week 5 Flashcards

1
Q

OCT vs FA what do they detect?

A

OCT: best way to detect changes in thickness

Fluorescein Angiography: only way to detect leakage

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2
Q

list some structures that might appear highly reflective on OCT?

A

horizontal structures, ERM, CWS, hemes, hard exudates, RPE hyperplasia, drusen, RPE atrophy, CNVM, retinal scars, choroidal nevi
*RPE dropout- this appears bright because there is more light from the retina getting though even though it’s a loss of pigment

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3
Q

what are some structures with low reflectivity?

A

vertical structures, fluid, cysts or cavities, shadowed areas, “ beneath a detachment ( RD or PED), vitreous

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4
Q

what 3 layers of OCT are hyperreflective?

A

ILM/ NFL and RPE are hyper-reflective

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5
Q

Band 1=

A

ELM- band slightly lighter in color than ONL

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6
Q

Band 2=

A

IS/OS- inner segment/outer segment junction- light band

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7
Q

Band 3=

A

outer segment tip= Verhoff’s membrane

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8
Q

Band 4=

A

RPE, possibly including Bruch’s

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9
Q

Vitreomacular traction puts you at risk for?

A

Macular hole

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10
Q

RPE contains what 2 types of pigment?

A

Melanin: does not change much after birth
Lipofuscin: increases with age

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11
Q

what is lipofuscin made of?

A

mainly derived from chemically modified residues of partially digested photoreceptor outer segments

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12
Q

Only OCT that can do autoFL?

A

spectralis OCT

Lipofuscin excitation: 300-600 nm

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13
Q

T/F: in the Macular Photocoagulation Study (MPS) study, those who got lasered, ended up with the same vision as the untreated group after 5 years ?

A

Yes, but it was better bw the 5 years

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14
Q

What were some of the findigns for the Macular Photocoagulation Study (MPS) study in regards to what laser should be used depending on where the CNV was?

A
  • Only use Argon on extrafoveal areas
  • For Jutxtafoveal areas use krypton laser (for lesions closer to fovea)
  • For subfoveal, IF you do choose to laser, use Krypton
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15
Q

which laser uses less thermal energy, ARgon or krypton?

A

krypton

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16
Q

What were 4 major risk factors (those who already have CNV in one eye- chance of happening in the fellow eye: ) associated with MPS study?

A

1) Five or more drusen
2) confluent drusen
3) retinal hyperpigmentation
4) systemic hypertension

Patients with all 4 risk factors =87% chance to develop wet AMD (CNV) in fellow eye within 5 years
-Eyes with none of the risk factors have less than 5% chance to develop in the other eye

17
Q

WHat steps are taken in photodynamic therapy?

A

Verteporforin administered as intravenous infusion (aka Visudyne)

  • binds to low density lipoprotein (LDL)
  • goes to choroid
  • absorbed by CNVM
  • then apply laser (10 mins after dye has been injected)
  • non-thermal infrared laser= no destruction of viable tissue – for no longer than 83 secs
  • oxygen free radicals are released
  • endothelial damage and thrombus occur
  • abnormal vessels occlude
18
Q

how often did photodynamic therapy have to be repeated

A
  • 1st year: 3-4 treatments

* 2nd year: 2-1 treatments

19
Q

what are some of the side effects of PDT?

A

pain associated with infusion= common
Visual disturbances= hallucinations
Photosensitivity reaction: had to be completely covered head to toe after treatment otherwise pts would get very sun-burnt
**Newer findings: PDT found to create “expression” of VEGF reason why repeated treatments are needed

20
Q

what was the outcome of Complications of Age-related Macular degeneration prevention trial (CAPT)?

A

Q: should they laser soft drusen? (Lasering drusen thins this aspect of Bruch’s causing increased permeability – goal is to restore normal transport between retina and choroid)
OUTCOME: No diff (nor harm but no benefit) in treating one eye vs untreated fellow eye for loss of 3 lines or more of acuity or progression to advanced AMD

21
Q

Macugen: cost, freq, why is it no longer first line?

A

Macugen (Pegaptanib)- breakthrough drug
1st anti-angiogenic drug approved for inhibiting VEGF with CNV formation ~2004
NOT FIRST LINE: Blocks VEGF of a particular isoform (doesn’t target all isoforms)
–Intravitreal injection every 6 weeks for 2 years  $$
–Approx. cost of $1,200 per injection

22
Q

Lucentis vs Avastin:

A

Lucentis done q3 months then q6 months/2 years (based on the PIER study) OR as needed basis (PRONTO study)
-Approx cost: $2000 per 0.3ml injection

Avastin:

  • Larger molecule with a longer ½ life
  • Approx cost: $50-150 for 0.3 ml injection
  • Much less $$, used once a month
23
Q

how does elyea compare to lucentis/avastin?

A

possibly superior to others,

Approx cost: $1,850 per injection, every 2 months

24
Q

List several possible side effects of intravitreal injections:

A
endophthalmitis
catarcts-traumatic
RD-if injection goes too far
myocardial infarction
IOP spike 
uveitis
25
If patient has a history of heart problems, choose which intravitreal injection?
If patient has a history of heart problems, choose Lucentis over Avastin; greater risk of MI with Avastin
26
what was the outcome of "The comparison of treatment trial (CATT)"?
Comparison between Lucentis and Avastin ~2009 | Results released in 2012: outcomes between the drugs are very similar, they work equally well
27
what were the outcomes of the Pier trial? Pronto trial?
Q: How often should anti VEGF be used? Inject 3x (1x a month), for 3 months, THEN: --PIER trial: 1x every 6 months for 2 years OR --PRONTO: as needed for the next 2 years (with regular f/u)
28
In what populations do you expect to see Idiopathic Central Serious Choriodopathy
o Males > females; 10:1 or 9:1 o Age 21-30 in males, 31-40 in females o Type A personalities, high achievers, people under high emotional stress o May have history of migraine or headaches
29
Describe the clinical presentation for central serous maculopathy: (VA, color VA, etc.)
o VA: sudden decrease in VA, no worse than 20/200 ; blurred , distortion or curved lines o Color vision: colors look less saturated; perform red desaturation test o Amsler grid: metamorphopsia present o Refractive Correction: shift to plus
30
Describe the appearance of central serous maculopathy:
- 1-4DD sized lesion | - elevated, round, or oval shaped, well defined
31
Describe the recovery process for central serous maculopathy: (time, VA, end result etc)
- Several weeks to several months (up to 6) for full recovery - Most will recover to 20/30 or better within 4-8 weeks - End result: RPE mottling/ loss of foveal reflex; vision not perfect, colors stay less saturated
32
How often does central serous recur?
1/3 to ½ of cases can relapse within the 1st year * Each time they get it, the VA will be more affected * *VA recovery has been noted to be worse in Mexican and Japanese populations
33
epidemiology of epiretinal membrane?
common in those over the age of 65, mostly age related cases, occurs equally in men and women, no racial component
34
pathophysiology of epiretinal membrane?
glial cells pile on top of ILM
35
what surgical option can you consider for ERM?
Membrane peel- vitrectomy and remove the epiretinal membrane | Very invasive and extreme surgery for very severe cases
36
what change in VA would you expect with VA for ERM
Decease in VA- mild to moderate decrease (from 20/20- to 20/80ish)