Physics/Radiopharm 2017 Flashcards

1
Q

Stats - reproducibility, population, reliability and bayes theorem

A

Reproducibility - ability to get the same research results or inferences, based on the raw data and computer programs provided by researchers.

Reliability - overall consistency of a measure. A measure is said to have a high reliability if it produces similar results under consistent conditions.

A population in statistics is a set of similar items or events which is of interest for some question or experiment.

Bayes theorem: The probability of event A (e.g., having breast cancer) given event B (having a positive mammogram) depends not only on the relationship between A and B (i.e., the accuracy of mammograms) but on the absolute probability (occurrence) of A not concerning B (i.e., the incidence of breast cancer in general), and the absolute probability of B not concerning A (i.e. the probability of a positive mammogram).

The absolutely crucial point to remember from Bayes’ theorem is that the prior probability (or pretest clinical assessment) is as important as the sensitivity and specificity of the diagnostic test in the determination of the post-test probability (the probability that the patient with a positive test truly has the disease).

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2
Q

60 Gbq in dose calibrator why measure less, how to fix, what amino acids why use them?

A

May measure less because of of incorrect radionuclide setting chosen, did not set to zero, high background, battery issue, constancy issue. Fix by performing QC such as constancy, set to zero, check voltage and battery. Dose calibrator is filled with argon and traces of halogen at high pressure. Its operating voltage is about 150 V.

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3
Q

10 % versus 20 % mediastinoscopy what relative risk reduction in % what NNT

A

ARR = ARC - ART = 0.20 - 0.10 = 0.10 = 10%

RRR = (ARC-ART)/ARC = (0.20 - 0.10) / 0.20 = 50%

NNT = 1/ARR = 1/0.10 = 10

AR (absolute risk) = the number of events (good or bad) in treated or control groups, divided by the number of people in that group

ARC = the AR of events in the control group
ART = the AR of events in the treatment group

ARR (absolute risk reduction) = ARC – ART

RR (relative risk) = ART / ARC

RRR (relative risk reduction) = (ARC – ART) / ARC

RRR = 1 – RR

NNT (number needed to treat) = 1 / ARR

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4
Q

How to produce Tc - 2 ways

A

Using Fission MOLY in generator
99Mo → 99mTc + β− + νe

Cyclotron produced
100Mo(p,2n)99mTc

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5
Q

Describe coincidence events and whether accepted (RC)

A

True, scatter, random.

True and Scatter events increase linearly with activity; random events increase with the square of activity.

To decrease random events: use 2D imaging with septa, reduce dose, scatter correction (delayed window method or singles method), reduce coincidence acceptance window.

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6
Q

High count rate what happens to lost counts, what about NaI crystal?

A

High count rate leads to Dead time, which refers to the time required to process individual detected events. Dead time is the period of time that a counter remains insensitive to count the next event after an event. Dead time reduces sensitivity, which reduces S/N ratio. Images are noisier due to dead time, but the spatial resolution is unchanged. Events that occur in the dead time are lost, and in paralyzable systems, extend the dead time even further.

A counting system can be classified as being paralyzable or non-paralyzable.

A non-paralyzable system is one for which, if an event occurs during the dead time of a proceeding event, then the second event is simply ignored with no effect on subsequently occurring events. Observed counting rate: RO = Rt/(1 + Rt τ)

A paralyzable system is one for which each event introduces a dead time, whether or not that event was actually counted. Therefore, an event occurring during the dead time of a proceeding event would not be counted but still would introduce its own dead time during which subsequent events could not be recorded. Most radiation detectors behave as paralyzable systems. RO =Rt e-Rt τ , ROmax = 1/(eτ)

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7
Q

Radioprotectors and dose rate factor

A

Most radioprotectors are sulfhydryl compounds. They contain a sulfhydrl group (S-H) attached to a short carbon chain with a reactive compound at the opposite end. The example from Hall et all is cysteamine:
SH−CH2−CH2−NH2
These agents are only effective on radiation types that require oxygen for ‘fixing’ - ie. that function through indirect action of radiation
Cytoprotective mechanisms of sulfylhydryl compounds:
1. Free radical scavenger
The sulfhydryl group may act by chemically reacting with free radicals generated by indirectly ionising radiation and preventing their interaction with DNA
2. Proton/hydrogen donor to aid in chemical repair of DNA damage
The sulhydryl group may donate a hydrogen atom to assist in DNA repair pathways.

