Duration from the first pale stool to portoenterostomy is prognostic in biliary atresia. Comparison with age at portoenterostomy

被引:8
作者
Nakamura, Hiroki [1 ]
Ara, Momoko [1 ]
Koga, Hiroyuki [1 ]
Miyano, Go [1 ]
Okawada, Manabu [1 ]
Doi, Takashi [1 ]
Lane, Geoffrey J. [1 ]
Okazaki, Tadaharu [1 ]
Urao, Masahiko [1 ]
Yamataka, Atsuyuki [1 ]
机构
[1] Juntendo Univ, Dept Pediat Gen & Urogenital Surg, Sch Med, Bunkyo Ku, 2-1-1 Hongo, Tokyo 1138421, Japan
关键词
Biliary atresia; Portoenterostomy; Postoperative prognosis; Stool color card; SPLENIC MALFORMATION SYNDROME; KASAI OPERATION; LIVER-TRANSPLANTATION; EXPERIENCE; FIBROSIS; CIRRHOSIS; JAUNDICE; OUTCOMES; IMPACT;
D O I
10.1016/j.clinre.2020.11.014
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Objective: Three criteria (age at first pale stool, age at portoenterostomy, and duration from the first pale stool to portoenterostomy) were assessed for prognostic value in biliary atresia. Methods: The medical records of 116 consecutive biliary atresia patients treated by portoenterostomy after liver transplantation became available in Japan in 1989 were identified and data from 96 were analyzed retrospectively for this study. The impact of each criterion on clearance of jaundice to normal levels (total serum bilirubin <= 1.2 mg/dL) and survival with the native liver as indicators of outcome were compared according to time (<= 30 days, 31-60 days, and >= 61 days). Results: Age at first pale stool was <= 30 days in 53, 31-60 days in 26, >= 61 days in 17; age at portoenterostomy was <= 30 days in 7, 31-60 days in 35, >= 61 days in 54, and duration preportoenterostomy was <= 30 days in 50, 31-60 days in 36, >= 61 days in 10. Survival with the native liver was not significantly influenced by age at first pale stool or age at portoenterostomy, but prolonged duration (>= 61 days) reduced survival with the native liver significantly (p = 0.003). Clearance of jaundice to normal levels was not affected by any criterion at any time. (C) 2020 Elsevier Masson SAS. All rights reserved.
引用
收藏
页数:14
相关论文
共 36 条
[1]  
Altman RP, 1997, ANN SURG, V226, P348, DOI 10.1097/00000658-199709000-00014
[2]  
Cazares J, 2020, Ashcraft's pediatric surgery, V7th, P679
[3]   Blood Tests to Diagnose Fibrosis or Cirrhosis in Patients With Chronic Hepatitis C Virus Infection A Systematic Review [J].
Chou, Roger ;
Wasson, Ngoc .
ANNALS OF INTERNAL MEDICINE, 2013, 158 (11) :807-+
[4]  
DAVENPORT M, 1993, SURGERY, V113, P662
[5]   The outcome of the older (≥100 days) infant with biliary atresia [J].
Davenport, M ;
Puricelli, V ;
Farrant, P ;
Hadzic, N ;
Mieli-Vergani, G ;
Portmann, B ;
Howard, ER .
JOURNAL OF PEDIATRIC SURGERY, 2004, 39 (04) :575-581
[6]   Surgical outcome in biliary atresia - Etiology affects the influence of age at surgery [J].
Davenport, Mark ;
Caponcelli, Enrica ;
Livesey, Emily ;
Hadzic, Nedim ;
Howard, Edward .
ANNALS OF SURGERY, 2008, 247 (04) :694-698
[7]   The biliary atresia splenic malformation syndrome: A 28-year single-center retrospective study [J].
Davenport, Mark ;
Tizzard, Sarah A. ;
Underhill, James ;
Mieli-Vergani, Giorgina ;
Portmann, Bernard ;
Hadzic, Nedim .
JOURNAL OF PEDIATRICS, 2006, 149 (03) :393-400
[8]   Diagnostic performance of quantitative magnetic resonance imaging biomarkers for predicting portal hypertension in children and young adults with autoimmune liver disease [J].
Dillman, Jonathan R. ;
Serai, Suraj D. ;
Trout, Andrew T. ;
Singh, Ruchi ;
Tkach, Jean A. ;
Taylor, Amy E. ;
Blaxall, Burns C. ;
Fei, Lin ;
Miethke, Alexander G. .
PEDIATRIC RADIOLOGY, 2019, 49 (03) :332-341
[9]   Stool Color Card Screening for Early Detection of Biliary Atresia and Long-Term Native Liver Survival: A 19-Year Cohort Study in Japan [J].
Gu, Yan-Hong ;
Yokoyama, Koji ;
Mizuta, Koichi ;
Tsuchioka, Takashi ;
Kudo, Toyoichiro ;
Sasaki, Hideyuki ;
Nio, Masaki ;
Tang, Julian ;
Ohkubo, Takayoshi ;
Matsui, Akira .
JOURNAL OF PEDIATRICS, 2015, 166 (04) :897-U431
[10]   Biliary atresia [J].
Hartley, Jane L. ;
Davenport, Mark ;
Kelly, Deirdre A. .
LANCET, 2009, 374 (9702) :1704-1713