| 1.
|
Discuss the gross anatomy and physiology of the central nervous and
immune systems as they relate to nuclear medicine studies. (I, VIII,
XVII)
|
| 2.
|
Describe the characteristics and causes of common pathologies of the
central nervous and immune systems related to nuclear medicine
procedures including susceptible populations and potential treatments.
(II, IX)
|
| 3.
|
List the indications for performing selected CNS imaging studies.
(III-VII)
|
| 4.
|
Compare and contrast the physical and chemical properties, kit and
dose preparation, dose and route of administration, biorouting and
dosimetry of each radiopharmaceutical used for selected CNS and immune
system imaging studies. (III-VII)
|
| 5.
|
Discuss the possible adverse reactions and contraindications for
selected CNS imaging studies. (III-VII)
|
| 6.
|
Describe patient preparation for selected CNS imaging studies.
(III-VII, X-XV, XVIII-XXIII)
|
| 7.
|
Describe equipment and basic procedures and processing utilized in
selected CNS imaging studies. (III-VII)
|
| 8.
|
Recognize normal, normal variants, abnormal findings, and artifacts on
CNS imaging studies. (III-VII)
|
| 9.
|
Discuss the diagnostic and prognostic value of selected CNS imaging
studies. (III-VII, X-XV, XVIII-XXIII)
|
| 10.
|
Discuss the interventions and additional procedures that may be added
to a basic functional brain SPECT study. (V)
|
| 11.
|
List the indications for performing selected immune system imaging
studies. (X-XV, XVII-XXIII)
|
| 12.
|
Discuss why a nuclear medicine study would be preferable to or
compliment other diagnostic modalities in various cases. (X-XV,
XVII-XXIII)
|
| 13.
|
Describe the radiopharmaceuticals used for selected immune system
imaging studies including the physical and chemical properties,
biorouting dose preparation, and route and method of administration.
(X-XV, XVII-XXIII)
|
| 14.
|
Specify the dose range for selected immune system imaging studies and
the resulting radiation doses to various organs and tissues. (X-XV,
XVII-XXIII)
|
| 15.
|
Describe patient preparation for selected immune system imaging
studies. (X-XV, XVII-XXIII)
|
| 16.
|
Describe the procedures for selected immune system imaging studies
including equipment, protocol, dose, administration technique,
administration-to-acquisition times, acquisition parameters, standard
positioning, special imaging adaptations, data processing and
potential pitfalls. (X-XV, XVII-XXIII)
|
| 17.
|
Recognize the normal distribution, normal variants and various
artifacts seen on selected immune system imaging studies and printed
images. (X-XV, XVII-XXIII)
|
| 18.
|
Discuss common causes of false-negative and false-positive thyroid
uptake results. (X-XV, XVIII-XXIII).
|
| 19.
|
Describe the physical properties of radionuclides as they relate to
therapeutic applications in nuclear medicine. (XVI)
|
| 20.
|
Discuss the basic concepts of radiobiology. (XVI)
|
| 21.
|
Discuss malignant and metastatic processes. (XVI)
|
|
|
|---|
I. Review of central nervous system (CNS) anatomy & physiology
A. Gross anatomy and function
B. Cellular anatomy and function
D. Cerebral spinal fluid production and flow
II. CNS Pathology: Characteristics, Causes, Population, and
Treatment
A. Inflammatory disease of the brain
D. Hematoma and contusion of the brain
E. Brain attack (ischemia and infarct due to cerebral vascular
disease)
1. Transient ischemic attack
4. Aneurym and hemorrhage
H. Traumatic brain injury
J. Neurological and psychiatric diseases
K. Communicating hydrocephalus
L. Non-communicating hydrocephalus
III. Cerebral vascular flow
a. Tc-99m sodium pertechnetate
b. Tc-99m DTPA (pentetate)
c. Tc-99m GH (gluceptate)
2. Physical and chemical characteristics
3. Kit and radiopharmaceutical preparation
4. Dose range and route of administration
C. Contraindications and adverse reactions
F. Basic procedure and processing
2. Dose range and administration technique
3. Acquisition parameters
4. Positioning and views, including adaptations
G. Interpretation of images
5. Diagnostic/Prognostic Value of the Study
c. prognostic risk factors based on diagnosis
IV. Planar Brain Imaging
a. Tc-99m sodium pertechnetate
b. Tc-99m DTPA (pentetate)
c. Tc-99m GH (gluceptate)
2. Physical and chemical characteristics
3. Kit and radiopharmaceutical preparation
4. Dose range and route of administration
C. Contraindications and adverse reactions
F. Basic procedure and processing
2. Dose range and administration technique
3. Acquisition parameters
4. Positioning and views, including adaptations
G. Interpretation of images
5. Diagnostic/Prognostic Value of the Study
c. prognostic risk factors based on diagnosis
V. Functional Brain SPECT
1. Historical tracer: Iodine-123 (I-123) IMP (d,
1-N-Isoprophyl-p-iodoamphetamine hydrochloride)
a. Tc-99m HMPAO (exametazime)
3. Physical and chemical characteristics
4. Kit and radiopharmaceutical preparation
