Engineering, 2013, 5, 114-117
http://dx.doi.org/10.4236/eng.2013.510B023 Published Online October 2013 (http://www.scirp.org/journal/eng)
Copyright © 2013 SciRes. ENG
A New Approach t o the Presentation of Myocardial
SPECT Images
—Radial Slices—Data Reduction without Loss of Information
Niloufar Darv ish1, Fatma Nadide Öçba1, Hamed Hamid Muhammed1*, Dianna Bone2
1School of Technology and Health STH, Royal Institute of Technology KTH, Alfred Nobels Allé 10,
SE-14152 Huddinge, Sweden
2Department of Clinical Physiology, Thoracic Clinics, Karolinska Hospital,
SE-17671 Stockholm, Sweden
Email: *hamed.muhammed@sth.kth.se
Received December 2012
ABSTRACT
Objective: SPECT data from myocardial perfusion imaging (MPI) are normally displayed as a set of three slices or-
thogonal to the left ventricular (LV) long axis. For data presentation, the images are orientated about the LV long axis.
Therefore, radial slices provide a suitable alternative to standard orthogonal slices, with the advantage of requiring few-
er slices to adequately represent the data.In this study, a semi-automatic method is developed for displaying MPI
SPECT data as a set of radial slices orientated about the LV axis. The aim is to reduce the number of slices viewed
without loss of information and independently from the heart size. Method: Standard short axis slices, orientated per-
pendicular to the LV axis, are utilized. The skeleton of the segmented myocardium is found and the true LV axis is de-
termined in each central long slice. The LV axis of the whole volume is determined by aligning the axes of all
slices. Result: Radial slices centered about this axis were generated by integration over a sector equal to the resolution
of the imaging system which was of the order of 1.2 cm. Therefore, assuming a mean LV diameter of 8 cm, 20 slices
were sufficient to represent a non-gated study. Gated information could be adequately displayed with 4 slices integrated
over an angle of 45˚. Conclusion:
Keywords: Myocardial Perfusion SPECT; Cardiac Left Ventricle; Radial Slices; Left Ventricular Long Axis
1. Introduction
Myocardial perfusion imaging (MPI) is a non-invasive
nuclear medicine technique used to study blood flow in
the left ventricular (LV) heart muscle. Images are ac-
quired using a gamma camera system following the in-
jection of a radiopharmaceutical during a cardiac stress
test [1]. At a subsequent examination, an injection is
given when the heart is in a resting state. Images from
the stress and rest examinations are then compared to
identify differences that may indicate ischemia, or other
abnormalities [1]. The method of choice for acquiring the
myocardial data is single photon emission tomography
[2].
A semi-automatic method for generating radial slices from SPECT MPI short axis
slices has been developed.
SPECT performed without any reference to heart
rhythm (MSPECT) provides the best quality images for
determining perfusion. Additional useful information
about LV function can be obtained with gated-SPECT
(GSPECT) studies, when the patient’s ECG is used to
control the acquisition [3]. In modern gamma camera
systems MSPECT and GSPECT projections can be ac-
quired simultaneously. Sets of slices orientated abou t the
long axis of the LV are reconstructed from projection
images. The standard slices presented for interpretation
are horizontal long axis (HLA), ver tical long axis (VLA)
and short axis (SA) (Figure 1).
Depending on the size of the LV, more than 30 slices
from each acquisition are needed to represent the heart
muscle, thus a considerable number of images must be
compared when making a diagnosis. To assist in this
problem, the polar presentation (bull’s eye) has been de-
veloped [4], but the display results in loss of information
and cannot completely replace the standard sets of slices.
An alternative approach would be to reconstruct radial
slices. Radial slices are orientated p arallel to the LV long
axis and arranged diametrically.
The central HLA and VLA slices are examples of
radial slices at 0˚ and 90˚ respectively. A set of radial
slices would, therefore, include the central HLA and
*Corresponding a uthor.