CLINICAL TECHNIQUES - Biometry and Pentacam and Microscopy Flashcards

1
Q

What is the difference between K1 and K2 readings in pentacams? What is Km? What is Kmax?

A

K1 - flattest meridian
K2 - steepest meridian
Km - mean power in diopters

Kmax - maximal K reading - its location tels you the apex of the cone

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2
Q

What is the Q-value in pentacam? What is normal Q-value range?

A

Q value - corneal shape
Normal is between -1 and 0

> 0 = oblate cornea
<-1 = prolate cornea (keratoconus)

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3
Q

Which unit assesses change in corneal thickness of the whole cornea of pentacams? What is it used for clinically?

A

Used to assess change in corneal thickness of the whole cornea - useful for ectatic disease.

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4
Q

What principal is used for confocal microscopy?

A

Principle of confocal single point of tissue illuminated by a point source of light whilst simulatenously imaged by a camera in the same plane

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5
Q

What is specular microscopy? What does it measure?

A

Provides objective measurement of corneal endothelial cells

  1. Parameters
  2. Density
  3. Coefficiency of Variation (>0.4 increased variation)
  4. Percentage of hexagonal cells (>50% pleomorphism, may not tolerate cataract surgery)
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6
Q

How wide is the field of view in colour fundus photography?

A

30-35 degrees

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7
Q

How wide is the field of view in colour fundus photography?

A

30-35 degrees

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8
Q

What are the causes of post-operative HYPERMETROPIC surprise (5)

A

Hypermetropic suprise –> greater axial length and/or reduced lens power.

  1. Previous unrecognised myopic refractive surgery
    1. Unrecognised staphyloma in a highly myopic eye (can occur if an A-scan is used instead of optical biometry) - overestimates the AL of the eye, leading to underestimation of the IOL power
  2. Use of a lower A constant than intended
  3. Post-operative cystoid macular oedema
  4. Use of biometry in keratoconus (as corneal power is typically overestimated)
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9
Q

What are the causes of MYOPIC refractive surprise? (4)

A
  1. Capsular block syndrome (accumulation of fluid between IOL and posterior capsule causing anterior displacement)
  2. AC shallowing
  3. Previously unrecognised hyperopic refractive surgery
  4. Errenously using higher A constant value –> higher IOL power than required for eye.
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10
Q

What is the difference between OCT and optical biometry in mechanism?

A

OCT: low coherence inferometry
Optical biometry: partial coherence inferometry where two co-axial partially coherent laser beams are used (infrared)

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11
Q

When should biometry be repeated (5)

A
  1. Axial length < 21.2 or > 26.6
  2. Difference in axial length >0.7mm
  3. Mean keratometry < 41D or >47D
  4. Difference in mean keratometry > 0.9D
  5. DeltaK (corneal astigmatism) > 2.5D
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12
Q

Which patients may not tolerate intraocular surgery in regards to specular microscopy findings?

A
  1. Corneas with low endothelial cell density
  2. Significant polymegathism (>0.40) - relates to coefficient of variation (increases in contact lens wear)
  3. high pleomorphism (>50% non-hexagonal cells)
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13
Q

What is the typical corneal compression from A scan biometry?

A

0.1-0.3mm

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14
Q

What strategy is used to detect the threshold stimulus intensity?

A

Bracketing

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