Outcome of biliary atresia after Kasai’s portoenterostomy: A 15-year experience

• Published in: Indian pediatrics 2017-04, Vol.54 (4), p.291-294
• Main Authors: Redkar, Rajeev, Karkera, Parag J., Raj, Vinod, Bangar, Anant, Hathiramani, Varun, Krishnan, Janani
• Format: Article
• Language: English
• Subjects: Biliary Atresia - epidemiology; Biliary Atresia - mortality; Biliary Atresia - surgery; Female; Humans; Infant; Jaundice; Male; Maternal and Child Health; Medicine; Medicine & Public Health; Pediatric Surgery; Pediatrics; Portoenterostomy, Hepatic - adverse effects; Portoenterostomy, Hepatic - mortality; Portoenterostomy, Hepatic - statistics & numerical data; Postoperative Complications; Research Paper
• ISSN: 0019-6061; 0974-7559
• DOI: 10.1007/s13312-017-1091-5

Objective To study the outcome of Biliary atresia after Kasai's portoenterostomy and clinical and biochemical factors affecting the outcome. Methods Medical record review of patients of biliary atresia operated from January 2000 to December 2014. The following data were collected and analyzed - sex, age at surgery, liver function tests, associated congenital anomalies, and clearance of jaundice (at 3 months). Final outcome was classified as alive, dead, or jaundice-free at last follow-up (minimum 1 year). Results 121 patients (61.9% males) were included; 32 (26.5%) were lost to follow-up at 1 year. At last follow-up, out of the 89, 42 (47.2%) were alive, 29 (32.6%) were jaundice-free, and 47 (52.8%) had died. The native liver survival rate at last follow up was 43.8%. 42 (47.2%) patients had complete clearance of jaundice at 3 months post-procedure. Jaundice-clearance rate was significantly high in patients alive (83.3% vs 16.7%, P