DOI:10.2214/AJR.07.3162
AJR 2008; 191:537-545
© American Roentgen Ray Society
MR Cholangiography for Evaluation of Hilar Branching Anatomy in Transplantation of the Right Hepatic Lobe from a Living Donor
Joon Seok Lim1,2,
Myeong-Jin Kim1,2,
Sungmin Myoung3,
Mi-Suk Park1,2,
Jin-Young Choi1,
Jin-Sub Choi4 and
Soon Il Kim4
1 Department of Diagnostic Radiology, Yonsei University Health System, 134
Shinchon-dong, Seodaemoon-ku, Seoul 120-752, Republic of Korea.
2 Institute of Gastroenterology, Yonsei University Health System, Seoul,
Republic of Korea.
3 Department of Biostatistics, Yonsei University Health System, Seoul, Republic
of Korea.
4 Department of Surgery, Yonsei University Health System, Seoul, Republic of
Korea.
Received September 11, 2007;
accepted after revision February 10, 2008.
Address correspondence to M. J. Kim
(kimnex{at}yuhs.ac.kr).
Abstract
OBJECTIVE. Our objective was to determine the utility of 3D T2 MR
cholangiography (MRC) for biliary visualization and predicting the number of
ductal orifices during right lobe harvesting for ductal anastomosis in liver
donors for right lobe transplantation.
MATERIALS AND METHODS. This study was composed of 33 donors who
underwent right lobectomy for transplantation. Preoperative MRC techniques
included 2D T2 MRC, 3D T2 MRC, and 3D contrast-enhanced T1 MRC. Qualitative
analyses were performed for ductal visualization in each technique. The
accuracies for predicting the numbers of orifices during right lobe harvesting
were evaluated for 2D T2 MRC alone and for various other combined sets. MRI
definitions of the predicted number of ductal orifices were compared with
surgical findings.
RESULTS. Mean visualization scores of all ducts for 3D T2 MRC were
significantly higher than for 2D T2 MRC and 3D contrast-enhanced T1 MRC. In
predicting the number of orifices, all combined sets showed significantly
higher accuracy than 2D T2 MRC. No significant difference in mean accuracies
was observed within the comparison of the combined sets.
CONCLUSION. Three-dimensional T2 MRC provided superior biliary
visualization than 2D T2 MRC and 3D contrast-enhanced T1 MRC. For predicting
the number of orifices, the combined set of 2D and 3D T2 MRC enabled better
accuracy than 2D T2 MRC alone and produced comparable results to other
combined sets.
Keywords: anatomy bile ducts liver transplantation MR cholangiopancreatography
Introduction
The evaluation of the biliary anatomy in donor candidates for
adult-to-adult living right lobe liver transplantation is essential because
the pattern of second-order biliary tract branching can affect the surgical
approach and biliary anastomotic technique or even preclude liver donation
[1,
2]. The standard MR examination
for defining biliary anatomy has been 2D T2-weighted MR cholangiography (MRC).
However, previous studies have reported difficulties in depicting the
nondilated normal bile ducts in potential living donors using 2D T2 MRC
[1,
3]. In an attempt to better
visualize the small caliber of normal-sized ducts, 3D contrast-enhanced
T1-weighted MRC (3D contrast-enhanced T1 MRC) has been implemented over the
past several years. And indeed, 3D contrast-enhanced T1 MRC using mangafodipir
trisodium or gadobenate dimeglumine has shown promising results in defining
intrahepatic biliary anatomy for liver transplantation
[4,
5]. However, mangafodipir
trisodium is no longer available in North American markets, and gadobenate
dimeglumine–enhanced MRC has a problematic disadvantage in that it
requires more than a 1-hour delay for ductal visualization.
Recently, several studies have reported that 3D T2 MRC can provide a
similar visualization rate for the bile duct as that of conventional 2D
techniques [6,
7]. However, to our knowledge,
the usefulness of 3D T2 MRC has not been assessed for the preoperative biliary
evaluation of living donor transplantation candidates. The standard method for
defining biliary visualization has been 2D T2 MRC, which has a relatively
short acquisition time (usually less than 2 minutes) and is available in all
MR equipment. So, to improve the diagnostic accuracy of biliary visualization,
a practical approach would be to combine the two or three examinations and to
compare the diagnostic accuracies in the variable combined sets with 2D T2
MRC.
Therefore, this study had a twofold purpose. The first was to determine the
utility of 3D T2 MRC for ductal visualization through comparison with 2D T2
MRC and 3D gadobenate dimeglumine–enhanced T1 MRC. The second was to
compare the diagnostic accuracies of ductal anastomosis for right lobe
transplantation in variable combined sets.
