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Published online before print April 3, 2003, 10.1148/radiol.2273020671
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Improved MR Coronary Angiography with Use of a New Rapid Clearance Blood Pool Contrast Agent in Pigs1

Martijn S. Dirksen, MD, Hildo J. Lamb, PhD, Patrik Kunz, PhD, Philippe Robert, MSc, Claire Corot, PhD and Albert de Roos, MD

1 From the Department of Radiology, Leiden University Medical Center, Albinusdreef 2, Rm 62, Post Zone C2-S, 2333 ZA Leiden, the Netherlands (M.S.D., H.J.L., P.K., A.d.R.); and Guerbet Research, Aulnay Sous Bois, France (P.R., C.C.). From the 2001 RSNA scientific assembly. Received June 6, 2002; revision requested July 30; revision received September 3; accepted October 25. Address correspondence to M.S.D. (e-mail: m.s.dirksen@lumc.nl).



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Figure 1. MR coronary angiography pulse sequences used in the present study. Upper row: native nonenhanced sequence with use of T2 preparation and navigator and breath-hold approaches. Lower row: contrast-enhanced sequences with use of navigator and breath-hold approaches. Note that for contrast-enhanced acquisitions, a 90° saturation preparation pulse was applied, whereas the T2 preparation pulse was omitted.

 


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Figure 2. A, P792 pharmacokinetics. The first-pass phase is followed by a steady-state phase and rapid renal clearance (data from one animal). P792 was below detection level after 59.5 minutes. B, Quantification of pharmacokinetics. C5/C0 represents P792 levels at 5 minutes after injection relative to P792 levels immediately after injection. The high C5/C0 ratio and the small distribution volume compared with that of gadoterate meglumine (Gd-DOTA) (26) illustrate the blood pool properties of P792 (data from two pigs). C, Molecular structure of P792 versus that of gadoterate meglumine (Gd-DOTA). P792 has four hydrophilic arms that prevent transcapillary diffusion. Alternatively, gadoterate meglumine may freely pass the capillary endothelium because of its small molecular size.

 


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Figure 3. Wash-out time series of MR coronary angiography with use of two types of contrast agents to illustrate the difference between blood pool contrast agents and extravascular contrast agents. Upper series: Application of a blood pool contrast agent (P792) results in selective enhancement of the blood pool during 15 minutes, whereas the background tissues remain unenhanced. Lower series: the conventional agent (gadoterate meglumine) extravasates within 1 minute, causing enhancement of the perivascular tissues, which makes it impossible to identify the coronary artery.

 


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Figure 4. MR images illustrate the main study results. The right coronary artery was imaged with a nonenhanced state-of-the-art T2 preparation technique (upper row); with P792 (middle row); and with gadoterate meglumine (lower row). Images were acquired with the navigator approach (each row shows four sections from a stack of 20). The arrow marks the right coronary artery on all images. Image acquisition was started immediately following bolus injection, with 8.5-second bolus arrival delay. Note the low signal intensity of the perivascular tissues on the P792-enhanced images with regard to the other two image types. Coronary background suppression appears most effective on the P792-enhanced images, thereby improving the conspicuity of the coronary vessel.

 





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