Determinants of life span after Kasai operation at the era of liver transplantation

被引:16
作者
Gauthier, F
Luciani, JL
Chardot, C
Branchereau, S
deDreuzy, O
Lababidi, A
Montupet, P
Dubousset, AM
Huault, G
Bernard, O
Valayer, J
机构
[1] UNIV PARIS 11, CHU BICETRE, DEPT ANESTHESIE REANIMAT, FAC MED, F-94275 LE KREMLIN BICETRE, FRANCE
[2] UNIV PARIS 11, CHU BICETRE, UNITE SOINS INTENSIFS ENFANTS, FAC MED, F-94275 LE KREMLIN BICETRE, FRANCE
[3] UNIV PARIS 11, CHU BICETRE, SERV HEPATOL PEDIAT, FAC MED, F-94275 LE KREMLIN BICETRE, FRANCE
关键词
biliary atresia; surgery; liver transplantation; BILIARY ATRESIA; POLYSPLENIA SYNDROME; PORTOENTEROSTOMY; SURGERY; SURVIVAL;
D O I
10.1620/tjem.181.97
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The aim of this work is to determine the influence of age, extrahepatic biliary lesions pattern (EHBP) and association to polysplenia syndrome (PS) on 10 years outcome of 164 patients with biliary atresia (BA) treated from 1984 to 1992 by initial Kasai operation (KO) and secondary liver transplantation (LT) when necessary. Actuarial crude survival without or after LT(CS), actuarial survival with native liver (NLS) and jaundice-free actuarial survival with native liver (JFS) were calculated from 1 to 10 years versus age (under/over 45 days), EHBP (favorable/unfavorable) and PX (no/yes). Overall 10-year CS is 70%, overall 10-year NLS and JFS are 14%. In univariate analysis, age at KO under 46 days, favorable EHBP (BA with patent gallbladder, and/or cystic dilatation of extrahepatic bile duct, or BA restricted to choledocus), and absence of PS are significant determinants of a better outcome regarding CS, NLS and JFS. EHBP is more discriminant than age. Influence of PX in this series is redundant with that of EHBP since 11/11 patients with PS had unfavorable EHBP.
引用
收藏
页码:97 / 107
页数:11
相关论文
共 24 条
  • [1] [Anonymous], 1984, HEPATOLOGY, V4, p107S
  • [2] DOES PREVIOUS ABDOMINAL-SURGERY ALTER THE OUTCOME OF PEDIATRIC-PATIENTS SUBJECTED TO ORTHOTOPIC LIVER-TRANSPLANTATION
    CUERVASMONS, V
    RIMOLA, A
    VANTHIEL, DH
    GAVALER, JS
    SCHADE, RR
    STARZL, TE
    [J]. GASTROENTEROLOGY, 1986, 90 (04) : 853 - 857
  • [3] DAVENPORT M, 1993, SURGERY, V113, P662
  • [4] PROGRESS IN THE TREATMENT OF BILIARY ATRESIA - A PLEA FOR SURGICAL INTERVENTION WITHIN THE 1ST 2 MONTHS OF LIFE IN INFANTS WITH PERSISTENT CHOLESTASIS
    EMBLEM, R
    STAKE, G
    MONCLAIR, T
    [J]. ACTA PAEDIATRICA, 1993, 82 (11) : 971 - 974
  • [5] LIVER-TRANSPLANTATION IN CHILDREN WITH BILIARY ATRESIA AND POLYSPLENIA SYNDROME
    FALCHETTI, D
    DECARVALHO, FB
    CLAPUYT, P
    DEGOYET, JD
    DEHEMPTINNE, B
    CLAUS, D
    OTTE, JB
    [J]. JOURNAL OF PEDIATRIC SURGERY, 1991, 26 (05) : 528 - 531
  • [6] GAUTHIER F, 1992, P 5 ISSBA, P121
  • [7] GAUTHIER F, 1992, P 5 ISSBA, P91
  • [8] Grosfeld J, 1994, Curr Opin Gen Surg, P168
  • [9] BILIARY ATRESIA AND THE POLYSPLENIA SYNDROME
    KARRER, FM
    HALL, RJ
    LILLY, JR
    [J]. JOURNAL OF PEDIATRIC SURGERY, 1991, 26 (05) : 524 - 527
  • [10] BILIARY ATRESIA REGISTRY, 1976 TO 1989
    KARRER, FM
    LILLY, JR
    STEWART, BA
    HALL, RJ
    [J]. JOURNAL OF PEDIATRIC SURGERY, 1990, 25 (10) : 1076 - 1081