Opthalmology Flashcards

(38 cards)

1
Q

Glaucoma vs Uveitis for Acute Painful Red Eye
How to differentiate ?

A

Glaucoma -
Dilated, Haloes

Uveitis -
Constricted Oval Pupil

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2
Q

Horners Syndrome

  1. Central Lesions
  2. Pre-Ganglionic
  3. Post-Ganglionic
A
  1. Anhydrosis of Face Arms Trunk

Stroke
Syringomyelia
Multiple sclerosis
Tumour
Encephalitis

  1. Anhydrosis of Face

Pancoast Tumour
Thyroidectomy
Trauma

  1. Post Ganglionic - No Anhydrosis

Carotid artery dissection
Carotid aneurysm
Cavernous sinus thrombosis
Cluster headache

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3
Q

What drug is used for Dilating Pupils in Horner’s Syndrome ?

A

Apraclonidine drops (an alpha-adrenergic agonist)

causes pupillary dilation in Horner’s syndrome due to denervation supersensitivity but produces mild pupillary constriction in the normal pupil by down-regulating the norepinephrine release at the synaptic cleft

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4
Q

Keith-Wagener’s Classification

A

Grade 1 – Silver wiring  

Grade 2 – + AV nicking 

Grade 3 – + flamed shape, dot and blot haemorrhages and cotton wool exudates 

Grade 4 – + papilloedema 

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5
Q

How to differentiate 1st/2nd order from 3rd order in Horner’s Syndrome ?

A

Apraclonidine drops 1st which will cause ipsilateral dilation and contralateral constriction = Confirming Horner

Then Hydroxyamphetamine drops will dilate pupils for 1st/2nd order

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6
Q

Glaucoma Pharmacology !!!

Watch Medicosis Video if needed

A

Alpha 1 Agonist –> Vasoconstriction so less Plasma filtered to make Aqueous Humor

Beta Blocker —> Prevent formation of Aqueous Humor by Panacinar Cells

OR Alpha 2 (Anti-sympathetic) which causes Less Noradrenaline release which will inturn not stimulate Beta Receptors so technically Beta Blockade

Alpha 2 agonist (Primary MOA)
OR PGF2 alpha (-prost) —> Dilate the Eye and Increase the Angle

Carbonic Anhydrase acts on PCT reduced water absorption and reduce plasma formation

Parasympathomimetic (Pilocarpine) which is a Muscarinic Agonist (M3) –> Increases the Angle and Promotes Drainage

  1. Any inhibitor / blocker –> reduce production
  2. Any agonist
    –> Increase outflow

Brimonidine (alpha 2 agonist) does both

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7
Q

Side Effects of Prostaglandin Analogues

A

Long Eye Lashes
Brown Iris Pigmentation

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8
Q

When not to give Alpha 2 Agonist ?

A

MOAI and TCA co-use

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9
Q

Diabetic Retinopathy Classification

NPDR
PDR
Maculopathy

A
  1. Mild NPDR

1 or more microaneurysm

  1. Moderate NPDR

microaneurysms

blot hemorrhages

hard exudates

cotton wool spots (‘soft exudates’ - represent areas of retinal infarction)

venous beading/looping

intraretinal microvascular abnormalities (IRMA) less severe than in severe NPDR

  1. Severe NPDR

blot haemorrhages and microaneurysms in 4 quadrants

venous beading in at least 2 quadrants

IRMA in at least 1 quadrant

  1. PDR

Neovascularization
Common in T1 DM

  1. Maculopathy

Macular oedema
Common in T2 DM

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10
Q

Treatment for NPDR PDR and Maculopathy

A

PDR

Neovascularization - Laser photocoagulation 

a. 50% experience reduction in Peripheral Vision
b. Decrease in NIGHT VISION)

Maculopathy

intravitreal VEGF inhibitors

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11
Q

Drugs that Precipitate Glaucoma

A

Anti-Cholinergic and TCA

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12
Q

Flashes in Which Conditions ?

A

Flashes in

Vitreous detachment (Flashes often on Temporal Side & Diabetics) + Weiss Ring

Retinal detachment (Peripheral to Central Shutdown)

Cataract

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13
Q

Holmes-Adie pupil

A

Dilated
Absent Knee Reflexes
Absent Eye Reflex

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14
Q
A

Marcus Gunn Pupil-Relative afferent pupillary defect-
defect is found by the ‘swinging light test’. It is caused by a lesion anterior to the optic chiasm i.e. optic nerve or retina, lesion btw optic chiasma & LGB is congruous defect and lesion posterior to LGB & occipital area is incongruous defect.
Finding: the affected and normal eye appears to dilated rather constricting when light is throw on the affected & constrict when light throw into the healthy eye.
Causes: retina: detachment, optic nerve: optic neuritis e.g. MS
Pathway of pupillary light reflex:
afferent: retina → optic nerve → lateral geniculate body(LGB) → midbrain
efferent: Edinger-Westphal nucleus (midbrain) → oculomotor nerve

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15
Q

Does Viral URTI associate with Blepharitis ?