Materials and Methods
Patients
Between April 2003 and July 2006, 33 healthy candidates underwent right
lobectomy for living adult-to-adult right-lobe liver transplantation. There
were a total of 23 men and 10 women (mean age, 30.7 years; age range,
18–51 years). Institutional review board approval was obtained for this
retrospective study. Informed consent was not required.
MRI Protocols
All candidates underwent MRI performed at 1.5 T using a torso phased-array
coil in one of two MR systems (Gyroscan Intera or Intera Achieva, Philips
Healthcare). Twenty-five MRC examinations were performed using the former, and
eight MRC examinations were performed using the latter. The donor candidates
were instructed to fast for 4 hours before the MRI examination. In addition to
undergoing MR cholangiography (described later in this article), the subjects
underwent routine MRI before and after IV administration of 0.1 mmol per
kilogram of body weight of gadobenate dimeglumine (MultiHance, Bracco)
injected by an automatic infusion system (Spectris MR injector, Medrad Europe)
at a rate of 2 mL/s.
Three methods for evaluating biliary anatomy were used, and no oral
contrast agent was administered. First, breath-hold 2D T2 MRC was performed
with a single-shot rapid acquisition with relaxation enhancement sequence
(RARE) (TR/TE, 2,025/800; field of view, 240 mm; section thickness, 40 mm;
matrix, 256 x 256; echo-train length, 256) in coronal oblique
orientations (–45° through 45° with 15° intervals) using the
single-section thick-slab technique. Seven images during seven breath-holds
were obtained during the acquisition time of 9 seconds per section, which
included scanning time and interleaved breathing time (total, 63 seconds).
Second, 3D T2 MRC images were obtained using a respiratory triggered 3D
T2-weighted rapid acquisition with relaxation enhancement sequence with
parallel acquisition technique in the coronal plane using the following
parameters: 1,600/650; refocusing flip angle, 90°; field of view,
240–280 mm with rectangular field of view; matrix, 256 x 250;
echo-train length, 128; slab thickness, 70 mm with 35 partitions and section
thickness of 2 mm; interpolation to 70 slices at 1-mm intervals; parallel
acquisition technique factor, 2; no phase wrap option; and acquisition time,
approximately 170 seconds. Rotating maximum-intensity-projection (MIP)
reconstructions of the 3D MR data were performed with a workstation to produce
19 coronal oblique MIP images (0–180°; slab thickness, 40 mm)
rotating about the z-axis in 10° increments.
Third, the donors were brought back for contrast-enhanced T1-weighted MRC
60 minutes after the MR angiography obtained after IV administration of
gadobenate dimeglumine. Three-dimensional volumetric breath-hold T1-weighted
fast-field-echo acquisitions of the central biliary system were obtained in
the coronal plane. The scanning parameters for the high-resolution sequences
that were performed with a limited coverage included 5.1/1.47; refocusing flip
angle, 40°; field of view, 340–380 mm with rectangular field of
view; matrix, 320 x 225; slab thickness, 40 mm with 20 partitions and a
section thickness of 2 mm; and interpolation to 40 slices at 1-mm intervals.
Acquisition time was kept under 25 seconds to facilitate breath-holding. In
addition, 19 coronal oblique MIP images (0–180°; slab thickness, 40
mm) were reconstructed.
Imaging Analysis of Biliary Tract Visualization
Three board-certified radiologists with subspecialty training in abdominal
imaging independently and retrospectively reviewed all source and
reconstructed MR images at a PACS (Centricity, GE Healthcare). The reviewers
had 8, 9, and 10 years of experience.
The 2D T2 MRC, 3D T2 MRC, and 3D contrast-enhanced T1 MRC images were
sequentially evaluated at separate sessions with a 2-week time difference
between reading sessions to reduce recall bias. Three-dimensional images
included source images and MIP images. A total of five biliary segments, the
common (one segment), right and left first-order branch (two segments), and
right second-order branch (two segments) bile duct segments were scored on a
4-point scale for each examination on the basis of previous literature
[7]. A score of 1 indicated
that the segment was not seen; a score of 2, that the segment was seen
faintly; a score of 3, that the segment was well seen, but the confluence or a
portion of the duct was not seen; and a score of 4, that there was excellent
visualization of the segment from its proximal commencement to its distal
confluence. Left secondary segmental duct visualization was not included
because it is not associated with right lobe harvesting. The degrees of
overall image quality were also scored in each examination as follows: 1, poor
quality with severe artifacts; 2, satisfactory quality with a few artifacts;
3, good quality with minimal artifacts; and 4, excellent quality without
artifacts.
