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AJR 2003; 181:467-474
© American Roentgen Ray Society


Vascular Complications After Living Related Liver Transplantation: Evaluation with Gadolinium-Enhanced Three-Dimensional MR Angiography

Bong Soo Kim1, Tae Kyoung Kim1, Dong Jin Jung1, Jung Hoon Kim1, In Young Bae1, Kyu-Bo Sung1, Pyo Nyun Kim1, Hyun Kwon Ha1, Sung Gyu Lee2 and Moon-Gyu Lee1

1 Department of Diagnostic Radiology, University of Ulsan, Asan Medical Center, 388-1 Poongnap-dong, Songpa-ku, Seoul, 138-736, Korea.
2 Department of Surgery, University of Ulsan, Asan Medical Center, Songpa-ku, Seoul, 138-736, Korea.

Received July 3, 2002; accepted after revision February 11, 2003.

 
Address correspondence to T. K. Kim.


Abstract
Top
Abstract
Introduction
Materials and Methods
Results
Discussion
References
 
OBJECTIVE. The purpose of this study was to evaluate the efficacy of gadolinium-enhanced three-dimensional (3D) MR angiography for detection of vascular complications in patients who have undergone living related liver transplantation.

MATERIALS AND METHODS. Seventy-six patients who underwent living related liver transplantation were evaluated with gadolinium-enhanced 3D MR angiography. All MR angiograms were assessed for patency of the hepatic artery and the portal vein using a four-point scale (grades I–IV). The results were correlated with conventional angiography (n = 23) and clinical follow-up with Doppler sonography (n = 53) for more than 6 months.

RESULTS. Seventy-three of 76 MR angiography procedures were technically adequate. When grades III (focal narrowing [> 50%] at the anastomotic site) and IV (abrupt cutoff at the anastomotic site with nonvisualization of the right [or left] hepatic artery distal to the anastomosis) were regarded as the diagnostic criteria for hepatic artery stenosis, the sensitivity, specificity, positive predictive value, negative predictive value, and accuracy of MR angiography were 100%, 74%, 29%, 100%, and 77%, respectively. In the portal vein, the sensitivity, specificity, positive predictive value, negative predictive value, and accuracy of MR angiography were 100%, 84%, 35%, 100%, and 85%, respectively, when grades III (narrowing [> 50%] without poststenotic dilatation) and IV (narrowing [> 50%] with poststenotic dilatation) were defined as criteria for portal vein stenosis.

CONCLUSION. MR angiography was sensitive but not specific in the detection of significant vascular stenosis after living related liver transplantation. However, normal MR angiography findings reliably exclude the possibility of significant stenosis.


Introduction
Top
Abstract
Introduction
Materials and Methods
Results
Discussion
References
 
Living related liver transplantation has recently been accepted as a realistic option for the treatment of end-stage liver disease in which harvesting of cadaver organs is limited [1, 2]. Advances in surgical techniques have contributed to the improved results of living related liver transplantation, which, however, has a high risk of vascular complications because of complex reconstruction of the hepatic artery and portal vein [35] (Fig. 1). Thus, a significant percentage of liver grafts is still lost from vascular complications after living related liver transplantation [611]. Early and accurate diagnosis of vascular complications is crucial for increasing the survival rate of the graft in living related liver transplantation because most stenoses or thromboses are treatable with interventional procedures. If untreated, many vascular complications may progress to severe hepatic failure or overwhelming biliary sepsis, resulting in graft failure. Recently, gadolinium-enhanced three-dimensional (3D) MR angiography has allowed assessment of the hepatic vasculature in patients who have undergone liver transplantation [12, 13]. However, the appropriate diagnostic criteria of MR angiography for diagnosing significant vascular abnormalities after living related liver transplantation are not yet known.



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Fig. 1. —Drawing shows living related liver transplant with right lobe graft. Three sites of vascular anastomosis are hepatic artery, portal vein, and hepatic vein.

 

The purpose of this study was to evaluate the efficacy of gadolinium-enhanced dual-phase 3D MR angiography for detecting vascular complications in patients who have undergone living related liver transplantation.


