Background: 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. Aim: We performed a national survey to investigate the listing criteria, comorbidities, and outcomes. Methods: In April 2022, we surveyed liver transplantation in primary sclerosing cholangitis nationwide for the last 15 years. Results: 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). Conclusions: 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.

Trends in liver transplantation for primary sclerosing cholangitis / 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; Burra, Patrizia; Viganò, Raffaella; Fornasiere, Ezio; Catanzaro, Elisa; Marrone, Giuseppe; Milana, Martina; Calleri, Alberto; Scorzoni, Chiara; Frassanito, Gabriella; Lionetti, Raffaella; Dibenedetto, Clara. - In: DIGESTIVE AND LIVER DISEASE. - ISSN 1590-8658. - 56:8(2024), pp. 1343-1349. [10.1016/j.dld.2024.01.175]

Trends in liver transplantation for primary sclerosing cholangitis

Baroni, Gianluca Svegliati;Scorzoni, Chiara
Membro del Collaboration Group
;
2024-01-01

Abstract

Background: 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. Aim: We performed a national survey to investigate the listing criteria, comorbidities, and outcomes. Methods: In April 2022, we surveyed liver transplantation in primary sclerosing cholangitis nationwide for the last 15 years. Results: 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). Conclusions: 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.
2024
Cholangiocarcinoma; Liver transplantation; PSC recurrence
File in questo prodotto:
File Dimensione Formato  
PIIS1590865824001944.pdf

Solo gestori archivio

Tipologia: Versione editoriale (versione pubblicata con il layout dell'editore)
Licenza d'uso: Tutti i diritti riservati
Dimensione 915.26 kB
Formato Adobe PDF
915.26 kB Adobe PDF   Visualizza/Apri   Richiedi una copia

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11566/348939
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 5
  • ???jsp.display-item.citation.isi??? 3
social impact