Overall Flashcards

1
Q

Is energy deposition stochastic for very small masses?

A

Yes (microdosimetry)

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2
Q

Is energy deposition stochastic for the mass elements that we are concerned with in this module?

A

No (stochastic fluctuations are negligible for the masses considered here)

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3
Q

The equation for energy imparted (epsilon) by ionising radiation to the matter in a given volume is equal to what?

A

R_in (radiant energy in) - R_out (radiant energy out) + sum of Q (sum of all changes in rest mass energy)

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4
Q

For the energy imparted equation, does the terms for radiant energy in and out include rest mass energy?

A

No

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5
Q

The absorbed dose (D) is the quotient of d(epsilon with dash on top) by dm, what do the terms mean?

A

epsilon dash is the mean energy imparted by ionising radiation to matter of mass dm

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6
Q

Sometimes we put D subscript med for for absorbed dose, why? (equivalent for kerma as well)

A

The absorbed dose generally depends on the medium (med) doing the absorbing

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7
Q

What is the units of absorbed dose?

A

Gray (Gy) or J kg^-1

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8
Q

What is a typical lethal whole body dose from ionising radiation?

A

5 J/kg (Gy)

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9
Q

What does Kerma stand for?

A

Kinetic energy released in matter

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10
Q

What is the equation for kerma?

A

Energy transferred (dE_tr) divided by dm (mass)

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11
Q

What is the energy transferred term in the kerma equation?

A

The sum of the initial kinetic energies of all the charged ionising particles liberated by uncharged ionising particles in matter of mass dm

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12
Q

What type of particles is kerma only defined for?

A

Indirectly ionising particles, which is usually photons

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13
Q

What is the units of kerma?

A

Gray or J/kg (same as absorbed dose)

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14
Q

Kerma is sometimes partitioned into two terms, what are these terms?

A

Collision kerma (K_c) and radiative kerma (K_r)

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15
Q

What does the radiative kerma refer to?

A

The part of kerma that includes the energy the charged particles will eventually re-radiate via bremsstrahlung photons

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16
Q

Collision kerma is related to total kerma by what equation that involves g and what does g stand for?

A

K_c = K (1-g), where g is the fraction of initial kinetic energy of the electrons that is re-radiated as bremsstrahlung in the particular medium of interest

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17
Q

What is cema (C)?

A

The charged particle equivalent of collision kerma (it stands for converted energy per unit mass) (i.e. instead of photons or uncharged particles, it is charged particles)

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18
Q

Particle fluence is a fundamental term to relate kerma or dose to the radiation field, what are these types of terms called in general?

A

Field quantities

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19
Q

What is the equation for the particle fluence?

A

dN (number of particles striking a finite sphere) divided by dA (cross sectional area)

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20
Q

What are the units of particle fluence?

A

m^-2 or cm^-2 (i.e number of particles per unit area)

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21
Q

Is fluence a scalar quantity and what does this mean?

A

Yes, so the direction of the radiation is irrelevant

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22
Q

An equivalent equation for fluence is the sum of the track lengths of the particles crossing the elementary sphere (sum of delta s) divided by what?

A

The volume of the sphere (dV)

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23
Q

What is the equation for fluence differential in energy?

A

D fluence divided by d energy

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24
Q

What is the energy fluence?

A

The product of fluence with energy

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25
Q

What is planar fluence?

A

The number of particles crossing a plane surface in either direction per unit area of the surface

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26
Q

What is the letter than symbolises fluence?

A

phi

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27
Q

What is the letter that symbolises energy fluence?

A

psi

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28
Q

What is the mass attenuation coefficient?

A

linear attenuation coefficient divided by the density (related to the probability of an interaction per unit effective length)

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29
Q

What is the mass energy transfer coefficient?

A

The probability of an energy transfer per unit effective length

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30
Q

What is the equation for the mass energy transfer coefficient?