Materials and Methods
Top
Abstract
Introduction
Materials and Methods
Results
Discussion
References
 
Patient Population
From August 1994 to June 2000, 243 patients with cirrhosis underwent living related liver transplantation at our institution. Of these 243 patients, MR angiography was performed in 98 patients. Twenty-two of these 98 patients were excluded because follow-up clinical or radiology data were not available. Therefore, 76 patients were included in this study. The study group consisted of 62 men and 14 women from 18 to 62 years old (mean age, 44 years). The interval between living related liver transplantation and MR angiography was 7 days–23 months (mean, 32 days).

The results of conventional angiography and follow-up Doppler sonography and clinical findings (i.e., laboratory findings including liver function tests and physical examinations) were used as the standard of reference. Patients with negative findings on conventional angiography or with no evidence of vascular complications on follow-up clinical and Doppler sonography for at least 6 months were regarded as having no vascular complications.

MR Angiography
MR angiography was performed with a 1.5-T scanner (Magnetom Vision, Siemens, Erlangen, Germany). A phased array torso coil or body coil was used in all patients. At first, peak arterial enhancement time was calculated using a test bolus method. The test bolus injection was performed with 1 mL of gadopentetate dimeglumine (Magnevist, Berlex Laboratories, Wayne, NJ) followed by a 30-mL saline flush. Using a test bolus injection, we chose a single-level axial image that best showed the porta hepatis, and sequential axial images were obtained at 1-sec intervals until 30 sec from the start of the gadolinium injection. A region of interest was positioned in the aorta at this level, and a time–intensity curve was obtained to determine the peak arterial enhancement time and the optimal injection-to-scanning delay time. A scanning delay was calculated according to a method described by Prince et al. [14].

Three-dimensional MR angiography was performed in the coronal plane using fast imaging with a steady-state free precession sequence during end-inspiratory breath-holding. We used two different versions of the fast imaging with a steady-state free precession sequence during the study period. The parameters of contrast-enhanced 3D MR angiography were as follows: TR/TE, 5/2 or 4.6/1.8; section thickness, 3 or 3.5 mm; slab thickness, 96 or 112 mm; number of partitions, 24 or 32; matrix size, 150 x 256 or 200 x 512; field of view, 350 or 400 mm; and acquisition time, 19 or 23 sec. Thirty milliliters of gadopentetate dimeglumine were administered with an automatic power injector (MRS-50, Nemoto, Tokyo, Japan; or Spectris, Medrad, Pittsburgh, PA) at a rate of 4 mL/sec followed by a 10-mL saline flush. The arterial phase was obtained by subtracting the unenhanced image from the enhanced arterial image. The second phases were set with an interscan delay of 20 sec after the arterial phase to fit the portal venous and hepatic venous phases. Zero-filling along the z-axis was performed to obtain 64 reconstructed sections overlapping by 50%. The entire examination required approximately 40 min.

Conventional Angiography
Conventional angiography (n = 23) was performed within 1 week (mean, 3.5 days). Digital subtraction angiography was performed with a 5-French selective visceral catheter by means of a common femoral arterial approach. Selective catheterization of the celiac trunk and the superior mesenteric artery was performed with injection of nonionic contrast medium ([iopamidol] Iopamiro 300, Bracco, Milano, Italy; or [iopromide] Ultravist 300, Schering, Berlin, Germany). In some cases, a vasodilator was administered to improve visualization of the portal venous system.

Direct portography was performed in six patients. A branch of the right portal vein was punctured in four patients and a branch of the left portal vein in two with a 21-gauge needle under fluoroscopic guidance. The needle was exchanged for a 4-French coaxial dilator and a 6-French sheath combination included in the introducer system. Portal venograms were obtained, and the pressure was measured in the portal vein before and after the portal venous anastomosis.

