Abstract

Introduction: Surgical treatment of biliary atresia (BA) is still based on sequential strategy with Kasai hepatoportoenterostomy (KP) followed by liver transplantation (LT), in case of complicated secondary biliary cirrhosis. Concerns have been expressed regarding the risks of LT related to previous KP, suggesting primary LT as an exclusive treatment of BA.Methods: Single-center retrospective analysis including 393 pediatric patients who underwent LT for BA from 1993 to 2018, categorized into two groups: with (KP) or without (NoKP) previous KP. Pre-LT clinical condition was estimated considering age at LT, time on waiting list, pediatric end-stage liver disease score (PELD), and presence of portal vein hypoplasia. Post-LT outcome was evaluated considering patient and graft survival rates, and need for early reoperation due to abdominal or graft-related complications (<45 days after LT).Results: Two-hundred ninety-six patients (75.3%) were categorized in the KP group, and 97 (24.7%) in the NoKP group. Median age at LT was 1.14 years in the KP group and 0.85 years in the NoKP group (p < 0.0001). PELD score was significantly less severe in KP patients (p < 0.05). One-year patient survival rates were 96.9 and 96.8% in the KP and NoKP groups, respectively (p = 0.43), and the corresponding graft survival was 92.5 and 94.8% (p = 0.97). The need for early reoperation was more frequent in the KP group (29.8%) vs. NoKP group (12.4%, p = 0.01). The rate of bowel perforation was non-significantly higher in the KP group (8.1%) vs. NoKP group (3.1%, p = 0.11).Conclusions: The sequential strategy including KP and LT allowed performing LT in patients with significant older age and better clinical conditions, when compared to those transplanted without previous KP. Patient and graft survivals were not impacted by previous KP. Although previous KP was associated with an increased rate of post-LT surgical complications, bowel perforation and bleeding did not occur significantly more frequently. Such results support the current strategy based on sequential treatment.

Highlights

  • Surgical treatment of biliary atresia (BA) is still based on sequential strategy with Kasai hepatoportoenterostomy (KP) followed by liver transplantation (LT), in case of complicated secondary biliary cirrhosis

  • The aim of the present study was to document the possible impact of a previous hepatoportoenterostomy in a large LT series for BA, testing the positive and negative consequences of KP on the clinical status at LT, as well as on post-LT overall outcome and surgical complications

  • Age at LT was significantly lower in patients in the NoKP group (p < 0.0001)

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Summary

Introduction

Surgical treatment of biliary atresia (BA) is still based on sequential strategy with Kasai hepatoportoenterostomy (KP) followed by liver transplantation (LT), in case of complicated secondary biliary cirrhosis. Current treatments of BA have been introduced within a few years’ interval around the 60s, when two surgical procedures were successively proposed: hepatoportoenterostomy by Morio Kasai in 1959 as an early approach to restore biliary drainage [7] and orthotopic liver transplantation (LT) by Thomas Starzl in 1963 for later management of end-stage biliary cirrhosis [8]. Sixty years later, these two procedures remain the cornerstones of therapeutic options, but the benefit/risk ratio of Kasai procedure (KP) in this therapeutic sequence is still debated [9, 10]. Only few studies have tried to systematically investigate whether LT outcomes are impacted by a previous KP, providing contradictory conclusions [18,19,20,21,22,23]

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