5. Dose range and route of administration
C. Contraindications and adverse reactions
F. Basic procedure and processing
2. Dose range and administration technique
3. Acquisition parameters
4. Positioning and views, including adaptations
5. Data processing (including co-registration and 3-dimensional
volumetric display)
G. Interventions in procedures
1. Vasodilators (acetazolamide)
2. Pyschological stress studies
3. Sensory stimulation studies
H. Interpretation of images and data
5. Diagnostic/Prognostic Value of the Study
c. prognostic risk factors based on diagnosis
VI. Brain tumor imaging
a. Thallium-201 thallous chloride
2. Physical and chemical characteristics
3. Kit and radiopharmaceutical preparation
4. Dose range and route of administration
C. Contraindications and adverse reactions
F. Basic procedure and processing
2. Radiopharmaceutical administration and technique
3. Acquisition parameters
4. Positioning and views, including adaptations
G. Interpretation of images and data
5. Diagnostic/Prognostic Value of the Study
c. prognostic risk factors based on diagnosis
VII. Cerebral Spinal Fluid (CSF) Studies
a. Historical tracer: Ytterbium-169 (Yb-169) DTPA (pentetate)
b. Current tracer: Indium-111 (In-111) DTPA (pentetate)
c. Physical and chemical characteristics
d. Radiopharmaceutical preparation
e. Dose range and route of administration
3. Contraindications and adverse reactions
a. physical and pathologic conditions
6. Basic procedure and processing
b. dose range and administration technique
c. acquisition parameters
d. positioning and views, including adaptations
7. Interpretation of images
e. Diagnostic/Prognostic Value of the Study
3. prognostic risk factors based on diagnosis
a. Historical tracer: Ytterbium-169 (Yb-169) DTPA (pentetate)
c. Physical and chemical characteristics
d. Radiopharmaceutical preparation
e. Dose range and route of administration
6. Contraindications and adverse reactions
a. physical and pathologic conditions
9. Basic procedure and processing
b. dose range and administration technique
c. acquisition parameters
d. positioning and views, including adaptations
e. data processing (including counting of pledgets in well
counters)
10. Interpretation of images and data
e. Diagnostic/Prognostic Value of the Study
3. prognostic risk factors based on diagnosis
a. Historical tracer: Yb-169 DTPA
3. Tc-99m HSA (human serum albumin)
c. Physical and chemical characteristics
d. Radiopharmaceutical preparation
e. Dose range and route of administration
3. Contraindications and adverse reactions
6. Basic procedure and processing
b. dose range and administration technique
c. acquisition parameters
d. positioning and views, including adaptations
7. Interpretation of images
e. Diagnostic/Prognostic Value of the Study
3. prognostic risk factors based on diagnosis
VIII. Oncology/Inflammation
A. Review of anatomy & physiology
2. Lymph node distribution
4. Inflammatory processes
IX. Pathology: Characteristics, Causes, Population, and
Treatment
a. In-111 oxine tagged white blood cells
b. Tc-99m hexametazime (HMPAO) tagged white blood cells
2. Physical and chemical characteristics
3. Kit and radiopharmaceutical preparation
4. Dose range and route of administration
C. Contraindications and adverse reactions
1. Physical or pathological conditions
4. laboratory equipment for tagging process
F. Basic procedure and processing
2. Dose range and administration technique
3. Acquisition parameters
4. Positioning and views, including adaptations
G. Interpretation of images
5. Diagnostic/Prognostic Value of the Study
c. prognostic risk factors based on diagnosis
X. Radiolabeled White Blood Cell Studies
a. In-111 oxine tagged white blood cells
b. Tc-99m hexametazime (HMPAO) tagged white blood cells
2. Physical and chemical characteristics
3. Kit and radiopharmaceutical preparation
4. Dose range and route of administration
C. Contraindications and adverse reactions
1. Physical or pathological conditions
4. laboratory equipment for tagging process
F. Basic procedure and processing
2. Dose range and administration technique
3. Acquisition parameters
4. Positioning and views, including adaptations
G. Interpretation of images
5. Diagnostic/Prognostic Value of the Study
c. prognostic risk factors based on diagnosis
XI. Gallium Imaging
1. Gallium-67 (Ga-67) citrate
2. Physical and chemical characteristics
3. Radionuclide preparation
4. Dose range and route of administration
C. Contraindications and adverse reactions
F. Basic procedure and processing
2. Dose range and administration technique
3. Acquisition parameters
4. Positioning and views, including adaptations
G. Interpretation of images
5. Diagnostic/Prognostic Value of the Study
c. prognostic risk factors based on diagnosis
XII. Antibody Receptor Imaging
a. In-111 satumomab penetide (for colon and ovarian cancer)
b. Tc-99m arcitumomab (for colon cancer
