Opthamology Flashcards

1
Q

Describe Acute Closed-angle Glaucoma, its symptoms, its cause, and management

A

A disease of middle years, in 25% acute uniocular attacks occur with headache, nausea and a painful red eye, often preceded by blurred vision or haloes around lights, at night.

Symptoms: Clouding (dull) of cornea, ciliary injection, large to cup to disc ratio. Unreactive partially dilated pupil

Cause: blocked flow of aqueous fro the anterior chamber via the canal of schlemn. Pupil dilatation at night worsens this. Intra-ocular pressure then rises to over 30mmHg (normal 15-20) the pupil becomes fixed and dilated and axonal death occurs.

Management:

  • Pilocarpine 2-4% drops/2h (miosis opens a blocked ‘closed’ drainage angle, + 500mg IV acetazolamide stat then 250mg/8h PO/IV (to decrease aqueous formation).
  • analgesia and antiemetics may be used.
  • Admit to monitor IOP.
  • Peripheral iridectomy is done once IOP is controlled
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2
Q

Describe Age-Related Macular Degeneration, its types, and treatment

A

It is the chief cause of registrable blindness, it occurs in elderly who present with deteriorating central vision. There is pigment, drusen and sometimes bleeding at the macula.

Can be classified into two types:

  • Dry ARMD, shows mainly drusen and degenerative changes at the macular and progresses slowly.
  • Wet ARMD, occurs when aberrant vessels grow from the choroid into the neuro-sensory retina and leak. Vision detioriates rapidly and visual distortion e.g. straight lines appearing wavy is a key feature.

Treatment:

  • Patients are advised to stop smoking and have a diet rich in green vegetables.
  • Intravitreal vascular endothelia growth factor (VEGF) inhibitors (bevacizumab aka avastin, ranibizumab) may be used in wet ARMD to increase acuity, decrease cell proliferation and formation of new blood vessels.
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3
Q

Describe cataracts, its presentation, treatment, and post-op complications.

A

Cloudy patches that develop in the lens of the eye. When a cataract is found measure fasting plasma glucose to exclude DM. Immature cataracts red reflex is intact.

Presentation: Blurred vision, unilateral cataracts are often unnoticed, but loss of stereopsis affects distance judgement. Bilateral cataracts cause gradual loss of vision +/- dazzle/glare.

Treatment:

  • Mydriatic drops (atropine), sunglasses, but if symptoms are troubling or lifestyle/driving restricted offer surgery.
  • Surgery involves ideally local (general if young, squeamish), small-incision surgery and phacoemulsion +/- intraocular lens implant.
  • Antibiotic and anti-inflammatory drops 3-6weeks post-op.

Post-op Complications: capsule thickening requiring capsulotomy, astigmatism, eye irritation, anterior evitis, vitreous haemorrhage, retinal detachment, glaucoma.

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4
Q

Describe Orbital Cellulitis, its presentation, causes, and its management.

A

Spread is typically via paranasal sinus infection (or eyelid, dental injury/infection).

Presentation: A child with inflammation in the orbit, fever, lid swelling, and decrease eye mobility.

Causes: staphs, Strep Pneumoniae, Strep Pyogenes, or Milleri.

Management:

  • Admit for prompt, CT, ENT and ophthalmic opinion + antibiotics +/- surgery to prevent extension to meninges or cavernous sinus.
  • Blindness is a risk from pressure on the optic nerve or thrombosis of its vessels. Rule out underlying rhabdomyosarcoma
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5
Q

What is the principle behind Panretinal Photocoagulation treatment in proliferative retinopathy?

A

Reduces the number of hypoxic peripheral retinal cells producing VEGF. This reduces overall oxygen consumption of the retina and the balance between oxygen supply and demand is reestablished. This causes new blood vessels to regress. The main side effects thus is poor peripheral vision and poor night vision due to rod destruction.

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6
Q

What is Presbyopia and briefly describe the mechanism

A

Age-related reduced near-acuity due to failing accommodation. The ciliary muscle reduces tension in the lens, allowing it to get more convex, for close focusing. Young lenses can go from far to near in 0.4s. With age, the lens stiffens and hence the need for glasses for reading. These changes start in the lens at 40yrs and are complete by 60yrs.

