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Technical Innovation |
1
Department of Radiology, MRI, New York University Medical Center, 530 First
Ave., HCC Basement, New York, NY 10016.
2
Department of Surgery, New York University Medical Center, New York, NY
10016.
Received August 23, 2000;
accepted after revision September 25, 2000.
Address correspondence to V. S. Lee.
Introduction
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State-of-the-art MR cholangiographic techniques typically rely on heavily T2-weighted turbo spin-echo techniques and have been shown to be highly accurate in the identification of biliary disease and in the detection of variant extrahepatic biliary anatomy relevant to laparoscopic cholecystectomy [6]. However, in our experience, the detection and definition of intrahepatic anatomic anomalies, particularly in nondilated systems, are often inadequate. An accurate, but invasive, alternative imaging techniqueendoscopic retrograde cholangiopancreatographyis associated with a quantifiable morbidity, which makes its use as a routine screening procedure difficult to justify in otherwise healthy donor candidates.
Mangafodipir trisodium is a safe and approved hepatobiliary MR contrast agent [7] that is administered intravenously and causes T1 shortening as a result of the paramagnetic effects of the manganese metal ion. The manganese is excreted primarily via the biliary system and therefore can theoretically be used as a biliary contrast agent with T1-weighted MR imaging. Because biliary stasis in the setting of strictures or common duct stones reduces the excretion of biliary manganese after mangafodipir trisodium injection, the clinical use of this contrast agent with cholangiography has been limited [8]. However, for normal nonobstructed systems, we have observed visible biliary enhancement within 10 min of IV injection. We describe a new method for defining intrahepatic ductal anatomy in liver transplant donor candidates, using a combination of mangafodipir trisodium contrast material and high-resolution volumetric three-dimensional (3D) T1-weighted gradient-echo imaging of the liver.
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Routine MR cholangiographic sequences were also performed and included axial and coronal half-Fourier acquisition single-shot turbo spin-echo images (TR/effective TE, infinite/62; refocusing angle, 140-160°; imaging matrix, 128-192 x 256; field of view, 300-375 mm with rectangular field of view depending on body habitus; slice thickness, 4 mm; number of slices per breath-hold, 15-20) and oblique coronal heavily T2-weighted turbo spin-echo images (2800/1100; flip angle, 150-180°; matrix, 240 x 256; field of view, 300-375 mm; section thickness, 20-60 mm with an optional rectangular field of view). All images were obtained during suspended respiration.
Subsequently, an IV injection of mangafodipir trisodium (Teslascan; Nycomed, Princeton, NJ) at a standard dose of 5 µmol/kg (0.1 mL/kg; maximum dose, 15 mL) was administered via a slow injection over 1-2 min followed by a 10-mL saline flush. From 10 to 15 min after injection, axial and coronal volumetric 3D spoiled gradient-echo acquisitions of the liver and biliary system were performed using two interpolated sequences with intermittent fat-suppression pulses. The first one was a higher resolution sequence that was performed coronally with limited coverage: TR/TE, 6.8/2.3; flip angle, 25-40°; matrix, 128-256 x 512; field of view, 350-450 mm (rectangular field of view depending on body habitus); and 24 partitions interpolated to 48 slices with a thickness of 1.5 mm or less. The second one was a lower resolution sequence that was performed axially to include the entire liver: TR/TE, 4.5/1.9; flip angle, 25-40°; matrix, 128-160 x 256; field of view, 300-375 mm using a rectangular field of view; and 80-112 partitions for a slice thickness of 2 mm or less [9]. Imaging time for all sequences was kept to less than 25 sec to facilitate breath-holding during the acquisition.
The imaging protocol was approved by our institutional review board, and informed consent was obtained from all patients.
The 3D image sets were viewed on a commercially available workstation (Virtuoso, Siemens Medical Systems; and Vitrea, Vital Images, Minneapolis, MN). Volume-rendering and maximum-intensity-projection displays are useful for evaluating the complex orthogonal relationships between the right lateral duct, which typically traverses the liver in the anteroposterior plane, and the right medial and left hepatic ducts, which typically lie in an oblique coronal plane (Figs. 1A,1B and 2A,2B,2C). Stereoscopic viewing of the 3D data sets (available on the Virtuoso workstation, Siemens) can be particularly helpful for visualization of 3D relationships in difficult cases.
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For the 10 patients examined so far, two independent MR radiologists have evaluated the conventional T2-weighted MR cholangiographic images and the mangafodipir trisodium-enhanced volumetric T1-weighted images for definition of biliary anatomy and the presence of anatomic variants [3, 4]. To date, only one patient (Fig. 1A,1B) has undergone right hepatectomy with intraoperative cholangiography. In this patient both the heavily T2-weighted coronal image and the mangafodipir trisodium-enhanced images predicted intraoperative findings accurately. Although an assessment of the accuracy of the method awaits further surgical confirmation, in our preliminary experience, we have observed that the mangafodipir trisodium-enhanced volumetric images of the liver can serve as a useful supplement to conventional T2-weighted MR cholangiographic images for the evaluation of right lobe donor candidates.
The high signal intensity of the biliary system after mangafodipir excretion produces excellent contrast when compared with the background liver parenchyma and hepatic vessels, the latter of which can be difficult to distinguish from bile ducts with some conventional T2-weighted MR cholangiographic methods. With two-dimensional T2-weighted images, the orthogonal relationships between the right medial duct, right lateral duct, left hepatic duct, and common hepatic duct can often be difficult to define with confidence (Fig. 2A,2B,2C). The use of volume-rendering algorithms for reconstruction of 3D data sets facilitates definition of these relationships for surgical planning. Transplantation surgeons at our institution review all cases using a 3D imaging workstation as part of the preoperative evaluation. The mangafodipir trisodium-enhanced 3D imaging method also provides improved resolution over that of conventional T2-weighted imaging by producing 3D images with a pixel size on the order of 1 x 2 x 1.5 mm. Given that the distinction between a normal pattern of biliary anatomy and biliary trifurcation may depend on differences in the position of the right lateral duct of less than 1 mm, image resolution can be critical for the accurate definition of biliary anatomy and, consequently, for the appropriate patient selection and exclusion (Fig. 2A,2B,2C).
Mangafodipir trisodium-enhanced T1-weighted MR imaging, particularly when performed using high-resolution volumetric T1-weighted imaging of the liver, may serve as a supplement to conventional MR cholangiographic methods; this method can facilitate the definition of intrahepatic bile duct anatomy in nonobstructed biliary systems such as that seen in healthy liver transplant donor candidates. It is hypothesized that this capacity will have a favorable impact on surgical results; however, studies to verify this hypothesis are needed. With our present protocol, both gadopentetate dimeglumine and mangafodipir trisodium contrast material are administered for evaluation of donor candidates to provide comprehensive evaluation of hepatic parenchymal and vascular anatomy as well as biliary anatomy, respectively. In the future, these studies could theoretically be performed with the use of a single contrast agent, such as a hepatobiliary gadolinium-based MR contrast agent, whereby dynamic T1-weighted imaging during bolus infusion can be used for evaluation of liver parenchyma and vascular anatomy and delayed imaging after biliary excretion can be used for cholangiography [10]. Investigational studies are warranted.
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