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Simplification of PET studies
Within the constraints of the tracer and the instrumentation, a number of
trade-offs must be evaluated in determining the final form of the model
[Carson 1991]:
- Is it necessary to measure the input function?
- Are arterial samples required for quantitation, or can it be done with
venous samples?
- Is continuous blood sampling necessary or can it be done with manual
samples?
- Is it necessary to measure the fractions of tracer metabolites in
plasma?
- How long PET scanning is needed?
- How many time frames we need, or is a single scan sufficient?
- Are multiple tracer injections under different conditions required?
- Can parameter estimates be calculated on a pixel-by-pixel basis to
generate a functional image?
Simplified methods must be validated for the clinical use. Example of such a
validation study has been performed by Krak et al. (2003).
Carson RE. The development and application of mathematical models in nuclear
medicine. J Nucl Med. 1991; 32: 2206-2208.
Krak NC, van der Hoeven JJM, Hoekstra OS, Twisk JWR, van der Wall E,
Lammertsma AA. Measuring [18F]FDG uptake in breast cancer during
chemotherapy: comparison of analytical methods. Eur J Nucl Med Mol Imaging
2003; 30: 674-681.