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Retina - 2

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Hypertensive Retinopathy

• Describe fundus findings associated withhypertensive retinopathy? – Constriction of retinal arterioles

 – Intraretinal hemorrhages

 – Cotton wool spots

 – Macular edema

 – Disc edema

 – Retinal neovascularization

• What are manifestations of hypertensivechoroidopathy?

 – Elschnig spots and Siegrist streaks

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Diabetic Retinopathy

• WESDR

 – IDDM 99% have retinopathy after 20 yr 

 – NIDDM 60% have retinopathy after 20 yr 

•DCCT – Tight glucose control decreases retinopathy in IDDM

• UKPDS

 – Glucose control decreases retinopathy in NIDDM

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Diabetic Retinopathy

• ETDRS – Focal laser indicated for CSME

• Retinal thickening at or within 500 mm of the foveal

center 

• Retinal thickening associated with hard exudate at or within 500 mm of the foveal center 

•  A zone of retinal thickening larger than 1 disc area

within 1 disc diameter of the foveal center 

 – PRP indicated for high risk PDR, not for NPDR (can

consider for severe NPDR) –  ASA does not affect vitreous hemorrhage

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Diabetic Retinopathy

• Describe the 4:2:1 rule – 4 quadrants of diffuse intraretinal hemorrhage and

microaneurysms

 – 2 quadrants of venous beading

 –1 quadrant of intraretinal microvascular abnormalities

• What is severe NPDR and what 1-year risk does

it carry for progression to high-risk PDR?

 – 1 of the above criteria

 – 15%

• What is very severe NPDR and what 1-year risk

does it carry for progression to high-risk PDR?

 – 2 of the above criteria

 – 45%

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Diabetic Retinopathy

• DRS - PRP reduces severe visual loss by 50% for high risk

PDR

 – Mild (1/4 to 1/3 disc area) NVD with vitreous hemorrhage

 – Moderate to severe NVD with or w/o vitreous hemorrhage

 – Moderate (1/2 disc area) NVE with vitreous hemorrhage

• DRVS - vitrectomy for nonclearing vitreous hemorrhage

 – Early vitrectomy beneficial for IDDM

 – Early (1 mo) same as late (6 mo) for NIDDM

• Other indications for surgery

 – Macula involving TRD

 – Combined TRD/RRD

 – Refractory macular edema with taut posterior hyaloid

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Sickle Cell Retinopathy

• Which form of sickle cell is associated with the mostserious ocular complications?

 – Hb SC

• What are the findings on nonproliferative sickle cellretinopathy?

 – Salmon patch hemorrhage (intraretinal hemorrhage)

 – Refractile spot (resorbed hemorrhage) – Black sunburst (RPE hypertrophy)

• What are the stages of proliferative sickle cell retinopathy?

 – I: arteriolar occlusions

 – II: arteriovenous anastomoses

 – III: sea-fan neovascularization – IV: vitreous hemorrhage

 – V: tractional retinal detachment

• What is the preferred treatment for PSR?

 – Peripheral scatter photocoagulation

 –Vitrectomy for non-clearing vitreous hemorrhage or RD

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ROP

• Describe the stages of ROP

 – 1: demarcation line

 – 2: elevated ridge

 – 3: ridge with extraretinal fibrovascular proliferation

 – 4: subtotal retinal detachment

•  A extrafoveal

• B involving fovea

 – 5: total retinal detachment

• Define plus disease – Retinal vascular dilation and tortuosity in the posterior pole

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ROP

• Define threshold ROP

 – Zone I or II

 – Extent of 5 contiguous or 8 non-contiguous clock

hours of extraretinal neovascularization

 – Plus disease

 – Threshold benefits from cryo or laser 

• STOP-ROP - oxygen level had no effect onprogression

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BVOS and CVOS

• Grid laser for macular edema

 – Beneficial for BRVO

 – Not beneficial for CRVO

• PRP laser for prevention of VH, NVG

 – Prophylactic laser not recommended

 – Laser once NV (iris, disc, retina) develops

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Ocular Ischemic Syndrome

• What percent carotid obstruction is typically

required to cause OIS?

