Sze G, Brant-Zawadzki M, McNamara M T, Haughton V M, Kumar A J, Maravilla K R, Aisen A M, Dreisbach J N, Bradley W G, Weinreb J C
Department of Diagnostic Imaging, Yale University Medical School, New Haven, Connecticut 06510.
Invest Radiol. 1993 Mar;28 Suppl 1:S49-55. doi: 10.1097/00004424-199303001-00006.
To investigate the safety and efficacy of the low-osmolar, nonionic contrast agent, gadodiamide injection (Omniscan, Sanofi Winthrop Pharmaceuticals, New York, NY), for magnetic resonance imaging (MRI) of the head and spine, a multicenter study involving 439 patients was done at 15 centers as part of a Phase II/III clinical trial. Unenhanced MRI scans were obtained after which the patients were injected with 0.1 mmol/kg gadodiamide, and the MRI was repeated. The patients' vital signs were monitored, and laboratory studies were conducted. Neurologic status was examined before and after the study. The images were evaluated for contrast enhancement. No patient had any significant adverse event or serious change in clinical status. Abnormalities were found in 80% (351) of all patients studied, and it was found that, in 75% (266) of these, the postgadodiamide injection images were improved or facilitated visualization of lesions compared with preinjection images. The investigators believe that, based on the results of this study, gadodiamide injection is safe and effective for imaging the head and spine. They suggest that future studies further assess and compare the safety parameters of gadodiamide injection with those of other nonionic and ionic gadolinium ligands.
为研究低渗非离子型造影剂钆双胺注射液(欧乃影,赛诺菲·温思罗普制药公司,纽约州纽约市)用于头部和脊柱磁共振成像(MRI)的安全性和有效性,作为一项II/III期临床试验的一部分,在15个中心对439例患者进行了一项多中心研究。先获取未增强的MRI扫描图像,之后给患者注射0.1 mmol/kg钆双胺,然后重复进行MRI检查。监测患者的生命体征,并开展实验室研究。在研究前后对患者的神经状态进行检查。对图像的对比增强情况进行评估。没有患者出现任何显著不良事件或临床状态的严重变化。在所有研究患者中,80%(351例)发现有异常情况,并且发现在其中75%(266例)患者中,注射钆双胺后的图像与注射前图像相比,病变的显示得到改善或更易于观察。研究者认为,基于本研究结果,钆双胺注射液用于头部和脊柱成像安全有效。他们建议未来的研究进一步评估并比较钆双胺注射液与其他非离子型和离子型钆配体的安全参数。