Prediction of the Number of Orifices During Right Lobe Harvesting
Two months after the qualitative visualization analyses, the same three
radiologists independently reviewed the uncombined set (2D T2 MRC) and the
three combined sets (2D T2 MRC and 3D T2 MRC, 2D T2 MRC and contrast-enhanced
T1 MRC, and the combined set of all three examinations) with a 2-week time
interval between the reading sessions for each set. They recorded the
predicted number of ductal orifices during right lobe harvesting (one or two;
at our institution, living donor transplantation is performed even if dual
orifices have been acquired during right lobe harvesting). The number of
ductal orifices was determined according to hilar branching anatomy. The
biliary anatomy bifurcation patterns were characterized into the patterns
previously described in the literature
[8]. Most notably, an emphasis
was placed on discerning whether there was a right hepatic duct. The junction
of the anterior segmental duct and the posterior segmental duct forming the
right hepatic duct and the right hepatic duct, in turn, joining the left
hepatic duct in the hilar confluence, were considered to be normal anatomy.
This type was regarded as the case in which the single duct-to-duct
anastomosis would be possible. However, there were three anatomic variations
in which the anterior and posterior segmental bile ducts did not form a right
hepatic duct, the posterior segmental duct joined the left hepatic duct, the
anterior segmental duct joined the left hepatic duct, and a three-branch-type
hilar confluence (trifurcation). The first two types were regarded as
requiring the acquirement of two orifices. In a trifurcation pattern, the
distinction between single and dual orifices was challenging, but our
reviewers determined it according to dominant similarity to normal anatomy or
aberrant insertion of the right segmental branch.
Each reviewer also recorded the diagnostic confidence on the predicted
number on a scale of 1–5: 1, not confident; 2, mildly confident; 3,
moderately confident; 4, highly confident; and 5, completely confident. The
MRI predictions of the number of ductal orifices during right lobe harvesting
were compared with the surgical findings.
Surgical findings during right lobectomy were obtained by reviewing the
operative records to determine the anastomosed number of ductal orifices as
the standard of reference. Of the 33 donors, 22 underwent intraoperative MRC.
During laparotomy, acquisitions of right hepatic ductal lumen for biliary
anastomosis were performed with a single lumen in 24 donors. However, in nine
donors, dual lumen acquisitions were performed because of aberrant biliary
ducts (right anterior duct to left duct: n = 2; right posterior duct
to left duct: n = 7). These results on the number of orifices during
right lobe harvesting were used as a reference standard to evaluate the
accuracy of our MRC imaging sets.
Statistical Analysis
Statistical analyses were performed by using SAS software, version 9.1
(Statistical Analysis System). Interobserver agreement for biliary tract
visualization scores was determined using a weighted kappa statistic.
Interobserver agreement was classified as follows: A kappa value of
0.00–0.20 was considered to indicate poor agreement; 0.21–0.40,
fair agreement; 0.41–0.60, moderate agreement; 0.61–0.80, good
agreement; and 0.81–1.00, excellent agreement.

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Fig. 1A —46-year-old male liver donor with normal right hepatic duct.
Anterior segmental, posterior segmental, right hepatic, and left hepatic ducts
are well visualized in 2D T2 MR cholangiography (MRC) (thick-slap) (A),
3D T2 MRC (maximum-intensity-projection [MIP]) (B), and 3D
contrast-enhanced T1 MRC (MIP) (C) images.
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Fig. 1B —46-year-old male liver donor with normal right hepatic duct.
Anterior segmental, posterior segmental, right hepatic, and left hepatic ducts
are well visualized in 2D T2 MR cholangiography (MRC) (thick-slap) (A),
3D T2 MRC (maximum-intensity-projection [MIP]) (B), and 3D
contrast-enhanced T1 MRC (MIP) (C) images.
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Fig. 1C —46-year-old male liver donor with normal right hepatic duct.
Anterior segmental, posterior segmental, right hepatic, and left hepatic ducts
are well visualized in 2D T2 MR cholangiography (MRC) (thick-slap) (A),
3D T2 MRC (maximum-intensity-projection [MIP]) (B), and 3D
contrast-enhanced T1 MRC (MIP) (C) images.
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Biliary tract visualization—Tests to determine significant
differences in mean visualization scores of the three examinations for common
bile ducts, branching ducts including bilateral first-order branches and right
second-order branches, and all ducts were performed using the Friedman test
(nonparameteric two-way analysis of variance by ranks for repeated measures).
The least significant difference (LSD) test was used for multiple post hoc
comparisons on common bile ducts, branching ducts, and all ducts. The same
statistical process was applied to compare the degree of image quality in the
three examinations. A p value of less than 0.05 was considered to
indicate a statistically significant difference.
