Literature DB >> 31141068

MULTIVARIATE ANALYSIS OF BILIARY FLOW-RELATED FACTORS AND POST-KASAI SURVIVAL IN BILIARY ATRESIA PATIENTS.

Alexandre Rodrigues Ferreira1, Thaís Costa Nascentes Queiroz1, Paula Vieira Teixeira Vidigal1, Raquel di Paula Ferreira1, David Campos Wanderley1, Eleonora Druve Tavares Fagundes1.   

Abstract

BACKGROUND: Biliary atresia represents the most common surgically treatable cause of cholestasis in newborns. If not corrected, secondary biliary cirrhosis invariably results.
OBJECTIVE: To evaluate, through multivariate analysis, the prognostic factors associated with the presence of biliary flow and survival with the native liver following Kasai portoenterostomy.
METHODS: The study analyzed data from 117 biliary atresia patients who underwent portoenterostomy and had suitable histological material for evaluation. A logistic regression model was used to assess the presence of biliary flow. Survival was investigated through Kaplan-Meier curves and Cox-adjusted models.
RESULTS: One third of patients achieved biliary flow and the median age at surgery was 81 days. Age at surgery, albumin, postoperative complications, biliary atresia structural malformation (BASM), liver architecture, larger duct diameter at porta hepatis, and cirrhosis (Ishak score) were the initial variables for the multivariate analysis. Age at surgery >90 days was the only variable associated with the absence of biliary drainage. Survival analysis revealed that the absence of biliary flow (P<0.0001), age at surgery >90 days (P=0.035), and the presence of BASM (P<0.0001), alone, could predict death or need for liver transplantation. Multivariate analysis demonstrated that the absence of biliary flow (P<0.0001 hazard ratio [HR] 6.25, 95% confidence interval [CI] 3.19-12.22) and the presence of BASM (P=0.014 HR 2.16, 95% CI 1.17-3.99) were associated with lowest survival with the native liver.
CONCLUSION: Age at surgery >90 days was associated with absence of biliary flow. The presence of biliary drainage and the absence of structural malformations are cornerstone features for higher survival rates with the native liver.

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Year:  2019        PMID: 31141068     DOI: 10.1590/S0004-2803.201900000-18

Source DB:  PubMed          Journal:  Arq Gastroenterol        ISSN: 0004-2803


  4 in total

1.  The usefulness of immunohistochemical staining of bile tracts in biliary atresia.

Authors:  Joanna Cielecka-Kuszyk; Maria Janowska; Małgorzata Markiewicz; Piotr Czubkowski; Anna Ostoja-Chyżyńska; Joanna Beata Bierła; Bożena Cukrowska; Joanna Pawłowska
Journal:  Clin Exp Hepatol       Date:  2021-03-25

2.  Biological and Histological Assessment of the Hepatoportoenterostomy Role in Biliary Atresia as a Stand-Alone Procedure or as a Bridge toward Liver Transplantation.

Authors:  Raluca-Cristina Apostu; Vlad Fagarasan; Catalin C Ciuce; Radu Drasovean; Dan Gheban; Radu Razvan Scurtu; Alina Grama; Ana Cristina Stefanescu; Constantin Ciuce; Tudor Lucian Pop
Journal:  Medicina (Kaunas)       Date:  2020-12-28       Impact factor: 2.430

Review 3.  Impact of early Kasai portoenterostomy on short-term outcomes of biliary atresia: A systematic review and meta-analysis.

Authors:  Changzhen Yang; Meng Ke; Yan Zhou; Hang Xu; Mei Diao; Long Li
Journal:  Front Surg       Date:  2022-09-01

Review 4.  Peri-Operative Liver Fibrosis and Native Liver Survival in Pediatric Patients with Biliary Atresia: A Systematic Review and Meta-Analysis.

Authors:  Ashkan Jahangirnia; Irina Oltean; Youssef Nasr; Nayaar Islam; Arielle Weir; Joseph de Nanassy; Ahmed Nasr; Dina El Demellawy
Journal:  Pediatr Gastroenterol Hepatol Nutr       Date:  2022-09-05
  4 in total

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