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8
Q

Define RBE, 2 factors that effect this (RC

A

Relative biologic effectiveness (RBE) of some test radiation (r) is the ratio D250/Dr, in which D250 and Dr are the doses of 250-kV x-rays and the test radiation, respectively, required to produce equal biologic effect. RBE = D250 / Dt = (Dose of 250 kVp X-rays) / (Dose of test radiation) to cause equivalent effect

RBE increases with LET to a maximum at about 100 keV/μm, thereafter decreasing with higher LET. For radiation with the optimal LET of 100 keV/μm, the average separation between ionizing events is similar to the diameter of the DNA double helix (2 nm). It can most efficiently produce double-strand breaks by a single track.

RBE depends on the following:
o Radiation quality (LET)
o Radiation dose
o Number of dose fractions
o Dose rate
o Biologic system or end point
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9
Q

Anatomy of central neck (RC)

A

Hyoid bone (superior)
Carotid arteries (laterally)
Superficial layer of deep cervical fascia (anteriorly)
Deep layer of deep cervical fascia (posteriorly)
Innominate artery on right and corresponding axial plane on left (inferior)

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10
Q

Rb-82 how it is taken up, % myocardial retention at rest and stress in an animal model (?rabbit) and two things that increase this retention

A

Rb-82 is a potassium analog and is taken up by myocardial cells via the Na+/K+ ATP transporter in a rapid and active manner. Myocardial extraction fraction 65%.

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11
Q

What 3 radiopharmaceuticals stop breastfeeding (kinda RC)

A

I-123 (NaI), I-131 (NaI), Ga-67 citrate

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12
Q

3 Causes of radiopharmaceutical breakdown (RC)

A

o Changes in temperature or pH
o Light
o Presence of oxidizing or reducing agents
o Radiolysis
o Decomposition of the radiopharmaceutical due to the action of a solvent

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13
Q

8 things for major spill (RC)

A

Notify all persons in area and clear the area
Leave fume hood running
Close off and secure spill area
Remove contaminated clothing and clean skin
Notify RSO
Clean spill working from outside in with protection
Put all contaminated stuff in radioactive waste
Wipe test for residual contamination as appropriate
Arrange bioassay if necessary
Submit written report

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14
Q

5 things to change spect to pet

A

More shielding for room
Source of radiopharmaceuticals from supplier
Consider purchasing cyclotron
Attenuation correction for PET/MR or PET/CT
Train technologists who are inexperienced in CT

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15
Q

2 pet generator produced radionuclides with parent named (RC)

A

82Sr/82Rb
25.4d/76s

o 68Ge/68Ga
271d/68m

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16
Q

Stochastic vs deterministic (cancer, cataracts, sterility) (RCish)

A

Deterministic effect: radiobiologic effect with a threshold dose; severity ↑ with radiation dose
Example: cataract, sterility, and skin erythema

Stochastic effect: radiobiologic effect where probability of occurrence ↑ with radiation dose, but severity independent of dose; no threshold dose
Example: cancer and heritable mutations

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17
Q

Linear No Threshold: define- 2 things that happen indicating this is wrong (RC)

A

Linear No Threshold Model assumes that the long term biological damage caused by ionizing radiation is directly proportional to the dose. All radiation is considered harmful with no safety threshold, and the sum of several small exposures are considered to have the same effect as one larger exposure.

Among humans, there is no evidence of a carcinogenic effect for acute irradiation at doses less than 100 mSv and for protracted irradiation at doses less than 500 mSv

Atomic bomb data do not provide solid arguments for the LNT model. dose response is not linear at doses less than 150 mSv. In fact, a quasi-threshold, or even a hormetic effect, may exist below this dose.

