Ann Liver Transplant.  2022 May;2(1):43-47. 10.52604/alt.21.0033.

Liver transplantation for young adult patients with post-Kasai portoenterostomy biliary atresia: Analysis of Korean Organ Transplantation Registry database

Affiliations
  • 1Department of Surgery, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea
  • 2Department of Surgery, Yonsei University College of Medicine, Seoul, Korea
  • 3Department of Surgery, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Korea
  • 4Department of Surgery, Korea University College of Medicine, Seoul, Korea
  • 5Department of Surgery, Ulsan University Hospital, University of Ulsan College of Medicine, Ulsan, Korea
  • 6Department of Surgery, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea

Abstract

Background
Some young adults with native liver after Kasai portoenterostomy (KPE) for biliary atresia (BA) have a long survival period. However, a considerable number of them finally require liver transplantation (LT) due to various BA-associated complications. This study aimed to analyze the outcomes of LT in adult patients with post-KPE BA using Korea Organ Transplantation Registry (KOTRY) database.
Methods
This study was a retrospective analysis of multi-center data using KOTRY database, including 14 adult patients who underwent LT in six institutions during a 7-year period from January 2014 to December 2020.
Results
All 14 patients underwent KPE at around 1 year of age. The mean ages at LT were 25.0±5.9 years. The mean model for end-stage liver disease score was 13.5±4.6. The main reasons for LT were advanced liver cirrhosis in nine and intractable cholangitis in five. All patients received living-donor LT. The mean graft-to-recipient body weight ratio was 1.21%±0.31%. All 14 patients are currently alive during the mean follow-up period of 32.3±17.1 months. Adult BA patients were being cared for by pediatric gastroenterologists in 3 institutions, by adult gastroenterologists in 1 institution, and undetermined in 2 institutions.
Conclusion
Young adult patients with BA are a unique group of patients requiring specialist care during the transition from pediatric to adult services. Living donor LT has been the main type of LT for these patients because of donor shortage in Korea. Similar to our previous single-center study, in the present study, LT outcomes in young adult BA patients were excellent. Therefore, LT should be considered in patients showing serious BA-associated complications.