A

The inelastic component linear attenuation coefficient divided by the density (interactions that result in energy transfer)

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31
Q

The mass energy absorption coefficient is the mass energy transfer but excluding which component of it?

A

The part of the initial kinetic energy of charged particles re-radiated as bremsstrahlung

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32
Q

When does the condition of charged particle equilibrium (CPE) apply?

A

The energy in equals the energy out and the energy imparted is just the net energy transferred

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33
Q

What is the bone dose enhancement?

A

The change in the absorbed dose when one goes from tissue to bone in a patient irradiated by a low-energy x-ray beam

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34
Q

The charged particle equilibrium condition is responsible for what region of the dose curve?

A

The build up region (skin sparing effect)

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35
Q

Is the dose build-up region longer or shorter for higher energy photons and why?

A

Longer because the secondary electrons are higher energy and travel further on average

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36
Q

Unlike stochastic photon behaviour, how do electrons lose energy?

A

Quasi-continuously through large numbers of Coulomb interactions

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37
Q

What is the total stopping power?

A

The rate of energy loss with distance and it is a sum of the electronic/collision stopping power and radiative stopping power

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38
Q

Why do we only consider collision stopping power within a dosimetry context?

A

Radiative stopping power is bremsstrahlung which carries the energy away and this only considers local energy deposition

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39
Q

What is the mass collision stopping power?

A

Collision stopping power divided by density

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40
Q

What is the analogue of charged particle equilibrium (CPE) which is for photons, for electrons?

A

Delta-ray equilibrium

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41
Q

What is the cavity referred to in cavity theory?

A

The detector

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42
Q

The detector signal is proportional to what?

A

The energy absorbed in its sensitive material

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43
Q

What is the goal of cavity theory?

A

Relate the average dose in the detector to that in the undisturbed medium for certain general classes of detector

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44
Q

What is the name and symbol for the coefficient that defines the ratio between the dose to the medium and the dose to the detector for a beam of quality Q?

A

Cavity factor and f_Q

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45
Q

Detectors can be split into large and small detectors, what is the size relative to?

A

Compared to the ranges of the dose-depositing charged particles

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46
Q

When are large detectors considered?

A

When lower energies are used, like orthovoltage/superficial x-rays, HDR brachytherapy, diagnostic imaging

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47
Q

When are small detectors considered?

A

When higher energies are used and so the electrons travel further

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48
Q

What is the cavity factor also called?

A

Mass-energy absorption coefficient ratio

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49
Q

Are TLDs (made of Lithium Fluroide) considered large or small detectors?

A

Large

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50
Q

For small detectors, the detector size is only a small fraction of the electron range, so what condition cannot be applied?

A

The charged particle equilibrium condition

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51
Q

What is the ideal voltage range for ionisation chambers (e.g. farmer chambers)?

A

200-400 V

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52
Q

What is the correction factor f_ion for?

A

To correct for ion recombination and whether all the ions have been detected

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53
Q

For ion chambers, what is the mean energy required to produce an ion pair in air per unit charge e in dry air for a wide range of energies?

A

33.97 eV / ion pair (or J/C)

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54
Q

Why are perturbation factor added to the equation for ion chamber dosimetry?

A

Departures from Bragg-Gray assumptions

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55
Q

What are the four effects of a real world ion chamber in water that cause changes to the electron fluence are corrected for by the perturbation factor?

A

The effect of displacing a volume of water with the chamber cavity (p_dis), the non-water equivalence of the chamber walls and any waterproofing material (p_wall), the effect of the central electrode (p_cel), and the in-scattering of electrons caused by the air cavity (p_cav)

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56
Q

Which perturbation effects are included in the perturbation factor for photon beams?

A

p_dis, p_wall, p_cel (significant for low energy photon beams - mostly diagnostic)

57
Q

Which perturbation effects are included in the perturbation factor for electron beams?

A

p_dis, p_cav

58
Q

Which perturbation effect means than Roos type chambers should be used for electron beams rather than farmer type chambers?

