Shams Rashid1, Fei Han1, Yu Gao1, Yingli Yang2, and Peng Hu1,3
1Radiological Sciences, University of California, Los Angeles, Los Angeles, CA, United States, 2Radiation Oncology, University of California, Los Angeles, Los Angeles, CA, United States, 3Biomedical Physics Graduate Program, University of California, Los Angeles, Los Angeles, CA, United States
Synopsis
We have developed a bSSFP-EPI cine sequence and
implemented it on a 0.35T MR system. The bSSFP-EPI cine sequence has reduced
acquisition duration compared to conventional bSSFP cine.
Purpose
Balanced steady state free precession (bSSFP) is considered
the workhorse for cardiac cine MRI owing to its superior contrast between blood
and myocardium1. Our institution recently installed a real time MRI-guided
radiotherapy system (ViewRay Inc., Oakwood Village, OH), which includes a 0.35T
superconducting MRI system and a Cobalt-60 radiotherapy system. Compared to
conventional cardiac imaging at 1.5T and higher, low-field cardiac imaging may
have additional benefits including reduced SAR, lower cost, and reduced banding
artifacts. In this work, we sought to evaluate the feasibility of a novel
bSSFP-EPI technique at 0.35T for cardiac cine imaging. The conventional bSSFP
sequence acquires a single echo in each TR. Consequently, the readout duration
is approximately one-third of the TR, which is typically 3-4ms, leading to a
low acquisition-efficiency2. However, if the bSSFP sequence is modified
to acquire multiple echoes from each TR using an echo planar imaging (EPI)
strategy, this may increase the acquisition-efficiency2. The major
drawback of this approach is increased banding artifacts2 arising
from the prolonged TR. However, banding artifacts are reduced at low field
strengths, such as 0.35T, and therefore bSSFP-EPI may be feasible at low field
strengths to substantially improve the acquisition efficiency without banding
artifacts. In this study, we developed a bSSFP-EPI cine sequence and evaluated it
on the ViewRay 0.35T MR scanner.
Methods
We modified a bSSFP cine sequence to acquire an EPIreadout
of 3-7 lines within each TR. The bSSFP-EPI sequence was implemented on the
ViewRay 0.35T system and was evaluated in 3 healthy volunteers. Sequence
parameters were: TR/TE: 8.1/2.4ms, FOV: 360mm, voxel size: 1.5x1.7x7mm3,
readout bandwidth: 772Hz/pixel, flip angles (FA): 70°, 90°, 110°, 130°, 150°.
Short axis cine images of the myocardium were acquired. Images were also
acquired using a conventional bSSFP cine sequence, with TR/TE: 3.8/1.9 ms (all
other parameters were matched). SNR of myocardium and blood pool were
calculated from the ratio of the mean tissue intensity to the standard
deviation of a background region. Blood-myocardium contrast-to-noise ratio
(CNR) was calculated from the difference between the blood-pool SNR and the
myocardium SNR. Normalized CNR was calculated by dividing CNR by the square
root of acquisition duration. CNR values between bSSFP-EPI and conventional bSSFP
images were compared using a paired t-test.Results
The sequence diagram and readout trajectory for the
bSSFP-EPI sequence is shown in Figure 1. The acquisition duration of the
bSSFP-EPI cine sequence (3 EPI lines per TR) was 17s (assuming heart rate of 60
beats-per-minute). The corresponding duration for the conventional bSSFP cine
sequence was 24s. No parallel imaging was used in any of our imaging
acquisition in this study.
Cine images in a healthy volunteer
acquired with bSSFP-EPI cine (3 EPI lines per TR, FA 130°) are shown in Figure
2 top row. Corresponding images acquired with conventional bSSFP cine are shown
in Figure 2 bottom row. The bSSFP-EPI provided similar images as conventional bSSFP
despite its shorter image acquisition time.
Cine images at multiple flip angles
acquired with bSSFP-EPI (3 EPI lines per TR) are shown in Figure 3 top row.
Corresponding conventional bSSFP cine images are shown in Figure 3 bottom row.
It is apparent that blood-myocardium contrast is higher at larger flip angles. The
cine images with up to 150° flip angle was possible due to the dramatically
reduced SAR at 0.35T. Cine images acquired with the bSSFP-EPI sequence with 5 and
7 EPI lines per TR are shown in Figure 4. Acquisition duration for both these
sequences was 15s.
Normalized blood-pool SNR,
myocardium SNR and blood-myocardium CNR values for different FA for bSSFP-EPI
(3 EPI lines per TR) and conventional bSSFP images are shown in Figure 5.
Discussion
This study demonstrates the feasibility of a bSSFP-EPI cine
sequence on a low-field MRI system. Imaging at a low field such as 0.35T is
prone to reduced SNR compared to 1.5T or higher. However, the results show that
the myocardium can be clearly delineated, and that the image quality of
bSSFP-EPI is similar to that of conventional bSSFP. Our images show in vivo bSSFP-EPI
acquisitions with a TR of up to 8.1ms without banding, owing to the lower field
strength and improved absolute off-resonance frequencies within the volume of
interest. The major advantage of bSSFP-EPI is its reduced acquisition duration,
and higher percentage of time per TR used in actual data acquisition, which
translated to higher CNR values despite its shorter acquisition time when
compared with conventional bSSFP.
Conclusion
We have developed a bSSFP-EPI cine sequence and demonstrated
its feasibility for diagnostic quality cardiac cine imaging at 0.35T.Acknowledgements
No acknowledgement found.References
1. Finn et al., Cardiac MR imaging: state of the technology,
Radiology 241:338 (2006)
2. Herzka et al., Multishot EPI-SSFP in the Heart, MRM
47:655 (2002)