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Trends in liver transplantation for primary sclerosing cholangitis.

Authors :
Morelli, Maria Cristina
Gambato, Martina
Martini, Silvia
Carrai, Paola
Toniutto, Pierluigi
Giannelli, Valerio
Donato, Francesca
Lenci, Ilaria
Pasulo, Luisa
Mazzarelli, Chiara
Ferrarese, Alberto
Rendina, Maria
Grieco, Antonio
Lanza, Alfonso Galeota
Baroni, Gianluca Svegliati
De Maria, Nicola
Marenco, Simona
Mameli, Laura
Ponziani, Francesca Romana
Vitale, Giovanni
Source :
Digestive & Liver Disease; Aug2024, Vol. 56 Issue 8, p1343-1349, 7p
Publication Year :
2024

Abstract

Primary sclerosing cholangitis is a cholestatic disease with a low prevalence in Italy. Indications for liver transplantation and the time of listing are not stated. We performed a national survey to investigate the listing criteria, comorbidities, and outcomes. In April 2022, we surveyed liver transplantation in primary sclerosing cholangitis nationwide for the last 15 years. From 2007 to 2021, 445 patients were included on waiting lists, and 411 had undergone liver transplants. The median age at transplantation was 46 years (males 63.9%); 262 patients (59%) presented an inflammatory bowel disease. Transplants increased over the years, from 1.8 % in 2007 to 3.0 % in 2021. Cholangitis (51%) and hepatic decompensation (45%) were the main indications for listing. The disease recurred in 81 patients (20%). Patient survival after the first transplant was 94 %, 86% and 84% at one, five, and ten years. Twenty-four died in the first year (50% surgical complications, 25% infections); 33 between one to five years (36% recurrence, 21% cholangiocarcinoma recurrence) and nine after five years (56% de novo cancer, 44% recurrence). Primary sclerosing cholangitis has been an increasing indication for transplantation in Italy. Cholangitis and decompensation were the main indications for listing. Recurrence and cancer were the leading causes of death. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
15908658
Volume :
56
Issue :
8
Database :
Supplemental Index
Journal :
Digestive & Liver Disease
Publication Type :
Academic Journal
Accession number :
178317146
Full Text :
https://doi.org/10.1016/j.dld.2024.01.175