Trans 012 Disturbances In Vision Flashcards

1
Q

Where does Retinal detachment occur?

A

Detachment occurs in the subretinal space (between RPE layer and rods & cones

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2
Q

Types of Retinal detachment

A

Non rhegmatogenous: fraction and exudative

Rhegmatogenous.

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3
Q

What type of Retinal detachment

 There is a leak in the blood vessels
• Breakdown of integrity of the vascular system of choroid and
/or retina
o Eclampsia&pre-eclampsia
o Tumorsofchoroidandretina
o Intraocular inflammation: choroidal effusion
▪ Vogt Koyang Harada Disease o Collagen Disease

A

Exudative detachment

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4
Q

 May humila sa retina kaya umangat
• Ischemic retinal disease causing fibroproliferative membrane
formation
o Diabetic Retinopathy
o Central Retinal Vein Occlusion (CRVO), Branch Retinal
Vein Occlusion (BRVO)
• Intraocular inflammation causing membrane formation
• Rhegmatogenous retinal detachment with proliferative
vietreoretinopathy (traction membranes)

A

TRACTION DETACHMENT

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5
Q

What retinal detachment has this symptom Symptoms:
o Blurry wavy vision, visual fields cuts, floaters and flashes
preceding blurry vision, NO PAIN, absence of symptoms is possible

• Pathophysiology
o Presenceofretinalbreak

o Theremaybevitreoustractiontotheretinalbreak
o Accumulation of fluid between RPE and photoreceptors

A

Take note: Pag nasa taas ang butas, retinal detachment is faster rhegmatogenous Retinal detachment

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6
Q

StageI:mildtomoderatearteriolarnarrowingorsclerosis
o Stage II: Moderate to marked arteriolar narrowing, with
focal or generalized narrowing, exaggerated light reflex,
and AV crossing changes
o Stage III: the above PLUS cottonwool spots, hard
exudates, retinal hemorrhages, extensive microvascular
changes, retinal edema
o StageIV:theabovePLUSdiscedema

What staging?

A

Keith Wagener Barker Staging of Hypertensive Retinopathy

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7
Q

W’hat stage in
Barker staging has

AV crossing changes

A

Stage 2

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8
Q

W’hat stage in

Barker staging has Cotton wool spots

A

Stage 3

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9
Q

W’hat stage in

Barker staging has disk edema

A

Stage 4

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10
Q

Av nicking versus venous elevation versus venue deviation

A

If an artery which is a thick muscular coat crosses a vein plus the effect of hypertension the changes in the wall will be harder. It will cause narrowing of the tips of the vein “pencil point” AV nicking
 The vein cross to the hard artery, the vein will be elevated. Venous elevation
 If the artery cross the vein it might delineate the path of the vein. Venous deviation

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11
Q

Deflection of retinal vein as it crosses the

arteriole.

A

Salus’ sign

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12
Q

Tapering of the retinal vein on either side

of the AV crossing.

A

Gunn’s sign

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13
Q

BankingoftheretinalveindistaltotheAV

crossing.

A

Bonnet’s sign

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14
Q

Causes
o Hypertension, arteriosclerosis, diabetes mellitus,
inflammation, collagen disease, hyperviscosity
syndromes
• Symptoms/signs
o Sudden painless blurring of vision, afferent pupillary defects

what disease?

A

Central Retinal vein occlusion

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15
Q

Treatment of the central Retinal vein occlusion if there is swelling of the macula

A

if there is swelling of the macula we inject

Anti-VEGF(vascular endothelial growth factor) medication

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16
Q

Causes:
o Emboli, thrombi, hemorrhage under an atherosclerotic
plaque, inflammation, spasm, dissecting carotid artery aneurysm, hypotension, hypertensive arterial necrosis, prolonged pressure on the globe
• One of the only 2 TRUE ophthalmologic emergencies!  The other one is chemical burns of the cornea
• Treatment:
o Loweringeyepressurestat,toimproveocularbloodflow  How to be resolve within 5 minutes

 Can also have a branch occlusion

A

CENTRAL RETINAL ARTERY OCCLUSION

17
Q

Risk factors of having diabetic retinopathy

A
Risk Factors
o DurationofDiabetes
o Glycemic control
o Age
o Type of diabetes
o Family Hx of DM
o Blood pressure
o Serum lipids
o Nutritional Factors/Obesity o Clotting Factors
o Renal Disease
18
Q

Types of diabetic retinopathy

A

Non proliterative and proliterative

19
Q

Mild, Moderate, Severe, Very Severe microaneurysms, retinal hemorrhages and hard and soft exudates, venous beading, IRMAs

Symptoms:
o Variablevisualdeficits/floaters
o Normal20/20visionpossible

A

Non proliterative

20
Q

Early, High Risk
o Retinal and disc neovascularization (NVE & NVD),
vitreous and pre-retinal hemorrhages, fibrovascular membranes

A

Proliferative Dr

21
Q

If there is macular

Edema, will there be loss of vision?

A

Yes

22
Q

induces regression of new vessels and reduces the
incidence of severe visual loss from proliferative diabetic
retinopathy by 50%. Several thousand regularly spaced laser burns are
applied throughout the retina outside the vascular arcades to reduce the angiogenic stimulus from ischemic areas

A

Pan-retinal photo-coagulation (prp)

23
Q

Treatment for macular edema

A

• Intravitrel anti-VEGF injections

24
Q

Reason for proliferation in diabetic retinopathy

A

Lack of oxygen

25
Q

The most common hereditary retinal dystrophy

A

RETINITIS PIGMENTOSA

26
Q
Clinical Manifestations
• Nyctalopia or night blindness
• Problems with peripheral vision
• Deteriorating vision
• Prolonged dark adaptation
• Contracted visual fields
• Abnormal ERG (Electroretinogram)

what disease?

A

RETINITIS PIGMENTOSA

27
Q

Classic triad of retinitis pigmentosa

A

classic triad of findings comprises of bone-spicule retinal pigmentation, arteriolar attenuation, and ‘waxy’ disc pallor.

28
Q

most common malignancy in childhood

A

Retinoblastoma

12-18 months to 5 years old

29
Q

2 types retinoblastoma

A

hereditary and sporadic

30
Q

Most common presenting sign retinoblastoma

A

leukocoria

31
Q

abnormality noted in the “retinoblastoma gene” at the q14

locus

A

Ch 13

32
Q

The most accepted treatment now for retinoblastoma

A

chemotherapy and debulking chemotherapy.

33
Q

Innermost layer of the choroid

A

Bruch’S membrane

34
Q

occlusive microvasculopathy characterized by multiple
retinal white areas around the optic nerve head and fovea
with paravascular clearing which may be associated with
intraretinal hemorrhages.

A

PURSTCHER’S RETINOPATHY

35
Q

It involves the choroid, Bruch membrane and retinal pigment epithelium
 Direct ruptures are located anteriorly at the site of impact and run parallel with the ora serrata

A

Choroidal rupture