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

被引:35
作者
Nio, Masaki [1 ]
Wada, Motoshi [1 ]
Sasaki, Hideyuki [1 ]
Tanaka, Hiromu [1 ]
Okamura, Atsushi [1 ]
机构
[1] Tohoku Univ, Grad Sch Med, Dept Pediat Surg, Aoba Ku, Sedai 9808574, Japan
关键词
Biliary atresia; Kasai operation; Long-term follow-up; Liver failure; Operative age; Cholangitis; EXPERIENCE; PREGNANCY; SURGERY;
D O I
10.1016/j.jpedsurg.2012.09.003
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Purpose: Following the Kasai operation, a number of patients have developed liver failure, even after long-term postoperative courses. We assessed the clinical parameters to clarify the early risk factors affecting late-presenting liver failure in biliary atresia. Materials and Methods: From 1955 to 1991, 277 patients underwent a Kasai operation. Among those patients, 92 survived with their native liver for more than 20 years, and 72 continue to survive with their native liver in good condition (Group 1). In 20 patients, persistent jaundice recurred after the age of 20 years (Group 2). The postoperative courses of these patients were assessed retrospectively, and the clinical parameters, including age at the time of the Kasai operation (AGE, days), the period required for jaundice to disappear (PJD, days), and the association with early cholangitis (CG), were compared between the 2 groups. Results: Of the 20 patients in Group 2, 8 survived after a liver transplantation (LTx). Eight patients had recurrent jaundice, including 4 on the waiting list for anLTx. Additionally, 2 patients died after anLTx at the ages of 22 and 39. Another patient died of liver failure at the age of 28. One patient died of massive esophageal variceal bleeding at the age of 29. Significant differences were confirmed with respect to AGE (Group 1 < Group 2, p < .001), PJD (Group 1 < Group 2, p < .001), and CG (Group 1: Group 2 = 47 %: 75 %, p = .028). Conclusions: A considerable number of adult patients developed liver failure, even after the age of 20 years. AGE, PJD, and CG were found to be risk factors affecting late-presenting liver failure. Therefore, close patient follow-up is essential, especially for long-term survivors with a late operative age and early postoperative complications. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:2179 / 2183
页数:5
相关论文
共 14 条
[1]   Biliary atresia: The King's College Hospital experience (1974-1995) [J].
Davenport, M ;
Kerkar, N ;
MieliVergani, G ;
Mowat, AP ;
Howard, ER .
JOURNAL OF PEDIATRIC SURGERY, 1997, 32 (03) :479-485
[2]   Twenty-Year Transplant-Free Survival Rate Among Patients With Biliary Atresia [J].
de Vries, Willemien ;
Homan-Van der Veen, Jenneke ;
Hulscher, Jan B. F. ;
Hoekstra-Weebers, Josette E. H. M. ;
Houwen, Roderick H. J. ;
Verkade, Henkjan J. .
CLINICAL GASTROENTEROLOGY AND HEPATOLOGY, 2011, 9 (12) :1086-1091
[3]   Clinical significance of 99mTc-DTPA-galactosyl human serum albumin liver scintigraphy in follow-up patients with biliary atresia [J].
Ishii, T ;
Nio, M ;
Shimaoka, S ;
Sane, N ;
Sasaki, H ;
Kimura, D ;
Hayashi, Y ;
Ohi, R .
JOURNAL OF PEDIATRIC SURGERY, 2003, 38 (10) :1486-1490
[4]   A PATIENT WITH BILIARY ATRESIA WHO DIED 28 YEARS AFTER HEPATIC PORTOJEJUNOSTOMY [J].
KASAI, M ;
OHI, R ;
CHIBA, T ;
HAYASHI, Y .
JOURNAL OF PEDIATRIC SURGERY, 1988, 23 (05) :430-431
[5]   Biliary atresia, the next generation: A review of liver function, social activity and sexual development in the late postoperative period [J].
Kuroda, T ;
Saeki, M ;
Nakano, M ;
Morikawa, N .
JOURNAL OF PEDIATRIC SURGERY, 2002, 37 (12) :1709-1712
[6]   Management of adult biliary atresia patients: should hard work and pregnancy be discouraged? [J].
Kuroda, Tatsuo ;
Saeki, Morihiro ;
Morikawa, Nobuyuki ;
Watanabe, Koji .
JOURNAL OF PEDIATRIC SURGERY, 2007, 42 (12) :2106-2109
[7]   Outcome in adulthood of biliary atresia: a study of 63 patients who survived for over 20 years with their native liver [J].
Lykavieris, P ;
Chardot, C ;
Sokhn, M ;
Gauthier, F ;
Valayer, J ;
Bernard, O .
HEPATOLOGY, 2005, 41 (02) :366-371
[8]   Cholangitis as a late complication in long-term survivors after surgery for biliary atresia [J].
Nio, M ;
Sano, N ;
Ishii, T ;
Sasaki, H ;
Hayashi, Y ;
Ohi, R .
JOURNAL OF PEDIATRIC SURGERY, 2004, 39 (12) :1797-1799
[9]   Five- and 10-year survival rates after surgery for biliary atresia: A report from the Japanese Biliary Atresia Registry [J].
Nio, M ;
Ohi, R ;
Miyano, T ;
Saeki, M ;
Shiraki, K ;
Tanaka, K .
JOURNAL OF PEDIATRIC SURGERY, 2003, 38 (07) :997-1000
[10]  
Nio M, 2000, Semin Pediatr Surg, V9, P177, DOI 10.1053/spsu.2000.18846