Literature DB >> 25064225

Liver transplantation following the Kasai procedure in treatment of biliary atresia: a single institution analysis.

Hideyuki Sasaki1, Hiromu Tanaka, Motoshi Wada, Takuro Kazama, Kotaro Nishi, Megumi Nakamura, Hironori Kudo, Naoki Kawagishi, Masaki Nio.   

Abstract

PURPOSE: This study aimed to assess outcomes of liver transplantation (LTx) in patients with biliary atresia (BA).
METHODS: The Kasai procedure was performed for 358 patients at Tohoku University Hospital between January 1955 and December 2013; 64 (17.9%) required LTx. These 64 patients were divided into 4 groups according to their age at the time of transplantation: Group 1, aged <2 years (n = 27); Group 2, aged 2-9 years (n = 16); Group 3, aged 10-19 years (n = 11); and Group 4, aged ≥20 years (n = 10). Clinical parameters were evaluated retrospectively.
RESULTS: Both living-donor (n = 57) and deceased-donor (n = 7) LTx were performed. Indications were irreversible jaundice (n = 53), intractable cholangitis (n = 3), hepatopulmonary syndrome (n = 6), portopulmonary hypertension (n = 1), and intestinal bleeding (n = 1). Jaundice occurred more frequently in Groups 1 and 2 than in Groups 3 and 4 (p = 0.031). Survival rates were 81.5, 100, 90.9, and 80% in Groups 1, 2, 3, and 4, respectively.
CONCLUSION: Although the overall LTx survival rate was satisfactory, some adult recipients experienced LTx-related difficulty. Close follow-up, meticulous assessment of physical and social conditions, presence of a multidisciplinary support system, and appropriate time course for LTx are all essential factors in the treatment of BA.

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Year:  2014        PMID: 25064225     DOI: 10.1007/s00383-014-3552-4

Source DB:  PubMed          Journal:  Pediatr Surg Int        ISSN: 0179-0358            Impact factor:   1.827


  11 in total

1.  Comparative analysis of live liver donation risk using a comprehensive grading system for severity.

Authors:  Paolo R O Salvalaggio; Talia B Baker; Alan J Koffron; Jonathan P Fryer; Lori Clark; Riccardo A Superina; Andres T Blei; Michael M Abecassis
Journal:  Transplantation       Date:  2004-06-15       Impact factor: 4.939

Review 2.  Current status of organ transplantation in Japan.

Authors:  H Egawa; K Tanabe; N Fukushima; H Date; A Sugitani; H Haga
Journal:  Am J Transplant       Date:  2011-11-04       Impact factor: 8.086

3.  Long-term outcome in type I biliary atresia.

Authors:  Masaki Nio; Nobuyuki Sano; Tomohiro Ishii; Hideyuki Sasaki; Yutaka Hayashi; Ryoji Ohi
Journal:  J Pediatr Surg       Date:  2006-12       Impact factor: 2.545

Review 4.  Hepatopulmonary syndrome--a liver-induced lung vascular disorder.

Authors:  Roberto Rodríguez-Roisin; Michael J Krowka
Journal:  N Engl J Med       Date:  2008-05-29       Impact factor: 91.245

5.  Five- and 10-year survival rates after surgery for biliary atresia: a report from the Japanese Biliary Atresia Registry.

Authors:  Masaki Nio; Ryoji Ohi; Takeshi Miyano; Morihiro Saeki; Kazuo Shiraki; Koichi Tanaka
Journal:  J Pediatr Surg       Date:  2003-07       Impact factor: 2.545

6.  Long-term efficacy of partial splenic embolization in children.

Authors:  Masaki Nio; Yutaka Hayashi; Nobuyuki Sano; Tomohiro Ishii; Hideyuki Sasaki; Ryoji Ohi
Journal:  J Pediatr Surg       Date:  2003-12       Impact factor: 2.545

7.  Risk factors affecting late-presenting liver failure in adult patients with biliary atresia.

Authors:  Masaki Nio; Motoshi Wada; Hideyuki Sasaki; Hiromu Tanaka; Atsushi Okamura
Journal:  J Pediatr Surg       Date:  2012-12       Impact factor: 2.545

8.  Present status of ABO-incompatible living donor liver transplantation in Japan.

Authors:  Hiroto Egawa; Satoshi Teramukai; Hironori Haga; Minoru Tanabe; Masanori Fukushima; Motohide Shimazu
Journal:  Hepatology       Date:  2008-01       Impact factor: 17.425

9.  Long-term outcome of children with biliary atresia who were not transplanted after the Kasai operation: >20-year experience at a children's hospital.

Authors:  Masato Shinkai; Youkatsu Ohhama; Hiroshi Take; Norihiko Kitagawa; Hironori Kudo; Kyoko Mochizuki; Tomoko Hatata
Journal:  J Pediatr Gastroenterol Nutr       Date:  2009-04       Impact factor: 2.839

Review 10.  Psychosocial stress and liver disease status.

Authors:  Cristin Constantin Vere; Costin Teodor Streba; Letitia Maria Streba; Alin Gabriel Ionescu; Felix Sima
Journal:  World J Gastroenterol       Date:  2009-06-28       Impact factor: 5.742

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  4 in total

1.  Liver transplantation in infants with biliary atresia: comparison of primary versus temporary abdominal closure.

Authors:  Nagoud Schukfeh; Anna-Charlotte Holland; Dieter P Hoyer; Anja Gallinat; Andreas Paul; Maren Schulze
Journal:  Langenbecks Arch Surg       Date:  2016-11-03       Impact factor: 3.445

2.  Association between mitochondrial and nuclear DNA damages and cellular senescence in the patients with biliary atresia undergoing Kasai portoenterostomy and liver transplantation.

Authors:  Yudai Nakajima; Yuto Yamazaki; Xin Gao; Masatoshi Hashimoto; Masaki Nio; Motoshi Wada; Fumiyoshi Fujishima; Hironobu Sasano
Journal:  Med Mol Morphol       Date:  2022-03-03       Impact factor: 2.309

3.  Analysis of the prognostic factors of long-term native liver survival in survivors of biliary atresia.

Authors:  Hideyuki Sasaki; Hiromu Tanaka; Motoshi Wada; Takuro Kazama; Megumi Nakamura; Hironori Kudo; Ryoji Okubo; Tsuyoshi Sakurai; Masaki Nio
Journal:  Pediatr Surg Int       Date:  2016-07-27       Impact factor: 1.827

4.  Telomere Length in Peripheral Blood Leukocytes Is Associated with Severity of Biliary Atresia.

Authors:  Wanvisa Udomsinprasert; Yong Poovorawan; Voranush Chongsrisawat; Paisarn Vejchapipat; Dong Zhan; Sittisak Honsawek
Journal:  PLoS One       Date:  2015-07-31       Impact factor: 3.240

  4 in total

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