c. In-111 capromab pendetide (for prostate cancer)
d. other approval radiopharmaceuticals
2. Physical characteristics
3. Chemical characteristics
4. Kit and radiopharmaceutical preparation
5. Dose range and route of administration
C. Contraindications and adverse reactions
1. Physical or pathologic conditions
F. Basic procedure and processing
2. Dose range and administration technique
3. Acquisition parameters
4. Positioning and views, including adaptations
5. Diagnostic/Prognostic Value of the Study
c. prognostic risk factors based on diagnosis
8. Diagnostic/Prognostic Value of the Study
c. prognostic risk factors based on diagnosis
XIII. Breast Imaging (Scintimammography)
2. Physical and chemical characteristics
3. Kit and radiopharmaceutical preparation
4. Dose range and route of administration
C. Contraindications and adverse reactions
F. Basic procedure and processing
2. Dose range and administration technique
3. Acquisition parameters
4. Positioning and views, including adaptations
G. Interpretation of images
5. Diagnostic/Prognostic Value of the Study
c. prognostic risk factors based on diagnosis
XIV. Sentinel Node Imaging
b. Tc-99m human serum albumin
2. Physical and chemical characteristics
3. Kit and radiopharamceutical preparation
4. Dose range and route of administration
C. Contraindications and adverse reactions
F. Basic procedure and processing
2. Dose range and administration technique
3. Acquisition parameters
4. Positioning and views, including adaptations
5. Diagnostic/Prognostic Value of the Study
c. prognostic risk factors based on diagnosis
XV. Lymphoscintigraphy
A. Indications Radiopharmaceutical
2. Physical and chemical characteristics
3. Kit and radiopharmaceutical preparation
4. Dose range and route of administration
E. Basic procedure and processing
2. Dose range and administration technique
3. Acquisition parameters
4. Positioning and views, including adaptations
F. Interpretation of data
5. Diagnostic/Prognostic Value of the Study
c. prognostic risk factors based on diagnosis
XVI. Introduction to Radionuclide Therapy
A. Review of radionuclide physical properties
B. Review of radiobiology
XVII. Review of immune system anatomy and physiology
XVIII. Pathology
3. metastatic bone cancer
XIX. Intracavitary Palliation
1. Phosphorus-32 (P-32) chromic phosphate
2. Physical and chemical characteristics
3. Radiopharmaceutical preparation
4. Dose range and route of administration
C. Contraindications and adverse reactions
1. Physical and pathologic conditions
D. Special radiation safety considerations and regulations
E. Patient preparation (including consent)
F. Equipment (for detection of tracer distribution)
G. Basic procedure and processing
2. Dose range and administration technique
3. Acquisition parameters
4. Positioning and views, including adaptations
8. Evaluation of tracer distribution
9. Prognostic Value (outcome)
XX. Bone Marrow Palliation
2. Physical and chemical characteristics
3. Radionuclide preparation
4. Dose range and route of administration
C. Contraindications and adverse reactions
1. Physical and pathologic conditions
D. Special radiation safety considerations and regulations
E. Patient preparation (including consent)
2. Dose range and administration technique
3. prognostic risk factors based on diagnosis
XXI. Ablation for Hyperthyroidism
1. Iodine-131 (I-131) sodium iodide
2. Physical and chemical characteristics
3. Radionuclide preparations
4. Dose range and route of administration
C. Contraindications and adverse reactions
1. Physical and pathologic conditions
D. Special radiation safety considerations and regulations
E. Patient preparation (including consent)
2. Dose range and administration technique
3. prognostic risk factors based on diagnosis
XXII. Thyroid Carcinoma Ablation
1. Iodine-131 sodium iodide
2. Physical and chemical characteristics
3. Radionuclide preparation
4. Dose range and route of administration
C. Contraindications and adverse reactions
1. Physical and pathologic conditions
D. Special radiation safety considerations and regulations
E. Patient preparation (including consent)
3. prognostic risk factors based on diagnosis
3. prognostic risk factors based on diagnosis
XXIII. Palliation of Metastatic Bone Pain
a. Strontium-89 (Sr-89) chloride
b. Samarium-153 (Sm-153) EDTMP
c. Rhenium-186 etidronate (HEDP)
2. Physical and chemical characteristics
4. Dose and route of administration
C. Contraindications and adverse reactions
1. Physical and pathologic conditions
D. Special radiation safety considerations and regulations
E. Patient preparation (including consent)
G. Basic procedure and processing
2. Dose range and administration technique
3. Acquisition parameters
4. Positioning and views, including adaptations
H. Interpretation of Images (if applicable)
3. Diagnostic/Prognostic Value of Study
c. prognostic risk factors based on diagnosis
|