Title: SNM99SimultaneousPET_SPECT
1Kinetic Modeling
Edward Di Bella Dmitri Riabkov Harshali
Bal Sathya Vijayakumar
2Outline
Introduction to kinetic modeling Challenges 1.
Formulation/selection of physiological model 2.
Obtaining accurate input functions 3. Noise
issues - optimal data groupings 4. Noise issues -
optimal reconstruction, non-linear optimization,
use of constraints Applications
3Introduction
- Examples of tracer kinetics
- Intravascular (99mTc-albumin, MS-325)
- Extracellular (gadolinium-DTPA)
- Intracellular (99mTc-Sestamibi, 99mTc-Teboroxime)
- More complex uptake and washout characteristics,
- including changes of state, binding (18FDG)
4Semi-quantitative Models
- Area under curve
- Upslope
- Percent Enhancement
5Two Compartments
Tissue - Interstitial (ve)
k
capillary
Vascular - plasma
Vascular - red blood cells
E extraction, F flow, t time volume
of extravascular space
6Axial concentration gradient
Tissue
capillary
Vascular - plasma (Cp)
Vascular - red blood cells (Hct)
7Model with capillary transit time
8Canine Study (LAD occlusion)
9Myocardial Perfusion with Contrast MRI
Region number
(e)
(d)
10Infarct - volume of distribution changes
Tissue - ve
Vascular - plasma (Cp)
Vascular - red blood cells
Normal
Infarct
11Myocardial viability
12MRI and PET Viability
- (Upper panels) Non-viable apical region shown
with FDG-PET, left, and contrast enhanced MRI,
right. (Lower panels) Non-viable inferoposterior
region shown with FDG-PET, left, and contrast
enhanced MRI, right. Arrows indicate regions of
non-viability.
13Input Function - challenges
- MRI
- Saturation
- Flow effects
- Dynamic PET and SPECT
- Blood binding
- Temporal sampling rate
- Solution Blind estimation of kinetic parameters
14Static SPECT
Dynamic SPECT
20-30s
90-100s
490-500s
290-300s
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18SUMMARY
- Kinetic modeling is a very useful approach with
many applications - Numerous important and interesting research
areas - Acquisition
- Automated robust processing
- Input function
- Modeling
- Visualization and use of parametric images