Alexander J Bondoc, Janice A Taylor, Maria H Alonso, Jaimie D Nathan, Yu Wang, William F Balistreri, Jorge A Bezerra, Frederick C Ryckman, Gregory M Tiao
OBJECTIVE: To determine whether portoenterostomy (PE) revision in patients afflicted with biliary atresia (BA) is a viable treatment option and, if so, identify which patients may benefit. BACKGROUND: BA, the most common cause of neonatal liver disease, results in biliary tract obstruction and hepatic fibrosis. Kasai PE is the initial surgical intervention performed and, if successful, restores drainage and preserves the native liver. Portoenterostomy failure warrants liver transplantation, but because of complications related to transplantation, treatment strategies to salvage the native liver may be beneficial...
March 2012: Annals of Surgery