haemorrhage
- Fibrous tissue forming Anterior to Retinal disc
- More common in Type 1 DM; 50% blind in 5 yrs.
MACULOPATHY
- Hard exudates & other ‘background’ changes on Macula

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12
Q

Which type of D Retinopathy is common in the following-
- Type 1 DM ??
- Type 2 DM ??

A
  • Proliferative D R
  • Maculopathy
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13
Q

How is Non-Proliferative D R classified ??

A

Mild NPDR
- >= 1 Microaneurysm
Moderate NPDR
- Microaneurysm
- Blot Haemorrhages
- Hard exudates
- Cotton Wool spots (Soft Exudates- represents the area of retinal infarction)
- Venous beading/ looping & Intraretinal Microvascular abnormalities (IRMA) less severe than in severe NPDR
SEVERE NPDR
- Blot haemorrhages & Microaneurysms in 4 quadrants
- Venous beading in at least 2 quad.
- IRMA in at least 1 quadrant

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13
Q

Rx. of Diabetic Retinopathy ??

A

Maculopathy: Intra-vitreal VEGF inhibitor
Proliferative D R:
- Panretinal Laser Photocoagulation
- Intra-vitreal VEGF inhibitors (eg. Ranibizumab
- Both can Slow down progression of PDR & improve visual acuity
NPDR
- Regular observation
- Severe/ Very Severe: Panretinal Laser Photocoagulation

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13
Q

Keith Wagener Classification of HTN Retinopathy ??

A

Stage 1:
- Arteriolar Narrowing & Tortuosity
- Silver wiring (Increased light reflex)
Stage 2: AV Nipping
Stage 3:
- Cotton-wool exudates
- Flame & Blot haemorrhages (These can collect around Fovea => ‘Macular Star’
Stage 4: Papilloedema

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14
Q

What is Retinitis pigmentosa ??

A

Primarily affects the PERIPHERAL Retina resulting in Tunnel vision
- 1st sign: Night blindness
- Tunnel/ Funnel vision
Fundoscopy: Black bone spicule- shaped pigmentation in the peripheral retina; Mottling of Retinal pigment epithelium

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15
Q

What is Refsum disease ??

A

Cerebellar ataxia + Peripheral Neuropathy + Deafness + Ichthyosis

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16
Q

What is Angioid Retinal Streaks ??

A

Irregular dark red streaks radiating from the optic nerve head
- due to Degeneration, Calcification & Breaks in BRUCH’s Memb.

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17
Q

Causes of Retinal Angioid Streaks ??

A
  • pseudoxanthoma elasticum
  • Ehler-Danlos syndrome
  • Paget’s disease
  • Sickle cell anaemia
  • Acromegaly
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18
Q

What is the MCC of blindness in the UK ??

A

Age-Related Macular Degeneration
- usually B/L condition
- Retinal Photoreceptors degeneration => Drusen formation
- MC in Increasing age (3x increase in >=75yrs) & in FEMALES
- Smoking (2x common)
- FAMILY Hx. (if 1st degree relative => 4x more common)
- IHD : HTN, Dyslipidaemia, DM

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19
Q

Presentation of ARMD ??

A

Subacute onset of Visual loss (typical)
- Reduced Visual Acuity (particularly: NEAR field objects)
- Dark adaptation difficulty + overall deterioration in vision at night
- Fluctuations in Visual fields (on a day to day basis)
- Photopsia: Flickering & Flashing light
- Glare around the objects

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20
Q

Ix. of ARMD ??

A

Slit-lamp Microscopy
- Initial IoC
- Accompanied by Colour Fundus Photography to provide a baseline against which changes over time is identified
Fluorescein Angiography
- used if Neovascular ARMD doubted as this can guide intervention with anti-VEGF therapy
Ocular Coherence Tomography
- 3D visualisation of Retina
- Reveals the areas of disease which aren’t visible to microscopy alone

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20
Q

Important Signs of ARMD ??

