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66 Cards in this Set
- Front
- Back
Describe the structure of the vitreous? |
• Virtually acellular • Viscous • Collagen framework, reinforces with hyaluronate |
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What percentage of the vitreous is water? |
98% |
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What is the volume of the vitreous in an emmertropic eye? |
4.5 ml |
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What are the Condensations of vitreous? |
• Anterior hyaloid membrane • Posterior hyaloid membrane • Cloquet’s canal |
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Where are the attachments of the vitreous? |
• Vitreous base- ora serrata
• Weigert’s ligament - attachment to posterior lens surface (anterior end of Cloquet’s)
• Vitreopapillary adhesions- Weiss ring
• Vascular adhesions (hence bleeds with PVD)
• Areas of vitreoretinal degeneration- Lattice degeneration, cystic retinal tufts |
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What are the changes that occur to the vitreous with age? |
• Vitreous gel liquefaction (syneresis) • Fluid filled cavities • Fluid dissects posterior hyaloid face from ILM • Remaining solid vitreous detaches inferiorly • Posterior Vitreous Detachment • Prevalence increases with age |
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What are the causes of posterior vitreous detatchement PVD? |
• myopia • ageing • trauma • inflammations • hereditary causes |
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What are the symptoms with PVD? |
• Photopsia
• Blurred vision- Haemorrhage
• Floaters- Spots, cobwebs or flies |
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What are some of the vitreous opactities that may be seen? |
• Muscae volitantes: remnants of hyaloid system • Syneresis • Weiss ring • Haemorrhage- Red blood cells • Tobacco dust: pigment cells • Inflammatory cells • Floaters seen more frequently against a bright background, are common |
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What percentage of |
• Without vitreous haemorrhage, 4% develop retinal breaks • With vitreous haemorrhage,20% develop retinal breaks |
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How do you investigate a PVD? |
• Full symptoms & history • Risk factors for retinal detachment • Visual acuity • Look fo rRAPD– absent • Look for cells in AC– absent • Measure IOP– equal between two eyes • Dilated fundus examination • Look for pigment in anterior vitreous • Ocular Coherence Tomograph OCT |
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What is shafer's sign? |
alludes to the clinical finding of pigment cells in the vitreous. |
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When might you see shafer's sign? |
• Symptoms of flashing lights and/or floaters of recent onset
• Suspect retinal tear/detachment |
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What is the set up to look for/at shafer's sign? |
• Dilated pupil • Direct focal illumination • Illumination normal to the cornea • Narrow slit-beam, small angle between observation and illumination • Moderate magnification ~ 15-24x |
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How would you examine the eye to look for shafer's sign? |
• Patient looks straight ahead • Focus on anterior vitreous • Ask patient to make horizontal and vertical saccades • Look for small, regular, brown particles |
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When looking at shafer's sign, what must you distinguish between? |
White cells Pigment cells |
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When looking at shafer's sign, whites cells are suggestive of what? |
Inflammation posterior uveitis |
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What would help to distinguish between white cells and pigment cells? |
Red free filter Red blood cells appear black |
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State the management of PVD. |
Education • give leaflets • if symptoms get worse or change return immediately |
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How do you manage PVD if there is a medium risk to retinal detatchement? |
Review in 6/12 time Education them on signs and symptoms to look our for |
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How do you manage PVD if there is a large risk to retinal detatchement? |
Refer as an emergency |
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What can cause vitreous haemorrhage? |
• Proliferative retinopathies • PVD • Trauma • Disciform macular degeneration |
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What are Proliferative rerinopathies? |
• Diabetes Mellitus • Retinal vein occlusion • Sickle cell retinopathy • Eale’s disease |
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What are the complications of vitreous haemorrhage? |
• Syneresis • Fibrosis→traction retinal detachment • Haemolytic (ghost cell) glaucoma • Synchisis scintillans • Ochre membrane |
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What is Asteroid Hyalosis? |
• Common degenerative condition • Calcium salts in vitreous • Highly mobile • Do not settle inferiorly whenpatient is immobile |
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When does asteroid Hyalosis increase? |
Increases with age 3% of those aged 75-86 |
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Who is Asteroid Hyalosis more common in? |
Men |
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What are the symptoms of asteroid Hyalosis? |
Usually asymptomatic |
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How would you investigate asteroid Hyalosis? |
• Visual acuity • Usually only slightly reduced • Dilated fundus examination • Association with diabetes? • Refer to GP for vascular workup |
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When would you refer a case of asteroid Hyalosis to the ophthalmologist? |
• Refer to ophthalmologist if visual acuity markedly reduced • Rare |
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What is Synchysis Scintillans? |
• Cholesterol crystals settle inferiorly when patient immobile
• May spill over into anterior chamber |
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What is Synchysis Scintillans associated with? |
Associated with long-standing vitreous haemorrhage in a blind eye |
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What are the symptoms of Acquired Maculopathies? |
• Reduced visual acuity - Particularly at near • Positive scotoma • Metamorphopsia - Micropsia - Macropsia • Colour vision? • Dark adaptation |
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How would you investigate symptoms of Acquired Maculopathies? |
• Visualacuity - Distance and near • Amsler chart • Colour vision • Dilated fundus examination - Volk lens (66D ideal) • Optical coherence tomography |
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Name some macula diseases. |
• Angioid streaks • ARMD • Central serous retinopathy • Choroidal folds • Cystoid macular oedema • Epiretinal membranes • Macular dystrophies • Macular holes • Myopic maculopathy • Sub-retinal Neovascular Membranes • Traumatic maculopathy |
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What is Angioid Streaks? |
• Small breaks in Bruch's membrane, that may become calcified and crack.