Conventional angiography was performed only in selected patients who were suspected of having vascular complications on the basis of clinical features and MR angiography and Doppler sonography findings. Clinical features suggestive of vascular complications were as follows: hepatic failure with rapid clinical deterioration (n = 3); development of a delayed bile leak due to ischemic necrosis of bile ducts (n = 3); an unexplained persistent increase in liver enzymes and coagulopathy (n = 9); and signs and symptoms of portal hypertension, persistent ascites, or gastrointestinal hemorrhage from varices (n = 8). Serial Doppler sonography and clinical follow-up were also available for those patients who underwent conventional angiography.

Doppler Sonography and Clinical Follow-Up
The remaining 53 patients underwent serial Doppler sonography and clinical follow-up for at least 6 months. Doppler sonography was performed by experienced radiologists with a commercially available unit (HDI 3000, ATL, Bothell, WA; or Sequoia, Acuson, Mountain View, CA) and a probe with frequencies of 3–7 MHz. Gray-scale sonography, color Doppler sonography, and spectral Doppler sonography were performed in all patients. The hepatic artery and portal vein were examined for patency and characteristics of the spectral waveforms. Doppler sonography was usually performed every 1–2 months after MR angiography. Doppler sonography criteria for hepatic artery stenosis were a resistive index less than 0.5 and a systolic acceleration time greater than 0.08 sec within the intrahepatic arteries or a focal systolic velocity of more than 2 m/sec at the stenotic site of the hepatic artery [15]. Doppler sonography criteria for portal vein stenosis were at least three- or four-fold velocity gradients across the anastomosis [16, 17].

Image Analysis
All MR angiography images were retrospectively analyzed by two reviewers in consensus to assess the patency of the transplanted hepatic artery and portal vein. During the period of review, no information was provided by conventional angiography, follow-up data, or Doppler sonography. The MR angiograms were interpreted at a work-station by viewing raw data, reformatted images, maximum-intensity-projection images, and the axial T1- and T2-weighted sequences. Findings of the hepatic artery on MR angiography were classified as grade I, normal (Fig. 2A, 2B); grade II, visualization of right (or left) hepatic artery distal to the anastomosis with nonvisualization of peripheral branches; grade III, focal narrowing (> 50%) at the anastomotic site with visible right (or left) hepatic artery distal to the anastomosis; and grade IV, abrupt cutoff at the anastomotic site with nonvisualization of the right (or left) hepatic artery distal to the anastomosis. Portal vein findings were classified as grade I, normal (Fig. 2A, 2B); grade II, mild narrowing (< 50%); grade III, narrowing (> 50%) without poststenotic dilatation; and grade IV, narrowing (> 50%) with poststenotic dilatation. Poststenotic dilatation means a fusiform dilatation distal to the anastomotic site of the portal vein without thrombosis.



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Fig. 2A. —39-year-old man who underwent living related liver transplantation with right lobe graft. Maximum-intensity-projection (MIP) image from gadolinium-enhanced MR angiography shows normal transplanted hepatic artery (arrow). Observers interpreted hepatic artery at anastomotic site as grade I.

 


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Fig. 2B. —39-year-old man who underwent living related liver transplantation with right lobe graft. MIP image from gadolinium-enhanced MR angiography shows patent portal vein (arrow) at anastomotic site. Observers interpreted portal vein as grade I.

 

The conventional angiograms were reviewed for the presence or absence of stenosis. Stenoses were interpreted as substantial if narrowing of the diameter of the hepatic artery was greater than 50%. On direct portography, a gradient of more than 5 mm Hg was considered a significant stenosis at the anastomotic site.


Results
Top
Abstract
Introduction
Materials and Methods
Results
Discussion
References
 