A
  • Amsler grid testing: Line perception distorted
  • Fundoscopy: Drusen, yellow areas of pigment deposition in Macular area => later confluences to form a Macular Scar
  • Wet ARMD: Well demarcated red patches may be seen which represent Intra-retinal or Sub-retinal fluid leakage or haemorrhage
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20
Q

ARMD classification ??

A

Dry Macular Degeneration
- 90% cases (MC)
- aka Atrophic
- Drusen (+)ve: Yellow round spots in Bruch’s membrane
WET Macular Degeneration
- 10% cases
- aka Exudative or Neovascular M D
- ‘CHOROIDAL Neovascularization’
- Leakage of Serous fluid & Blood can result in rapid vision loss
EARLY ARMD
- Non-exudative, age-related maculopathy
- Drusen & alteration to Retinal Pigment Epithelium
LATE ARMD
- Neovascularization, Exudative

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21
Q

Which ARMD can worsen after Laser Photocoagulation ??

A

Sub- Foveal ARMD (causes Acute Vision Loss)

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21
Q

Rx. of ARMD ??

A

Anti-VEGF therapy
- Limits progression of Wet ARMD; should be given in 1st 2 months of Dx.
- Ranibizumag, Bevalizumab, Pegaptanib
Laser Photocoagulation
- Slows progression
- Risk of Acute Vision Loss after Rx. which is particularly increased in pts. with Sub-Foveal ARMD
Combination of Zinc + Anti-oxidant Vit. A, C & E reduces progression in 1/3rd pts.

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22
Q

What is Optic Atrophy ??

A

Pale, well demarcated disc on Fundoscopy; usually B/L
- Causes GRADUAL Vision loss
- It is a descriptive term, it is Optic Neuropathy that results in Vision loss

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23
Q

Causes if Optic Atrophy ??

A

Acquired
- Multiple Sclerosis
- Papilloedema (Long standing)
- Raised IOP (Glaucoma, Tumour)
- Retinal damage (Choroiditis, Retinitis pigmentosa) & ISCHAEMIA
- Toxins: Tobacco, Quinine, Methanol, Arsenic, Lead
- Vit. B1, B2, B6 & B12 deficiency
CONGENITAL Causes
- Friedreich’s Ataxia
- Mitochondrial disorder (Leber’s OA)
- Wolfram’s synd. (DI DM OA D)

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24
Q

Features of Optic Neuritis ??

A
  • Multiple Sclerosis (commonest association)
  • Diabetes. - Syphilis
    Features
  • U/L decrease in Visual acuity over hours to days
  • Pain worse on eye movement
  • Red Desaturation (Poor discrimination of colours)
  • RAPD & Central Scotoma
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24
Q

Rx. & Prognosis of Optic Neuritis ??

A

High-dose STEROIDS
Recovery takes 4- 6 wks
Prognosis
- MRI: if > 3 white-matter lesions, 5-year risk of developing MS is 50%

24
Q

What is Papilloedema ??

A

Optic Disc Swelling caused by increased ICP. Almost always B/L
Features-
- 1st sign: Venous Engorgement
- Loss of Venous Pulsation (many normal pts. do not have this)
- Optic Disc margin Blurring
- Elevation of optic disc
- Loss of Optic Cup
- PATON’s Line: Concentric/ Radial Retinal lines cascading from optic disc

24
Q

Causes of Papilloedema ??

A
  • Space-occupying lesion: Neoplastic, Vascular
  • Malignant HTN
  • Idiopathic ICH
  • Hydrocephalus
  • Hypercapnia
    Rare causes: Hypoparathyroidism, Hypocalcaemia, Vit.-A toxicity
25
Q

What is Posterior Vitreous Detachment ??

A

Separation of Vitreous memb. from Retina which can rarely lead to tears & detachment of Retina
- Most pts. are > 65 yrs old
- FEMALE preponderance

26
Q

RF for Posterior Vitreous Detachment ??

A

As we age, the vitreous fluid in the eye becomes less viscous & thus does not hold its shape as well
- High myopia (myopic eye has a longer axial length than normal)

27
Q

C/F of Posterior Vitreous Detachment ??

