Monitoring and compensating phase imperfections in cine balanced steady-state free precession.

PURPOSE: To analyze and correct for eddy current-induced phase imperfections in cardiac cine balanced steady-state free precession (bSSFP) imaging. METHODS: Eddy current-induced phase offsets were measured for different phase-encoding schemes using a higher order dynamic field camera. Based on these measurements, offset phases were corrected for in postprocessing and by run-time phase compensation applying radiofrequency phase increments and additional compensatory gradient areas. The findings were validated using numerical simulations, phantom experiments, and in vivo cardiac scans. RESULTS: Depending on the phase-encoding scheme, significant eddy current-induced phase offsets were detected. Time-varying phase offsets were observed at subsequent excitations leading to steady-state distortions and hence to profile-dependent amplitude modulations in k-space. Taking into account measured k-space trajectories algebraic image reconstruction allowed compensating imperfect spatial encoding. Correction of amplitude modulations was successfully accomplished by run-time phase compensation. CONCLUSION: Using magnetic field monitoring, artifacts in cine balanced steady-state free precession caused by uncompensated eddy current fields can be significantly reduced.

Linear Response Equilibrium versus echo-planar encoding for fast high-spatial resolution 3D chemical shift imaging.

In this work Linear Response Equilibrium (LRE) and Echo-planar spectroscopic imaging (EPSI) are compared in terms of sensitivity per unit time and power deposition. In addition an extended dual repetition time scheme to generate broad stopbands for improved inherent water suppression in LRE is presented. The feasibility of LRE and EPSI for assessing cholesterol esters in human carotid plaques with high spatial resolution of 1.95×1.15×1.15 mm(3) on a clinical 3T MR system is demonstrated. In simulations and phantom experiments it is shown that LRE has comparable but lower sensitivity per unit time relative to EPSI despite stronger signal generated. This relates to the lower sampling efficiency in LRE relative to EPSI as a result of limited gradient performance on clinical MR systems. At the same time, power deposition of LRE is significantly reduced compared to EPSI making it an interesting niche application for in vivo high field spectroscopic imaging of metabolites within a limited bandwidth.