Seventy-three MR angiography examinations (96%) were technically satisfactory. The three remaining examinations were inadequate because of excessive patient motion. Vascular complications were identified in 13 patients (18%) on conventional angiography. Hepatic artery stenosis was present in seven patients and portal vein stenosis, in six. Sixty-three patients had no vascular complications—that is, the findings on conventional angiography were negative in 10, and no evidence of vascular complications was present on Doppler sonography and at the clinical follow-up in 53 patients. The mean length of time for those patients who underwent serial Doppler sonography and clinical follow-up was 13 months. Among the 53 patients, 40 remained asymptomatic during the follow-up period. The others developed increased liver enzymes (n = 7), intermittent fever (n = 4), and abdominal pain (n = 2). In the seven patients with increased liver enzymes, acute rejection (n = 3), chronic rejection (n = 2), and recurrent hepatitis (n = 2) were proven at liver biopsy. In the four patients with intermittent fever, three had anastomotic stricture that required balloon dilatation, and the remaining patient had intraabdominal abscesses. In the two patients with abdominal pain, one had bile peritonitis with anastomotic leakage, and the other had intestinal obstruction caused by an adhesive band. All patients underwent Doppler sonography at least three times during the follow-up period (mean, 4.4). In the Doppler sonography and clinical follow-up group, 49 patients had normal findings on all Doppler sonograms. A tardus–parvus waveform within the intrahepatic arteries was seen in two examinations (one had a resistive index of 0.47 and a systolic acceleration time of 0.07 sec; the other had a resistive index of 0.49 and a systolic acceleration time of 0.06 sec) and a three-fold velocity gradient across the anastomosis of the portal vein was seen in two examinations. However, in all these patients, a normal waveform and a normal-ranged velocity were seen on follow-up of serial Doppler sonography.

We analyzed the MR angiography findings that were technically adequate in 73 patients. Observers classified the MR angiography findings for the hepatic artery in 39 patients (53%) as grade I, 10 (14%) as grade II, 19 (26%) as grade III, and five (7%) as grade IV. Three patients (3/19, 16%) who were classified as grade III (Fig. 3A, 3B) and four patients (4/5, 80%), as grade IV (Fig. 4A, 4B) had hepatic artery stenosis. All patients who were classified as grade IV on MR angiography did not actually have complete occlusion but had a stenosis visualized on conventional angiography. When grade IV alone was regarded as the diagnostic criterion for hepatic artery stenosis, the sensitivity, specificity, positive predictive value, negative predictive value, and accuracy of MR angiography were 57%, 99%, 80%, 96%, and 95%, respectively. When grades III and IV were defined as the diagnostic criteria for hepatic artery stenosis, the total number of lesions in the hepatic artery shown on MR angiography was 24, and the sensitivity, specificity, positive predictive value, negative predictive value, and accuracy of MR angiography were 100%, 74%, 29%, 100%, and 77%, respectively (Table 1). Among the seven false-positive cases from the 23 MR angiograms with correlative conventional angiography for the hepatic artery, a direct comparison of findings on MR angiography and conventional angiography confirmed the presence of surgical clips in three (Fig. 5A, 5B).



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Fig. 3A. —60-year-old man with hepatic artery stenosis after living related liver transplantation with left lobe graft. Maximum-intensity-projection image from gadolinium-enhanced MR angiography shows diffuse narrowing of hepatic artery (arrows) at anastomotic site. Observers interpreted hepatic artery as grade III.

 


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Fig. 3B. —60-year-old man with hepatic artery stenosis after living related liver transplantation with left lobe graft. Conventional hepatic angiogram shows hepatic arterial stenosis (arrows) at anastomotic site.

 


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Fig. 4A. —45-year-old man with hepatic arterial stenosis and pseudoaneurysm after living related liver transplantation with right lobe graft. Maximum-intensity-projection image from gadolinium-enhanced MR angiography shows abrupt cutoff of proper hepatic artery (arrow) just beyond its origin. Observers interpreted hepatic artery as grade IV.

 


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Fig. 4B. —45-year-old man with hepatic arterial stenosis and pseudoaneurysm after living related liver transplantation with right lobe graft. Conventional angiogram shows severe narrowing of hepatic artery (solid arrow) and pseudoaneurysm (open arrow) at anastomotic site.

 

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TABLE I MR Angiography Grade and the Number of Hepatic Artery Stenoses Confirmed on Conventional Angiography

 


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Fig. 5A. —40-year-old man who underwent living related liver transplantation with right lobe graft. Maximum-intensity-projection image from gadolinium-enhanced MR angiography shows focal signal loss (arrow) of hepatic artery at anastomotic site. Observers interpreted hepatic artery as grade III.

