Parallel transmission of spokes pulses is a promising way of mitigating flip-angle inhomogeneity in 2D imaging at ultra-high-field MRI. Bipolar slice-selective gradient is often used to minimise the overall duration of these pulses, making them more resilient to off-resonance related artefacts, but they are prone to errors caused by RF-gradient timing mismatch. In this study, we present a mathematical description for the effect of such delay on bipolar-gradient composite excitations. We demonstrate the effect with both flip-angle maps and EPI images. Finally, we propose a navigator approach to estimate the delay and show two effective ways of eliminating these errors.
A time delay of $$$\Delta{t}$$$ between a symmetric RF pulse and its slice-selective gradient5-12 (Fig. 1) gives rise to a phase difference $$$\Delta\phi$$$ between the odd and even sub-pulses in a bipolar composite excitation: $$\Delta\phi=2\gamma{G_{z}}\Delta{t}z=4\pi{BW}\Delta{t}\frac{z}{\Delta{z}},(1)$$ where $$$\gamma$$$ is the gyromagnetic ratio, $$${G_{z}}$$$ is the slice-selective gradient amplitude, $$$z$$$ is the distance of the slice from the isocentre, $$$BW$$$ is the bandwidth of the RF pulse and $$$\Delta{z}$$$ is the slice thickness. The actual achieved excitation pattern (effective flip-angle) will deviate from the expectation when $$$\Delta\phi$$$ is not accounted for during the pulse design.
We propose a dual-echo navigator as shown in Fig. 2 to measure the delay, and subsequently eliminate the error. This is demonstrated with in vivo experiments on a 7 T whole-body MR scanner (MAGNETOM, Siemens Healthineers, Erlangen, Germany) with a 8Ch-pTX/32Ch-Rx coil (Nova Medical, Wilmington, MA, USA). Data were acquired using SMS-pTX EPI4,13, and flip-angle maps were measured by PreSat-TFL14. 2-spoke pulses (flip-angle=45˚, $$$\Delta{z}$$$=3.0 mm, BWTP=4.0, $$${G_{z}}$$$=32.62 mT/m, sub-pulse spacing=1.36 ms, sub-pulse duration=0.96 ms) were calculated in a slice-by-slice fashion4, using B0 maps obtained by dual-echo 3D GRE15 and B1+ sensitivity maps collected by a transmit phase-encoded15,16, T2 and T2* compensated version of DREAM17. Two different correction methods are demonstrated here: 1) by removing the time delay directly; 2) or by applying the corresponding slice-position dependent phase differences (Eq. 1) to the sub-pulses. In each case the flip-angle homogeneity [normalised root-mean-square error (NRMSE)] is evaluated and compared with the prediction as well as mono-polar (fly-back) excitations which served as reference.
Near-perfect agreement between the observed flip-angles and predictions is achieved with both correction approaches. Fig. 3 shows the flip-angle maps of 2-spoke pulses at five different slice positions. Fly-back spokes (NRMSE=0.096), bipolar spokes with -6 μs correction of the RF-gradient starting time (NRMSE=0.093) and with slice-dependent RF phase correction according Eq. 1 (NRMSE=0.091) all agree well with each other and the pulse optimisation’s prediction.
Fig. 4 shows the excitation errors as a function of the imposed relative RF-gradient starting time in the bipolar excitations where the slice-position dependent phase is clearly seen. Good agreement is seen between the predicted NRMSE (circle), the measured NRMSE of the fly-back spokes, and both the delay-corrected and slice-phase corrected bipolar spokes.
The proposed navigator (Fig. 2d) measured a time delay of 12.6 µs between the echoes, corresponding to a $$$\Delta{t}$$$ value of 6.3 μs, which agreed well with the estimate from the flip-angle maps.
Fig. 5 demonstrates the application of 2-spoke multi-band pulses in a SMS-EPI sequence with slice-acceleration factor 2. Application of the timing correction resulted in accurately excited EPI images with bipolar dual-spokes SMS-2 excitations.
In comparison with the fly-back spokes, the shorter duration of the bipolar spokes results in increased robustness against signal intensity drop in regions where B0 inhomogeneity is known to be severe, e.g. above the frontal sinus and the ear canals. The lower signal intensity and lower flip-angle seen in the CP-mode excitation (Fig. 5e) in the temporal lobes and the cerebellum confirm the expected benefits of flip-angle homogenisation with spokes excitations.
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