Literature DB >> 34057595

Preoperative risk factors for the early failure of the Kasai portoenterostomy in patients with biliary atresia.

Mauro Ariel Capparelli1, Victor Hugo Ayarzabal2, Esteban Tomas Halac3, Horacio Alberto Questa2, Maria Julia Minetto3, Guillermo Cervio3, Marcelo Eugenio Barrenechea2.   

Abstract

PURPOSE: Biliary atresia is managed surgically by the Kasai portoenterostomy (KP). It has been reported by some groups that the outcomes of patients who have an early failed KP requiring a liver transplant (LTx) within the first year of life are worse than the outcomes of patients who undergo a primary LTx. The aim of this study was to identify preoperative parameters that could help predict what patients are at risk for the early failure of the procedure.
MATERIALS AND METHODS: We conducted a retrospective chart review of all patients who underwent a KP between January 2008 and May 2018. The following preoperative parameters were analyzed: age at KP, anatomical variant of the biliary atresia, degree of liver fibrosis, CMV status, and PELD score. The main outcome of the study was the early failure of the KP (EF-K), which was defined as the need for LTx before 1 year of age, or BA-related death before 1 year of age. Second, we analyzed the risk factors associated with death without LTx within the first year of life.
RESULTS: A total of 58 patients were included in the analysis. The native liver survival (NLS) was 56.5% and 48% at 1 and 5 years post KP, respectively. Overall survival (OS) was 79% and 76% at 1 and 5 years post KP, respectively. Early failure of KP occurred in 23 (39.7%) patients. OS in this group was 47% and 40% at 1 and 5 years, respectively. On the contrary, the OS of the remaining 35 (60.3%) patients was 100% at 1 and 5 years (P < 0.0001). When we compared all preoperative parameters, the only predictor of EF-K was the PELD score. When we analyzed the cases in the EF-K group who died without LTx, we found that the significant predictors were the cystic variant, a degree of liver fibrosis >4, and the PELD score. Nevertheless, on multivariate analysis, only PELD score was found as a statistically significant variable.
CONCLUSION: Due to bad prognosis found in EF-K patients, we believe that it could be reasonable to offer them a primary LTx. PELD score was found to be the strongest preoperative parameter that allows predicting which patient will likely have an early failed KP. Further prospective and multicenter studies are needed to reinforce these results.

Entities:  

Keywords:  Biliary atresia; Kasai failure; Kasai portoenterostomy; Liver transplant; Native liver survival

Year:  2021        PMID: 34057595     DOI: 10.1007/s00383-021-04933-y

Source DB:  PubMed          Journal:  Pediatr Surg Int        ISSN: 0179-0358            Impact factor:   1.827


  21 in total

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Authors:  Riccardo Superina; John C Magee; Mary L Brandt; Patrick J Healey; Greg Tiao; Fred Ryckman; Frederick M Karrer; Kishore Iyer; Annie Fecteau; Karen West; R Cartland Burns; Alan Flake; Hanmin Lee; Jeff A Lowell; Pat Dillon; Paul Colombani; Richard Ricketts; Yun Li; Jeffrey Moore; Kasper S Wang
Journal:  Ann Surg       Date:  2011-10       Impact factor: 12.969

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Journal:  J Pediatr Surg       Date:  2018-11-26       Impact factor: 2.545

3.  Outcomes of biliary atresia in the Nordic countries - a multicenter study of 158 patients during 2005-2016.

Authors:  Mikko P Pakarinen; Lars Søndergaard Johansen; Jan F Svensson; Kristin Bjørnland; Vladimir Gatzinsky; Pernilla Stenström; Antti Koivusalo; Nina Kvist; Markus Almström; Ragnhild Emblem; Sigurdur Björnsson; Torbjörn Backman; Runar Almaas; Hannu Jalanko; Björn Fischler; Jørgen Thorup
Journal:  J Pediatr Surg       Date:  2017-09-05       Impact factor: 2.545

4.  The limited prognostic value of liver histology in children with biliary atresia.

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Review 6.  Biliary atresia and liver transplantation: results and thoughts for primary liver transplantation in select patients.

Authors:  Riccardo Superina
Journal:  Pediatr Surg Int       Date:  2017-10-13       Impact factor: 1.827

Review 7.  Japanese Biliary Atresia Registry.

Authors:  Masaki Nio
Journal:  Pediatr Surg Int       Date:  2017-10-16       Impact factor: 1.827

8.  Elevated expression of Bmi1 in hepatocellular carcinoma with bile duct tumor thrombi.

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Journal:  Hepatogastroenterology       Date:  2013 Nov-Dec

9.  The impact of hepatic portoenterostomy on liver transplantation for the treatment of biliary atresia: early failure adversely affects outcome.

Authors:  Sophoclis P Alexopoulos; Melanie Merrill; Cindy Kin; Lea Matsuoka; Fred Dorey; Waldo Concepcion; Carlos Esquivel; Andrew Bonham
Journal:  Pediatr Transplant       Date:  2012-03-30

10.  Improving outcomes of biliary atresia: French national series 1986-2009.

Authors:  Christophe Chardot; Chantal Buet; Marie-Odile Serinet; Jean-Louis Golmard; Alain Lachaux; Bertrand Roquelaure; Frédéric Gottrand; Pierre Broué; Alain Dabadie; Frédéric Gauthier; Emmanuel Jacquemin
Journal:  J Hepatol       Date:  2013-02-08       Impact factor: 25.083

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Review 1.  Peri-Operative Liver Fibrosis and Native Liver Survival in Pediatric Patients with Biliary Atresia: A Systematic Review and Meta-Analysis.

Authors:  Ashkan Jahangirnia; Irina Oltean; Youssef Nasr; Nayaar Islam; Arielle Weir; Joseph de Nanassy; Ahmed Nasr; Dina El Demellawy
Journal:  Pediatr Gastroenterol Hepatol Nutr       Date:  2022-09-05
  1 in total

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