Literature DB >> 9149343

Japanese Biliary Atresia Registry, 1989 to 1994.

M Ibrahim1, T Miyano, R Ohi, M Saeki, K Shiraki, K Tanaka, T Kamiyama, M Nio.   

Abstract

The Japanese Biliary Atresia Society founded in 1980 for the aim of investigations of all aspects of biliary atresia (BA), started a nationwide registry of BA patients in 1989. A total of 626 cases were registered from 1989 to 1994. The male to female ratio was 0.58. Corrective surgery was performed in 603 patients. Regarding the type of obstruction, 63 cases were Type I, atresia of the common bile duct, 9 were Type II, atresia of the hepatic ducts, and 543 were Type III, atresia of the porta hepatis. As initial corrective procedures, original Roux-en Y, Suruga II and Roux-en Y with intestinal valve were mainly employed. Jaundice cleared in 346 patients (57%) and decreased in 131, while it persisted in 120. The 5-year-follow-up showed that 34 patients, 49% of the patients who were followed up, were alive without jaundice, while 28 (41%) are dead. Thirty five, 33% of the patients who were entered to the Registry, were lost to follow-up.

Entities:  

Mesh:

Year:  1997        PMID: 9149343     DOI: 10.1620/tjem.181.85

Source DB:  PubMed          Journal:  Tohoku J Exp Med        ISSN: 0040-8727            Impact factor:   1.848


  9 in total

1.  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.

Authors:  Riccardo Superina; John C Magee; Mary L Brandt; Patrick J Healey; Greg Tiao; Fred Ryckman; Frederick M Karrer; Kishore Iyer; Annie Fecteau; Karen West; R Cartland Burns; Alan Flake; Hanmin Lee; Jeff A Lowell; Pat Dillon; Paul Colombani; Richard Ricketts; Yun Li; Jeffrey Moore; Kasper S Wang
Journal:  Ann Surg       Date:  2011-10       Impact factor: 12.969

2.  Indication for redo hepatic portoenterostomy for insufficient bile drainage in biliary atresia: re-evaluation in the era of liver transplantation.

Authors:  T Hasegawa; T Kimura; T Sasaki; A Okada; S Mushiake
Journal:  Pediatr Surg Int       Date:  2003-04-03       Impact factor: 1.827

Review 3.  Surgical modifications, additions, and alternatives to Kasai hepato-portoenterostomy to improve the outcome in biliary atresia.

Authors:  Shilpa Sharma; Devendra K Gupta
Journal:  Pediatr Surg Int       Date:  2017-10-04       Impact factor: 1.827

Review 4.  Liver biopsy in modern clinical practice: a pediatric point-of-view.

Authors:  Nadia Ovchinsky; Roger K Moreira; Jay H Lefkowitch; Joel E Lavine
Journal:  Adv Anat Pathol       Date:  2012-07       Impact factor: 3.875

Review 5.  Biliary atresia: recent progress.

Authors:  Mikelle D Bassett; Karen F Murray
Journal:  J Clin Gastroenterol       Date:  2008-07       Impact factor: 3.062

Review 6.  Screening and outcomes in biliary atresia: summary of a National Institutes of Health workshop.

Authors:  Ronald J Sokol; Ross W Shepherd; Riccardo Superina; Jorge A Bezerra; Patricia Robuck; Jay H Hoofnagle
Journal:  Hepatology       Date:  2007-08       Impact factor: 17.425

Review 7.  Biliary atresia.

Authors:  Christophe Chardot
Journal:  Orphanet J Rare Dis       Date:  2006-07-26       Impact factor: 4.123

8.  Laparoscopic Kasai portoenterostomy can be a standard surgical procedure for treatment of biliary atresia.

Authors:  Chiyoe Shirota; Akinari Hinoki; Takahisa Tainaka; Wataru Sumida; Fumie Kinoshita; Kazuki Yokota; Satoshi Makita; Hizuru Amano; Yoichi Nakagawa; Hiroo Uchida
Journal:  World J Gastrointest Surg       Date:  2022-01-27

9.  Ultrasonographic findings of type IIIa biliary atresia.

Authors:  Seung-Seob Kim; Myung-Joon Kim; Mi-Jung Lee; Choon-Sik Yoon; Seok Joo Han; Hong Koh
Journal:  Ultrasonography       Date:  2014-06-10
  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.