Prediction of the number of orifices—Interobserver agreement
for diagnostic confidence for predicting the number of orifices on all four
imaging sets was determined with the weighted kappa statistic. Interobserver
agreement was classified according to the previously mentioned criteria. Tests
for significant differences in mean accuracies and diagnostic confidences were
performed using nonparametric tests (Kruskal-Wallis test and Friedman test,
respectively). Mean accuracies and mean confidences of the three reviewers
regarding the predicted number of orifices were compared among the four image
sets using the LSD test. A p value of less than 0.05 was considered a
statistically significant difference.
Results
Biliary Tract Visualization
The kappa values for the interobserver agreement of biliary tract
visualization ranged from fair to good for 2D T2 MRC, 3D T2 MRC, and
contrast-enhanced T1 MRC (Table
1). The acquired kappa values for the degree of image quality also
ranged from fair to good for all three techniques
(Table 1).

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Fig. 2A —35-year-old male liver donor with aberrant biliary anatomy.
Two-dimensional T2 MR cholangiography (MRC) (A) and 3D T2 MRC
(B) images show aberrant biliary anatomy with right posterior duct
draining into left hepatic duct. Anterior (arrowhead, A,
B, and D) and posterior segmental branches (arrow,
A, B, and D) are well delineated in both sequences, but
right segmental branches are not delineated on 3D contrast-enhanced T1 MRC
(C) image. Intraoperative cholangiogram (D) confirmed aberrant
biliary anatomy.
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Fig. 2B —35-year-old male liver donor with aberrant biliary anatomy.
Two-dimensional T2 MR cholangiography (MRC) (A) and 3D T2 MRC
(B) images show aberrant biliary anatomy with right posterior duct
draining into left hepatic duct. Anterior (arrowhead, A,
B, and D) and posterior segmental branches (arrow,
A, B, and D) are well delineated in both sequences, but
right segmental branches are not delineated on 3D contrast-enhanced T1 MRC
(C) image. Intraoperative cholangiogram (D) confirmed aberrant
biliary anatomy.
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Fig. 2C —35-year-old male liver donor with aberrant biliary anatomy.
Two-dimensional T2 MR cholangiography (MRC) (A) and 3D T2 MRC
(B) images show aberrant biliary anatomy with right posterior duct
draining into left hepatic duct. Anterior (arrowhead, A,
B, and D) and posterior segmental branches (arrow,
A, B, and D) are well delineated in both sequences, but
right segmental branches are not delineated on 3D contrast-enhanced T1 MRC
(C) image. Intraoperative cholangiogram (D) confirmed aberrant
biliary anatomy.
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Fig. 2D —35-year-old male liver donor with aberrant biliary anatomy.
Two-dimensional T2 MR cholangiography (MRC) (A) and 3D T2 MRC
(B) images show aberrant biliary anatomy with right posterior duct
draining into left hepatic duct. Anterior (arrowhead, A,
B, and D) and posterior segmental branches (arrow,
A, B, and D) are well delineated in both sequences, but
right segmental branches are not delineated on 3D contrast-enhanced T1 MRC
(C) image. Intraoperative cholangiogram (D) confirmed aberrant
biliary anatomy.
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Mean visualization scores of all ducts were significantly different on the
Friedman test (2D T2 MRC, 3.56 ± 0.36 [SD]; 3D T2 MRC, 3.75 ±
0.33, and contrast-enhanced T1 MRC, 3.19 ± 0.37; F value, 26.82;
p < 0.0001) (Figs.
1A,
1B,
1C,
2A,
2B,
2C, and
2D). There were also
significant differences in the mean visualization scores of the common and
branching ducts (common duct, F value, 4.92; p = 0.0007; branching
duct, F value, 24.71; p < 0.0001). In multiple comparisons, the
mean scores for all ducts at both 2D T2 MRC and 3D T2 MRC were significantly
higher than for 3D contrast-enhanced T1 MRC (p < 0.05)
(Fig. 3A). The mean score of 3D
T2 MRC for visualization of all ducts was significantly higher than that of 2D
T2 MRC (p < 0.05). For visualization of the branching ducts, both
2D and 3D T2 MRC again showed better results when compared with 3D
contrast-enhanced T1 MRC (p < 0.05). Two-dimensional T2 MRC and 3D
T2 MRC showed comparable results. For common duct visualization, there was no
significant difference between either of the T2 MRC techniques and 3D
contrast-enhanced T1 MRC. However, the mean score of 3D T2 MRC was
significantly higher than that of 2D T2 MRC.

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Fig. 3A —Graphs show multiple comparisons of mean visualization scores
and image quality for three MR cholangiography (MRC) techniques. White bars =
2D T2 MRC, light gray bars = 3D T2 MRC, dark gray bars = 3D contrast-enhanced
T1 MRC, error bars indicate SD, asterisk indicates p < 0.05 in
comparison of techniques. Branching ducts included bilateral first-order
branches and right second-order branches. Overall ducts included a total of
five segments. Graph shows mean visualization scores of common duct, branching
ducts, and all ducts in three MR cholangiography techniques.