 – 90%

• Describe the symptoms

 – Gradual visual loss

 –  Aching pain

 – Prolonged recovery following bright light exposure

• What are anterior segment findings?

 – Iris neovascularization (67%)

 –  AC cellular reaction (20%)

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Ocular Ischemic Syndrome

• Describe the posterior segment findings – Narrowed arteries

 – Dilated, non-tortuous veins

 – Mid-peripheral retinal hemorrhages, microaneurysms

 – Neovascularization

• What are the fluorescein angiographic findings?

 – Delayed choroidal filling (60%)

 – Delayed arteriovenous transit (95%)

 –Vascular staining (85%)

• What is the 5-year mortality rate and what is the

most common cause of death?

 – 40%

 – Cardiovascular disease

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Coats Disease

• Describe the clinical findings – Telangiectatic vessels, microaneurysms

 – Fusiform capillary dilation

 – Exudative retinal detachment

 – Capillary non-perfusion• What is the mode of transmission?

 – Not hereditary

• What is the percentage of cases affecting males?

 – 85%• What treatments are employed to halt

progression?

 – Cryotherapy or photocoagulation

 –Retinal reattachment surgery

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Retinal Arterial Macroaneurysm

• What percentage of cases are associated with

systemic hypertension?

 – 67%

• What are causes of visual loss?

 – Intra- or subretinal hemorrhage

 – Vitreous hemorrhage

 – Macular edema/exudation

 

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Posterior Vitreous Detachment

• What percentage of patients with acute

symptomatic PVD have a retinal tear?

 – 15%

• What percentage of patients with vitreous

hemorrhage associated with PVD have a

retinal tear?

 – 70%

 

20 t ti

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Retinal Breaks

• What percentage of the population will

develop a retinal detachment over their 

lifetime?

 – 0.07%

• What types of retinal breaks should be

treated?

 – Symptomatic horseshoe tears

 – Retinal dialysis

 

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Retinal Detachment

• What is optimal timing for surgery? – Mac on - 87% ≥ 20/50 

 – Mac off - 30-50% ≥ 20/50 

• < 1 wk 75% ≥ 20/70 

• 1-8 wk 50% ≥ 20/70 

• Define subclinical retinal detachment –

Subretinal fluid extends more than 1DD fromthe break

 – Subretinal fluid extends no more than 2DDposterior to the equator 

 

60 yo asymptomatic

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Retinoschisis

• What is the typical location in the fundus?

 – Inferotemporal

• What layer is affected in typicalretinoschisis? – Outer plexiform

 – (reticular retinoschsis, juvenile retinoschisis in NFL)

• How can schisis be differentiated from

RD? –  Absolute scotoma

 – No associated tear/tobacco dust

 – Smoother surface

 – Laser scars

 

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Hereditary Hyaloidoretinopathies

• Describe features of Jansen and Wagner 

disease –  Autosomal dominant transmission

 – Optically empty vitreous

 – Equatorial and perivascular lattice

 – Myopia, strabismus, cataract

• Which of the above conditions is

associated with retinal detachment? – Jansen disease

 

Stickler Syndrome

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Stickler Syndrome

• Describe the features of Stickler 

Syndrome –  Autosomal dominant transmission

 – Myopia, glaucoma, cataract

 – Orofacial findings

• Midfacial flattening• Pierre-Robin malformation (micrognathia,

cleft palate, glossoptosis)

 – Skeletal abnormalities

• Joint hyperextensibility•  Arthritis

• Spondyloepiphyseal dysplasia

 – High incidence of RD, giant retinal tear, PVR

 

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FEVR 

• What is the mode of inheritance of familial

exudative vitreoretinopathy?

 –  Autosomal dominant

• Describe the clinical features – Normal birth weight/gestational age

 – Failure of the temporal retina to completely vascularize

 – Peripheral fibrovascular proliferation

 – Traction retinal detachment – Subretinal exudate or exudative detachment

 – Late-onset rhegmatogenous detachment