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7
Q

Describe Diabetic Retinopathy, pathogenesis, signs, types, and management.

A

Pathogenesis is through microangiopathy in capillaries, precapillary arterioles and venules which causes occlusion +/- leakage. Diabetics should be regularly screened and assessed for any diabetic retinopathy.

Background: microvascular haemorrhage, blot haemorrhages, hard exudates
Pre-proliferative: Cotton wool spots (ischaemia)
Proliferative: New vessel formation
maculopathy e.g. Leakage of vessels close to macula cause oedema and can significantly threaten vision

Management:

  • Those with severe NPDR, proliferative, or ,maculopathy need urgent assessment and treatment.
  • good control of diabetes is treatment of choice
  • pan-retinal photocoagulation is treatment occasionally anti-VEGF may be used in macular oedema.
  • vitreous haemorrhage may require vitrectomy if does not clear
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8
Q

Describe the pupillary light reflex, relative afferent pupillary defect test, and causes of abnormal light reflex.

A

Light detection by the retina is passed to the brain via the optic nerve (afferent pathway) and pupil constriction is mediated by the Oculomotor nerve (efferent pathway). The sympathetic nervous system is responsible for pupil dilatation via the ciliary nerves.

RAPD (Marcus-Gunn pupil): On beaming a light to the normal eye, both pupils constrict ( direct and consensual reaction) if on swinging the light to the affected eye the pupil dilates as it has an afferent lesion.

Causes of an afferent defect:

  • optic neuritis
  • optic atrophy
  • retinal disease
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9
Q

What are some causes of a fixed dilated pupil?

A
  • IIIrd nerve lesion i.e. Cavernous sinus lesion, superior orbital fissure syndrome, diabetes, posterior communicating artery aneurysm
  • mydriatics
  • trauma e.g. Blow to iris
  • acute glaucoma
  • coning i.e uncal herniatiom
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10
Q

Describe Central Retinal Vein Occlusion (CRVO), its causes/associations, symptoms, and management.

A

It is commoner than arterial occlusion. Incidence increases with age.

Causes/associations: Arteriosclerosis, hypertension, diabetes, polycythaemia, glaucoma.

Symptoms: Unilateral painless visual loss, it is less sudden than arterial occlusion. Fundoscopy shows stormy sunset appearance, with swollen optic disc, flame-like haemorrhages.

Management:

  • refer within 24hrs to ophthalmology
  • if ischaemia anti-VEGF and panretinal photocoagulation may have a role
  • monitor non-ischaemic as may progress
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11
Q

Describe Central Retinal Artery Occlusion (CRAO), its symptoms, and management

A

Occlusion is often thrombo-embolisation i.e. From clot, tumour, infective.

Symptoms: Sudden, unilateral, painless visual loss within seconds of occlusion. In 90% visual acuity is finger-counting or worse. Retina appears white with a cherry red spot at the macula.

Management:

  • exclude temporal arteritis
  • look for signs of cause
  • if seen with 6h aim to increase retinal blood flow by reducing ocular pressure.
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12
Q

Describe blind registration

A

A person is eligible to register as blind if their acuity is less than 3/60 or higher but with substantial visual field loss i.e. Glaucoma. Those greater than this but less than 6/60 can register as partially sighted.

It is the responsibility of the local authority. Application is made by consultant ophthalmologist and is voluntary, not statutory.

Registering as blind entitles one to extra tax allowances, reduced TV licences, travel concession, access to talking books.

The Royal National Institute for the Blind will advise on aids, such as guide dogs.

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13
Q

Describe Anterior uveitis, it symptoms, causes, tests, and management

A

The uvea is the pigmented part of the eye (iris, ciliary body, choroid). The iris and ciliary body make up the anterior uvea.

Symptoms: Acute, painful red eye, photophobia, decreased acuity (due to aqueous precipitates), lacrimation (no sticky discharge unlike conjunctivitis), circumcorneal congestion (ciliary congestion), small pupil though may also be irregular or partially dilated.

Causes: Ankylosing spondylitis, stills, sarcoid, behcets, crohns, UC, herpes, TB, syphilis, HIV MS, lymphoma

Tests: Talbot’s test is +ve I.e. Pain increases on convergence as patients watch a finger approach their nose, slit lamp show white precipitates on back of cornea, and anterior chamber cells.