 


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Fig. 5B. —40-year-old man who underwent living related liver transplantation with right lobe graft. Conventional angiogram shows normal hepatic artery at anastomotic site. Note multiple surgical clips (arrow) adjacent to anastomosis.

 

Observers classified the MR angiography findings for the portal vein in 47 patients (64%) as grade I, nine (12%) as grade II, 12 (16%) as grade III, and five (7%) as grade IV. Three patients (3/12, 25%) with findings classified as grade III and three patients (3/5, 60%) with findings classified as grade IV (Fig. 6A, 6B) were found to have portal vein stenosis. When grades III and IV were defined as the diagnostic criteria for portal vein stenosis, the total number of lesions of the portal vein found on MR angiography was 17 (Table 2), and the sensitivity, specificity, positive predictive value, negative predictive value, and accuracy of MR angiography were 100%, 84%, 35%, 100%, and 85%, respectively.



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Fig. 6A. —41-year-old man with portal vein stenosis after living related liver transplantation with right lobe graft. Maximum-intensity-projection image from gadolinium-enhanced MR angiography shows severe narrowing (solid arrow) of portal vein with poststenotic dilatation. Observers interpreted portal vein as grade IV. Note dilated coronary vein (open arrow) due to portal hypertension.

 


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Fig. 6B. —41-year-old man with portal vein stenosis after living related liver transplantation with right lobe graft. Transhepatic portogram shows high-grade stenosis of portal vein and retrograde flow in coronary vein. Pressure gradient between prestenotic and poststenotic regions is 10 mm Hg. After balloon angioplasty and placement of Wallstent (Schneider, Minneapolis, MN, and Buelach, Switzerland), portal vein at anastomotic site is widely patent and pressure gradient across stenosis decreased to 1 mm Hg (not shown).

 

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TABLE 2 MR Angiography Grade and the Number of Portal Vein Stenoses Confirmed on Conventional Angiography

 

We also analyzed the overall results in 76 patients that included suboptimal examinations due to excessive patient motion. When grades III and IV were defined as the diagnostic criteria for hepatic artery stenosis, the sensitivity, specificity, positive predictive value, negative predictive value, and accuracy of MR angiography were 100%, 74%, 28%, 100%, and 76%, respectively. When grades III and IV were defined as the diagnostic criteria for portal vein stenosis, the sensitivity, specificity, positive predictive value, negative predictive value, and accuracy of MR angiography were 100%, 83%, 33%, 100%, and 84%, respectively.


Discussion
Top
Abstract
Introduction
Materials and Methods
Results
Discussion
References
 
Although surgical advances have contributed to the improved results of living related liver transplantation, vascular complications are still common. Hepatic artery thrombosis and stenosis are devastating complications after liver transplantation and can cause biliary necrosis and graft failure [10, 11, 18]. The incidence of hepatic artery thrombosis in several reports varies from 7.4% to 26%, with a higher incidence in pediatric transplantation [68, 10, 11]. Hepatic artery stenosis occurs in 5–11% of transplant recipients and generally occurs at the surgical anastomotic site within 3 months after transplantation [11]. Portal vein stenosis is uncommon, usually occurring at the anastomotic site in only 0.5–3.0% of recipients of transplants, and inferior vena cava complications occur in fewer than 1% [911]. In particular, living related liver transplant patients have a high risk of vascular complications for the hepatic artery and portal vein because of the complex vascular reconstruction required [1, 35, 19]. The detection of vascular complications is important because most stenoses or thromboses are frequently treatable with interventional procedures, but if untreated, many vascular complications may progress to graft failure [1012, 18, 20].