Hormesis: Upregulation of protective mechanisms at the cell and tissue levels by low doses likely also operates against carcinogenic factors other than ionizing radiation and against spontaneous cancer, as demonstrated in various experiments in vitro and in vivo. Indeed, a dose of 10 mGy reduces the rate of spontaneous transformation in culture cells below the background level.

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18
Q

Electron capture, what else comes out, another electron capture isotope and does this cause transmutation (RC

A

Electron capture: p+ + e- → n + νe + Q

Neutrino carries away some of the energy, and when the orbital vacancy is filled, either characteristic x-ray or Auger electron is emitted. ↑Z favours EC. Larger elements favour EC as the K-shell is closer to the nucleus and more easily captured.

Some EC radiopharmaceuticals: Tl-201, Ga-67, I-123, I-125, In-111, Xe-127. Se-75

Yes, transmutations.

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19
Q

Cell phases in order of sensitivity

A

Cells in S-phase are typically radioresistant, those in late G2 and M phase are relatively sensitive.

From least radiosensitive to most radiosensative:
S; G1; early G2; late G2; M

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20
Q

Backprojection what is issue, how to fix, what is method used

A

Simple backprojection has inherent 1/r blurring. Fix it by using Filtered Backprojection. Ramp filter selectively amplifies high-frequency components relative to low-frequency components. The filter removes the 1/r blurring and star artifact present in simple backprojection and sharpens image detail, but it also amplifies high-frequency noise components in the image.

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21
Q

Transport index define and maximum dose for 3 package types (RC)

A

Transport Index (TI) = dose rate measurement at 1 meter in uSv/hr divided by 10

White I - maximum TI <0.05
Yellow II - 1.0
Yellow III - 10

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22
Q

Components of DTPA kit and relative proportions and why?

A

Main components: DTPA and stannous chloride
10^5-10^8 mol DTPA : 10^3-10^6 mol Sn2+ : 1 mol 99mTc

o Need enough Sn2+ to reduce all 99mTc
o Need greater amount of chelate to drive chemical equilibrium to form chelated complexes, and prevent Sn and Tc colloid formation

o pentasodium or calcium trisodium salt of DTPA – chelating agent
o stannous chloride dihydrate in lyophilized from - reducing agent of Tc-99mO4-
o ascorbic acid – stabilizer

Tin:
Too much: Hydrolysis of tin increases, may precipitate some of the reduced Tc-99m to form Tc-99m-Sn-colloid and other Sn-complexes, reducing yield of the labeled chelate
Too little: Incomplete reduction of Tc-99m to desired oxidation state and lower yield, and results in an increase in free pertechnetate.

Pertechnetate:
Too high a concentration with O2 can lead to radiolysis and the production of free radicals, which will interact with the chelates to form free pertechnetate. However kit limits are well below this.

The pH is adjusted to 3.9-4.1 with sodium hydroxide and/or hydrochloric acid prior to lyophilization. No bacteriostatic preservative is present

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23
Q

Effective dose for NEW and public

A

A NEW is any person who in the routine performance of their profession, business or employment will expect to be exposed to more than the prescribed limit of ionizing radiation for the general public (>1 mSv)
b) What is dose limit for NEW?
100 mSv over 5 years with a maximum of 50 mSv in any one year
c) What is dose limit for public?
1 mSv per year
The dose limit for pregnant workers is 4 mSv from the time the pregnancy is declared to the end of the term.

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24
Q

P32 route, 1/2 life and decay

A
P32 sodium orthophosphate
Dose/route: 6-12 mCi IV
Half-life: 14.3 days
Decay: Pure beta emitter
βmax: 1.71MeV
Range: 8 mm ST, 3mm bone
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25
Q

Relative front

A

Relative front (Rf) is the ratio of the distance traveled by given compound within a solution during paper chromatography or ITLC, to the distance traveled by the solvent.