A

The in scattering effect (p_cav)

59
Q

Are the perturbation effects all above or below one?

60
Q

What is the sensitive volume of ion chambers usually filled with?

A

Ordinary air

61
Q

In ion chamber dosimetry, what is the dose related measured quantity?

62
Q

In ion chamber dosimetry, what is the dose rate related measured quantity?

A

Current, I

63
Q

If the voltage across an ion chamber is low, what effect could occur? (think about charge vs voltage graph)

A

Ion recombination, so the collected charge is lower than expected for the ionisation chamber region

64
Q

If the voltage across an ion chamber is high, what effect could occur? (think about charge vs voltage graph)

A

Charge multiplication, so the collected charge is higher than expected for the ionisation chamber region

65
Q

In the energy imparted equation for epsilon, what is the radiant energy in and out?

A

The sum of the energies (excluding rest mass energies) of all charged and uncharged ionising particles either entering (in) or leaving (out) the volume

66
Q

In the energy imparted equation for epsilon, what is the sum of Q term?

A

The sum of all the changes of the rest mass energy of nuclei and elementary particles that occur in the volume (Q>0 = decrease of rest energy)

67
Q

For questions that use the energy imparted equation for epsilon, does the creation of photons (e.g. radioactive decay or pair production) mean a positive or negative Q in the equation?

68
Q

Whilst kerma only considers the initial kinetic energies of charged particles created in the volume (if created outside it doesn’t count), how does this differ to dose?

A

Dose considers the energy deposited in the volume element, regardless of whether the particle was created inside or outside the volume element.

69
Q

For absorbed dose calculations, highlight the charged particle tracks that are inside the volume element, what should be highlighted for kerma calculations?

A

Circle the charged particles that are generated in the volume element

70
Q

To note the difference between absorbed dose and kerma: Absorption of energy does not take place in the same location as what?

A

The transfer of energy

71
Q

What is the equation for cema?

A

dE_l / dm, where dE_l is the mean energy lost in electronic collisions by the primary charged particles

72
Q

For charged particles, most of the energy loss is directly absorbed, but how is the energy of uncharged particles imparted to matter?

A

Through a two step process: energy transfer then energy absorption

73
Q

What is the difference between kerma and cema?

A

Cema involves the energy lost in electronic collisions by the incoming charged particles, whereas kerma involves the energy imparted to outgoing charged particles

74
Q

All codes of practice have standard nomenclature, what does N_D,w,Q0 mean?

A

The calibration factor in terms of absorbed dose to water for a dosimeter at a reference beam quality Q_0

75
Q

All codes of practice have standard nomenclature, what does M_Q mean?

A

Reading of a dosimeter at quality Q, corrected for influence quantities other than beam quality

76
Q

All codes of practice have standard nomenclature, what does k_pol mean?

A

Factor to correct the response of an ionisation chamber for the effect of a change in polarity of the polarising voltage applied

77
Q

All codes of practice have standard nomenclature, what does k_s mean?

A

Factor to correct the response of the ionisation chamber for the lack of complete charge collection due to ion recombination

78
Q

All codes of practice have standard nomenclature, what does k_Q,Q0 mean?

A

Factor to correct for the difference between the response of an ionisation chamber in the user beam quality compared to the reference beam quality

79
Q

Which factor in the dose equation with the calibration factor do the perturbation factors contribute to?

80
Q

What are the methods for the standard lab calibration for air kerma?

A

Ionisation chamber, free air chamber

81
Q

What are the methods for the standard lab calibration for absorbed dose to water?

A

Graphite calorimeter, water calorimeter, ionisation chamber, Fricke dosimeter

82
Q

Where the reference quality is cobalt-60, what is omitted from the standard nomenclature terms?

83
Q

How is energy (quality) for MV photons defined in the UK and IAEA?

