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7/28/2019 Retina - 2
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Retina Review
Part 2
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35 yo on multiple BP meds
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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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47 yo 20/20 referred by internist
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62 yo diabetic
20/60
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33 yo diabetic 20/30 OU
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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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35 yo African American male
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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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Baby
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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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71 yo woman h/o POAG
20/30
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75 yo 20/80
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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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60 yo
Scotoma for
one wk
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65 yo sudden decreased vision OU x 4hr
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65 yo decreased vision x 3d
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Central Retinal Artery Occlusion
• What percentage of eyes have vision <20/400? – 66%
• With NLP vision, what diagnosis must be
considered? – Ophthalmic artery occlusion
• What is the leading cause of death in patients
with CRAO? – Cardiovascular disease
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82 yo NLP
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Central Retinal Artery Occlusion
• What percentage of CRAO is accounted
for by giant cell arteritis?
– 1-2%
• What are some methods used as therapy
for CRAO?
– Ocular massage
– Anterior chamber paracentesis
– Administration of carbogen
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85yo chronic pain and redness OD
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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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35 yo asymptomatic
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Retinal Vasculitis
• What is the differential diagnosis of retinal
vasculitis?
– Giant cell arteritis Multiple sclerosis
– Sarcoidosis Syphilis
– Behcets disease Pars planitis
– Lupus Toxoplasmosis
– Polyarteritis Idiopathic
– Inflammatory Bowel Dz
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8 yo boy; parents noted leukocoria
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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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40 yo 20/40 OU
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Idiopathic Juxtafoveal Telangiectasis
• What are the 3 clinical groups
– Unilateral juxtafoveal telangiectasis
– Bilateral juxtafoveal telangiectasis
– Bilateral juxtafoveal telangiectasis with capillary
obliteration
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45 yo h/o HTN
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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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50 yo c/o floater
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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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20 yo myope, asymptomatic
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60 yo c/o flashes
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60 yo c/o flashes
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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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60 yo asymptomatic
Retinoschisis
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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
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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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3 mo old term baby
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FEVR
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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