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26
Q

1/2 lives I-125, I-131, I-123, Ga-67, Ga-68, Y-90, Tl-201, In-111, Sr-89, Mo-99, ?Tc-99m (RC)

A

I-125 (59 days), I-131 (8 days), I-123 (13.2 hours), Ga-67 (78 hours), Ga-68 (68 minutes), Y-90 (64 hours), Tl-201 (73 hours), In-111 (67 hrs), Sr-89 (50.5 days), Mo-99 (66 hours), Tc-99m (6 hours)

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27
Q

Quenching gas, where is it and what does it have to do? (RC)

A

Ionized quenching gas that can recombine with electrons without giving off UV radiation (by dissociating into molecular fragments)
Absorb UV radiation inhibiting further ionization.
Electron donor

Quenching gas is used in a Geiger Mueller counter to prevent additional avalanche ionization from
positive ion cloud. They are commonly made from
o heavy organic vapors (alcohol) - more effective but can be used up because molecular fragments do not recombine after dissociation
o halogen gases (Cl2) – recombine after dissociation so essentially unlimited lifetime in GM counter
gives up electrons easily to neutralize positive ions, converting ion cloud into ionized molecules of quenching gas
when ionized quenching gas molecules are neutralized by electrons, they de-energize themselves by dissociating into molecular fragments instead of emitting UV photons
strong absorbers of UV radiation

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28
Q

Weighting factors for photon, electron, alpha and 1st 1/2 of neutrons

A

Equivalent dose = absorbed dose x Wr (radiation weighting factor)
Wr = 1 for x-ray, gamma ray, electrons, positrons
Wr = 2 OR 5 for proton (Sorenson P406)
Wr = 20 for alpha, fission and heavy nuclei
Wr = 5-20 depending on neutron energy

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29
Q

CT photon effects and which one dominates > 100 keV

A

Photoelectric effect at < 100 keV
Compton scatter begins to dominate > 100 keV
Pair production at > 10 MeV

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30
Q

Ra 223, 1/2 life, what is eventual stable daughter, how much energy and how many alphas?

A
Ra-223: t½ of 11.4 days, eventual stable daughter: Lead-207 (Pb-207), after six-stage decay.
Energy range: 5-7.5 MeV  
# of particles: 4 alpha particles
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31
Q

2 factors that can decrease PET resolution

A

Resolution = √((Rrange)2 + (Rdetector)2 + (Rnon-colinear)2 )

Rsys = √((Rins)2 + (Rscatter)2 + (Rnon-colinear)2 )

32
Q

Intrinsic efficiency and factors that effect?

A

Intrinsic efficiency (ε) – efficiency with which detector absorbs incident radiation events and converts them into potentially usable detector output signal; determined by detector thickness and composition/density and by type and E of radiation – with increased E need increased crystal thickness

o Decreases with increasing E
o Increases with increasing thickness of detector
o Increases as detector density and Z increase (stopping power)

Detector Efficiency: D = g x e x f x F

g: geometric efficiency of the detector – efficiency with which detector intercepts radiation emitted from the source, determined mostly by detector size and distance from source.
e: intrinsic efficiency with which detector absorbs incident photons and converts them to potentially usable detector output signal

33
Q

Intrinsic resolution and factors that effect? (RC)

A

Intrinsic resolution refers to how well the crystal and PMT system localize an interaction in the crystal. Dependent on:

(1) Crystal Size: the smaller the crystal, the higher the resolution. This is the primary limiting factor that determines spatial resolution of the PET scanner
(2) Positron range prior to annihilation: The positron will travel a short distance before annihilation with electron. Energetic positrons may travel several mm in tissue before undergoing annihilation. Therefore, the detected event may be some distance from the actual location of the radionuclide. Resolution loss is about 0.5 – 2 mm, depending on the isotope.
(3) Non-colinearity. Annihilation photons are not exactly 180 apart. Because of the residual kinetic energies of the positron and negative electron. Results in 2 – 3 mm loss of resolution. Loss of resolution is a function of distance between the detectors. X=d/2 tan (0.25). (Example: For 100 cm diameter, the loss is 2.2mm)
(4) Depth of interaction effect: as a source moves away from the centre of the FOV, the apparent width of the detector element becomes d’ = dcosO + x sinO
(5) Sampling: in practice, 2 samples are usually acquired per detector element width.
(6) Reconstruction filters: PET images can be reconstructed with higher cut-off frequencies (because higher detection efficiency leads to less noise), and thus, final spatial resolution generally is superior to SPECT images.
(7) Detector ring diameter: the closer the detectors are to each other and to the source, the greater the resolution. Unfortunately, the smaller the diameter of the scanner ring, the more likely scattered and random coincidences will be recorded. ?? Does ring diameter affect spatial resolution???
(8) Scattered and random coincidences

