Dosimetry in Radiotherapy Flashcards

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1
Q

State and explain the three ways to measure ionising radiation used in radiotherapy.

A

Ionisation - collect ion-pairs produced in air.
Calorimetry - ionising particle shares its energy with many others and eventually ions recombine. Energy ends up as heat.
Chemical effects - Free radicals produced by ionising particles cause chemical changes.

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2
Q

How does a Free-Air ionisation chamber measure dose?

A
  • Photon beam passes between parallel plates with a high polarising voltage between then
    • Voltage must be high enough to separate +ve and -ve ions before they recombine.
  • X-Ray produce electrons which cause ionisation
  • Mas f air in collecting volume, dm, defined by guard plate and beam geometry
  • Ion (not electrons0 are collected and measured.
  • Energy to create ion pair is known, so dose can be calculated.
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3
Q

What will happen if the voltage between the plates is not high enough?

A

The measured charge will be proportional to the voltage.

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4
Q

What beam energies are Free-Air ionisation chambers suitable for?

A

kV beam qualities. Rance of photo- and Compton electrons from MV energies would require a 4m plate separation to reach electronic equilibrium.

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5
Q

Where is the primary standard kept?

A

At the NPL

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6
Q

What does a primary standard do?

A

A primary standard makes and absolute measurement from first principles. All other devices are calibrated to the primary standard through a traceability chain.

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7
Q

What advantage does a thimble chamber have compared to a free-air chamber when measuring MV beam qualities?

A

Smaller (air shell “compressed” to solid “air-equivalent” graphite) so more practicable.

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8
Q

What are large ionisation chambers used for ad why?

A

Used for environmental monitoring.

Very sensitive, but poor spatial resolution.

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9
Q

What are small ionisation chambers used for an why?

A

Used for fine resolution scanning.

Good spatial resolution, but small signal.

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10
Q

When would a parallel plate chamber be used?

A

Parallel plate chambers are thin in the gradient direction for better resolution, but with a large detecting volume for decent signal.
Used for measurements in high dose gradient fields (e.g. electron beams, kV beams, build up regions of MV beams)
Thimble chamber would be too big and would measure contributions from other parts of the high gradient field.

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11
Q

How do calorimeters measure dose?

A

Dose = Energy/Mass = E/m
E=mc x dT
E/m = specific heat capacity x temperature rise = Dose
Temperature rise measured using very sensitive thermistors.

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12
Q

What advantage do calorimeters have over ionisation chambers?

A

Directly measure absorbed dose.

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13
Q

What type of calorimeter does the NPL use for their primary standard?

A

Graphite

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14
Q

Why isn’t a water calorimeter used?

A
  • Specific heat capacity too high (1Gy ~ 0.24mK temperature increase)
  • Difficulties with impurities adding heat defects.
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15
Q

How id the dose in the graphite calorimeter converted into a dose in water?

A

Uses ratio of electron densities (Photon fluence scaling theorem)

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16
Q

What temperature rise is caused by a dose of 1Gy in a graphite calorimeter?

A

1.5mK

17
Q

What is needed to ensure an acceptable level of precision?

A
  • Method capable of measuring dT of 10^-6K (~mGy)
  • Thermal isolation of the core
  • Maintain jacket and main body at a constant temperature.
18
Q

Describe one modern ay of measuring the temperature rise in a graphite calorimeter.

A

Core temperature kept constant by reducing current in a heating circuit.
D=VIt/M

19
Q

What is a secondary standard?

A

High-quality dosemeter owned by hospitals that is sent to be calibrated against the MPL primary standard.
NPL provide correction factor tp convert dose readings made with secondary standard to accurate dose measurements.
All other field instruments in the hospital are then cross-calibrated against this.

20
Q

How is a field instrument cross-calibrated?

A
  • Field instrument and secondary standard placed at 10cm in same perspex phantom.
  • Both irradiated with the same beam (should receive same dose)
  • Ratio of reading from field instruments and secondary standard taken.
  • Repeated 12 times with position of the chambers swapped after each three readings.
21
Q

What is the quality dependant factor?