84
Q

Why is the effective point of measurement for an ionisation chamber not at the centre? (closer to entrance region by 0.6 r)

A

Generally more electrons will come from the top

85
Q

How is energy (quality) for lower energy photons defined?

A

Half value layer (HVL)

86
Q

What are the three levels of dose measurement?

A

Quick check, calibration (traceable to a national standard) and definitive calibration

87
Q

How can a quick check of dose measurement be performed and is the calibration directly traceable to the national standard?

A

Any dose measuring device and no

88
Q

What should you do for calibrations of dose measurement (broad)?

A

There is a detailed protocol to follow and all factors should be recorded. Calibrations should be reviewed regularly

89
Q

What are the action levels for calibration of dose measurements?

A

2% to consider recalibration when possible and 3% to suspend treatments

90
Q

When is a definitive calibration of dose measurement used (general) and what is it used for?

A

Whenever there is a potential break in calibration history and it forms a baseline for subsequent confirmatory measurements

91
Q

When are specific times that definitive calibrations should be done for linacs?

A

Commissioning, following major repair that may affects its calibration, following the replacement of radioactive sources and where the link with the previous calibration has been broken

92
Q

Other than external beam radiotherapy treatment machines, what other equipment requires definitive calibration?

A

Radiation dose measuring equipment

93
Q

Individual patient QA can be done for IMRT treatments with different centres having different frequencies, what are the different approaches to frequency of this?

A

Do individual patient QA for: all IMRT patients, no patients, representative sample or only for unusual cases

94
Q

What are some benefits of audits?

A

Identifies necessary changes, ensures procedures of followed, conforms to ISO9000, avoids drifts to procedures, identifies hardware changes and ensures uniformity between centres

95
Q

What are the different types/levels of audit?

A

Local (e.g. new machine), national (e.g. IPEM networks), international (e.g. IAEA) and clinical trials

96
Q

What is mostly used for in vivo dosimetry?

A

TLDs and diodes (sometimes also MOSFETs, OSL, gafchromic film and portal imager)

97
Q

What is in vivo dosimetry in radiotherapy?

A

Measurements made on the patient during treatment and it often involves placing detectors on the skin to measure surface dose

98
Q

Roughly what percentage differences from the expected doses does in vivo dosimetry identify?

99
Q

Where can we measure the dose for in vivo dosimetry?

A

Surface, exit or intracavity

100
Q

What factors are in vivo dosimeters dependent on and could affect the readings?

A

Dose rate, energy, temperature, incident angle, detector degradation

101
Q

How are in vivo dosimeters calibrated?

102
Q

What are some of the clinical uses of in vivo dosimetry?

A

Independent check of MU calculations, TBI/TSET calcs, intracavitary doses, OAR doses, errors in patient setup, non-standard cases where doses may be difficult to predict

103
Q

How are TLDs calibrated?

A

A batch of 100-150 TLDs get uniformly irradiated and then the mean thermoluminescence reading of the batch is used generate correction factors

104
Q

What are the pros of TLDs?

A

Dose rate independent, read out temp is high compared to room/patient temp, no directional dependence

105
Q

What are the cons of TLDs?

A

Readings aren’t real time (couple hours of processing), destructive read out, one dimensional readings

106
Q

What are diodes made of and what does this mean?

A

Silicon and they have a higher Z than water, so the photoelectric effect will be dominant for lower energies, so they will be overly sensitive in the kV range

107
Q

Why do diodes need calibrating regularly?

A

They lose sensitivity due to radiation damage

108
Q

Are diodes temperature dependent and what does this mean for in vivo dosimetry using them?

A

Yes and the response will change if the temperature of the diode changes when placed on patient skin

109
Q

Do diodes have angular dependence?

110
Q

What in vivo dosimetry type are MOSFETs used for? (rarely used)

A

Cavity readings

111
Q

What does OSL stand for?

A

Optically Stimulated Luminescence

112
Q

Are OSLs similar to TLDs and how are they different?