34
Q

Why is uniformity more important in spect? (RCish)

A

Uniformity is more important in SPECT because even small variations in non-uniformities can cause major artifact in reconstructed images

Non-uniformity artifact in SPECT: concentric full rings
Centre of rotation offset: non-concentric, full circle near centre of FOV, partial circle in periphery

In planar imaging, non-uniformities of a few percent are acceptable for producing images of diagnostic quality. In SPECT, even small non-uniformities can lead to major artifacts in reconstructed images and flood-field uniformities of 1% or less are desirable.

35
Q

3 gamma camera qc and frequency

A

Uniformity (Daily)
o Intrinsic with a point source placed 5x detector face width away, collimator off

Energy Peak (Daily)
o Tc-99m point source 
o Set to 140 +/- 10% window

Resolution (weekly)
o Bar phantom with a flood source

36
Q

Diagram with big hole in bottom of flood and asked what is issue and subsequent artifact on spect

A

Photomultiplier tube malfunction. PM tube defect on SPECT will create a nonuniformity artifact.

37
Q

4 important pet crystal characteristics

A
Density (g/cm3)
Effective Z
Decay time (nsec)
Photon yield (per keV)
Index of refraction
Hygroscopic
Peak emission (nm)
38
Q

4 important amyloid imaging characteristics not related to isotope

A

Binding characteristics
o Beta amyloid plaque
o Neurofibrillary tangles consisting of tau protein
What regions
o Posterior temporo-parietal and posterior cingulate gyrus
Pathologic finding with potential for in vivo imaging
o Beta amyloid plaque imaging is currently being investigated (e.g. with agents like 18Fflorbetapir, 18Fflorbetaben, 18Fflutemetamol), but combined beta amyloid plaque and neurofibrillary tangle agents may be better (e.g., 18F-FDDNP)

39
Q

4 kinds of radioactive deca

A

Beta decay: n → p+ + e- + ṽe + Q
Positron decay: p+ → n + e+ + νe + Q
Electron capture: p+ + e- → n + νe + Q
Internal conversion: α = e/γ

40
Q

What is Compton effect (RC)

A

Compton scatter: photon interaction with outer shell electron resulting in deflection of photon and ejection of electron. Compton scatter can reduce intrinsic spatial resolution

41
Q

4 pet F-18 isotopes

A

18F-FDG, 18F-FES, 18F-FLT, 18F-FDOPA, 18F-choline, 18F-acetate

42
Q

Highest cause of background radiation (RC)

A

Latest estimations for US population is NCRP report 160 (2009), based on 2006 exposure
o Inhaled Radon-222 and Radon-220 (thoron) are technically internal dose
2.3 mSv/a
Others
o K-40: 4 kBq, 0.17 mSv/a
o Uranium/thorium series (U-238, U-234, Th-232, Pu-239): 0.12 mSv/a
o C-14: 3.7 kBq, 0.12 μSv/a

43
Q

Gso, lso, bgo, Na I list in increasing numeric order (effective z, density, attenuation in cm) (RCish)

A

If asked increasing density: NaI < CsI < LaBr3 < GSO < BGO < LSO

If asked increasing Z: NaI < LaBr3 < CsI < GSO < LSO < BGO

If asked increasing attenuation coefficient: NaI < CsI < LaBr3 < GSO < LSO < BGO

44
Q

Can following radiation effects be due to in utero exposure (sterility, microcephaly, cancer, neurological impairment, cataracts- y or n)

A
Sterility - N?? No specific mention in BEIR VII; 
Microcephaly - Y
Cancer - Y
Neurological impairment - Y
Cataracts - Y
45
Q

Direct vs indirect and what is worst indirect oxidant

A

Direct action: radiation directly interacts with DNA (typically high LET)