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The mean degree of image quality of the three techniques was significantly
different on the Friedman test (2D T2 MRC, 3.05 ± 0.67; 3D T2 MRC, 3.19
± 0.51; and contrast-enhanced T1 MRC, 3.53 ± 0.51; F value,
52.06; p < 0.0001). In multiple comparisons, 3D contrast-enhanced
T1 MRC showed significantly better image quality when compared with 2D T2 MRC
or 3D T2 MRC (p < 0.05) (Fig.
3B). No significant difference was observed between 2D T2 MRC and
3D T2 MRC.

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Fig. 3B —Graphs show multiple comparisons of mean visualization scores
and image quality for three MR cholangiography (MRC) techniques. White bars =
2D T2 MRC, light gray bars = 3D T2 MRC, dark gray bars = 3D contrast-enhanced
T1 MRC, error bars indicate SD, asterisk indicates p < 0.05 in
comparison of techniques. Branching ducts included bilateral first-order
branches and right second-order branches. Overall ducts included a total of
five segments. Graph shows mean scores of image quality of each technique.
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Prediction of the Number of Orifices During Right Lobe Harvesting
The mean accuracies of predicting the number of orifices in the four sets
of imaging techniques were significantly different on the Kruskal-Wallis test
(2D T2 MRC alone, 94.95% ± 3.50%; combined set of 2D T2 MRC and 3D T2
MRC, 98.99% ± 1.75%; 2D T2 MRC and 3D contrast-enhanced T1 MRC, 100.00%
± 0.00%; and all techniques, 100.00% ± 0.00%; F value, 6.97,
p = 0.0029). The LSD test for multiple comparisons of mean accuracies
showed that all combined sets showed significantly higher accuracy than 2D T2
MRC alone (p < 0.05) (Figs.
4A,
5A,
5B,
5C,
5D,
5E,
5F,
6A,
6B, and
6C). No significant difference
was observed within the comparison of three combined sets (p >
0.05).

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Fig. 4A —Multiple comparisons of mean accuracy and diagnostic
confidence for four sets of MR cholangiography (MRC) imaging techniques.
Technique 1 = 2D T2 MRC alone, technique 2 = combined set of 2D T2 MRC and 3D
T2 MRC, technique 3 = combined set of 2D T2 MRC and 3D contrast-enhanced T1
MRC, and technique 4 = combined set of all three techniques. Error bars
indicate SD; asterisk indicates p < 0.05 in comparison of
techniques. No significant difference was observed within comparison of
combined sets for both accuracy and diagnostic confidence. Graph shows mean
accuracy of 2D MRC alone and three combined sets for prediction of ductal
orifice number during right lobe harvesting.
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Fig. 5A —30-year-old male liver donor who underwent single lumen
acquisition during right lobe harvest. Two-dimensional T2 MR cholangiography
(MRC) (A), maximum-intensity-projection (MIP) image of 3D T2 MRC
(B), source image of 3D T2 MRC (C), MIP image of 3D
contrast-enhanced T1 MRC (D), and source image of 3D contrast-enhanced
T1 MRC (E) show normal anatomy in which junction of anterior segmental
duct and posterior segmental duct forms right hepatic duct (arrow).
All reviewers predicted that acquisition of single lumen would be possible
during right lobe harvesting on sets of all four techniques. Intraoperative
cholangiogram (F) confirmed normal anatomy (arrow), and
acquisition of single lumen was performed.
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Fig. 5B —30-year-old male liver donor who underwent single lumen
acquisition during right lobe harvest. Two-dimensional T2 MR cholangiography
(MRC) (A), maximum-intensity-projection (MIP) image of 3D T2 MRC
(B), source image of 3D T2 MRC (C), MIP image of 3D
contrast-enhanced T1 MRC (D), and source image of 3D contrast-enhanced
T1 MRC (E) show normal anatomy in which junction of anterior segmental
duct and posterior segmental duct forms right hepatic duct (arrow).
All reviewers predicted that acquisition of single lumen would be possible
during right lobe harvesting on sets of all four techniques. Intraoperative
cholangiogram (F) confirmed normal anatomy (arrow), and
acquisition of single lumen was performed.
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Fig. 5C —30-year-old male liver donor who underwent single lumen
acquisition during right lobe harvest. Two-dimensional T2 MR cholangiography
(MRC) (A), maximum-intensity-projection (MIP) image of 3D T2 MRC
(B), source image of 3D T2 MRC (C), MIP image of 3D
contrast-enhanced T1 MRC (D), and source image of 3D contrast-enhanced
T1 MRC (E) show normal anatomy in which junction of anterior segmental
duct and posterior segmental duct forms right hepatic duct (arrow).