A
  • Sudden Appearance of Floaters (a ring of floaters TEMPORAL to Central vision)
  • Flashes of light (Peripheral vision field) & Blurred vision
  • Cobweb across vision
  • Dark curtain descending down in vision (means there is Retinal detachment)
    WEISS Ring on Ophthalmoscopy (detached vitreous memb. around the Optic N form a ring-shaped floater
28
Q

Ix. & Rx. of Posterior Vitreous Detachment ??

A

Suspected pts. Examined by an ophthalmologist in < 24hrs to rule out Retinal tear/ detachment
Rx.-
- Will not cause permanent vision loss
- No Rx.- as symptoms gradually improve over 6 months
- a/w Retinal Tear: Sx. is required

28
Q

Retinal Detachment features ??

A
  • Dense shadow that starts Peripherally progresses to the Central vision
  • Veil of Curtain over Vision Field
  • Distortion of Straight lines
  • Central Vision Loss
28
Q

Vitreous Haemorrhage Features ??

A

Large Bleed => Sudden Vision loss
Moderate Bleed => Numerous dark spots
Small Bleed => Floaters

29
Q

What is Holmes-Adie Pupil ??

A

Benign condition; MC seen in FEMALES.
- U/L in 80% cases
- Dilated pupils
- Once the pupil is constricted, it remains as such for a long time
- Light reflex: Absent
- Accommodation: Slowly reactive

30
Q

What is Holmes-Adie Syndrome ??

A

Holmes-Adie Pupil + Absent Ankle/ Knee reflex

31
Q

What are the features of Horner’s Syndrome ??

A
  • Miosis + Ptosis + Anhidrosis
  • Enophthalmos (due to Narrow Palpebral aperture rather than True Enophthalmos)
32
Q

How to differentiate b/w Congenital & Acquired Horner’s Syndrome ??

A

Congenital= Horner’s + Heterochromia

33
Q

What is Apraclonidine test ??

A

Alpha-adrenergic AGONIST is used
- Horner’s eye = causes MYDRIASIS (due to denervation supersensitivity)
- Normal eye = Mild MIOSIS (by down-regulating the NE release at Synaptic cleft)

34
Q

What is Argyll Robertson Pupils ??

A

“ARP” : Accommodation Reflex PRESENT
PRA- Pupillary Reflex Absent
- Small Irregular pupils
- No light response
Causes: DM, Neurosyphilis

35
Q

What is Marcus Gunn pupil ??

A

RAPD is identified by ‘Swinging Light Test’
- Site of Lesion: Anterior to Optic Chiasm (O N or Retina)
Affected eye & Normal eye DILATE when light is shone on the Affected eye
Causes
- Retina: Detachment
- Optic N : Optic Neuritis (eg. MS)

36
Q

Elaborate the Pathway of Pupillary light reflex

A

Afferent: Retina => O N => Lateral Geniculate body => Midbrain
Efferent: Edinger-Westphal N (mid brain) => Oculomotor N

37
Q

What are the Ocular manifestations of Rheumatoid Arthritis ??

A

Seen in 25% of pts. with RA
- Keratoconjunctivitis Sicca (MC)
- Episcleritis (Erythema)
- Scleritis (Erythema + Pain)
- Corneal ulceration
- Keratitis
Iatrogenic Cause:
- Steroid induced Cataract
- Chloroquine Retinopathy

38
Q

What is Anterior Uveitis ??

A

aka IRITIS a/w HLA-B27
- Inflammation of Anterior portion of Uvea: IRIS + CILIARY Body
Associated Conditions:
- Ank. Spon.
- Reactive Arthritis
- IBD (UC & CD)
- Behcet’s disease
- Sarcoidosis: B/L may be seen

39
Q

Features & of Anterior Uveitis ??

A
  • Acute onset Red eye
  • Ocular discomfort & Pain
  • PHOTOPHOBIA, Lacrimation
  • Blurred vision
  • Ciliary Flush: ring of red spreading outwards
  • Hypopyon: pus & inflam. cells in the anterior chamber
  • Visual acuity initially normal => Impaired
40
Q

Rx. of Anterior Uveitis ??

