Beam Modelling & Inhomogeneity Corrections Flashcards

1
Q

What is the goal of commissioning and clinical acceptance testing?

A

To determine a set of values for the adjustable parameters that generate calculated dose distributions.

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2
Q

What are some examples of adjustable parameters?

A
  1. a set of energies
  2. off-axis beam softening
  3. off-axis changes in the in-air photon fluence
  4. photon fluence through the
    collimators.
  5. Scatter from the flattening filter;
  6. Scatter from the beam
    modifiers
  7. The dimensions of the photon source
  8. Electron contamination
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3
Q

What is PDD?

A

Percentage of the absorbed dose at any depth ‘d’ to the absorbed dose at a fixed reference depth ‘do’ along the central axis of the beam.

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4
Q

What is beam modelling?

A

Acquisition and comparison of the Linac and TPS profiles

What the treatment planning system provides compared to the actual recorded data from the Linac

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5
Q

Profile Analysis?

A
  • Field size
  • Depth
  • Wedges
  • Off-axis factors
  • As the depth increases the the difference between the TPS measured and recored increases
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6
Q

What are algorithms?

A

A procedure for solving a mathematical problem in a finite number of steps that frequently involves repetition of an operation.

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7
Q

Why do we need dose algorithms?

A

Measurements are performed under these conditions

  • -> Fixed square field
  • ->Fixed depth
  • ->homogenous medium
  • ->Flat surface

Don’t represent the real world!

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8
Q

How is the effect of inhomogeneity calculated?

A

-Indirectly, through a correction factor.

OR

-Directly, inherent to the algorithm.

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9
Q

Isodose distributions in patients are determined by?

A
  1. Correction/measurement based algorithms

2. Model based algorithms

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10
Q

What are types of corrections for contour irregularities?

A
  • –> Effective SSD
  • —>TAR (tissue air ratio)
  • –> TMR (tissue maximum ratio)
  • –>isodose shift method
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11
Q

What are types of corrections for tissue inhomogeneities?

A
  • ->TAR (tissue air ratio)
  • –>Effective path lengths
  • ->Batho power law method
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12
Q

What is the TAR (tissue air ratio method)?

A

-Ratio of dose (Dd) at a given point in phantom to the dose in free space (Dfs) at the same point.

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13
Q

What is the TAR equation?

A

CF=TAR (z-h, Aq)/TAR(z, Aq)

CF= Correction factor
z=depth
h=Thickness of missing tissue
A=Field size

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14
Q

What is the effective path length?

A

•Models the primary dose variation.
•Unreliable for regions of e- disequilibrium (lung treated
with high energy photons).
•Best for dose calculation far away from inhomogeneity

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15
Q

Why is optimising the linac performance important?

A
  1. PDD- Beam Quality/Energy
  2. Output
  3. Flatness
  4. Symmetry
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16
Q

Which methods correct for inhomogeneities?

A
  1. TAR method
  2. Effective paths lengths
  3. Batho power law method; 4. Equivalent TAR method
17
Q

What is the Batho power law method?

A

Accounts for both primary beam attenuation and scatter changes in water, below a single inhomogeneous slab.

18
Q

What is a limitation of the Batho power method?

A

Works well below a large inhomogeneous layer with e- density less than that of tissue.
􏰀 If the e- density is greater than that of tissue, the method over-estimates the dose.

19
Q

What is the equivalent TAR method (ETAR)?

A

correctly accounts for the primary component of dose

􏰀 It ignores changes in scattered dose

20
Q

What is a limitation of the equivalent TAR method?

A

It ignores changes in scattered dose