All reviewers predicted that acquisition of single lumen would be possible
during right lobe harvesting on sets of all four techniques. Intraoperative
cholangiogram (F) confirmed normal anatomy (arrow), and
acquisition of single lumen was performed.
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Fig. 5D —30-year-old male liver donor who underwent single lumen
acquisition during right lobe harvest. Two-dimensional T2 MR cholangiography
(MRC) (A), maximum-intensity-projection (MIP) image of 3D T2 MRC
(B), source image of 3D T2 MRC (C), MIP image of 3D
contrast-enhanced T1 MRC (D), and source image of 3D contrast-enhanced
T1 MRC (E) show normal anatomy in which junction of anterior segmental
duct and posterior segmental duct forms right hepatic duct (arrow).
All reviewers predicted that acquisition of single lumen would be possible
during right lobe harvesting on sets of all four techniques. Intraoperative
cholangiogram (F) confirmed normal anatomy (arrow), and
acquisition of single lumen was performed.
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Fig. 5E —30-year-old male liver donor who underwent single lumen
acquisition during right lobe harvest. Two-dimensional T2 MR cholangiography
(MRC) (A), maximum-intensity-projection (MIP) image of 3D T2 MRC
(B), source image of 3D T2 MRC (C), MIP image of 3D
contrast-enhanced T1 MRC (D), and source image of 3D contrast-enhanced
T1 MRC (E) show normal anatomy in which junction of anterior segmental
duct and posterior segmental duct forms right hepatic duct (arrow).
All reviewers predicted that acquisition of single lumen would be possible
during right lobe harvesting on sets of all four techniques. Intraoperative
cholangiogram (F) confirmed normal anatomy (arrow), and
acquisition of single lumen was performed.
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Fig. 5F —30-year-old male liver donor who underwent single lumen
acquisition during right lobe harvest. Two-dimensional T2 MR cholangiography
(MRC) (A), maximum-intensity-projection (MIP) image of 3D T2 MRC
(B), source image of 3D T2 MRC (C), MIP image of 3D
contrast-enhanced T1 MRC (D), and source image of 3D contrast-enhanced
T1 MRC (E) show normal anatomy in which junction of anterior segmental
duct and posterior segmental duct forms right hepatic duct (arrow).
All reviewers predicted that acquisition of single lumen would be possible
during right lobe harvesting on sets of all four techniques. Intraoperative
cholangiogram (F) confirmed normal anatomy (arrow), and
acquisition of single lumen was performed.
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Fig. 6A —38-year-old male liver donor who underwent dual-lumen
acquisition during harvesting of right lobe. Right anterior and posterior
segmental branches do not seem to be separated on 2D T2 MR cholangiography
(MRC) (A) image. Two reviewers incorrectly interpreted that single
lumen acquisition would be possible. However, maximum-intensity-projection
(MIP) images of 3D T2 MRC (B) and 3D contrast-enhanced T1 MRC
(C) depicted well absence of common right hepatic duct (arrowhead,B and C, right anterior segmental duct; arrow,B and C, right posterior segmental duct). Dual-lumen
acquisition was performed during right lobe harvesting.
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Fig. 6B —38-year-old male liver donor who underwent dual-lumen
acquisition during harvesting of right lobe. Right anterior and posterior
segmental branches do not seem to be separated on 2D T2 MR cholangiography
(MRC) (A) image. Two reviewers incorrectly interpreted that single
lumen acquisition would be possible. However, maximum-intensity-projection
(MIP) images of 3D T2 MRC (B) and 3D contrast-enhanced T1 MRC
(C) depicted well absence of common right hepatic duct (arrowhead,B and C, right anterior segmental duct; arrow,B and C, right posterior segmental duct). Dual-lumen
acquisition was performed during right lobe harvesting.
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Fig. 6C —38-year-old male liver donor who underwent dual-lumen
acquisition during harvesting of right lobe. Right anterior and posterior
segmental branches do not seem to be separated on 2D T2 MR cholangiography
(MRC) (A) image. Two reviewers incorrectly interpreted that single
lumen acquisition would be possible. However, maximum-intensity-projection
(MIP) images of 3D T2 MRC (B) and 3D contrast-enhanced T1 MRC
(C) depicted well absence of common right hepatic duct (arrowhead,B and C, right anterior segmental duct; arrow,B and C, right posterior segmental duct). Dual-lumen
acquisition was performed during right lobe harvesting.
|
|
The scores of diagnostic confidences in each imaging set were also
statistically evaluated. The acquired kappa values ranged from fair to
moderate (Table 1). Mean
confidences of the four techniques were significantly different on the
Friedman test (2D T2 MRC alone, 4.51 ± 0.62; combined set of 2D T2 MRC
and 3D T2 MRC, 4.93 ± 0.16; 2D T2 MRC and 3D contrast-enhanced T1 MRC,
4.89 ± 0.25; and all techniques, 4.95 ± 0.12; F value, 8.14,
p < 0.0001). The LSD test for multiple comparisons of mean
confidences showed that no significant difference was observed within the
comparison of three combined sets (p > 0.05). In a comparison
between the combined sets and 2D T2 MRC, all combined sets showed
significantly higher confidence than 2D T2 MRC (p < 0.05) (Figs.