A

Urgent Ophthalmology referral
- Cycloplegics (DILATES pupil => relieves pain & photophobia): Atropine, Cyclopentolate
- Steroids eye drops

41
Q

Features of Blepharitis ??

A

Meibomian gland secretes oil which prevents rapid evaporation of tears
- B/L symptoms
- Grittiness & Discomfort, particularly around lid margin
- Sticky eyes in the morning
- Staph. Infection: Red Eyelid margins & Swollen eyelids
- STYES & CHALAZIONS are common

41
Q

What is Blepharitis ??

A

Inflammation of Eyelid MARGINS
- Meibomian gland dysfunc. (common POSTERIOR blepharitis) or
- Seborrhoeic Dermatitis or
- Staph. infection (less common; ANTERIOR blepharitis)
More common in pts. with Rosacea

42
Q

Rx. of Blepharitis ??

A

Hot Compresses 2x a day (to Soften the lid margins)
Lid Hygiene- mechanical removal of debris
- Cotton wool buds dipped in a mixture of cooled boiled H2O + Baby shampoo (OR)
- NaHCO3 + Cooled, boiled H2O
Artificial Tears

43
Q

What is Herpes Zoster Ophthalmicus ??

A

Reactivation of Varicella Zoster virus in the area supplied by Trigeminal V1
- Vesicular rash around the eye (may or may not involve the eye itself)
- Hutchinson’s sign: Rash on the tip of the nose; indicates nasociliary involvement & is a strong indicator of ocular involvement

44
Q

Rx. of Herpes Zoster Ophthalmicus ??

A

Oral Antivirals for 7 to 10 days
- Ideally started within 72 hrs
- IV Antivirals (Very Severe infection)
Topical Corticosteroids (used to treat any secondary inflammation of eye)
Ocular involvement (Ophthalmology review)
Complications: Ptosis, Post Herpatic Neuralgia, Keratitis, Conjunctivitis, Episcleritis, Anterior uveitis

45
Q

What is Keratitis ??

A

Inflammation of CORNEA. (Microbial Keratitis is sight threatening)
Causes
- Bacterial, Fungal, Amoebic, Parasitic
- Herpes Simplex Keratitis
- Environmental

46
Q

C/F of Keratitis ??

A

Red eye: Pain & Erythema
Photophobia
Foreign body, Gritty sensation
Hypopyon

47
Q

Name the causes for the following regarding Keratitis-
- Bacterial
- Amoebic
- Parasitic
- Environmental

A
  • Stap. aureus (typical) & P aeruginosa (in Contact lens wearers)
    Acanthamoebic keratitis
  • 5% of all cases
  • Eye exposure to soil & contaminated H2O
  • Pain out of proportion to findings
    River blindness- Onchocercal Keratitis
    Environmental
  • Photokeratitis: Welder’s arc eye
  • Exposure keratitis
  • Contact Lens Acute Red Eyes- CLARE
47
Q

Rx. of Keratitis ??

A

Topical Abx.- QUINOLONES (1st line)
Pain: Cycloplegics (eg. Cyclopentolate
Contact lens wearers
- Same day referral to an Eye Specialist for Slit-Lamp Examination to rule out Microbial cause

47
Q

What is Herpes Simplex Keratitis ??

A

Most commonly presents with a DENDRITIC Corneal Ulcer
- Red, Painful eye, Epiphora, Visual Acuity (Decreased)
- Fluorescein stain: EPITHELIAL Ulcer
Rx.-
- Immediate referral to Opthalmology
- Topical ACICLOVIR

48
Q

What is Dacryocystitis ??

A

Infection of Lacrimal Sac
- Epiphora + Swelling & Erythema at the inner canthus of eye
Rx.-
- Systemic Abx.
- IV Abx. if a/w Periorbital Cellulitis

49
Q

What is Orbital Cellulitis ??