Management:

  • Aim to prevent damage from prolonged inflammation as it can lead to disruption of the flow of aqueous and so cause glaucoma +/- adhesions between iris and lens.
  • Prednisolone drops 0.5-1%/2h help reduce inflammation
  • to prevent adhesions keep dilated wit cyclone tollgate 0.5%/8h unless very mild.
  • Intravitreal and biological agents such as anti-TNF show promise adalimumabhas a role.
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14
Q

Describe conjunctivitis, its symptoms, and management.

A

The conjunctiva (the layer that covers the front of the eye) Is red and inflamed usually due to adenoviruses, bacteria, or allergies.

Symptoms: Red inflamed conjunctiva on palpating of the globe the vessels may be moved over the sclera. Acuity, pupillary responses are unaffected. Eyes itch and burn and lacrimation often with sticky discharge.

Management:

  • usually self-limiting
  • Chloramphenicol 0.5% drops/4-6h are often used
  • try antihistamine drops for allergic conjunctivitis
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15
Q

Describe optic neuritis, it’s causes, signs, and management

A

Causes: MS, syphilis, diabetes, vitamin b12 deficiency drugs e.g. Amiodarone, ethambutol, isoniazid

Symptoms:

  • Unilateral loss of acuity occurs over hours or days.
  • Colour vision is affected, reds appear less red
  • pain, eye movement hurts.
  • The pupil shows an afferent defect.
  • Disc size is normal in 60%, swollen in 23% and blurred or hyperaemic in 18%

Management:

  • recovery is usually over 2-6 weeks
  • in acute setting methylprednisolone for 3days is recommended
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16
Q

Describe Horner’s syndrome and some causes

A

Occurs on disrupting sympathetic fibres, so the pupil is miotic (smaller), and there is partial pots is, and the pupil does not dilate in the dark. Unilateral facial anhydrosis is may indicate a lesion proximal to the carotid plexus.

Causes:

  • posterior inferior cerebellar artery or basilar artery occlusion
  • MS
  • cavernous sinus thrombosis
  • Pancoasts tumour
  • Hypothalamic lesions
  • Cervical adenopathy
  • mediastinal masses
  • pontine syringomyelia
  • aortic aneurysm
17
Q

Describe retinitis pigmentosa and its symptoms.

A

This is the most prevalent inherited degeneration in the retina. Due to degeneration of rod photoreceptors. Sporadic types are more common (mostly autosomal recessive, though autosomal dominant types has better prognosis, X-linked is rarest but worst prognosis) Through life, 25% retain the ability to read, with reduced visual fields.

Symptoms:

  • initially deceased night vision due to loss of rod photoreceptors
  • ring scotoma
  • loss of peripheral vision first then central vision
18
Q

Describe Retinal detachment, its symptoms, and management

A

May be rhegmatogenous (Greek for break, occur when retinal tear leads to fluid accumulation and separation of retinal layer), or secondary due to fibrous bands in diabetes or melanoma. May also occur by trauma e.g. Cataract surgery. If a retinal break is identified before a detachment, cryo/laser retinopexy may be preventative

Symptoms: The four ‘F’s, floaters, flashes, field loss, fall in acuity. It presents painless. Ophthalmoscopy shows grey opalescent retina ballooning forward. Note course of venules and retinal fold.

Management:

  • urgent referral for surgery, vitrectm and Gas tamponade or silicone oil.
  • Cryotherapy/laser coagulation is used to secure the retina.
  • Post-op re-detachment occurs in 5-10%
19
Q

Describe episcleritis and it management

A

Inflammation below the conjuctiva in the episclera is often seen with an inflammatory nodule. Bilateral in 30%. The sclera may look blue below a focal cone-shaped wedge (with the thin end towards the pupil) of engorged vessels which can be moved over the area unlike in scleritis. The eye aches and is tender, visual acuity is OK.

Management: Topical or systemic NSAIDs

20
Q

Describe scleritis

A

Rarely the sclera itself may be inflamed and pain is significant. There is generalised inflammation and oedema of the conjunctiva and scleral thinning tends to be due to vasculitis, refer to specialist.

21
Q

Describe blepharitis, symptoms and management.

A

+/- style, Lid inflammation e.g. Due to staphs, seborrhoeic dermatitis or rosacea.

