Table 2.
Aspect | Consensus |
---|---|
Pre-localization method | Chemical shift displacement less than 2% per ppm. 3 T: semi-LASER with OVS (preferred) or OVERPRESS with VSS. 1.5 T: semi-LASER with OVS (preferred) or PRESS with VSS. |
Echo and repetition time | TE as short as possible (typically 30 ms). Longer TEs may be preferred for lactate detection (144 or 288 ms) and enhanced lipid suppression. TR 1.5 s at 1.5 T, 2.0 s at 3 T. |
Matrix dimensions, nominal voxel dimensions and sampling parameters | 16x16 matrix with 10 mm in-plane resolution and 15 mm slice thickness. 1 average per phase encoding step. Spectral sampling of 1024 complex data points at 2000 Hz spectral width at 1.5 T or 3 T. |
k-space sampling and preprocessing | 2D phase-encoded Cartesian sampling over an elliptical or circular k-space mask. K-space zero-filling (interpolation) to twice the acquired number of points. Hamming filter. Reduction of subcutaneous lipid contamination (e.g. Papoulis-Gerchberg algorithm). |
Water reference acquisition | Should be acquired where possible. Collect with the same sequence parameters as the water-suppressed scan, but without water suppression. Typically, to reduce scan time, a lower resolution scan is acceptable and interpolated post-acquisition to match the metabolite resolution |
B0 shimming hardware | 2nd order shim coils with adequately powered amplifiers are recommended at 1.5 T and 3 T. |
B0 shimming algorithm | Methods incorporating shim strength limits and instability counter-measures are preferred over unconstrained approaches. |