Literature DB >> 29216021

Long-term Results and Quality of Life Assessment in Biliary Atresia Patients: A 35-Year Experience in a Tertiary Hospital.

Carol Wing Yan Wong1, Patrick Ho Yu Chung, Paul Kwong Hang Tam, Kenneth Kak Yuen Wong.   

Abstract

OBJECTIVES: To review long-term transplant-free survival and quality of life (QOL) of patients with biliary atresia (BA).
METHODS: A retrospective study reviewing all patients with Kasai operation between January 1, 1980 and December 31, 2015 was performed to evaluate the transplant-free survival. Subgroup analysis of patients older than 20 years was carried out to assess the QOL using the Short Form-36 Health Survey and incidences of disease-related complications. Comparison between patients with native and transplanted liver was performed using two-tailed independent samples t-test (P value < 0.05, significant).
RESULTS: The 20-year Kaplan-Meier transplant-free survival of the 141 patients in our study was 51%. The subgroup analysis of long-term survivors revealed a trend of increased prevalence of complications like esophageal varices, portal hypertension, and recurrent admissions in the patient groups with raised serum bilirubin (SB).Thirty-one patients were successfully contacted for QOL assessment, 26 (16 with native liver and 10 with transplanted liver) responded (76.5%). BA patients who were documented to have active complications have a significantly lower vitality score (50.7 vs 57.5, P = 0.015). There was no statistically significant difference in the scores between the transplanted group and the disease-free control group. However, the native liver group achieved a lower score in both the general health section (42.9 vs 49.6, P = 0.029) and the overall physical component (49.6 vs 54.4, P = 0.037).
CONCLUSIONS: A significant proportion of our patients survive with their native liver for more than 20 years. These long-term survivors may suffer from complications that impair their QOL. They require continuous life-long care.

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Mesh:

Year:  2018        PMID: 29216021     DOI: 10.1097/MPG.0000000000001854

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


  3 in total

1.  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

2.  Outcome of biliary atresia among Saudi children: A tertiary care center experience.

Authors:  Sinan Holdar; Badr Alsaleem; Ali Asery; Abdulrahman Al-Hussaini
Journal:  Saudi J Gastroenterol       Date:  2019 May-Jun       Impact factor: 2.485

3.  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

  3 in total

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