Progress in living donor liver transplantation for biliary atresia and challenges faced: A thirty-year single institutional experience.

ABO incompatible transplants Adult Biliary atresia (BA) Kasai's portoenterostomy (KP) Living donor liver transplantation (LDLT) Retransplantation

Journal

Journal of pediatric surgery
ISSN: 1531-5037
Titre abrégé: J Pediatr Surg
Pays: United States
ID NLM: 0052631

Informations de publication

Date de publication:
Nov 2022
Historique:
received: 01 12 2021
revised: 28 02 2022
accepted: 09 03 2022
pubmed: 9 4 2022
medline: 19 10 2022
entrez: 8 4 2022
Statut: ppublish

Résumé

Biliary atresia (BA) is the most common indication for liver transplantation in the pediatric population, and living donor liver transplantation (LDLT) and deceased donor liver transplantation (DDLT) have been established as a radical treatment for BA .The aim of this study was to clarify the long term outcomes and risk factors affecting the LDLT outcomes, as well as the challenges faced. Between 1990 and 2019, 666 BA patients underwent LDLT in our institution and were enrolled in this study. Data regarding the recipient's age, anatomic findings of the biliary tree at Kasai's portoenterostomy, basic characteristics at transplantation, transplant profiles, donor characteristics, and outcomes of LDLT were analyzed. The 1-, 5-, 10-, 15-, 20-, and 25-year graft survival rates of BA patients who underwent LDLT were 88.1%, 85.4%, 81.5%, 78.9%, 76.6%, and 75.5%, respectively. The transplant era, age at transplantation, ABO incompatible transplant, and presence of pulmonary vascular complications were identified as significant risk factors for overall graft survival. When the study period was divided into the first (1990-1999) and second (2000-2019) phases and re analyzed, the outcomes of ABO-incompatible transplants and LDLT for adult BA patients remained inferior to others in the second phase. The 20-year graft survival rate in patients who underwent re transplantation in the second phase was 54.2%. The outcomes of LDLT in children are generally good, but the immunosuppression procedures need to be further improved for ABO-incompatible cases in the future. Further improvements in LDLT results for adult patients and re transplantation remain challenges to be addressed in this field, and future attempts, including revision to the organ allocation system of deceased donors, are necessary. Level III (case control study).

Sections du résumé

BACKGROUND BACKGROUND
Biliary atresia (BA) is the most common indication for liver transplantation in the pediatric population, and living donor liver transplantation (LDLT) and deceased donor liver transplantation (DDLT) have been established as a radical treatment for BA .The aim of this study was to clarify the long term outcomes and risk factors affecting the LDLT outcomes, as well as the challenges faced.
METHODS METHODS
Between 1990 and 2019, 666 BA patients underwent LDLT in our institution and were enrolled in this study. Data regarding the recipient's age, anatomic findings of the biliary tree at Kasai's portoenterostomy, basic characteristics at transplantation, transplant profiles, donor characteristics, and outcomes of LDLT were analyzed.
RESULTS RESULTS
The 1-, 5-, 10-, 15-, 20-, and 25-year graft survival rates of BA patients who underwent LDLT were 88.1%, 85.4%, 81.5%, 78.9%, 76.6%, and 75.5%, respectively. The transplant era, age at transplantation, ABO incompatible transplant, and presence of pulmonary vascular complications were identified as significant risk factors for overall graft survival. When the study period was divided into the first (1990-1999) and second (2000-2019) phases and re analyzed, the outcomes of ABO-incompatible transplants and LDLT for adult BA patients remained inferior to others in the second phase. The 20-year graft survival rate in patients who underwent re transplantation in the second phase was 54.2%.
CONCLUSIONS CONCLUSIONS
The outcomes of LDLT in children are generally good, but the immunosuppression procedures need to be further improved for ABO-incompatible cases in the future. Further improvements in LDLT results for adult patients and re transplantation remain challenges to be addressed in this field, and future attempts, including revision to the organ allocation system of deceased donors, are necessary.
LEVEL OF EVIDENCE METHODS
Level III (case control study).

Identifiants

pubmed: 35393118
pii: S0022-3468(22)00216-0
doi: 10.1016/j.jpedsurg.2022.03.009
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

649-655

Informations de copyright

Copyright © 2022. Published by Elsevier Inc.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare no conflicts of interest in association with the present study.

Auteurs

Tatsuya Okamoto (T)

Department of Surgery, Graduate School of Medicine, Kyoto University, Kyoto 606-8507, Japan. Electronic address: okamotot@kuhp.kyoto-u.ac.jp.

Hideaki Okajima (H)

Department of Surgery, Graduate School of Medicine, Kyoto University, Kyoto 606-8507, Japan; Department of Pediatric Surgery, Kanazawa Medical University, Kanazawa, Japan.

Eri Ogawa (E)

Department of Surgery, Graduate School of Medicine, Kyoto University, Kyoto 606-8507, Japan.

Mari Sonoda (M)

Department of Surgery, Graduate School of Medicine, Kyoto University, Kyoto 606-8507, Japan.

Elena Yukie Uebayashi (EY)

Department of Surgery, Graduate School of Medicine, Kyoto University, Kyoto 606-8507, Japan.

Takashi Ito (T)

Department of Surgery, Graduate School of Medicine, Kyoto University, Kyoto 606-8507, Japan.

Satoru Seo (S)

Department of Surgery, Graduate School of Medicine, Kyoto University, Kyoto 606-8507, Japan.

Koichiro Hata (K)

Department of Surgery, Graduate School of Medicine, Kyoto University, Kyoto 606-8507, Japan.

Toshihiko Masui (T)

Department of Surgery, Graduate School of Medicine, Kyoto University, Kyoto 606-8507, Japan.

Kojiro Taura (K)

Department of Surgery, Graduate School of Medicine, Kyoto University, Kyoto 606-8507, Japan.

Shinji Uemoto (S)

Shiga University of Medical Science, Otsu, Japan.

Etsurou Hatano (E)

Department of Surgery, Graduate School of Medicine, Kyoto University, Kyoto 606-8507, Japan.

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