Gadolinium-enhanced 3D MR angiography has recently become an alternative means of accurate, noninvasive, and rapid evaluation for hepatic vascular disease because image quality can be improved with thinner sections and shorter TRs, resulting in a faster scanning time and fewer motion artifacts from incomplete breath-holding. Improved temporal resolution and repeated sequences after contrast administration allow optimal and separate enhancement of the arteries and veins [21]. A growing body of literature supports the accuracy of 3D MR angiography compared with that of conventional angiography. There has been good agreement between conventional angiography and gadolinium-enhanced 3D MR angiography for the depiction of arterial and venous abnormalities, despite some limitations in small intrahepatic arteries [22]. MR angiography has been reported to have excellent results in the detection of hemodynamically significant stenosis in the renal and aortoiliac arteries (> 50%), although other researchers have found that MR angiography does a poor job of revealing mild stenosis [23]. MR angiography shows a higher sensitivity and accuracy than conventional angiography for the detection of thrombosis or the assessment of vessel patency in any part of the portal venous system [24]. Glockner et al. [13] reported that all cases of hepatic artery and portal vein thrombosis after liver transplantation were detected on MR angiography with no false-positive or false-negative interpretations. The study by Glockner et al. showed that the sensitivity of MR angiography for moderate to severe arterial stenosis after liver transplantation was 86%, with one false-negative and three false-positive interpretations and that there was a discrepancy in estimating the degree of stenosis.

In our study, we evaluated the utility of the criteria for detection of hepatic artery and portal vein stenoses in recipients who underwent living related liver transplantation. Our results indicate that gadolinium-enhanced 3D MR angiography is technically accessible and useful for the evaluation of vascular complications after living related liver transplantation. When an abrupt cutoff at the anastomotic site with nonvisualization of the right (or left) hepatic artery distal to the anastomosis was regarded as the diagnostic criterion for hepatic artery stenosis, the sensitivity and specificity of MR angiography were 57% and 99%, respectively. This finding may have been related to the small amount of contrast material flowing into the intrahepatic artery through the stenosis at the anastomotic site. When the diagnostic criteria for hepatic artery stenosis included focal narrowing at the anastomotic site with visible intrahepatic artery and abrupt cutoff at the anastomotic site with nonvisualization of the intrahepatic artery, we achieved 100% sensitivity and 74% specificity. The results of our study indicate that MR angiography tends to overestimate hepatic artery stenosis. This fact might be explained by the following factors. First, the susceptibility artifact from the surgical clips adjacent to the hepatic arterial anastomotic site creates focal signal loss of the hepatic artery, mimicking stenosis. Second, low-flow states can play an important role in creating false-positive findings of arterial disease. Low-flow states are caused by the inflow of small amounts of contrast material into the intrahepatic artery due to elevated end-organ resistance (i.e., recent transplanted edematous liver, graft rejection) or a decrease of systemic (i.e., systemic hypotension) or localized (i.e., splenic artery steal) blood volume [25]. Third, because of the small size of the lobar hepatic artery in living related liver transplantation grafts, subtle vascular signals could not be distinguished from background signals in a small vessel, thereby producing an overestimation of the amount of stenosis [26]. Therefore, we suggest that this MR angiography finding should be assessed together with the patient's clinical course, the natural history of the hepatic artery stenosis, and Doppler sonography findings before considering conventional angiography.

When narrowing (> 50%) of the portal vein was regarded as the diagnostic criterion for portal vein stenosis, we achieved 100% sensitivity and 84% specificity. MR angiography clearly depicts anastomotic narrowing of the portal vein. In addition, MR angiography may be performed to evaluate the extent and degree of the portosystemic collateral vessels resulting from portal hypertension. Our results show high sensitivity and specificity in the detection of more than 50% of the portal vein stenoses. However, we found a high false-positive rate with the results of portal vein stenosis. For this reason, it is important that a diagnosis of portal vein stenosis correlate with both the clinical findings and Doppler sonography. Most cases of portal vein stenosis are accompanied by symptoms of portal hypertension—that is, varices, upper gastrointestinal hemorrhage, splenomegaly, massive ascites, hepatic failure, and intestinal swelling [11]. It is important that the criteria used in Doppler sonography to identify patients with portal vein stenosis are direct gray-scale sonography depictions of portal vein narrowing in diameter and an acceleration of flow at the stricture (> 3–4 times the peak velocity of the nonstenotic portion) on Doppler sonography. In our study, patients with poststenotic dilatation on MR angiography had fewer false-positive findings than those without poststenotic dilatation. This fact suggests that poststenotic dilatation of the portal vein is caused by turbulent flow immediately distal to the stenosis because of long-standing severe stenosis.

