Porter David A, Heidemann Robin M
Siemens AG, Healthcare Sector, Erlangen, Germany.
Magn Reson Med. 2009 Aug;62(2):468-75. doi: 10.1002/mrm.22024.
Single-shot echo-planar imaging (EPI) is well established as the method of choice for clinical, diffusion-weighted imaging with MRI because of its low sensitivity to the motion-induced phase errors that occur during diffusion sensitization of the MR signal. However, the method is prone to artifacts due to susceptibility changes at tissue interfaces and has a limited spatial resolution. The introduction of parallel imaging techniques, such as GRAPPA (GeneRalized Autocalibrating Partially Parallel Acquisitions), has reduced these problems, but there are still significant limitations, particularly at higher field strengths, such as 3 Tesla (T), which are increasingly being used for routine clinical imaging. This study describes how the combination of readout-segmented EPI and parallel imaging can be used to address these issues by generating high-resolution, diffusion-weighted images at 1.5T and 3T with a significant reduction in susceptibility artifact compared with the single-shot case. The technique uses data from a 2D navigator acquisition to perform a nonlinear phase correction and to control the real-time reacquisition of unusable data that cannot be corrected. Measurements on healthy volunteers demonstrate that this approach provides a robust correction for motion-induced phase artifact and allows scan times that are suitable for routine clinical application.
单次激发回波平面成像(EPI)作为临床磁共振成像(MRI)扩散加权成像的首选方法已得到广泛认可,因为它对磁共振信号扩散敏感化过程中出现的运动诱导相位误差敏感度较低。然而,该方法容易因组织界面处的磁化率变化而产生伪影,并且空间分辨率有限。并行成像技术的引入,如GRAPPA(广义自校准部分并行采集),减少了这些问题,但仍存在显著局限性,特别是在3特斯拉(T)等更高场强下,而这些场强正越来越多地用于常规临床成像。本研究描述了读出分段EPI与并行成像的结合如何用于解决这些问题,即在1.5T和3T下生成高分辨率扩散加权图像,与单次激发情况相比,显著减少磁化率伪影。该技术使用来自二维导航器采集的数据进行非线性相位校正,并控制对无法校正的不可用数据的实时重新采集。对健康志愿者的测量表明,这种方法为运动诱导相位伪影提供了强大的校正,并允许适合常规临床应用的扫描时间。