4B,
7A,
7B,
7C,
7D, and
7E).

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Fig. 4B —Multiple comparisons of mean accuracy and diagnostic
confidence for four sets of MR cholangiography (MRC) imaging techniques.
Technique 1 = 2D T2 MRC alone, technique 2 = combined set of 2D T2 MRC and 3D
T2 MRC, technique 3 = combined set of 2D T2 MRC and 3D contrast-enhanced T1
MRC, and technique 4 = combined set of all three techniques. Error bars
indicate SD; asterisk indicates p < 0.05 in comparison of
techniques. No significant difference was observed within comparison of
combined sets for both accuracy and diagnostic confidence. Graph shows mean
diagnostic confidence of 2D MRC alone and three combined sets for prediction
of ductal orifice number during right lobe harvesting.
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Fig. 7A —21-year-old male liver donor with normal biliary anatomy. On
2D T2 MR cholangiography (MRC) image, right ductal anatomy is not well
delineated. All three reviewers had relatively lower confidence.
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Fig. 7B —21-year-old male liver donor with normal biliary anatomy. All
three reviewers had relatively lower confidence, but all techniques combined
showed relatively higher confidence grade in predicting single lumen
acquisition: maximum-intensity-projection (MIP) image of 3D T2 MRC (B);
source image of 3D T2 MRC (C); source image of 3D contrast-enhanced T1
MRC (D). Arrowhead indicates anterior segmental branch, short arrow
indicates posterior segmental branch, and long arrow indicates right hepatic
duct.
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Fig. 7C —21-year-old male liver donor with normal biliary anatomy. All
three reviewers had relatively lower confidence, but all techniques combined
showed relatively higher confidence grade in predicting single lumen
acquisition: maximum-intensity-projection (MIP) image of 3D T2 MRC (B);
source image of 3D T2 MRC (C); source image of 3D contrast-enhanced T1
MRC (D). Arrowhead indicates anterior segmental branch, short arrow
indicates posterior segmental branch, and long arrow indicates right hepatic
duct.
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Fig. 7D —21-year-old male liver donor with normal biliary anatomy. All
three reviewers had relatively lower confidence, but all techniques combined
showed relatively higher confidence grade in predicting single lumen
acquisition: maximum-intensity-projection (MIP) image of 3D T2 MRC (B);
source image of 3D T2 MRC (C); source image of 3D contrast-enhanced T1
MRC (D). Arrowhead indicates anterior segmental branch, short arrow
indicates posterior segmental branch, and long arrow indicates right hepatic
duct.
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Fig. 7E —21-year-old male liver donor with normal biliary anatomy.
Intraoperative cholangiogram confirmed normal anatomy, and acquisition of
single lumen was performed. Arrowhead indicates anterior segmental branch,
short arrow indicates posterior segmental branch, and long arrow indicates
right hepatic duct.
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Discussion
The results of the present study showed that 3D T2 MRC enables
significantly better visualization of all bile ducts than 2D T2 MRC or 3D
contrast-enhanced T1 MRC. Three-dimensional MR techniques of these MRC
examinations have potential advantages over 2D imaging including the capacity
to provide thinner sections without interslice gaps and a higher
signal-to-noise ratio (SNR). These advantages of the 3D T2 MRC may be the
reason that it showed better visualization of all bile ducts than 2D T2 MRC.
However, the 3D contrast-enhanced T1 MRC showed lesser visualization grade
than 2D MRC despite the 3D acquisitions that were used. This result is curious
and seemingly contradictory to the previous report
[9] that there was no
difference in biliary visualization between excretory T1-weighted MRC and 2D
T2 MRC. Such a discrepancy may be caused by the differences in the biliary
segments included. Papanikolaou et al.
[9] included only the
extrahepatic bile duct for comparison of biliary visualization. In the common
duct visualization of our study, there was no significant difference in
visualization between 2D T2 MRC and contrast-enhanced T1 MRC, similar to their
results. In addition, this discrepancy might be attributed to the use of
ultralong echo-trains in turbo spin-echo sequences on T2 MRC that provide
selective ductal visualization with better background suppression in
comparison with T1-weighted imaging
[8].
