RANZCO Ophthalmic Sciences flashcards
RANZCO Ophthalmic Sciences · Build recall with a focused review session.
32 cards. Read the term and the definition here. The deck at the top of this page is optional.
- Snell's law
- n1 sin i = n2 sin r, where n1 and n2 are refractive indices of the two media and i and r are the angles of incidence and refraction measured from the normal.
- Thin lens power
- The power of a thin lens in dioptres equals 1/f, where f is the focal length in metres; a shorter focal length corresponds to a higher power.
- Aqueous outflow pathway
- Aqueous humour flows from the anterior chamber through the trabecular meshwork into Schlemm canal, then collector channels and episcleral veins; obstruction raises intraocular pressure.
- Phototransduction cascade
- Light isomerises 11-cis-retinal to all-trans-retinal, activating rhodopsin and transducin, reducing cGMP, closing cation channels, and hyperpolarising the photoreceptor.
- Apoptosis versus necrosis
- Apoptosis is ATP-dependent, caspase-mediated, and non-inflammatory; necrosis involves membrane rupture, cell swelling, and inflammation.
- Topical drop bioavailability
- Only about 1-5% of a topically applied eye drop reaches intraocular tissues; punctal occlusion reduces nasolacrimal drainage and systemic absorption.
- Relative afferent pupillary defect
- A relative afferent pupillary defect is detected with the swinging flashlight test and indicates asymmetric optic nerve or severe retinal dysfunction.
- Optic neuritis features
- Optic neuritis causes painful subacute monocular visual loss, reduced colour vision, a relative afferent pupillary defect, and often a swollen optic disc; it is associated with multiple sclerosis.
- Bitemporal hemianopia
- Bitemporal hemianopia is loss of both temporal visual fields and localises to the optic chiasm, often from a pituitary lesion compressing the crossing nasal fibres.
- Horner syndrome
- Horner syndrome consists of ptosis, miosis, and anhidrosis from sympathetic pathway interruption; postganglionic lesions may cause ipsilateral facial flushing.
- Third nerve palsy
- A pupil-involving third nerve palsy suggests a compressive lesion such as a posterior communicating artery aneurysm; a pupil-sparing palsy is more often microvascular.
- Papilloedema
- Papilloedema is bilateral optic disc swelling caused by raised intracranial pressure; it is usually painless and may cause transient visual obscurations.
- Cover-uncover test
- The cover-uncover test detects heterotropia by observing the uncovered eye's movement; the alternate cover test detects heterophoria and the total deviation.
- Esotropia and exotropia
- Esotropia is inward deviation of the eye and exotropia is outward deviation; hypertropia is upward deviation of one eye.
- Amblyopia causes
- Amblyopia results from visual deprivation, strabismus, or anisometropia during the critical period and is treated with refractive correction, occlusion, or atropine penalisation.
- Extraocular muscle innervation
- The oculomotor nerve supplies the medial rectus, inferior rectus, superior rectus, and inferior oblique; the trochlear supplies the superior oblique and the abducens the lateral rectus.
- Incomitant strabismus
- In paralytic strabismus the deviation varies with direction of gaze and is greatest in the field of action of the paretic muscle, a pattern called incomitance.
- Bacterial keratitis
- Bacterial keratitis presents with a corneal infiltrate, often a hypopyon, and risk factors include contact lens wear and trauma; urgent scrapings and fortified antibiotics are indicated.
- Acanthamoeba keratitis
- Acanthamoeba keratitis occurs in contact lens wearers with water exposure, causes severe pain and a ring infiltrate, and is diagnosed by culture on non-nutrient agar with Escherichia coli.
- Dendritic ulcer
- A dendritic corneal ulcer with terminal bulbs indicates herpes simplex keratitis; topical corticosteroids are contraindicated during epithelial disease.
- Keratoconus
- Keratoconus is progressive corneal thinning and ectasia causing irregular astigmatism; management includes rigid gas-permeable lenses and corneal collagen cross-linking.
- Acute angle-closure glaucoma
- Acute angle-closure glaucoma causes severe pain, halos, nausea, and a mid-dilated fixed pupil; treatment is pressure-lowering medication followed by laser peripheral iridotomy.
- Glaucomatous optic disc cupping
- Glaucomatous cupping shows an increased cup-to-disc ratio, neuroretinal rim thinning, and sometimes disc haemorrhage, reflecting progressive optic nerve damage.
- Prostaglandin analogues
- Prostaglandin analogues lower intraocular pressure by increasing uveoscleral outflow and can cause iris darkening, eyelash lengthening, and periorbital skin pigmentation.
- Open-angle glaucoma risk factors
- Primary open-angle glaucoma risk factors include age, African ancestry, family history, elevated intraocular pressure, myopia, and thin central corneal thickness.
- Cherry-red spot
- A cherry-red spot appears when retinal pallor surrounds the preserved fovea, classically in central retinal artery occlusion, and is accompanied by sudden painless visual loss.
- Retinal detachment
- Rhegmatogenous retinal detachment occurs when a retinal break allows vitreous fluid to separate the neurosensory retina from the retinal pigment epithelium.
- Diabetic retinopathy signs
- Non-proliferative diabetic retinopathy shows microaneurysms, dot-blot haemorrhages, hard exudates, and cotton-wool spots; proliferative disease shows neovascularisation.
- Orbital cellulitis
- Orbital cellulitis causes proptosis, pain, restricted eye movement, and fever; it is an emergency requiring intravenous antibiotics and imaging, unlike preseptal cellulitis.
- Basal cell carcinoma
- Basal cell carcinoma is the most common eyelid malignancy; it is locally invasive, rarely metastasises, and is treated by complete surgical excision.
- Leukocoria
- Leukocoria is a white pupillary reflex requiring urgent evaluation for retinoblastoma, congenital cataract, and other causes of visual axis opacity.
- Retinopathy of prematurity screening
- Retinopathy of prematurity screening is indicated for infants with birth weight under 1500 g or gestational age under 32 weeks, with examinations starting a few weeks after birth.