A

Nope !!!

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16
Q

Pupils Dilated in which conditions ?

HoT COP ATTACK with a GUN

A

Holmes Adie
Traumatic Iridoplegia
Congenital
Oculomotor nerve palsy
Pheochromocytoma
Atropine
Tropicamide
TCA
Amphetamine
Cocaine
Marcus gun/RAPD

17
Q

Dacryocystitis Treatment

A

Systemic Abx –> IV if Periorbital Cellulitis

18
Q

Pinguecula ?
What does it Progress into ?

A

Benign yellow-white thickening which is usually bilateral and caused by ultraviolet (UV) exposure.

Progresses into Pterygium Surfers Eye - raised, fleshy, triangular-shaped growth that starts in the corner of your eye

19
Q

What’s a Chalazion ?

A

Meibomian cyst - Painless

20
Q

Most Common Ocular Manifestation in RA ?

A

Keratoconjunctivitis Sicca

21
Q

Herpes Simplex Keratitis Investigation ?

A

Fluorescein Staining –> Dendritic Ulcers

22
Q

1st line for Chronic Open Angle Glaucoma ?

A

Lantanoprost
Prostaglandin Analogues !!!!!!!

vs Open Angle if Acute
IV Carbonic Anhydrase and Timolol

23
Q

Treatment of ARMD ?

Investigations ?

A

If Dry - Watch and Wait
If Wet - Anti VEGF

Slit Lamp is the Investigation of Choice +/- Colour fundus photography

Once Wet ARMD suspected –> fluorescein angiography +/- indocyanine green angiography

Optical coherence tomography - To show 3D Retina

24
Q

Hypermetria or Myopia

Risk Factor for Acute vs Chronic Open Angle Glaucoma ?

A

Acute - Asians / Hypermetria / Anti Cholinergic or Antidepressants / 55-70

Chronic - Africans / Myopia / >40

25
Strongest Risk Factor for ARMD ?
Smoking !!!
26
Retinitis Pigmentosa
Night Blindness + Tunnel Vision Fundoscopy - black bone spicule-shaped pigmentation in the peripheral retina, mottling of the retinal pigment epithelium Associated diseases Refsum disease: cerebellar ataxia, peripheral neuropathy, deafness, ichthyosis Usher syndrome abetalipoproteinemia Lawrence-Moon-Biedl syndrome Kearns-Sayre syndrome Alport's syndrome
27
Optic Neuritis 1. Features 2. Investigation of Choice 3. Treatment
Red Saturation + Central Scotoma + Ophthalmoplegia + RAPD NO VISION LOSS !!!!! MRI with Gadolinium Contrast Steroids
28
What pathologies cause Tunnel Vision (CHOP P GR)
Choroidoretinitis Hysteria Optic Atrophy 2ry to tabes dorsalis Papilloedema Glaucoma Retinitis pigmentosa
29
Pathologies about Angloid Retinal Streaks
SPACE sickle-cell anaemia Paget's disease pseudoxanthoma elasticum acromegaly calcification and breaks in Bruch's membrane Ehler-Danlos syndrome
30
CRVO vs CRAO Fundocopy Changes
CRVO - Stormy Sunset - Multiple Hemorrhages CRAO - Cherry Red Spot
31
Orbital Cellulitis Tx
1. IV antibiotics --> risk of cavernous sinus thrombosis and intracranial spread
32
Orbital Cellulitis Risk Factors
Risk Factor 1. Lack of Hemophilus influenzae type b (Hib) vaccination
33
Preseptal vs Orbital Cellulitis
Reduced visual acuity, proptosis, ophthalmoplegia/pain with eye movements in Orbital Cellulitis
34
Angloid Retinal Streaks on Fundoscopy
Irregular dark red lines radiating from the optic nerve.
35
Vitamin AC and E are given in ARMD. So when is it contraindicated to give this ?
In SMOKERS but its not ACE its only Beta-Carotene
36
Herpes Zoster Opthamicus 1. Treatment 2. Predictor of Ocular Involvement
1. Oral Acyclovir 2. Hutchinson's Sign
37
Optic Atrophy
Acquired MS papilloedema (longstanding) raised intraocular pressure (e.g. glaucoma, tumour) retinal damage (e.g. choroiditis, retinitis pigmentosa) ischaemia toxins: tobacco amblyopia, quinine, methanol, arsenic, lead nutritional: vitamin B1, B2, B6 and B12 deficiency Congenital causes Friedreich's ataxia mitochondrial disorders e.g. Leber's optic atrophy DIDMOAD - the association of cranial Diabetes Insipidus, Diabetes Mellitus, Optic Atrophy and Deafness (also known as Wolfram's syndrome)
38