Official Course
Description: MCCCD Approval: 5-27-2008 |
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DMI281
2008 Fall – 2012 Fall |
LEC
1.5 Credit(s) 1.5 Period(s) 1.5 Load Occ |
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Nuclear
Medicine PET I |
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Positron
emission tomography (PET) and Integrated positron emission tomography/computed
tomography (PET/CT). Basic principles of operation and design of positron
imaging systems and quality control necessary for the equipment. Positron
coincidence detection and positron imaging using gamma camera and high energy
collimators. Production and characteristics of positron emitters. Prerequisites: DMI251 or certified
nuclear medicine technologist or permission of Nuclear Medicine Technology
Program Director. |
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Cross-References:
ICE281 |
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Go to Competencies Go to Outline
MCCCD
Official Course Competencies: |
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DMI281 2008
Fall – 2012 Fall |
Nuclear Medicine PET I |
1.
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Discuss basic designs and principles that enable the
construction of images using, Positron Emission Tomography (PET), and/or
Integrated PET/CT imaging systems and integrated PET/CT. (I) |
2.
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Describe the Quality Control necessary for PET and PET/CT.
(I) |
3.
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Compare and contrast acquisition parameters of selected
types of imaging including SPECT, PET, and planar imaging. (I) |
4.
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Give a step-by-step explanation of the back projection
method of reconstruction, taking into consideration various correction
parameters. (I) |
5.
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Describe iterative reconstruction. (I) |
6.
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Discuss the selection criteria related to the open frame
and axial collimators used in positron imaging. (I) |
7.
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Describe the 511 keV collimators
used on SPECT systems to acquire images using positron-emitting
radionuclides. (I) |
8.
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Describe the components of PET, integrated PET/CT and
Positron Coincidence Detection (PCD) systems. (I) |
9.
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List conditions or pathologies for which tomographic
imaging procedures are advantageous over planar imaging. (I) |
10.
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State radiopharmaceutical requirements that must be
satisfied in order to perform a PET, PCD, or PET/CT studies. (I) |
11.
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Discuss the activity limitations related to open frame and
axial collimators. (I) |
12.
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Describe the factors the must be considered when selecting
a filter. (I) |
13.
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Describe how annihilation allows for PET, PET/CT and PCD
imaging. (I) |
14.
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Compare the sensitivity, resolution, and signal-to-noise
ratio for the three methods of imaging with 511 keV
photons. (I) |
15.
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List the studies that can be performed satisfactorily
using each method of imaging. (I) |
16.
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Discuss the physical and chemical characteristics of
positron emitters that make them appropriate for nuclear medicine procedures.
(II) |
17.
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Describe the methods and radiation protection procedures
necessary for preparing and administering positron emitters. (II) |
18.
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Describe the allowable dose ranges and calibration
requirements according the NRC regulations. (III) |
19.
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Calculate specific dose concentration and volume for
pediatric and adult patients. (III) |
20.
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Use decay formulas and decay factor tables to account for
radioactive decay. (III) |
21.
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Discuss the different methods used to calculate pediatric
dosages, the advantages and disadvantages of each method including the
importance of utilizing minimum and maximum dose limits. (III) |
Go to Description Go to top of
Competencies
MCCCD
Official Course Outline: |
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DMI281 2008
Fall – 2012 Fall |
Nuclear Medicine PET I |
I. Positron Imaging Systems
A. Dedicated Positron
Emission Tomography (PET) 1. Basic principles of
operation 2. Sensitivity/deadtime 3. Spatial resolution 4. System configurations 5. Time of flight (TOF) 6. Annihilation coincidence
detectors 7. Crystal characteristics 8. Signal-to-noise ratio
(SNR) 9. Quantitation 10. Attenuation correction 11. Suitable studies 12. Quality Control for PET
and PET/CT B. Integrated PET/CT 1. Basic principles of
operation 2. Sensitivity/deadtime 3. Spatial resolution 4. System configuration 5. Time of flight 6. Annihilation coincidence
software 7. Crystal characteristics 8. Signal-to-noise ratio 9. Attenuation correction 10. Collimators a. Open frame b. Axial 11. Dose range limitations 12. Mode acquisition 13. AIterative
reconstruction 14. Attenuation correction 15. Coincidence timing unit
16. Angle of acceptance 17. Rebinding of data 18. Crystal thickness 19. Limitations 20. Suitable studies C. Positron imaging using
gamma camera and high energy collimators Positron Coincidence Detection (PCD)
1. Basic priciples of operation 2. Sensitivity/deadtime 3. Spatial resolution 4. System configuration a. Collimator design b. Camera head adaptation 5. Signal-to-noise ratio 6. Limitations 7. Suitable studies D. Positron Imaging Systems
1. Positron Emission
Tomography (PET) 2. Positron Coincidence
Detection (PCD) 3. Integrated PET/CT II. Preparing
Positron-Emitters A. Production 1. Generator systems 2. Cyclotron systems B. Characteristics of
positron emitters 1. Physical 2. Chemical C. Biochemical
characteristics 1. 11C 2. 15O 3. 13N 4. 18F 5. Rb-82 6. NaFBone
Scanning with PET 7. Other D. Synthesis of
radiopharmaceuticals E. Quality control of
radiopharmaceuticals F. Administration 1. Intravenous 2. Gaseous III. Dose Determination A. Dose range 1. Factors affecting dose
determination a. Organ or system size b. Photon flux c. Radiation dose 2. NRC acceptable ranges 3. Nuclear Regulatory
Commission (NRC) calibration requirements B. Calculation of dose to
be administered 1. Specific concentration 2. Volume to be
administered 3. Dilution of doses 4. Adjusting unit doses 5. Accounting for decay a. Decay calculation b. Decay factor tables |