Results 51 to 60 of about 1,713 (227)
Pediatric liver transplantation from neonatal donors [PDF]
Sixteen recipients of neonatal liver grafts were compared with 114 contemporaneous pediatric recipients of grafts from older donors. Graft and patient survival were worse in the neonatal group although the differences were not statistically significant ...
Bismuth H +9 more
core +1 more source
Our study of 489 pediatric living donor liver transplants demonstrated a low hepatic artery thrombosis rate of 1%. Age and cold ischemia time emerged as significant risk factors. Notably, performing a double hepatic artery anastomosis was safe but did not decrease the incidence of biliary complications such as strictures or leaks.
Carolina Magalhães Costa +18 more
wiley +1 more source
Background Total parenteral nutrition (TPN) and biliary atresia (BA) are common causes of cholestasis in infancy. The diagnosis of BA is time sensitive due to an inverse correlation between age at intervention (hepatic portoenterostomy - HPE) and ...
Atu Agawu +4 more
doaj +1 more source
Introduction Biliary atresia (BA) is a life-threatening disease with persistent neonatal cholestasis and progressive liver fibrosis. Timely non-invasive diagnosis of BA can result in early hepatic portoenterostomy (HPE) and better prognosis. Quantitative
Yan Luo +6 more
doaj +1 more source
Abstract Aim This retrospective study aimed to assess the efficacy of prophylactic antibiotics in preventing ascending cholangitis following Kasai portoenterostomy (KPE). Data from 72 patients treated across four tertiary centres in Israel from 2008 to 2018 were analysed.
Yael Brody +6 more
wiley +1 more source
Abstract Background Vitamin K (VK) prophylaxis refers to the administration of VK to newborns to prevent neonatal VK deficiency bleeding (VKDB), which is characterized by intracranial hemorrhage (ICH). This study investigated the relationship between VK prophylaxis methods and VKDB in biliary atresia (BA).
Ryuji Okubo +16 more
wiley +1 more source
Current management of biliary atresia based on 35 years of experience at a single center
OBJECTIVE: The prognosis of patients with biliary atresia undergoing Kasai portoenterostomy is related to the timing of the diagnosis and the indication for the procedure.
Wagner de Castro Andrade +5 more
doaj +1 more source
Background: Biliary atresia (BA) is a progressive obstructive hepatic disease that requires early diagnosis and the prompt initiation of treatment. Although portoenterostomy (PES) is usually performed as the initial surgical procedure, the liver damage ...
Atsushi Higashio +6 more
doaj +1 more source
Neuropsychological development of children with biliary atresia after liver transplantation
Background. In young children, the most common liver disease leading to transplantation is biliary atresia. Liver transplantation has fundamentally improved the survival rate of children with biliary atresia. Studies on developmental outcomes in children
A. V. Syrkina +7 more
doaj +1 more source
The aim of the study was to find associations between the levels of liver injury serum markers and the selected liver, peripheral leukocytes, and plasma immune characteristics in biliary atresia (BA) children. Twenty‐five newly diagnosed BA children aged 4–30 weeks and 12 age‐matched controls were included (for leukocytes characteristics) and 19 BA ...
Anna Helmin-Basa +8 more
wiley +1 more source

