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26 - World Journal of Gastroenterology

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Li GL et al . Biliary complications in rat liver transplantation<br />

Table 1 Incidence rates <strong>of</strong> biliary complications in different groups<br />

Groups n Abscess Sludge EBD IBD Total<br />

Group A 41.7% e (25/60)<br />

A1 30 <strong>26</strong>.70% (8/30) 13.30% (4/30) <strong>26</strong>.70% (8/30) 13.30% (4/30) 33.30% (10/30)<br />

A2 30 43.30% (13/30) 20% (6/30) <strong>26</strong>.70% (8/30) 10% (3/30) 50% a (15/30)<br />

Group B 32.50% (13/40)<br />

B1 10 10% (1/10) 0 30% (3/10) 0 30% (3/10)<br />

B2 10 10% (1/10) 0 20% (2/10) 10% (1/10) 20% (2/10)<br />

B3 10 30% (3/10) 20% (2/10) 40% (4/10) 10% (1/10) 50% c (5/10)<br />

B4 10 20% (2/10) 10% (1/10) 30% (3/10) 10%t (1/10) 30% (3/10)<br />

Group C 5 0 0 0 0 0 0<br />

Total 105 <strong>26</strong>.70% (28/105) 12.40% (13/105) <strong>26</strong>.70% (28/105) 9.52% (10/105) 36.20% (38/105)<br />

Some rats had two (or more) kinds <strong>of</strong> biliary complications at the same time. a P < 0.05 vs A1; c P < 0.05 vs B1, B2 and B4; e P < 0.05 vs groups B and C EBD:<br />

Extrahepatic biliary dilatation; IBD: Intrahepatic biliary dilatation.<br />

between the control and the experimental groups were<br />

analyzed using analysis <strong>of</strong> variance. P < 0.05 was considered<br />

statistically significant.<br />

RESULTS<br />

Operation time and success rate<br />

In transplantation groups, the anhepatic phase was 13.7<br />

± 1.06 min, and cold ischemia time was 50.5 ± 8.6 min.<br />

There was no significant difference between A1 and A2 in<br />

operating time (P > 0.05). And the time for biliary reconstruction<br />

was almost the same among all groups (P > 0.05).<br />

Recipients surviving at least 24 h were considered as<br />

success. The success rate <strong>of</strong> ROLT was 98.3% (59/60).<br />

Only one case in A1 died from bleeding at SHIVC 8 h after<br />

operation.<br />

Biliary complications<br />

The incidence rate <strong>of</strong> biliary complications was 41.7% in<br />

Group A, which was much higher than that in Group B<br />

(32.5%) and Group C (0%), with significant differences<br />

among the three groups (P < 0.05). After transplantation,<br />

A2 had a higher incidence <strong>of</strong> biliary complications than<br />

A1 (50% vs 33.3%, P < 0.05). B3 had the highest incidence<br />

<strong>of</strong> biliary complications among the groups without<br />

orthotopic liver transplantation (P < 0.05). No biliary<br />

complication was found in the sham-operation group.<br />

General observation<br />

The color <strong>of</strong> urine turned yellow in the rats with biliary<br />

complications. Other complications were dried hair, reaction<br />

retardation, reduced appetite and activities, and eye<br />

bleeding in some rats.<br />

Gross anatomy<br />

Biliary complications consisted <strong>of</strong> abscess, intrahepatic and<br />

extrahepatic biliary dilatation and biliary sludge. Abscess<br />

(35%) was most frequently seen in Group A, compared<br />

with dilatation <strong>of</strong> extrahepatic bile duct (25%) in Group<br />

B. B3 had the highest incidence <strong>of</strong> biliary complications in<br />

non-transplantation groups (50% vs 30%, 20% and 30% )<br />

and extrahepatic biliary dilatation and abscess were two <strong>of</strong><br />

the most important complications in this group (Table 1).<br />

WJG|www.wjgnet.com<br />

Histopathology<br />

In the samples with biliary complications, infiltration <strong>of</strong> a<br />

large number <strong>of</strong> mononuclear cells in the portal area was<br />

the most common change, followed by dilatation <strong>of</strong> bile<br />

ducts. Cellular infiltration <strong>of</strong> biliary wall and degeneration<br />

<strong>of</strong> epithelial cells, dilatation <strong>of</strong> the central vein could also<br />

be seen. Some samples even showed vacuolar degeneration,<br />

necrosis and fibrous tissue hyperplasia. In samples<br />

with severe biliary dilatation, the normal bile duct structure<br />

had completely disappeared, with a large number <strong>of</strong> infiltrated<br />

inflammatory cells.<br />

Serology<br />

The serum levels <strong>of</strong> AST, ALT, TBIL, DBIL, GGT and<br />

ALP in Group A and Group B were significantly higher<br />

than in Group C, particularly AST and TBIL, with significant<br />

difference among the three groups (P < 0.05). Significant<br />

difference could be easily observed between ductduodenum<br />

reconstruction groups and duct-duct reconstruction<br />

groups (A2 vs A1, B3 vs B1, and B4 vs B2, P <<br />

0.05). Among non-transplantation groups, the serological<br />

changes, especially the bilirubin level, were more remarkable<br />

in groups with hepatic artery ligation than in those<br />

without (B1 vs B2 and B3 vs B4, P < 0.05) (Table 2).<br />

DISCUSSION<br />

Biliary complication is the second most common cause <strong>of</strong><br />

graft dysfunction in liver transplantation with an incidence<br />

rate <strong>of</strong> as high as 64% [1-9] . Biliary complications may be<br />

related to various factors, including hepatic artery thrombosis<br />

or stenosis, technical reasons, as well as ischemia-reperfusion<br />

injury and immunological injury. High incidence<br />

<strong>of</strong> biliary complication has made biliary reconstruction the<br />

“Achilles heel” <strong>of</strong> liver transplantation.<br />

It has been proved that hepatic artery plays an important<br />

role in blood supply <strong>of</strong> bile duct, the artery must be<br />

reconstructed when injured or cut during operation. In the<br />

early 90s, Engermann et al [12] showed that reconstruction<br />

<strong>of</strong> the hepatic artery can significantly reduce the incidence<br />

<strong>of</strong> biliary complications such as biliary fistula and biliary<br />

obstruction after ROLT. But with the cuff method introduced<br />

in 1973, ROLT without hepatic artery (HA) recon-<br />

3142 July 14, 2011|Volume 17|Issue <strong>26</strong>|

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