National Heart and Lung Institute, Imperial College London
Doi
Abstract
Magnetic resonance imaging of myocardial perfusion during the first-pass of
a contrast agent has been proved valuable for the detection of coronary artery
disease. During contrast enhancement, transient dark rim artifacts are sometimes
visible in the subendocardium, mimicking real perfusion defects and complicating
diagnosis.
This thesis studied several different mechanisms behind dark rim artifacts
with the aim of exploring possible solutions to minimise them and potentially
improve the accuracy of perfusion methods.
An in-depth review of current myocardial perfusion imaging techniques is
presented. This is followed by a comprehensive study of dark rim artifacts, with
realistic phantom and numerical simulations, and in vivo measurements. Simulations
for the most common perfusion sequences are made, showing that
Gibbs, myocardial radial-motion, and frequency-offsets are capable of creating
endocardial signal-loss, although dependent on many sequence parameters.
Frequency-offsets during first-pass of contrast agentwere measured in vivo; results
show negligible intra-voxel signal dephasing, although careful frequency
adjustments need to be considered for the b-SSFP and h-EPI sequences.
The investigations on dark rim artifacts lead to the development of an ultrafast
but robust sequence suitable for first-pass myocardial perfusion imaging,
and the assessment of its in vivo performance. The sequence was a multi-slice
single-shot spin-echo EPI sequence accelerated by a reduced phase-encode
FOV (zonal excitation), and parallel imaging R=2. When tested in clinical volunteers
with CA at rest, the sequence yielded a reasonable CNR with a very short
acquisition time, although spatial resolution needs to be improved