In terms of image quality, our results also showed that 3D
contrast-enhanced T1 MRC could produce better image quality than 2D T2 MRC or
3D T2 MRC. Recently, several studies on 3D contrast-enhanced T1 MRC have
reported increased SNR relative to 2D T2 MRC
[9,
10]. In addition, the better
image quality in 3D contrast-enhanced T1 MRC may be due to lack of image
blurring related to long echo-trains and artifacts by overlapping
fluid-containing structures. A lesser degree of respiration artifacts than
occurs in 3D T2-weighted imaging, which requires longer acquisition time, may
be another causative factor. Between 2D T2 MRC and 3D T2 MRC, there was no
significant difference of overall image quality. Although a breath-holding
technique for the acquisition of 2D T2 MRC could have provided better image
quality than 3D T2 MRC, higher SNR and better resolution in 3D T2 MRC might
play a complementary role in improving overall image quality.
With regard to the prediction of the number of bile duct orifices exposed
and requiring anastomosis during the right lobe harvest, our study results
showed that the combination of two or three imaging techniques (2D T2 MRC and
3D T2 MRC or 2D T2 MRC and 3D contrast-enhanced T1 MRC or all three imaging
techniques) may significantly improve the accuracy and confidence for
predicting the number of bile duct orifices exposed compared with 2D T2 MRC
alone. The advantages of 3D imaging such as 3D T2 MRC or 3D contrast-enhanced
T1 MRC included higher spatial resolution when compared with 2D T2 MRC. The
complex orthogonal relationships between the right anterior duct, right
posterior duct, left hepatic duct, and common hepatic duct make it difficult
to predict the orifice number with confidence on conventional 2D MR images.
The higher spatial resolution of 3D imaging can be helpful when, for example,
distinguishing among a normal short right hepatic duct (candidate for single
lumen acquisition), trifurcation (possible candidate for single lumen
acquisition), and right anterior or posterior duct draining into the left
hepatic duct (which requires dual lumen acquisition during right lobe
harvesting) and consequently selecting the appropriate patient and surgical
plan.
Several studies have reported the usefulness of the combination of 2D
T2-weighted imaging and mangafodipir trisodium MR cholangiography for making a
better evaluation of the hilar bile duct anatomy
[5,
11,
12]. However, this approach
requires the combined use of two different contrast agents (manganese agent
for MRC and gadolinium-based agent for MR angiography). The combination of
imaging techniques in our study (3D T2 MRC and 3D contrast-enhanced T1 MRC)
did not require the additional contrast agent for MR angiography because
ductal anatomy can be depicted on the delayed phase images obtained after MR
angiography acquisition using gadobenate dimeglumine as the contrast
agent.
Nevertheless, the use of the added imaging techniques is not without
potential disadvantages. The additional imaging sequences inevitably require
additional acquisition time. Particularly, the 3D contrast-enhanced T1 MRC
requires a 60- to 90-minute delay for biliary contrast agent excretion before
imaging. In the comparison between the three combined sets (2D T2 MRC and 3D
T2 MRC or 2D T2 MRC and 3D contrast-enhanced T1 MRC or all three imaging
techniques), there was no significant difference. Therefore, it may be more
logical to acquire the added sets of 3D T2 MRC than the added sets of 3D
contrast-enhanced T1 MRC or both sequences. Contrast-enhanced T1 MRC may be
limitedly helpful only when both 2D and 3D T2 MRC findings have poor imaging
quality with severe artifacts.
Our study has some limitations. First, our study population was relatively
small. Second, for biliary ductal visualization, we compared 3D images (3D T2
MRC and 3D contrast-enhanced T1 MRC) only with an established thick-slab
heavily T2-weighted method
[13,
14] and not with conventional
2D single-shot half-Fourier turbo spin-echo images. Usually, 2D T2 MRC may
include either a thick-slab method or thin single-shot half-Fourier turbo
spin-echo images. However, the addition of a thin-slice 2D T2 MRC sequence to
thickslice 2D T2 MRC would further increase the examination time for the 2D T2
MRC and may not be appropriate for our aim of evaluating the biliary
visualization of three comparable MR sequences.
In summary, we have shown that 3D T2 MRC significantly enables the best
visualization of all bile ducts, and 3D contrast-enhanced T1 MRC provides the
best image quality. For predicting the number of orifices as the ultimate goal
of the ductal visualization, the combined set of 2D and 3D T2 MRC enabled
better accuracy and diagnostic confidence than 2D T2 MRC alone and produced
comparable results to other combined sets. Therefore, we suggest the
combination sets of 2D T2 MRC and 3D T2 MRC for the preoperative biliary
anatomy evaluation of living liver donor candidates for right lobe
harvesting.
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