• Usually bilateral
• 50% related to systemic disorders of connective tissue |
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Describe what Angioid Streaks may look like. |
• Dark, irregular lines radiating from ONH which end abruptly posterior to the equator
• May interlink around ONH
• May cause sub-retinal neovascular membranes which may bleed |
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What are Angioid Streaks associated with? |
• Pseudoxanthoma elasticum • Marfan’s syndrome • Paget’s disease • Sickle cell anaemia & thalassaemia • Lead poisoning • Acromegaly |
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How would you manage/treat Angioid Streaks? |
• Systemic evaluation - If not already diagnosed • Observation • Advice - Avoid contact sports - Wear safety spectacles • Intravitreal Anti-VEGF if choroidal new vessels |
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What is Central serous retinopathy? |
A condition where fluid builds up behind the retina in the eye. It can cause sudden or gradual vision loss as the central retina detaches. |
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At what age would you see central serious retinopathy? |
20-45 yrs |
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Who is central serous retinopathy more common in? |
Males
Myopia |
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What is the pathogenesis of central serous retinopathy? |
• Breakdown of blood retinal barrier
• Fluid accumulates in subretinal space
• Sometimes associated with RPE detachment |
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What are the symptoms of central serous retinopathy? |
• Blurred central vision • Metamorphopsia & micropsia |
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What are the signs of central serous retinopathy? |
• VA 6/9 – 6/18 - often improves with a +1D lens • Positive central or paracentral scotoma • Red desaturation • Small serous sensory retinal detachment of macula • Sometimes associated with an optic pit |
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What is Central Serous Chorioretinopathy? |
when fluid builds up under the retina.
This can distort vision. The fluid leakage comes the choroid. |
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What is the prognosis of Central Serous Chorioretinopathy? |
• 90% spontaneously resolve • 33% recur |
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What is the treatment/management for Central Serous Chorioretinopathy? |
• Refer to an Ophthalmologist routinely Treatment • Usually conservative • Occasionally photocoagulation indicated |
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What are the Choroidal folds? |
• Hypermetropia • Ocular disease • Orbital disease |
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What are the ocular diseases that cause choroidal folds? |
• Scleral buckling
• Scleritis
• choroidal masses
• Oculartrauma
• Papilloedema |
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What are the orbital diseases that cause choroidal folds? |
• Thyroid eye disease • Tumours • Cellulitis |
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What is this? |
Cystoid Macular Oedema |
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What is Cystoid Macular Oedema? |
Henle’s layer is unsupported around macula allowing extracellular fluid to accumulate |
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What is the source of leak in Cystoid Macular Oedema? |
• Maular capillaries • Forms “flower-petal” arrangement as a result of radiation of cone fibres |
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What might Cystoid Macular Oedema develop? |
Intreretinal cysts |
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What are the symptoms of Cystoid Macular Oedema? |
• Reduced visual acuity • Metamorphopsia • Micropsia |
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What are the signs of Cystoid Macular Oedema? |
• Loss of the foveal depression, thickening of the retina. • Multiple cystoid areas in the sensory retina • Red-free light using a fundus contact lens |
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What are the causes of Cystoid Macular Oedema? |
• Diabetic & hypertensive retinopathy • Macroaneurysms & telangiectasia • Tumours • Retinitis pigmentosa • Irvine-Gass syndrome |
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What is the prevalence of macular hole? |
3 : 1000 F >M Aged 60 - 70 |
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What are the symptoms of macular hole? |
• Present as visual loss when one eye is covered
• Minimal symptoms otherwise metamorphopsia |
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What are the signs of macular hole? |
• Full thickness retinal hole • Cuff surrounding subretinal fluid • Deposits at base |
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What are the causes of macular hole? |
• Idiopathic • Myopia • Trauma |
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What is this? |
Myopic degeneration |
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What is Myopic degeneration? |
• In very large eyes, retina & choriocapillaris are thinned • Myopic macular degeneration results |
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What are the early findings of Myopic degeneration? |
• PPA • Thinned macular RPE • Tilted disc |
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What are the late findings of Myopic degeneration? |
• Lacquer cracks (breaks in Bruch’s membrane) • Macular haemorrhages • CNV • Macular atrophy • Peripheral & macular holes predispose to RD |