A

Infection of Fat & Muscle ‘Posterior to the Orbital Septum’ within the orbit but NOT involving the globe
- Caused by URTI from the Sinuses & carries High Mortality

50
Q

Risk Factors for Orbital Cellulitis ??

A

Childhood (7 to 12 years)
Previous Sinus Infection
Lack of HiB vaccination
Recent eyelid infection/ Insect bite on eyelid (Periorbital Cellulitis)
Ear/ Facial Infection

51
Q

Difference b/w Orbital Cellulitis & Periorbital (Preseptal) Cellulitis ??

A

It is a less serious superficial infection Anterior to the Orbital septum (due to superficial tissue injury)
- It can progress to O Cellulitis

Reduced visual acuity, Proptosis, Ophthalmoplegia/ Pain with eye movt are NOT consistent with Preseptal C

51
Q

Presentation of Orbital Cellulitis ??

A

Redness & Swelling around the Eye
Severe Ocular pain
Visual disturbance
Proptosis
Ophthalmoplegia/ Pain on Eye movt.
Eyelid edema & Ptosis
Drowsiness +/- N & V (Meningeal involvement)

52
Q

Ix. & Rx. of Orbital Cellulitis ??

A

CT with Contrast
Blood culture & Swab
- MC bacterial cause: Strept., Staph. aureus, HiB
Complete Oph. Assessment

Rx: Admit + IV Antibiotics

53
Q

What is Glaucoma ??

A

Optic neuropathies a/w raised IOP. This can be classified based on whether the peripheral iris i covering the trabecular meshwork (as drainage of aq. humour occurs through this from anterior chamber of eye)

53
Q

What is Primary Open Angle Glaucoma ??

A

The Iris is clear of the meshwork; the trabecular network functionally offers an increased resistance to aqueous outflow => increased IOP
- Increases with age
- 1st degree relative have a 16% chance of developing disease

54
Q

Features of POAG ??

A

Slow rise in IOP => Symptomless for a long period
- Typically presents after an IOP measurement during a routine test.
Raised IOP > 24 mmHg (Goldmann type Applanation Tonometry)
Visual field defect
Pathological ‘Cupping’ of optic disc

54
Q

Ix. done for POAG ??

A
  • Automated Perimetry: To assess visual field
  • Slit-lamp examination
  • Applanation Tonometry
  • Central Corneal Thickness
    (CCT) measurement
  • Gonioscopy: Assesses Peripheral Anterior chamber configuration & depth
55
Q

Rx. of POAG ??

A

Eye drops: To lower IOP
- 1st line: PGs analogue
- 2nd line: Beta-blockers, Carbonic anhydrase inhibitor or Sympathomimetic drops
- More advanced: Sx or Laser Rx

56
Q

What is Acute Angle Closure Glaucoma ??

A

Increased IOP secondary to IMPAIRED Aqueous humour outflow
MC among
- Hypermetropia
- Pupillary Dilatation
- Lens growth a/w age

57
Q

Features of AACG ??

A
  • Severe pain: Ocular or Head
  • Decreased Visual acuity
  • C/F worse on Mydriasis (Watching TV in a dark room)
  • Hard, Red eyes
  • Halos around light
  • SEMI-DILATED Non-reactive pupil
  • Corneal oedema => dull/ hazy cornea
  • N & V; even Abd. pain
58
Q

Rx. of AACG ??

A

Emergency; so urgent referral to ophthalmologist
- Direct Parasympathomimetics (eg.- Pilocarpine => causes contraction of ciliary muscles => Trabecular meshwork opens up => Increased outflow
- Beta- blocker: (eg. Timolol => decreased Aq. h production)
- Alpha-2 agonist: Apraclonidine => Dual mechanism => decreases Aq. H synthesis & increases Uveoscleral outflow
IV Acetazolamide (reduces aq. secretion)

59
Q

Definitive Rx. of AACG ??

A

Laser Peripheral Iridotomy
- Tiny hole peripheral iris => Aq. H flowing to the ang;e