4.3 Article

Biliary complications in pediatric liver transplantation: findings of percutaneous transhepatic cholangiography in a large single-center cohort

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PEDIATRIC RADIOLOGY
卷 52, 期 6, 页码 1061-1074

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SPRINGER
DOI: 10.1007/s00247-021-05278-3

关键词

Biliary; Children; Complications; Interventional radiology; Liver; Percutaneous transhepatic cholangiography; Transplantation

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This study retrospectively analyzed the prevalence of biliary complications after pediatric liver transplantation and the efficacy of percutaneous transhepatic cholangiography in their management. The results showed a high incidence of biliary complications, and percutaneous transhepatic cholangiography played an important role in diagnosis and treatment.
Background Although biliary complications after orthotopic liver transplantation represent a common source of morbidity and mortality, decreasing graft survival, consensus is lacking on their management in the pediatric population. Objective The aim of this study was to present the prevalence of such biliary complications and their interventional radiologic management with representative images. Materials and methods This retrospective study reports our experience with percutaneous transhepatic cholangiography in the management of biliary complications after orthotopic liver transplantation in pediatric patients. This study enrolled all pediatric patients (<18 years old) who underwent percutaneous transhepatic cholangiography for the management of biliary complications after orthotopic liver transplantation at a tertiary care center between January 2010 and December 2020. Diagnosis of biliary complications and indication to perform percutaneous transhepatic cholangiography were based on clinical, laboratory or radiologic data. Results Among the 301 orthotopic liver transplantations, 78 (26%) developed biliary complications that were managed by interventional radiology: these included 52 (17.3%) biliary strictures, 19 (6.3%) bile leaks, 5 (1.7%) biliary stones, 1 (0.3%) iatrogenic biliary obstruction and 1 (0.3%) vanishing syndrome. The median time interval between orthotopic liver transplantation and the diagnosis of biliary complications was 6.0 years (interquartile range [IQR] 8.2 years). Percutaneous transhepatic cholangiography and biliary duct catheterization were successful in all cases, with low rates of complications that were variable among subgroups. Conclusion A wide spectrum of biliary complications can occur after pediatric orthotopic liver transplantation. In this large single-center experience, we highlight the value of percutaneous transhepatic cholangiography in their diagnosis and management. Percutaneous treatments in pediatric patients are safe and effective, providing resolution or serving as a bridge to surgery, including re-transplantation.

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