Fabian, JuneBotha, JeanVan der Schyff, Francisca.Terblanche, Alberta J2022-09-252022-09-252019-12-09van der Schyff F, Terblanche Alberta J, Botha JF. Improving Poor Outcomes of Children With Biliary Atresia in South Africa by Early Referral to Centralized Units. JPGN. 2021; 2( 2): e073. DOI: 10.1097/PG9.0000000000000073https://hdl.handle.net/10539/33336Https//doi.org//10.54223/uniwitwatersrand-10539-33336All children with BA who were managed at SBAH between June 2007 and July 2018 were included. Parameters measured centered on patient demographics, timing of referral and surgical intervention, immediate and long-term outcomes of surgery, and follow-up management.Biliary atresia (BA) is a progressive fibrosing cholangiopathy of infancy, the most common cause of cholestatic jaundice in infants and the top indication for liver transplantation in children. Kasai portoenterostomy (KPE) when successful may delay the requirement for liver transplantation, which in the majority offers the only cure. Good outcomes demand early surgical intervention, appropriate management of liver cirrhosis, and in most cases, liver transplantation. These parameters were audited of children with BA treated at the Steve Biko Academic Hospital (SBAH) in Pretoria, South Africa.data published in June Fabian et al. on behalf of the African Research in Kidney Disease (ARK) Working Group. Methods and reporting of kidney function: a systematic review of studies from sub-Saharan Africa. Clinical Kidney Journal. 2019. sfz089, https://doi.org/10.1093/ckj/sfz089Hepatic TransplantationHepatic TransplantationDataset