Keyword

Portal hypertension; Cholangitis; Liver cirrhosis; Portoenterostomy; Adolescent

Reference

1. Livesey E, Cortina Borja M, Sharif K, Alizai N, McClean P, Kelly D, et al. 2009; Epidemiology of biliary atresia in England and Wales (1999-2006). Arch Dis Child Fetal Neonatal Ed. 94:F451–F455. DOI: 10.1136/adc.2009.159780. PMID: 19457876.
2. Davenport M, Ong E, Sharif K, Alizai N, McClean P, Hadzic N, et al. 2011; Biliary atresia in England and Wales: results of centralization and new benchmark. J Pediatr Surg. 46:1689–1694. DOI: 10.1016/j.jpedsurg.2011.04.013. PMID: 21929975.
3. Bijl EJ, Bharwani KD, Houwen RH, de Man RA. 2013; The long-term outcome of the Kasai operation in patients with biliary atresia: a systematic review. Neth J Med. 71:170–173.
4. Lykavieris P, Chardot C, Sokhn M, Gauthier F, Valayer J, Bernard O. 2005; Outcome in adulthood of biliary atresia: a study of 63 patients who survived for over 20 years with their native liver. Hepatology. 41:366–371. DOI: 10.1002/hep.20547. PMID: 15660386.
5. Namgoong JM, Hwang S, Ahn CS, Moon DB, Ha TY, Song GW, et al. 2021; Indications and outcomes of liver transplantation for post-Kasai biliary atresia in young adults. Korean J Transplant. 35:177–182. DOI: 10.4285/kjt.21.0018.
6. Hsu EK, Mazariegos GV. 2017; Global lessons in graft type and pediatric liver allocation: a path toward improving outcomes and eliminating wait-list mortality. Liver Transpl. 23:86–95. DOI: 10.1002/lt.24646. PMID: 27706890. PMCID: PMC6767049.
7. Sasaki H, Tanaka H, Wada M, Kazama T, Nakamura M, Kudo H, et al. 2016; Analysis of the prognostic factors of long-term native liver survival in survivors of biliary atresia. Pediatr Surg Int. 32:839–843. DOI: 10.1007/s00383-016-3934-x. PMID: 27464487.
8. Samyn M, Davenport M, Jain V, Hadzic N, Joshi D, Heneghan M, et al. 2019; Young people with biliary atresia requiring liver transplantation: a distinct population requiring specialist care. Transplantation. 103:e99–e107. DOI: 10.1097/TP.0000000000002553. PMID: 30461724.
9. Nio M, Sano N, Ishii T, Sasaki H, Hayashi Y, Ohi R. 2004; Cholangitis as a late complication in long-term survivors after surgery for biliary atresia. J Pediatr Surg. 39:1797–1799. DOI: 10.1016/j.jpedsurg.2004.08.021. PMID: 15616933.
10. Kyoden Y, Tamura S, Sugawara Y, Yamashiki N, Matsui Y, Togashi J, et al. 2008; Outcome of living donor liver transplantation for post-Kasai biliary atresia in adults. Liver Transpl. 14:186–192. DOI: 10.1002/lt.21344. PMID: 18236393.
11. Kumagi T, Drenth JP, Guttman O, Ng V, Lilly L, Therapondos G, et al. 2012; Biliary atresia and survival into adulthood without transplantation: a collaborative multicentre clinic review. Liver Int. 32:510–518. DOI: 10.1111/j.1478-3231.2011.02668.x. PMID: 22098694.
12. Uchida Y, Kasahara M, Egawa H, Takada Y, Ogawa K, Ogura Y, et al. 2006; Long-term outcome of adult-to-adult living donor liver transplantation for post-Kasai biliary atresia. Am J Transplant. 6:2443–2448. DOI: 10.1111/j.1600-6143.2006.01487.x. PMID: 16889600.
13. Kang SH, Hwang S, Ahn CS, Kim KH, Moon DB, Ha TY, et al. 2020; Changes in the indications for living donor liver transplantation: single-institution experience of 3,145 cases over 10 years. Korean J Transplant. 34:47–54. DOI: 10.4285/kjt.2020.34.1.47.
14. Ha HS, Hong JJ, Kim IO, Lee SR, Lee AY, Ha TY, et al. 2019; Deceased donor liver transplantation under the Korean model for end-stage liver disease score-based liver allocation system: 2-year allocation results at a high-volume transplantation center. Korean J Transplant. 33:112–117. DOI: 10.4285/jkstn.2019.33.4.112.
15. Park HS, Lee JM, Hong K, Han ES, Hong SK, Choi Y, et al. 2021; Impact of model for end-stage liver disease allocation system on outcomes of deceased donor liver transplantation: a single-center experience. Ann Hepatobiliary Pancreat Surg. 25:336–341. DOI: 10.14701/ahbps.2021.25.3.336. PMID: 34402433. PMCID: PMC8382855.
16. Namgoong JM, Hwang S, Kim DY, Ha TY, Song GW, Jung DH, et al. 2020; Whole liver deceased donor liver transplantation for pediatric recipients: single-center experience for 20 years. Korean J Transplant. 34:249–256. DOI: 10.4285/kjt.20.0036.
17. Namgoong JM, Hwang S, Ahn CS, Kim KH, Moon DB, Ha TY, et al. 2020; Korea-nationwide incidence of pediatric deceased donors and single-institutional status of liver transplantation using pediatric donor liver grafts. Korean J Transplant. 34:178–184. DOI: 10.4285/kjt.2020.34.3.178.
18. Bae SK, Akamatsu N, Togashi J, Ichida A, Kawahara T, Maki H, et al. 2019; Hepatitis B virus recurrence after living donor liver transplantation of anti-HBc-positive grafts: a 22-year experience at a single center. Biosci Trends. 13:448–455. DOI: 10.5582/bst.2019.01283. PMID: 31666441.
19. Cholongitas E, Papatheodoridis GV, Burroughs AK. 2010; Liver grafts from anti-hepatitis B core positive donors: a systematic review. J Hepatol. 52:272–279. DOI: 10.1016/j.jhep.2009.11.009. PMID: 20034693.
20. Wong TC, Fung JY, Cui TY, Lam AH, Dai JW, Chan AC, et al. 2019; Liver transplantation using hepatitis B core positive grafts with antiviral monotherapy prophylaxis. J Hepatol. 70:1114–1122. DOI: 10.1016/j.jhep.2019.03.003. PMID: 30871981.
21. Suehiro T, Shimada M, Kishikawa K, Shimura T, Soejima Y, Yoshizumi T, et al. 2005; Prevention of hepatitis B virus infection from hepatitis B core antibody-positive donor graft using hepatitis B immune globulin and lamivudine in living donor liver transplantation. Liver Int. 25:1169–1174. DOI: 10.1111/j.1478-3231.2005.01165.x. PMID: 16343068.
Full Text Links
  • ALT
Actions
Cited
CITED
export Copy
Close
Share
  • Twitter
  • Facebook
Similar articles
Copyright © 2025 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr