Literature DB >> 30095577

Prognosis of Biliary Atresia After 2-year Survival With Native Liver: A Nationwide Cohort Analysis.

Mauri Witt1, Daan B E van Wessel1, Ruben H J de Kleine2, Janneke L M Bruggink1, Jan B F Hulscher1, Henkjan J Verkade3.   

Abstract

OBJECTIVES: The aim of the study is to determine the prognosis of patients with biliary atresia after 2 years of native liver survival (NLS) and to identify prognostic factors for continued NLS after 2 years of age.
METHODS: We retrospectively analyzed perioperative, laboratory, and outcome parameters of all biliary atresia patients in The Netherlands between January 1987 and June 2015 with NLS of at least 2 years. We compared parameters between patients who continued to have their native liver (NLS+) to those who did not, either by transplant or death (NLS-).
RESULTS: We included 100 patients. Upon a median follow-up of 16.4 years, NLS ended in 37% by liver transplantation (LTx) and in 6% by (pre-transplant) mortality. NLS rates at 5, 10, 15, 18 years of age were 89%, 72%, 60%, 54%, respectively. Corresponding overall survival rates were 98%, 90%, 87%, 87%, respectively. Six months post-Kasai, NLS+ patients had higher clearance of jaundice (COJ) rate, significantly lower total and direct serum bilirubin, aspartate-aminotransferase and alkaline phosphatase levels, compared with NLS- patients (each P < 0.05). Cox regression could only assess a significant effect of COJ on continued NLS. Main indications for LTx after the age of 2 were irreversible jaundice and portal hypertension.
CONCLUSIONS: Eighty-seven percent of patients with 2-year NLS reach adult age and more than 50% with their native liver. A pre-transplant mortality of 6%, however, exists among patients who reach the age of 2 years with their native livers. Early life parameters, other than COJ, did not have a significant effect on continued NLS after 2 years of age.

Entities:  

Mesh:

Year:  2018        PMID: 30095577     DOI: 10.1097/MPG.0000000000002130

Source DB:  PubMed          Journal:  J Pediatr Gastroenterol Nutr        ISSN: 0277-2116            Impact factor:   2.839


  7 in total

1.  Home-based color card screening for biliary atresia: the first steps for implementation of a nationwide newborn screening in Germany.

Authors:  Omid Madadi-Sanjani; J Blaser; G Voigt; J F Kuebler; C Petersen
Journal:  Pediatr Surg Int       Date:  2019-07-25       Impact factor: 1.827

2.  Revisiting long-term prognostic factors of biliary atresia: A 20-year experience with 81 patients from a single center.

Authors:  Damla Hanalioğlu; Hasan Özen; Asuman Karhan; Ersin Gümüş; Hülya Demir; İnci N Saltık-Temizel; Saniye Ekinci; İbrahim Karnak; Arbay O Çiftçi; Feridun C Tanyel; Aysel Yüce
Journal:  Turk J Gastroenterol       Date:  2019-05       Impact factor: 1.852

Review 3.  Biliary Atresia: A Complex Hepatobiliary Disease with Variable Gene Involvement, Diagnostic Procedures, and Prognosis.

Authors:  Consolato M Sergi; Susan Gilmour
Journal:  Diagnostics (Basel)       Date:  2022-01-27

4.  A Nomogram Predicting the Prognosis of Children With Biliary Atresia After Hepatoportoenterostomy.

Authors:  Jin-Qiao Liu; Wen-Juan Chen; Meng-Jie Zhou; Wen-Feng Li; Ju Tang; Qi-Chang Zhou
Journal:  Front Pediatr       Date:  2021-02-24       Impact factor: 3.418

5.  Modeling Outcomes in Children With Biliary Atresia With Native Liver After 2 Years of Age.

Authors:  Veena Venkat; Vicky L Ng; John C Magee; Wen Ye; Kieran Hawthorne; Sanjiv Harpavat; Jean P Molleston; Karen F Murray; Kasper S Wang; Nisreen Soufi; Lee M Bass; Estella M Alonso; Jorge A Bezerra; M Kyle Jensen; Binita M Kamath; Kathleen M Loomes; Cara L Mack; Philip Rosenthal; Benjamin L Shneider; Robert H Squires; Ronald J Sokol; Saul J Karpen
Journal:  Hepatol Commun       Date:  2020-10-03

6.  A Novel Model for Predicting the Clearance of Jaundice in Patients With Biliary Atresia After Kasai Procedure.

Authors:  Yimao Zhang; Qi Wang; Siyu Pu; Junxiang Wang; Bo Xiang; Juxian Liu; Shuguang Jin
Journal:  Front Pediatr       Date:  2022-01-31       Impact factor: 3.418

7.  Low gamma-glutamyl transpeptidase levels at presentation are associated with severity of liver illness and poor outcome in biliary atresia.

Authors:  Song Sun; Shan Zheng; Chun Shen; Rui Dong; Kuiran Dong; Jingying Jiang; Yifan Yang; Gong Chen
Journal:  Front Pediatr       Date:  2022-09-23       Impact factor: 3.569

  7 in total

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