Symptoms: eyes having burning itching red margins with scales on the lashes.

Management:

  • cleaning eye especially crust of lashes, baby shampoo
  • fusidic acid, steroid drops, oral doxycycline have a role
  • if style hot compresses
22
Q

Describe chronic simple glaucoma, its symptoms, screening, and treatment.

A

Can lead to blindness and may be asymptomatic and so screening of at risk groups is necessary. If IOP raised life-long follow up needed.

Symptoms: Asymptomatic, Visual field loss, increased cup to disc ratio, scotomata.

Screening if:

  • older than 35 with FHx
  • Afro-Caribbean
  • Myopia
  • Diabetic/thyroid eye disease

Screening entails multiple stimulus static visual field screening, documenting optic disc cupping and increased IOP.

Treatment:

  • Reduce IOP by 30% of baseline. Surgery if drugs fail
  • Prostaglandin analogues (latanoprost) acts to increased uveoscleral outflow, SEs include red eye, iris colour change, periocular skin pigmentation, eyelash growth
  • B-blockers (timolol) to decrease production of aqueous. SEs include bradycardia, bronchospasm, dry eyes
  • alpha-adrenergic agonists (brimonidine) decreased production of aqueous and increased uveoscleral outflow SEs include lethargy, dry mouth
  • Carbonic Anhydrase inhibitors (acetazolamide) decreased production of aqueous SE include lassitude, dyspepsia, Hypokalaemia,
  • Miotics (pilocarpine) decrease resistance to aqueous outflow it cause miosis and reduce acuity and brow ache from ciliary muscle spasm.
  • Surgery, trabeculectomy s a filtration surgery that establishes a pressure valve at the limbus so aqueous can flow into a conjunctival bleb.
23
Q

What is an Argyll-Robertson pupil?

A

Occurs in neurosyphillis and diabetes. There is bilateral miosis, pupil irregularity, and no response to light, but the is response to accomodation (The prosit tunes pupil accommodate buts does not react). The iris is spongy and pupils dilate poorly, and there may be ptosis.

24
Q

Describe Charles Bonnet Syndrome and its risk factors.

A

Characterised by persistent or recurrent complex hallucinations (usually visual or auditory) occurring in clear consciousness. This is usually against a background of visual impairment. In sight is usually preserved. Must occur in absent of any other significant neuropsychiatric disturbance.

Risk factors: Advanced age, peripheral visual impairment (ARMD, Glaucoma, cataract), social isolation, sensory deprivation, early cognitive impairment.

25
Q

Describe Oculogyric crisis, it’s causes, symptoms, and management.

A

A dystonias reaction to certain drugs or in medical condition characterised by prolonged involuntary upward deviation of the eyes.

Causes:

  • Drugs e.g. Neuroleptics, carbamazepine, cisplatin, levodopa, lithium, Nifedipine, metoclopramide, domperidone, certirizine.
  • Tourette’s syndrome, MS, Neurosyphilis, Trauma, Parkinson’s, Kernicterus.

Symptoms: restlessness, agitation, malaise, extreme sustained upward deviation of the eyes, widely opened mouth with tongue protrusion, ocular pain.

Management:
-IV antimuscarinic e.g. Procyclidine usually effect within 5-30 minutes.

26
Q

Describe Keratoconus, it’s symptoms, and management.

A

The cornea bulges and becomes conical in shape on lateral viewing due to corneal thinning. More common in people with allergic disease, Down’s, Connective tissue disorders

Symptoms: visual distortion, causes multiple ‘ghost’ images, photophobia, Fleischer rings due to haemosiderin deposition.

Management:

  • Rigid Gas Permeable contact lenses, to correct vision.
  • refer to ophthalmology for monitoring
  • if severe deterioration Corneal cross-linking if under 35yrs.
27
Q

Describe Blepharospasm, it’s symptoms, and management

A

Involuntary contraction of the orbicularis oculi. Stress is an important exacerbating factor. May be caused by neuroleptic drugs, Parkinson’s disease, progressive supra nuclear palsy, paraneoplastic or idiopathic.

Symptoms: Tight eyes, often preceded by exaggerated blinking. Other dystonias may be present. Usually starts unilaterally becoming bilaterally.

Management:
-Botulinum neurotoxin