A

Due to chamber construction, response varies with beam energy (or quality).
The secondary standard chamber is calibrated against the MPL chamber at a number of different beam qualities and a calibration curve is produced.

22
Q

What is the quality index of a beam?

A

Same as the TPR(20/10) (i.e. Tissue Phantom Ratio a depths of 20cm and 10cm.)

23
Q

What other correction factors are applied to calibrations of chambers?

A

k(tp) - correction for temperature and pressue (1013.25/P x T/293.15)
k(ion) - correction for ion recombination
k(elec) - correction for electrometer reading
k(lin) - correction for linearity wrt dose.

24
Q

How is k(ion) quantified?

A

Measure charge collected at different polarising voltages as recombination increases at lower voltages.

25
Q

How do TLDs record the absorbed dose?

A
  • TLDs contain lattice impurities which give additional energy levels to the electrons in the lattice.
  • These energy levels are meta-stable so act as traps for the electrons.
  • When irradiated the electrons jump from the valence to the conduction band and then some fall into the traps.
  • Heating the material releases the electrons from the traps where they initially move to the conduction band before falling into the valence band and emit light.
  • The light recorded from the TLD is proportional to the absorbed dose.
26
Q

What are advantages of TLDs over other dose-measuring devices?

A
  • Linear response over wide range (0.001-1Gy)
  • Sensitivity is almost energy independent (MV range)
  • Small size provides high resolution
  • No leads, batteries or connectors required.
27
Q

What are disadvantages of TLDs over other dose-measuring devices?

A
  • Must be calibrated
  • Fade with time after irradiation (typically <10%/yr)
  • Careful annealing is required between uses to ensure TLD returns to the original condition (wrt e-traps)
  • Affected by previous thermal and radiation history.
  • Reader constancy difficult to maintain over long periods.
28
Q

What is the most commonly used material for TLDs?

A

Lithium Fluoride

29
Q

What are some uses for TLDs?

A

Commissioning and QA

  • Small fields
  • Surface Dose/High-Dose gradients
  • Superficial X-Ray Therapy backscatter
  • Internal dose in phantoms

Patient Dosimetry

  • Total body Irradiation
  • Total skin irradiation
  • Eye dose estimates

Personal Dosimetry

  • Multi-chip badges
  • Single chip finger holders
30
Q

What is the equation that represents the interaction in a radiographic film?

A

gamma + Halide(-) -> Halide + e

e + Ag(+) -> Ag

31
Q

What is the equation that represents the interaction in radiochromic film?

A

gamma + n(C3R2) -> [C3R2]n

32
Q

What is the active component in radiochromic film?

A

Lithium pentacosa-12, 12-diynoate

33
Q

What are advantages of film dosimetry?

A
  • Good spatial resolution (grains ~ 100um, only limited by aperture size of scanner)
  • Convenient for aspects of Linac comissioning & QC
  • Can be calibrated of absolute dose measurement
  • Geometry well suited for dose mapping (thin, flat, large area)
34
Q

What are disadvantages of film dosimetry?

A
  • Silver Halide film requires wet processing (must be well controlled and consistent)
  • Silver halide film sensitivity is energy dependent ( high Z - preferential absorption of photons <150kV)
  • Radiochromic film: dose sensitive to scan parameters.
35
Q

What are the four parts of radiographic film?

A
  • Supercoat: Protect emulsion from damage
  • Emulsion: Contains Silver Halide
  • Adhesive
  • Base: Provides stability
36
Q

What is the grain density of radiographic film?

A

10^9 to 10^12 grains/cm^2

37
Q

How does Radiochromic film differ from radiographic?

A
  • Radiochromic is self-developing
  • Sensitivity is independent of photon energy
  • More expensive per sheet, but no processing costs
  • Tissue equivalent
  • Can be immersed in water.
38
Q

What other chemical dosimetery is available?

A

Fricke solutions and Alanine