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16 Cards in this Set
- Front
- Back
It's a full-thickness defect (tear/hole/split) in the sensory retina which may occur with or without detachment of the retina
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retinal break
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It's a separation of the photoreceptors from the underlying RPE.
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retinal detachment
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What are the 3 main types of retinal detachment (RD)?
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1. Rhegmatogenous RD
- tear in the retina 2. Tractional RD - pulling out from the RPE 3. Exudative RD - fluid in the RPE |
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A specific type of RD which occurs when a retinal break allows liquefied vitreous to seep into the potential space between the NSR & RPE.
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Rhegmatogenous RD
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Formation of a Rhegmatogenous RD requires what 3 things?
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1. A FULL thickness retinal break
2. Traction holding the break open 3. Liquefied vitreous |
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What are some CAUSES of retinal breaks?
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- Mechanical tearing: something can "tug" on the retina, ripping it.
- Atrophic hole formation: the retina itself can degenerate (wither away) |
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What are some examples of retinal breaks?
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1. Posterior Vitreous Detachment (PVD)
2. Trauma 3. Developmental/Degenerative abnormalities 4. Traction induced by fibrovascular proliferation (Ex: Diabetic Retinopathy) |
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This is a normal age-related process, whereby vitreous gel liquefies over time
- Probably due to accumulated toxic effects of light irradiation and metabolic waste products - Will happen in ALL eyes eventually - Usually WITHOUT causing RD! |
Vitreal Synchysis
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Refers to a normal age-related process, whereby the solid vitreous gel collapses/contracts forward while liquid fills retrohyaloid space
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Posterior Vitreous Detachment (PVD)
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PVD is accompanied by what 2 characteristics?
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1. Synchysis
- liquefaction of vitreous 2. Syneresis - shrinkage or contraction of vitreous |
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Pt c/o of:
1) Flashes (photopsia) - it's observed when retina is tugged on as gel pulls away 2) Floaters - observed when moving vitreous opacities cast a shadow on the retina: 1. Single large floater (Weiss Ring) 2. Cobwebs (condensation of collagen fibers) 3. Shower of small dark spots (RBC's) Signs: 1. Easier to see Weiss Ring 2. Vitreous hemorrhage 3. Difficult but not impossible to observe detached/condensed vitreous gel at slit lamp What's the Dx & Tx? |
a) Posterior Vitreous Detachment (PVD)
b) Tx: 1. Must rule out RD in symptomatic patients - Careful DFE - Look for associated signs/symptoms of RD 2. Monitor closely while "flashes" persist 3. Reassurance - NO cure for annoying floaters - will become LESS noticeable over time |
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What are some SYMPTOMS of RD?
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1. NOT all patients are symptomatic!
2. Majority of spontaneous cases notice "flashes" and/or floaters with preceding PVD. - "Flashes" may disappear if a piece of retina (operculum) tears away completely 3. A "curtain" or "shadow" in vision may be seen to progress centrally - initially location signals that of primary retinal break |
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What are some SIGNS of RD?
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1. RAPD may be present if RD is extensive
2. IOP may be slightly LOWER than fellow eye 3. Mild iritis is common 4. Pigment cells in anterior vitreous - Shafer's sign or "tabacco dust" 5. Retinal Breaks - most often found in superotemporal quadrant - may appear as complete/incomplete flap tears, operculated tears, dialysis, holes |
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What's the major clinical differences between a fresh RD vs long-standing RD?
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a) Fresh RD
- Elevated retina has a translucent appearance - Appears "wrinkled" - Seen to undulate with eye movements b) Long-standing RD - Detached retina becomes thinned & atrophied - Intraretinal cysts may form - Demarcation lines |
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Pt c/o:
- Flashes - Floaters - A "curtain"/"shadow" in central vision Signs: - RAPD - Lower IOP in affected eye - Mild iritis - Shafer's sign/Tabacco dust = pigment cells in anterior vitreous What's the Dx and Tx? |
a) Retinal Detachment
b) Tx: 1. Most RD's will progress to severe permanent vision loss without treatment 2. Successful reattachment depends on permanent closure of retinal breaks responsible in a timely fashion 3. Reattachment techniques will be discussed in detail by retinal specialist - Pneumatic retinopexy (gas bubble tamponade - Scleral Buckling (with/without fluid drainage) |
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What are some diagnostic methods for Rhegmatogenous RD?
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1. Suspicion should be aroused when typical symptoms are described
2. Evaluation must include careful DFE w/BIO - Scleral indentation may be appropriate 3. B-scans useful when media opacities obscure view 4. Slit-lamp lenses may be helpful |