Preoperative risk factors for the early failure of the Kasai portoenterostomy in patients with biliary atresia
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Medicine,Surgery,Pediatrics, Perinatology and Child Health
Link
https://link.springer.com/content/pdf/10.1007/s00383-021-04933-y.pdf
Reference23 articles.
1. Davenport M, Ong E, Sharif K, Alizai N, McClean P, Hadzic N et al (2011) Biliary atresia in England and Wales: results of centralization and new benchmark. J Pediatr Surg 46:1689–1694. https://doi.org/10.1016/j.jpedsurg.2011.04.013
2. Superina R, Magee JC, Brandt ML, Healey PJ, Tiao G, Ryckman F et al (2011) The anatomic pattern of biliary atresia identified at time of kasai hepatoportoenterostomy and early postoperative clearance of jaundice are significant predictors of transplant-free survival. Ann Surg 254:577–585. https://doi.org/10.1097/SLA.0b013e3182300950
3. Superina R (2017) Biliary atresia and liver transplantation: results and thoughts for primary liver transplantation in select patients. Pediatr Surg Int 33:1297–1304. https://doi.org/10.1007/s00383-017-4174-4
4. Wang Q, Yan L, Zhang M, Wang W, Zhao J, Jin S (2013) Can primary LDLT be the alternative first line treatment for infant patients with biliary atresia? Hepatogastroenterology. https://doi.org/10.5754/hge12956
5. Alexopoulos SP, Merrill M, Kin C, Matsuoka L, Dorey F, Concepcion W et al (2012) The impact of hepatic portoenterostomy on liver transplantation for the treatment of biliary atresia: early failure adversely affects outcome. Pediatr Transplant 16:373–378. https://doi.org/10.1111/j.1399-3046.2012.01677.x
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