Multidetector CT permits a more rapid acquisition of thinly collimated images than is possible with conventional CT. In addition, the high quality of 3D images can be obtained with volume data. In this regard, the use of 3D images and narrow collimation of section thickness will provide more valuable information about the vascular structure of the transplanted liver and allow detailed examination of the liver parenchyma and extrahepatic tissues. Multiplanar CT has been used to show the dilated pancreatic duct and common bile duct, but the normal or minimally dilated duct may not be visualized [27]. Although nonionic contrast agents have been used to opacify the minimally dilated biliary tree, their use is associated with an increased iodine load in patients [28].

MR imaging combined with MR cholangiography and MR angiography can be an effective diagnostic method in the postoperative workup of a patient who has undergone liver transplantation; provide a more comprehensive evaluation of the transplanted liver; reveal abnormalities of vascular structure; and depict bile ducts, liver parenchyma, and extrahepatic tissues. An important advantage of MR imaging is the low toxicity of its contrast agents; hence, MR angiography can be used, particularly in patients with renal insufficiency. Finally, the amount of radiation exposure associated with an imaging technique must be considered, particularly in young patients, when selecting an imaging modality for a patient who has undergone liver transplantation.

We recognize that our study has specific limitations. First, the definitive proof of patency or stenoses on conventional angiography was not obtained in all patients. Although normal findings on Doppler sonography do not entirely exclude vascular abnormalities because the clinical scenario evolves and the patients return for repeated Doppler sonography of the transplanted liver, it may become apparent that a more definitive diagnostic evaluation of the hepatic arterial system and the portal venous system should be undertaken. Therefore, negative findings on serial Doppler sonography and the absence of clinical symptoms during the follow-up period might prompt us to regard these patients as not having any hemodynamically significant vascular abnormalities. Second, our study was retrospective. We think that further prospective, blinded studies will be needed to determine the applied sensitivity and specificity of the discriminatory criteria selected in the retrospective review. Third, 30 mL of gadopentetate dimeglumine might be insufficient, resulting in the high number of false-positive findings. Using higher doses of IV contrast material may improve vascular signal intensity and diagnostic image quality in low-flow states and deserves further investigation. Fourth, the use of a 4-mL/sec rate with a 10-mL saline flush in our study might be less effective for imaging of the portal venous system. The use of a lower volume rate (2 mL/sec) with a larger volume (> 30 mL) of saline flush might have improved the portal venous phase images [29].

Assessment of the clinical course and Doppler sonography are the first steps for evaluation of vascular complications in patients who have undergone liver transplantation in most hospitals. We suggest a new algorithm using MR angiography that has a high sensitivity and an excellent negative predictive value for the detection of clinically significant vascular stenosis: If a patient has both normal Doppler sonography and clinical findings, a simple follow-up is required. If a patient has both abnormal Doppler sonography and abnormal clinical findings, conventional angiography is recommended. MR angiography is useful and rules out the possibility of vascular complications when Doppler sonography and clinical findings are discordant (Fig. 7).



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Fig. 7. —Diagram of algorithm for evaluation of vascular complications after living related liver transplantation shows that MR angiography is useful when Doppler sonography and clinical findings are discordant.

 

In conclusion, gadolinium-enhanced 3D MR angiography can be a useful, noninvasive technique for evaluating vascular complications in patients who have undergone living related liver transplantation. MR angiography was sensitive but not specific for detection of clinically significant stenosis after living related liver transplantation. However, normal MR angiography findings reliably exclude the possibility of stenosis.


Acknowledgments
 
We thank Bonnie Hami, Department of Radiology, University Hospitals Health System, Cleveland, OH, for editorial assistance in preparing this manuscript.


References
Top
Abstract
Introduction
Materials and Methods
Results
Discussion
References
 

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