Characteristics of Clinical Beams: Photons Flashcards

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1
Q

Define the Tissue-Phantom Ratio.

A

Ratio of the dose obtained at a fixed field size and SSD, but with different thicknesses of “tissue” between the surface and the detector.

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2
Q

How does the beam profile change with increasing depth?

A
  • Beam and penumbra widen
  • Flattest beam at 10cm (with flattening filter)
  • Before 10cm beam is “horny”
  • After 10cm beam is peaked
  • Horniness and Peakedness increase with distance from 10cm depth.
  • Dose is reduced as with PDD.
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3
Q

How does a geometric penumbra arise?

A
  • Photon source is not a point source

- Photons from opposite edges of soucre can pass through collimators giving beams in overlapping locations

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4
Q

What does the width of the geometric penumbra depend on?

A
  • width of extended source

- position of collimators

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5
Q

What does the width of the transmission penumbra depend on?

A

energy of the beam

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6
Q

What happens if the jaw face is not parallel to the divergent beam?

A
  • at larger field sizes the path through the collimators is shorter
  • penumbrae becomes larger
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7
Q

How do dosimetric penumbra change with increasing energy?

A
  • lower energies have more lateral scatter

- dosimetric penumbrae reduce at higher energies as ther is more forward scatter

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8
Q

What two factors affect the dose to patient when beam size is increased?

A
  • incident beam (more photons incident to patient)

- scatter within patient

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9
Q

What percentage of the dose to the patient comes from head scatter?

A

3-4%

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10
Q

Where does head scatter come from?

A

mainly the flattening filter, but some contribution from collimators

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11
Q

How does the patient scatter factor (Sp) relate to the head scatter factor (Sc) and the field size factor (St)?

A

Sp = St/Sc

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12
Q

What is a monitor unit?

A

dose measured in the monitor chmaber in the linac head that gives a fixed dose (1cGy) under the departmental reference conditions (fixed SSD, field size and depth)

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13
Q

What happens to the isodose plot in the patient as the energy of the beam increases?

A

Greater penetration

Less side scattered dose - loss of side lobes on the isodose plot.

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14
Q

How is a percentage depth dose (PDD) curve obtained from and isodose plot?

A

Linear profile of the dose down the central axis of the plot.

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15
Q

How does an increase in energy affect the PDD?

A
  • Greater depth of d(max)
  • Shallower drop off after d(max)
  • Shallower build up region
  • Lower entrance surface dose
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16
Q

What are the major characteristics of a clinical photon beam?

A
  • Build up region
  • Point of max dose
  • Normalisation point (5, 7 or10cm, depends on centre)
  • Dose reduction with depth
  • Penumbra
  • Beam profiles at depth
  • Dose from scatter (linac head and patient) and leakage
17
Q

What causes the build-up effect in a clinical beam?

A
  • Photons interact at different depths in the tissue and generate secondary electrons.
  • At each interaction, the recoils electrons travel (mostly) forward and deposit dose
  • As more tracks overlap, the dose builds up until Charged Particle EquillibriumM (CPE) is reached.
  • A steady state would be reached if there was not photon attenuation (absorption or scatter)
  • Dose>0 at the surface due to back0-scattered electrons and electron contamination.
18
Q

How dose increasing the beam size affect the PDD?

A

Increases the dose at depth due to:

  • More photons reaching the patient from the source
  • More scattered electrons to the measurement point from the irradiated volume.
19
Q

How does increasing the SSD affect the PDD?

A

Increases dose at depth > d(max) (i.e. shallower drop-off)

Absolute dose would decrease with increase of SSD, but percentage dose relative to a fixed point increases

20
Q

How does the TPR vary with increasing field size?

A
  • Steeper build-up region
  • Lower depth of TPR(max)
  • Shallower fall-off after TPR(max)
21
Q

Why is there a steeper fall-off from the TPR compared to a PDD?

A
  • TPR does not have an Inverse Square Law effect

- Scatter conditions of the TPR and PDD are different.

22
Q

How is the beam size defined on a beam profile?

A

Defined at the Full-Width Half-Maximum

23
Q

How are the penumbra defined on a beam profile?

A

Difference between the 80% and 20% dose points.

24
Q

How is the wedge angle defined?

A

Wedge angle is the angle between the isodose line and the normal to the central axis at 10cm deep.

25
Q

What are the three causes of penumbrae in a clinical beam?

A
  • Geometric
  • Transmission trough collimators
  • Scatter in Patient.
26
Q

Concerning MV photon percentage depth doses, Which one of these statements is true?

a) The depth of maximum dose is a function of beam energy and field size
b) The increase in PDD with beam energy is due to increased lateral scattering of the incident photons
c) A 30cm increase in SSD has a negligible effect on the PDD
d) Surface dose decreases with increasing field size
e) Changes in PDD with field size are mainly due to differences in collimator/head scatter

A

a

27
Q

Concerning radiation beam geometry, which of these is true?

a) The dose at any depth is greatest on the central axis
b) At 100cm SSD, field size is defined by the width of the 95% isodose line at the patient surface
c) Only scattered photons can reach outside the geometric field edge
d) An increase in source to secondary collimator distance increases the geometric penumbra
e) Penumbra widths are expected to decrease as the beam energy increases from 4MV to 8MV

A

e