Choledochoduodenostomy in pediatric liver transplantation
Article first published online: 9 JAN 2011
© 2011 John Wiley & Sons A/S
Volume 15, Issue 3, pages 237–239, May 2011
How to Cite
Campsen, J., Zimmerman, M. A., Narkewicz, M. R., Sokol, R. J., Mandell, M. S., Kam, I., Dovel, D. and Karrer, F. M. (2011), Choledochoduodenostomy in pediatric liver transplantation. Pediatric Transplantation, 15: 237–239. doi: 10.1111/j.1399-3046.2010.01338.x
- Issue published online: 15 APR 2011
- Article first published online: 9 JAN 2011
- Accepted for publication 2 April 2010
- pediatric liver transplant;
- Roux-en-Y choledochojejunostomy;
- biliary reconstruction;
Campsen J, Zimmerman MA, Narkewicz MR, Sokol RJ, Mandell MS, Kam I, Dovel D, Karrer FM. Choledochoduodenostomy in pediatric liver transplantation. Pediatr Transplantation 2011: 15: 237–239. © 2011 John Wiley & Sons A/S.
Abstract: Reconstruction of the bile ducts during pediatric liver transplantation is generally performed by a Roux-en-Y CDJ because direct duct-to-duct anastomosis CC is often not possible. Anastomosis of the donor liver bile duct to the duodenum CDD provides another option. We provide preliminary evidence that CDD is an alternative technique for biliary reconstruction when CC is not possible in pediatric liver transplant recipients that have a hostile abdomen or to preserve bowel length.
Methods: From 2007 to 2008, a total of 19 pediatric cadaveric liver transplants were performed at our center. Four of the 19 had a bile duct reconstruction by CDD.
Results: CDD reconstruction was used in patients who received a liver transplant for a diagnosis of PSC, congenital hepatic fibrosis, biliary atresia, and Alagille syndrome. The ages of the patients were 17 and 10 yr and 10 and 17 months. Three grafts were whole cadaveric livers, and one was a reduced left lobe. CDD was used to revise a prior anastomosis in one patient who had a previous Roux-en-Y that was unusable during the retransplant, and another to repair a stricture in a second patient with a CC. We also performed a CDD in a patient with a hostile abdomen from previous surgery, and another patient to avoid short gut syndrome that a Roux-en-Y may have created. All patients are alive with functioning grafts with a follow-up of at least one yr. None of the patients developed clinically significant biliary complications (leak, stricture, cholangitis).
Conclusion: Our preliminary experience suggests that CDD is an option for biliary reconstruction in pediatric transplant patients with hostile abdomens or to preserve bowel length.