Beyond the Pediatric end-stage liver disease system: Solutions for infants with biliary atresia requiring liver transplant

doi:10.3748/wjg.v20.i32.11062

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Aug 28, 2014 (publication date) through Nov 8, 2024

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World Journal of Gastroenterology

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1007-9327

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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA

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World J Gastroenterol. Aug 28, 2014; 20(32): 11062-11068
Published online Aug 28, 2014. doi: 10.3748/wjg.v20.i32.11062

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Figure 1 Diagram of split liver transplant. The left lateral segment is donated to a child and the right trisegmental graft is designated for an adult.

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Figure 2 Outcomes in the current era of biliary atresia and ways to improve patient outcomes. KP: Kasai portoenterostomy; NLS: Native liver survival; LT: Liver transplant; LRD: Living related donor; ILT: Incompatible donor liver transplant.

Citation: Tessier MEM, Harpavat S, Shepherd RW, Hiremath GS, Brandt ML, Fisher A, Goss JA. Beyond the Pediatric end-stage liver disease system: Solutions for infants with biliary atresia requiring liver transplant. World J Gastroenterol 2014; 20(32): 11062-11068
URL: https://www.wjgnet.com/1007-9327/full/v20/i32/11062.htm
DOI: https://dx.doi.org/10.3748/wjg.v20.i32.11062