Direct is more likely to cause double strand breaks (can lead to direct death from cytoxic effect of exposed dbl strands)

Indirect action: radiation (typically low LET) interaction with other molecules (primarily H20), producing free radicals (H2O2 and OH), that cause DNA damage

Indirect generally easier to repair, as usually constitutes single strand breaks (can lead to frameshifts and substitutions

46
Q

4 Rs of radiology (RC)

A
The “four Rs” of Radiobiology are:
Repair of sublethal damage
Reassortment of cells within the cell cycle
Repopulation
Reoxygenation
47
Q

BMD windowing 2 methods

A

Voltage switching (e.g. Hologic) - continuously switch voltage between high and low values

K-edge filtering (e.g. GE, Norland) - Use carefully chosen metal filter (thin sheet of a special metal) to create two separate energy peaks in x-ray spectrum

48
Q

When’d to repeat precision measurements in BMD (RC)

A

After basic scanning skills have been learned
After 100 patients have been scanned
When a new DXA system is installed
Whenever their skill level has changed

49
Q

What is the manipulated variable in experiment design

A

AKA independent variable
Condition or variable that you change in your experiment
Does not depend on any other variable in the experiment

Dependent variable
Condition that you measure in the experiment

50
Q

What is and How to calculate standard deviation

A

SD is used to quantify the amount of variation

= SQRT (variance)

51
Q

2 kinds of breathing correction techniques (RC)

A

Pressure sensor elastic belt around abdomen
Infrared stereovision system tracking motion of thoracic markers
Active breathing control (verbal instruction)
Spirometer measuring flow of respired air
Nasal thermistor
Inflatable chest cuff

52
Q

Impact of changing from 16 frames to 8 frames on MPI and explain

A

Reducing frame rate from 16 frames to 8 frames results in:
Underestimation of EDV
Overestimation of ESV
Underestimation of LVEF

Explanation (same source):
For gated SPET imaging, image data are acquired in synchrony with the ECG signal using a specific number of intervals, from R wave to R wave.
Counts accumulated during each of these intervals generate individual images
Each individual image is subsequently reconstructed into a tomographic set
Inverse relationship between the temporal resolution (i.e., number of frames per cardiac cycle) of gated images and the count density in each gated frame
Aquisition of 16 frames instead of 8 frames per cycle should improve the temporal resolution of the cardiac contraction and consequently allow more accurate determination of LV systolic function
Higher temporal resolution of SPET should result in more accurate determination of end-systolic and end-diastolic frames and hence more accurate assessment of ventricular volumes

53
Q

Increase acceptance window 100% for rr of 1000ms , what is window and what is effect on curve and images

A

R-R interval 1000 ms
Acceptance window of 100% = accept beats with duration of 500-1500 ms

Cardiac beat length acceptance window:
the peak or R point of each QRS complex in the ECG triggers the binning of counts into projection images
If a “fixed temporal resolution framing” approach is employed, usually based on a sampling of the beats at the beginning of a gated SPECT acquisition, all gating intervals will be set to the same temporal length
For example, in 8-frame gating, the 8 intervals will span 125 milliseconds each if the expected heartbeat duration (R-R computer) is 1 second
Because the actual time between successive R points (R-R patient) typically varies during the course of the acquisition, and particularly because of the impact of PVCs on systolic function and the systolic and diastolic timing noted, if there is no “bad beat” rejection, an error in the function measurements will be embedded in the data, with the magnitude of the error being proportional to the frequency of the premature beats

a beat length acceptance window of 20% allows accumulation of data from cardiac beats of 900 to 1100 milliseconds’ duration. An acceptance window of 100%, on the other hand, allows accumulation of data from beats with duration in the range of 500 to 1500 milliseconds

54
Q

3 causes of soft tissue mdp uptake (RC)

A
Trauma/burns/frostbite/overexertion/ischemia
Myositis ossificans
Rhabdo
Polymyositis/dermatomyositis
Calcific tendonitis
Muscular dystrophy
55
Q

3 ways to reduce dose post exposure (RC)

A

Things like frequent voiding, laxative, thyroid blocking, etc?

