T. Obi et al., 2.5-D simultaneous multislice reconstruction by series expansion methods from Fourier-rebinned PET data, IEEE MED IM, 19(5), 2000, pp. 474-484
Citations number
24
Categorie Soggetti
Radiology ,Nuclear Medicine & Imaging","Eletrical & Eletronics Engineeing
True three-dimensional (3-D) volume reconstruction from fully 3-D data in p
ositron emission tomography (PET) has only a limited clinical use because o
f its large computational burden. Fourier rebinning (FORE) of the fully 3-D
data into a set of 2-D sinogram data decomposes the 3-D reconstruction pro
cess into multiple 2-D reconstructions of decoupled 2-D image slices, thus
substantially decreasing the computational burden even in the case when the
2-D reconstructions are performed by an iterative reconstruction algorithm
. On the other hand, the approximations involved in the rebinning combined
with the decoupling of the image slices cause a certain reduction of image
quality, especially when the signal-to-noise ratio of the data is low.
We propose a 2.5-D Simultaneous Multislice Reconstruction approach, based o
n the series expansion principle, where the volume is represented by the su
perposition of 3-D spherically symmetric bell-shaped basis functions. It ta
kes advantage of the time reduction due to the use of the FORE (2-D) data,
instead of the original fully 3-D data, but at the same time uses a 3-D ite
rative reconstruction approach with 3-D basis functions. The same general a
pproach can be applied to any reconstruction algorithm belonging to the cla
ss of series expansion methods (iterative or noniterative) using 3-D basis
functions that span multiple slices, and can be used for any multislice sin
ogram or list mode data whether obtained by a special rebinning scheme or a
cquired directly by a PET scanner in the 2-D mode using septa. Our studies
confirm that the proposed 2.5-D approach provides a considerable improvemen
t in reconstruction quality, as compared to the standard 2-D reconstruction
approach, while the reconstruction time is of the same order as that of th
e 2-D approach and is clinically practical even on a general-purpose comput
er.