Myocardial perfusion imaging is clinically established for the detection of myocardial ischemia and requires rapid imaging to monitor the uptake of a contrast-agent in the heart. Spatial resolution or coverage is commonly increased by exploiting temporal correlations, at the risk of inducing temporal blurring. Here, we investigate the use of simulteaneous multi-slice imaging for high spatial-only acceleration. Outer-volume-suppression using multi-band saturation-slabs (MB-OVS) were used to facilitate high multi-band factors. Phantom results, show through signal suppression outside region-of-interest with MB-OVS. In-vivo results show robust image quality throughout the contrast uptake and washout with 9-slice LV coverage at a temporal resolution <550ms.
Perfusion imaging was performed at three cardiac phases in the proposed sequence (Fig. 1), each following a non-selective saturation and a short saturation-delay. FLASH imaging with linear reordering is employed for data acquisition. Simultaneous multi-band excitation of three slices was performed with RF phase-cycling7. MB-OVS pulses are played directly prior to and interleaved with the imaging pulses, to obtain optimal suppression of extra-cardiac tissue suppression. MB-OVS consists of a slab-selective 90° pulse to two slabs (on chest and back) followed by 200µs gradient spoiling. Multiple RF pulse shapes (Fig. 2) were investigated for MB-OVS saturation. For both MB-OVS and MB excitation pulses, constant phase shifts were added to each band to minimize B1+ peak amplitude.
Imaging was performed at 3T (Siemens Magnetom Prisma). Phantom images were acquired to confirm the efficiency of MB-OVS using various RF pulses. In-vivo first-pass perfusion imaging was performed with injection of 0.05 mmol/kg gadobutrol (Gadovist) at 4 mL/s, followed by a 10-mL saline flush. 3-fold MB acceleration, 3-fold uniform in-plane acceleration, and partial-Fourier=7/8 were utilized for an overall 10-fold acceleration. MB-OVS preparation was interleaved between every 9 imaging pulses. The imaging parameters were: FOV=320x320mm2, resolution=1.7x1.7mm2, slice-thickness=8mm, TR/TE/FA=2.9/1.7ms/12°, temporal resolution=163ms, saturation time=150ms. 3 separate MB slice-stacks were acquired within each heart-beat, for a total of 9-slice coverage. A 1-second reference low-resolution scan (6x6 mm2) of 3 slices and at 3 cardiac phases, during free-breathing, was used to generate coil sensitivity profiles. Iterative non-linear reconstruction was performed for each MB slice using a B1-weighted approach with in-plane TV-regularization.
The proposed technique enables a 10-fold acceleration acquisition of myocardial perfusion images with 9-slice coverage, 1.7mm in-plane resolution, and a 163ms temporal resolution, suggesting the total acquisition can be confined to <500ms. Furthermore, the reconstruction technique only relies on spatial information, avoiding issues with temporal blurring or need for motion compensation. Additional improvements in reconstruction quality and higher acceleration rates may be possible using more advanced regularization techniques10.
MB processing of Cartesian data has a simple characterization in terms of FOV/MBFactor shifts in image space. Thus, the use of OVS has an intuitive interpretation, in removing extra-cardiac structure for reduced fold-over artifacts due to slice acceleration. While this also enables a simple reconstruction framework, the linear ordering used in 2D Cartesian acquisitions necessitates interleaving of the OVS pulses, limiting their duration. To obtain good signal suppression at a minimal pulse duration we used an MB approach to excite multiple saturation slabs simultaneously. This allowed its interleaving into the acquisition pulse train, while avoiding contrast disruption.
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