56
Q

4 benefits of negative ion cyclotron (RC)

A

a. stripping foil is near 100% efficient, so get less radioactivity in the housing.
b. Better beam optics.
c. The foil can also split a beam, so you can create 2 different products at once.
d. Smaller than positive ion cyclotrons
e. Disadvantage: need a lower-pressure vacuum

57
Q

3 kinds of radiolabelling (RC)

A

BEIBER

Bifunctional chelates - In111 DTPA

Excitation labelling - I123 labelled compounds

Introduction of a foreign label - Tc99, In111 labelled cells

Biosynthesis - Co-57 B12

Exchange of isotopes - 131 MIBG, C14

Recoil labelling - H3 labelled compounds, Iodinated compounds

58
Q

What determines whether nuclide is stable or unstable? 2 ways in which a proton-rich radionuclide can become more stable (RC)?

A

Ratio of neutrons to protons

Ways a proton rich RN can become more stable:
Positron decay
Electron capture

59
Q

Why thallium doped NaI?

A

Tl doping (0.1-0.4 mol %) adds activation centres that makes NaI crystal an efficient scintillator at room temperature (vs. liquid nitrogen temperatures)

Also decreases self-absorption.

60
Q

2 advantages of Technegas over Aerosol Tc-99m-DTPA?

A

Smaller particle size

Behaves as true gas, allowing nanosized particles to penetrate deep into alveoli

Remain bound to lining of alveoli, resulting in stable image

Less central airways deposition

Ability to perform ventilation SPECT

Little degradation or translocation across pulmonary alveolar bed

61
Q

What is the difference between paralyzable and non-paralyzable? Name a detector system that is paralyzable? Which of paralyzable vs. non-paralyzable gives higher count loss at high dose rates?

A

A non-paralyzable system is one for which, if an event occurs during the dead time of a proceeding event, then the second event is simply ignored with no effect on subsequently occurring events

A paralyzable system is one for which each event introduces a dead time, whether or not that event was actually counted. Therefore, an event occurring during the dead time of a proceeding event would not be counted but still would introduce its own dead time during which subsequent events could not be recorded.

Most radiation detectors behave as paralyzable systems.

62
Q

In what form is 18F produced in the cyclotron? How is it extracted?

A

F-18 is produced by irradiation of O-18 water with protons in a cyclotron and recovered as F-18 sodium fluoride by passing the irradiated water target mixture through a carbonate type anion exchange resin column. Water passes through, but F18-(-) is retained on the column.
O-18(p,n) F-18 reaction

Also variant recall: 2 ways of making F-18? 1 adv and 1 disadv of each
a. O18(p,n) gives fluoride ion in aqueous solution, higher specific radioactivity and better for FDG production, but O18 water is expensive.

b. Ne20(d,α) gives elemental fluorine gas, cheap and better for F-dopa production, but lower specific radioactivity

63
Q

Define “specific activity” and “concentration”

A

Specific activity: proportion of a sample that contains only the radioactive form of the atom, expressed in Bq/g.

Concentration: Abundance/volume; abundance of a material is most commonly mass or moles

64
Q

Define dead time. What is the consequence of dead time for imaging?

A

“the period of time that a counter remains insensitive to count the next event after an event.” (Saha). Dead time reduces sensitivity, which reduces S/N ratio. Images are noisier due to dead time, but the spatial resolution is unchanged. Events that occur in the dead time are lost, and in paralyzable systems, extend the dead time even further.

65
Q

2 methods of testing linearity in a dose calibrator

A

Decay method (large dose of 99mTc measure decay every 6 hours over 72 hours, point on the graph that deviated most from the line <10%)

Shielding method (series of lead shield, various thickness, apply correction and average, the result that deviates the most must deviate <10%)

66
Q

What is the linear no threshold model?

2 Examples at cellular level that counter this?

A

inear no threshold - model that assumes that the long term biological damage caused by ionizing radiation is directly proportional to the dose. All radiation is considered harmful with no safety threshold, and the sum of several small exposures are considered to have the same effect as one larger exposure.

