Unit 6 - VMT, CMO, ret dystrophies Flashcards

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1
Q

What are the 5 symptoms of VM disorders?

A
  1. Gradual loss of V/A
  2. Difficulty with binocular s/v
  3. Distortion
  4. Central scotoma
  5. Monocular diplopia
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2
Q

What is the general management of VM disorders?

A
  1. Patient counselling/reassurance
  2. Vitrectomy with macula peel if sig symptoms
  3. Combined vity with mac peel and phaco
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3
Q

What ocular investigations should be conducted on VM disorders?

A
  1. Amsler
  2. OCT
  3. Photography (red-free will show sudden changes in vessel direction)
  4. FFA to exclude other causes
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4
Q

What is NICE guidance on the use of Jetrea in VM disorders?

A

Can be used if macula hole is <=400microns or there are severe symptoms and if ERM not present

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5
Q

What are the cons of Jetrea?

A

Has shown to loosen zonules in mice.

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6
Q

How are macula holes classified by size?

A

By size horizontal measurement along narrowest point:

  • Small <250 mics (95% surgical success)
  • Medium (250-400) 85-90% surgical success
  • Large (>400microns) 25-50% success
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7
Q

How are macula holes classified by cause?

A

Primary initiated by VMT Secondary due to disease or trauma

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8
Q

How are pseudo-holes different?

A
  1. Invaginated foveal edges
  2. Associated ERM
  3. No loss in retinal tissue
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9
Q

What is an ERM?

A

Fibrocellular proliferation contracting as a sheet over the surface of the ILM

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10
Q

How often are ERM’s bilateral?

A

10-35% of the time

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11
Q

What are the 5 ocular risks of developing an ERM?

A
  1. RD
  2. RVO
  3. DR
  4. Trauma
  5. Uveitis
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12
Q

What are the clinical signs of an ERM?

A
  1. Wrinkling of superficial light reflexes
  2. White, thick membrane structure visible
  3. Translucent membrane with distortion and angulation of retinal blood vessels
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13
Q

How many cases of VMT spontaneously resolve?

A

15-50%

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14
Q

What does jetrea target

A

Fibronectin laminin and collagen

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15
Q

How long after resolution do VMT symptoms continue after resolution?

A

6-9 months

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16
Q

How often does CMO occur after ICCE?

A

5-15%

17
Q

What is the proposed pathogenesis of CMO?

A

Cytokines released by inflammatory cells break down blood-retinal barrier causing capillary leakage

18
Q

What other proposed causes of CMO are there?

A
  1. VMT
  2. Vitreous inflammation
  3. Disc swelling
  4. Prostaglandin release in vitreous
  5. Lens removal
19
Q

What factors put you at risk of CMO?

A
  1. Diabetes
  2. Capsular rupture
  3. ERM
  4. Previous uveitis, RVO or RD
20
Q

What are the clinical signs of CMO?

A
  1. Macula thickening
  2. Loss of foveal depression
  3. 3-4 large central cysts
  4. Vitreous cells
  5. Central yellow spot
21
Q

What FFA appearance will you see in CMO?

A

FFA will show leakage from perifoveal caps

Late leakage into fovea with a petalloid appearance

Mild optic disc leakage

22
Q

What is the differential diagnosis of CMO?

A
  1. Diabetic maculopathy
  2. BRVO
  3. Exudative ARMD
  4. Radiation retinopathy
23
Q

When should treatment be considered for CMO?

A

if Reduced v/a and clinical macula oedema

24
Q

What are the treatments for CMO?

A

1) Topical NSAID’s e.g Ketorala (acular) for 6/52
2) Acetazolamide twice daily for 6/52
3) Intravitreal triamincinolone, can be given intraoperatively in susceptible patients or post-surgery as a sub-tenons injection
4) Vitrectomy

25
Q

Why does acetazolamide work in CMO?

A

It increases the action or the RPE pump

26
Q

What are the long terms complications of CMO?

A

Multiple remissions can result in photoreceptor death.