Bile-Tagged 3D Magnetic Resonance Colonography After Exclusive Intravenous Administration of Gadobenate Dimeglumine, a Contrast Agent with Partial Hepatobiliary Excretion

2001 ◽  
Vol 36 (10) ◽  
pp. 619-623 ◽  
Author(s):  
MICHAEL V. KNOPP ◽  
Frederik L. GIESEL ◽  
Jannis RADELEFF ◽  
Hendrik VON TENGG-KOBLIGK
2008 ◽  
Vol 43 (4) ◽  
pp. 236-242 ◽  
Author(s):  
Francesco Sardanelli ◽  
Alfonso Fausto ◽  
Anastassia Esseridou ◽  
Giovanni Di Leo ◽  
Miles A. Kirchin

2007 ◽  
Vol 106 (4) ◽  
pp. 557-566 ◽  
Author(s):  
Matthew J. Kuhn ◽  
Piero Picozzi ◽  
Joseph A. Maldjian ◽  
Ilona M. Schmalfuss ◽  
Kenneth R. Maravilla ◽  
...  

Object The goal in this article was to compare 0.1 mmol/kg doses of gadobenate dimeglumine (Gd-BOPTA) and gadopentetate dimeglumine, also known as gadolinium diethylenetriamine pentaacetic acid (Gd-DTPA), for enhanced magnetic resonance (MR) imaging of intraaxial brain tumors. Methods Eighty-four patients with either intraaxial glioma (47 patients) or metastasis (37 patients) underwent two MR imaging examinations at 1.5 tesla, one with Gd-BOPTA as the contrast agent and the other with Gd-DTPA. The interval between fully randomized contrast medium administrations was 2 to 7 days. The T1-weighted spin echo and T2-weighted fast spin echo images were acquired before administration of contrast agents and T1-weighted spin echo images were obtained after the agents were administered. Acquisition parameters and postinjection acquisition times were identical for the two examinations in each patient. Three experienced readers working in a fully blinded fashion independently evaluated all images for degree and quality of available information (lesion contrast enhancement, lesion border delineation, definition of disease extent, visualization of the lesion's internal structures, global diagnostic preference) and quantitative enhancement (that is, the extent of lesion enhancement after contrast agent administration compared with that seen before its administration [hereafter referred to as percent enhancement], lesion/brain ratio, and contrast/noise ratio). Differences were tested with the Wilcoxon signed-rank test. Reader agreement was assessed using kappa statistics. Significantly better diagnostic information/imaging performance (p < 0.0001, all readers) was obtained with Gd-BOPTA for all visualization end points. Global preference for images obtained with Gd-BOPTA was expressed for 42 (50%), 52 (61.9%), and 56 (66.7%) of 84 patients (readers 1, 2, and 3, respectively) compared with images obtained with Gd-DTPA contrast in four (4.8%), six (7.1%), and three (3.6%) of 84 patients. Similar differences were noted for all other visualization end points. Significantly greater quantitative contrast enhancement (p < 0.04) was noted after administration of Gd-BOPTA. Reader agreement was good (κ > 0.4). Conclusions Lesion visualization, delineation, definition, and contrast enhancement are significantly better after administration of 0.1 mmol/kg Gd-BOPTA, potentially allowing better surgical planning and follow up and improved disease management.


2017 ◽  
Vol 5 (6) ◽  
pp. 1090-1100 ◽  
Author(s):  
Taofeng Zhu ◽  
Xiuqin Ma ◽  
Ruhua Chen ◽  
Zhijun Ge ◽  
Jun Xu ◽  
...  

The intravenous administration of atta@Fe3O4@Ru nanocomposites to a rabbit model resulted in a marked and negatively enhanced T2-weighted MRI.


2021 ◽  
Vol 49 (7) ◽  
pp. 030006052110297
Author(s):  
Milan Vajda ◽  
Jana Dědková ◽  
Maja Stříteská ◽  
Jiří Jandura ◽  
Pavel Ryška

Enhancement of the subarachnoid space after intravenous administration of gadolinium contrast agent is not common. Enhancement usually occurs in pathological conditions that increase the permeability of the blood–cerebrospinal fluid barrier, most notably in meningitis. We herein describe possible subarachnoid enhancement in patients with no apparent effect on the meninges. These patients had clinical signs of Meniere’s disease and underwent specific magnetic resonance imaging of the inner ear to possibly visualize endolymphatic hydrops. The endolymphatic space can be noninvasively imaged by intravenous administration of contrast agent, usually at a double dose, 4 hours before the scanning process. During this time, the contrast agent penetrates not only the perilymph but also the subarachnoid space, where the highest concentration occurs after 4 hours according to some studies.


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