Makowski Marcus R, Wiethoff Andrea J, Ebersberger Hans U, Botnar René M, Razavi Reza, Schaeffter Tobias, Greil Gerald F
King's College London BHF Centre, Division of Imaging Science, Biomedical Research Centre of Guy's and St. Thomas' NHS Foundation Trust, London, UK,
Int J Cardiovasc Imaging. 2015 Feb;31(2):409-16. doi: 10.1007/s10554-014-0565-y. Epub 2014 Nov 11.
The aim of this prospective study is to compare the performance of 2D time-resolved phase-contrast (PC) MRI prior to and after the administration of an intravascular (gadofosveset-trisodium) and extravascular (gadopentetate-dimeglumine) contrast agent in the same patient in the cardiovascular system. This study was approved by the ethics committee (Study-Number-07/Q0704/2) and registered with the MedicinesAndHealthcareProductsRegulatoryAgency (MHRA-Study-Number-28482/0002/001-0001, EudraCT-Number-2006-007042). All patients signed an informed consent. 20 patients were examined using a 1.5T MR-scanner and 32-channel-coil-technology. Gadopentetate-dimeglumine (GdD) and gadofosveset-trisodium (GdT) were administered in the same patient on consecutive days. Image quality, velocity-to-noise-ratios (VNRs) and standard-deviation of blood-flow-velocities (phase-noise) were compared between GdT, GdD and non-contrast-enhanced imaging. On both days pre- and post-contrast-scans were performed. The administration of GdT significantly improved the delineation of the perfused lumen and the VNR compared to GdD and non-contrast-enhanced imaging. Standard deviations of through-plane and in-plane velocity-measurements (phase-noise) were significantly reduced after GdT administration (p < 0.05). No significant differences (p > 0.05) were measured regarding absolute flow values prior to and after the administration of GdD and GdT. PC flow imaging benefits from the administration of an intravascular contrast agent by improving the delineation of the perfused lumen and reducing phase noise in flow measurements.
这项前瞻性研究的目的是在同一患者的心血管系统中,比较血管内(钆布醇三钠)和血管外(钆喷酸葡胺)造影剂给药前后二维时间分辨相位对比(PC)MRI的性能。本研究已获得伦理委员会批准(研究编号:07/Q0704/2),并在药品和医疗产品监管局注册(MHRA研究编号:28482/0002/001 - 0001,欧盟临床试验数据库编号:2006 - 007042)。所有患者均签署了知情同意书。使用1.5T MR扫描仪和32通道线圈技术对20名患者进行了检查。钆喷酸葡胺(GdD)和钆布醇三钠(GdT)在同一患者身上连续两天给药。比较了GdT、GdD和非增强成像之间的图像质量、速度噪声比(VNR)和血流速度标准差(相位噪声)。在造影剂注射前后的两天均进行了扫描。与GdD和非增强成像相比,GdT的给药显著改善了灌注腔的描绘和VNR。GdT给药后,层面内和层面间速度测量的标准差(相位噪声)显著降低(p < 0.05)。在GdD和GdT给药前后,绝对流量值方面未测得显著差异(p > 0.05)。PC血流成像通过改善灌注腔的描绘和降低血流测量中的相位噪声,从血管内造影剂的给药中获益。