Kaplan G D, Aisen A M, Aravapalli S R
Department of Radiology, University of Michigan, Ann Arbor 48109-0030.
J Magn Reson Imaging. 1991 Jan-Feb;1(1):57-62. doi: 10.1002/jmri.1880010107.
The safety and efficacy of a newly developed intravenous formulation of the nonionic contrast agent gadolinium diethylenetriaminepentaacetic acid-bis(methylamide), formulated as gadodiamide injection, was investigated. In 30 patients who underwent spin-echo magnetic resonance (MR) imaging before and after contrast agent enhancement, the enhanced images had characteristics judged similar to those of images enhanced by means of available gadolinium compounds. In 15 patients, contrast agent administration was of major diagnostic help, either revealing lesions not apparent without enhancement or providing important lesion characterization. In 12 patients, the lack of abnormal enhancement patterns was important in excluding the presence of disease. In three patients, the contrast agent did not provide information additional to that obtained with the unenhanced T1- and T2-weighted images. No clinically significant changes were observed in vital signs, neurologic status, or laboratory results. The authors conclude that, in this limited series, gadodiamide injection proved to be a safe and useful MR imaging contrast agent for evaluation of the central nervous system and surrounding structures.
对新开发的非离子型造影剂钆双胺二乙三胺五乙酸双甲酰胺静脉制剂(即钆双胺注射液)的安全性和有效性进行了研究。在30例接受造影剂增强前后自旋回波磁共振(MR)成像的患者中,增强后的图像具有与现有钆化合物增强的图像相似的特征。在15例患者中,造影剂的使用对诊断有很大帮助,要么显示出未增强时不明显的病变,要么提供重要的病变特征。在12例患者中,缺乏异常增强模式对于排除疾病的存在很重要。在3例患者中,造影剂未提供除未增强的T1加权和T2加权图像所获得信息之外的其他信息。生命体征、神经状态或实验室检查结果均未观察到具有临床意义的变化。作者得出结论,在这个有限的系列研究中,钆双胺注射液被证明是一种用于评估中枢神经系统及其周围结构的安全且有用的MR成像造影剂。