- Poster presentation
- Open Access
CAIPIRINHA-accelerated 2D bSSFP imaging with improved banding behavior using Gradient-Controlled Local Larmor Frequency (GC-LOLA)
© Speier et al. 2016
- Published: 27 January 2016
- Larmor Frequency
- Slice Position
- Healthcare GmbH
- bSSFP Sequence
- bSSFP Imaging
Cardiac MRI often requires a careful trade-off between SNR, spatio-temporal resolution and slice coverage. Providing fast acquisitions, high SNR and flow/motion robustness, bSSFP has become the dominant sequence. Drawbacks are high SAR levels and sensitivity to B0 inhomogeneities. For improving slice coverage, MS-CAIPIRINHA  has emerged as a standard method. By simultaneously scanning multiple slices, it provides acceleration in slice direction with minimal SNR penalty.
When combining MS-CAIPIRINHA with bSSFP, the sequence steady-state and contrast have to be maintained. Two methods are available: The first  employs RF-based multi-slice encoding , generating slice-specific shifts in the bSSFP pass-band structure effectively reducing the off-resonance robustness by a factor of two. The second  applies balanced gradient encoding during readout, potentially increasing the sensitivity to eddy currents for small inter-slice distances because encoding changes from excitation to excitation.
We propose a new method, called gradient-controlled local larmor adjustment (GC-LOLA), that eliminates the drawback of the RF-encoded combination in two steps: (1) By slightly unbalancing the slice select gradient, the Larmor frequency is made locally dependent, which compensates the relative shift between the pass-bands. (2) In addition, the RF phase cycles are modified to shift the centers of the aligned pass-bands to resonance. The method is illustrated in Figure 1 for two slices S0 and S1 at slice positions D0 and D1. The pass-band shifts are fully corrected by unbalancing the slice gradient by the moment M, distributed evenly on slice pre- and rephaser, and subtracting the residual off-resonance ΦG from the RF phase increments in both slices. To test the concept, phantom and in-vivo measurements were performed using a bSSFP sequence prototype, modified in-house to support MS-CAIPIRINHA and GC-LOLA (MAGNETOM Aera and Skyra, Siemens Healthcare GmbH, Erlangen).
Our preliminary results indicate that GC-LOLA stabilizes MS-CAIPIRINHA-accelerated bSSFP with respect to field inhomogeneities, without the need for toggled gradients from TR to TR.
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