For second part, not sure if they are getting at radiation hormesis: Paradoxical, beneficial effect of low dose ionizing radiation in biological systems
Possible mechanisms:
o Stimulation of defense mechanisms like antioxidant formation and DNA repair, leading to better repair of damage after subsequent high dose radiation
o Activation of anticancer immune functions
o Bystander effect to eradicate neighbouring cells with genomic instability

OR true DNA repair mechanisms:
Base excision repair (single stranded breaks) - repairs damage to a single nitrogenous base by deploying enzymes called glycosylases.These enzymes remove a single nitrogenous base to create an apurinic or apyrimidinic site (AP site). Enzymes called AP endonucleases nick the damaged DNA backbone at the AP site. DNA polymerase then removes the damaged region using its 5’ to 3’ exonuclease activity and correctly synthesizes the new strand using the complementary strand as a template

Nucleotide excision repair (single stranded breaks)- repairs damaged DNA which commonly consists of bulky, helix-distorting damage, such as pyrimidine dimerization caused by UV light. Damaged regions are removed in 12–24 nucleotide-long strands in a three-step process which consists of recognition of damage, excision of damaged DNA both upstream and downstream of damage by endonucleases, and resynthesis of removed DNA region

Non-homologous end joining (double stranded breaks) - DNA Ligase IV, a specialized DNA ligase that forms a complex with the cofactor XRCC4, directly joins the two ends

Homologous recombination (double stranded breaks) - requires the presence of an identical or nearly identical sequence to be used as a template for repair of the break. The enzymatic machinery responsible for this repair process is nearly identical to the machinery responsible for chromosomal crossover during meiosis. This pathway allows a damaged chromosome to be repaired using a sister chromatid (available in G2 after DNA replication) or a homologous chromosome as a template

67
Q

3 radiopharmeuticals that have so much breast uptake that complete breastfeeding cessation is recommended.

A
Radiopharmaceuticals with > 3 weeks breastfeeding cessation recommended:
I131-NaI
I131-MIBG
Ga-67
I123-NaI
I123-MIBG
68
Q

Name 2 generator produced PET tracers

A

82Sr /82Rb: 25.4d (EC)/76s (EC/β+)
68Ge/68Ga: 271d (EC)/68m (EC/β+)
81Rb/81mKr : 4.6h (EC/β+)/13.1s (EC/IT)
62Zn/62Cu: 9.3 hours/9.7 min

69
Q

If a particle undergoes positron decay (or EC, B-, alpha) does it transmutate?

A

Yes

Transmutation happens when parent radionuclide (X) and daughter product (Y) are different chemical elements.

Isomeric transition and internal conversion don’t transmutate

70
Q

what’s common between positron and EC in terms of decay and what factor favours EC?

A

Both in low N:P ratio nuclides, results in Z-1 transmutation and are isobaric

↑Z favours EC
In both positron forms a neutron, both isobaric decay with transmutation, one by the emission of positron and neutrino (positron decay), the other by capture of K-shell electron by the nucleus and subsequent X-ray or Auger emission (EC). Larger elements favour EC as the K-shell is closer to the nucleus and more easily captured

71
Q

Two decay modes for a proton rich nucleus. What orbital process can occur after this? Emission that can accompany electron capture is?

A

For EC, get hole in an inner electron orbital shell, results in emission of characteristic X-ray or Auger electron

72
Q

Does the emission from a proton-rich isotope lead to transmutation?

A

Yes, EC or positron decay, resulting in Z-1

73
Q

List 3 ways of dealing with internal contamination.

A

Depends on the tracer. Most commonly:
Potassium iodide, PTU, Tapazol, thyroid monitoring (if I131)
Hydration, EDTA, EDTA for many others

Also, internal contamination considered a major spill, need to do the routine procedures required for major spill (inform RSO, etc).

74
Q

Define DREF, RBE

A

Dose and Dose-Rate Effectiveness Factor - ratio between the radiation detriment from high doses/rates and that from low doses/rates

75
Q

Name a radionuclide that undergoes EC.

A
Thallium
Gallium-67
Indium
I123
\+ most PET tracers