RT3 - Clinical use of dosimetry equipment Flashcards
What could you use for clinical dosimetry in RT (x5)
- Ion chamber
- Semiconductor Diode
- TLD
- Film
- Chemical
Ion chamber vs Diode:
Asbolute Dose
Ion Chamber
- Density & atomic number close to water, minimum perturbation of energy fluence
Diode
- Higher density Z leads to significant perturbation of energy fluence
- Ocer-response to low energies
Ion chamber vs Diode:
PDDs
Ion Chamber
- Ideal, flat energy response
Diode
- High resolution (small active volume) is useful (particularly in build-up region) but response varies with energy
Ion chamber vs Diode:
Ouput factors
Ion Chamber
- Spectral variation over field sizes not issue
- physical size of collecting volume is bad for small field sizes (loss of electronic equilibrium)
- Smaller volume reduces sensitivity
Diode
- Size of active component menas you can measure small fields
- Sensitive
- Variation in spectrum small enough to ignore over small range of field sizes
Ion chamber vs Diode:
Penumbra (beam profile)
Ion chamber
- Acceptable but low res due to large collecting volume
Diode
- Steep dose gradients need high res, use a diode for beam profile
Principle of Thermoluminescence
- Impurities in material’s latice prodeuces additional energy levels (a few eV below conduction band). Meta-stable to trap electrons
- Radiation excites electrons into conduction band, relax back but some get trapped
- Heating material results in trapped electrons premoted to conduction band and relaxing back to valence emitting light
- Light collected ∝ absorbed dose
Advantages of TLDs
- Linear response with dose over wide range
- Sensitivity is nearly energy independent
- Small size (2mm) = high res
- No leads/connections needed
Disadvantages of TLDs
- Need to be calibrated
- Fade with time
- Annealing is needd to return electrons to traps
- Affected by history of thermal and radiation
- Difficult to keep constant over long periods
Uses of TLDs
- Commisioning & QA
- small fields, surface & high dose/rates, internal phantom dose
- Patient Dosimetry
- Total body irradiation (TBI)
- Skin
- Eyes
- Personal Dosimetry
- Multi-chip badges
What is TBI?
How do you do dosimetry?
Total Body Irradiation
- TLD sachets at several location on patient
- Additional sachets irradiated at known dose for clibration
- Results compared to expected
2 Types of film dosimetry?
- Radiographic
- Radiochromic (GafC)
Advantages of Film?
- Good spat res
- Convenient for QA and commisioning
- Calibrated for absolute dose
- Geometry is good for dose mapping (thin, flat, large area)
Disadvantgaes of Film?
- Wet processing, not very consistent
- Sensitivity is energy dependent (PE proportial to z^3)
- dose is sensitive to scan parameters
How does Radiographic film work?
- Silver halide crystals become opaque when irradiated
- Detected optically
- Optical density vs Dose = charichteristic curve
How does Radiochromic film (GafC) work?
- Exposure causes reaction between polymers, transparent layer becomes opaque in proportion to dose
- Self-developing & scanned (direction is impoertant)
- Sensitivity independent of energy
- Expensive
- Tissue equiv
- Can go in water
Uses of Gafc
- Star shots (isocentric test)
- PDD for shallow depths
- Light vs rad field size
- Picket fence tests
Chemical Dosimetry principles
- Ionising radiation = cascade of secondary electrons, tranfers energy to molecules, ionisation excitation and breaking of chemical bonds
- Reactive species produce stable products that you measure
Two types of chemical dosimetry
- Fricke Solutions - Radiation oxidises fe2+ to fe3+. Absorption specrophotometry used to assess ratio proprtional to dose. 3D dose distribution.
- Alanine - Solid-state cylindrical pellets, irradiation = free radicals, dose determine from EPR spectrum. Used for individual patient dosimetry
Why are chambers better than TLD film and chemical methods?
Other methods are:
- Fiddly & time consuming
- Need calibrations
- Cosly
- Full of errors
Only realy useful as checks in QA or audit.