A

Very similar but for OSLs, the stored energy is released by light irradiation rather than heating

113
Q

What can automatic segmentation be used for?

A

Outlining OARs automatically during treatment planning

114
Q

What is the difference between the CT scans between diagnostic and radiotherapy planning?

A

Flat-topped couch to attach immobilisation equipment to, wide-bore to accommodate different treatment positions, reference position lasers, indexing system (zero position from lasers), high kV

115
Q

What is the outer material and central electrode of Farmer chambers made of?

A

Outer material - graphite
Central electrode - aluminium

116
Q

Are Farmer chambers used for relative or absolute dosimetry typically?

117
Q

What are PinPoint chambers used for?

A

Water tank measurements

118
Q

What are the pros and cons of pinpoint chambers when considering its size?

A

It is small so it has a high resolution (small volume averaging) but worse SNR as less ionisation events in sensitive volume so more intense beam required

119
Q

What type of ionisation chamber is the NACP chamber?

A

Parallel plate

120
Q

Why are Roos chambers often used for daily use as a parallel plate chamber compared to NACP or Markus chambers?

A

They are more robust

121
Q

What are the purpose of guard rings in cylindrical ionisation chambers and parallel plate chambers?

A

In cylindrical ionisation chambers, to avoid leakage current in the insulator and in parallel plate chambers, it defines the effective collection volume

122
Q

Why are water phantoms used?

A

Similar properties to tissue, directly relates to the chain of calibration and matches treatment planning system (TPS) reference conditions

123
Q

What is the purpose of build-up cups?

A

To create electronic equilibrium (energy dependent), only measure primary radiation (avoid phantom scatter)

124
Q

Why are brass build-up caps used instead of other materials of lower atomic number?

A

They can be smaller (thinner walls) to reach electronic equilibrium (electron path length smaller in higher Z material)

125
Q

What type of detector is used for CT scans?

A

Pencil ionisation chambers (central electrode like Farmer chambers)

126
Q

What is measured for CT scanner output using pencil ionisation chambers?

127
Q

Which ion chambers are used for absolute dosimetry?

A

Large volume detectors, soft x-ray, pencil chambers, Farmer, Roos (can use Markus)

128
Q

Which ion chambers are used for relative dosimetry?

A

Build-up caps, Markus, PinPoint, TLD (can use Farmer)

129
Q

What is the main application/motivations for measuring dose distributions?

A

Treatment planning system beam modelling (profiles, PDDs), machine performance characterisation (flatness, symmetry), patient specific QA, commissioning new techniques, in-vivo dosimetry

130
Q

What equipment can be used for measuring dose distributions?

A

Plotting tanks (e.g. water tanks),

131
Q

What are arrays and what are they for?

A

Lots of detectors in rows and columns (e.g. ion chambers or diodes) to measure multiple points in the field size rather than just one

132
Q

What other method of measuring dose distributions is similar to diode or ion-chamber arrays?

133
Q

What are the dosimetry issues with using EPIDs for measuring dose distributions?

A

Lack of build up, sensitive to contaminant electrons, not water equivalent material, scatter from detector assembly, over-response at low energies

134
Q

What are the practical issues with using EPIDs for measuring dose distributions?

A

Image artefacts if poorly calibrated, ghosting (previous irradiation leaves a faint response), saturation, not independent from linacs or TPS for QA considerations

135
Q

What dosimeters with high spatial resolution can be used for measuring dose distributions?

A

Film (e.g. radiochromic, radiographic), digital luminescent radiography (computed radiography), gel (3D)

136
Q

Why are films, computed radiography and gel for measuring dose distributions less convenient compared to digital detector arrays?

A

Not real-time measurements and the dosimetry is sensitive to processing conditions

137
Q

What applications is radiochromic film used for in radiation dosimetry?

A

When high dose gradients and small fields are used, penumbra and build up regions, IMRT/VMAT, stereotactic radiotherapy, brachy, protons, low energy electrons