Impact of different ischemia times on biliary stricture after living donor liver transplantation with biliary atresia.


Journal

Liver transplantation : official publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society
ISSN: 1527-6473
Titre abrégé: Liver Transpl
Pays: United States
ID NLM: 100909185

Informations de publication

Date de publication:
01 06 2023
Historique:
received: 08 11 2022
accepted: 04 01 2023
medline: 19 5 2023
pubmed: 8 2 2023
entrez: 7 2 2023
Statut: ppublish

Résumé

Biliary atresia (BA) is the most common indication for pediatric liver transplantation, and biliary stricture (BS) remains an Achilles' heel for pediatric living donor liver transplantation (LDLT). We investigated the impact of different ischemia times on BS after LDLT in patients with BA. We retrospectively analyzed patients (<18 y) with BA who underwent LDLT between January 2016 and December 2020. Cases with hepatic artery thrombosis, bile leakage, early BS (<2 wk), and early death (<3 mo) were excluded. In all, 572 cases were included. A total of 26 cases (4.55%, 26/572) developed BS: 25 patients with anastomotic stricture and 1 patient with anastomotic stricture combined with left hepatic duct stricture. In addition, the time to diagnosis of BS ranged from 1.8 to 53.0 months (mean, 13.0 mo and median, 8.2 mo) after transplantation. A multivariate logistic regression analysis showed that arterial ischemia time (AIT), per 10 minutes (OR=1.222, 95% CI: 1.007-1.438, p =0.04) was the only independent risk factor for the development of BS after LDLT in patients with BA. What is more, the 5-year cumulative risk of BS between the AIT ≥40 minutes and AIT <40 minutes groups was 2.79% versus 10.57%. AIT was the only independent risk factor for the development of BS after LDLT with BA, and AIT ≥40 minutes would increase the 5-year cumulative risk of BS in our study. A shorter AIT, especially AIT <40 minutes, should be kept to decrease BS.

Identifiants

pubmed: 36748552
doi: 10.1097/LVT.0000000000000092
pii: 01445473-202306000-00008
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

607-617

Informations de copyright

Copyright © 2023 American Association for the Study of Liver Diseases.

Références

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Auteurs

Shengqiao Zhao (S)

First Central Clinical school, Tianjin Medical University, Tianjin, China.

Zhixin Zhang (Z)

First Central Clinical school, Tianjin Medical University, Tianjin, China.

Zhuyuan Si (Z)

First Central Clinical school, Tianjin Medical University, Tianjin, China.

Chong Dong (C)

First Central Clinical school, Tianjin Medical University, Tianjin, China.

Chao Sun (C)

Department of pediatric transplantation, Organ transplantation center, Tianjin Key Laboratory of organ transplantation, Tianjin First Central Hospital, Tianjin, China.

Kai Wang (K)

Department of pediatric transplantation, Organ transplantation center, Tianjin Key Laboratory of organ transplantation, Tianjin First Central Hospital, Tianjin, China.

Wei Zhang (W)

Department of pediatric transplantation, Organ transplantation center, Tianjin Key Laboratory of organ transplantation, Tianjin First Central Hospital, Tianjin, China.

Weiping Zheng (W)

Department of pediatric transplantation, Organ transplantation center, Tianjin Key Laboratory of organ transplantation, Tianjin First Central Hospital, Tianjin, China.

Xinzhe Wei (X)

Department of pediatric transplantation, Organ transplantation center, Tianjin Key Laboratory of organ transplantation, Tianjin First Central Hospital, Tianjin, China.

Wei Gao (W)

Department of pediatric transplantation, Organ transplantation center, Tianjin Key Laboratory of organ transplantation, Tianjin First Central Hospital, Tianjin, China.

Zhongyang Shen (Z)

Department of pediatric transplantation, Organ transplantation center, Tianjin Key Laboratory of organ transplantation, Tianjin First Central Hospital, Tianjin, China.

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