Improving high-resolution MR bold venographic imaging using a T1 reducing contrast agent

Recently, a new imaging method was proposed by Reichenbach et al (Radiology 1997;204:272–277) to image small cerebral venous vessels specifically. This method, referred to as high‐resolution blood oxygen level‐dependent venography (HRBV), relies on the susceptibility difference between the veins and...

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Published inJournal of magnetic resonance imaging Vol. 10; no. 2; pp. 118 - 123
Main Authors Lin, Weili, Mukherjee, Pratik, An, Hongyu, Yu, Yingjing, Wang, Yi, Vo, Katy, Lee, Benjamin, Kido, Daniel, Haacke, E.M.
Format Journal Article
LanguageEnglish
Published New York John Wiley & Sons, Inc 01.08.1999
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Summary:Recently, a new imaging method was proposed by Reichenbach et al (Radiology 1997;204:272–277) to image small cerebral venous vessels specifically. This method, referred to as high‐resolution blood oxygen level‐dependent venography (HRBV), relies on the susceptibility difference between the veins and the brain parenchyma. The resulting phase difference between the vessels and the brain parenchyma leads to signal losses over and above the usual T2* effect. At 1.5 T, a rather long TE (roughly 40 msec) is required for this cancellation to become significant, leading to enhanced susceptibility artifacts and a long data acquisition time. In this study, we examine the utility of incorporating a clinically available T1 reducing contrast agent, Omniscan (Sanofi Winthrop Pharmaceuticals, NY, NY), with the HRBV imaging approach to reduce susceptibility artifacts and imaging time while maintaining the visibility of cerebral veins. Using a double‐dose injection of Omniscan, we were able to reduce TE from 40 to 25 msec. This led to a decrease in TR from 57 to 42 msec, allowing a 26% reduction in data acquisition time while maintaining the visibility of cerebral venous vessels and reducing susceptibility artifacts. J. Magn. Reson. Imaging 1999;10:118–123, 1999. © 1999 Wiley‐Liss, Inc.
Bibliography:ArticleID:JMRI2
Siemens Medical Systems
NIH - No. NS35147
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RSNA
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ISSN:1053-1807
1522-2586
DOI:10.1002/(SICI)1522-2586(199908)10:2<118::AID-JMRI2>3.0.CO;2-V