The efficacy of kasai operation for biliary atresia: A single institutional experience

Jer Nan Lin*, Kuei Liang Wang, Jiin Haur Chuang

*Corresponding author for this work

Research output: Contribution to journalJournal Article peer-review

25 Scopus citations

Abstract

To assess the efficacy of Kasai operation for biliary atresia, 60 cases during a 14-year period (1976 to 1989) at this institution were reviewed. Thirty-four (56.7%) underwent operation within 90 days of life, 11 (18.3%) between 90 and 120 days and 15 (25.0%) beyond 120 days. Fifty-six underwent hepaticoportojejunostomy and 4 underwent hepaticoportocholecystostomy. Follow-up was 1 to 14 years (mean, 7.2 years). The postoperative follow-up of these 60 patients was categorized into five groups: group A (16 patients, 26.7%) was characterized by survival > 3 years and without jaundice; group B (3 patients, 5.0%) was defined as survival > 3 years, but with jaundice; group C (11 patients, 18.3%) was defined by survival but follow-up <3 years, (this group was further divided into C1 [7 patients, 11.7%] if anicteric and C2 [4 patients, 6.7%] if icteric); group D (2 patients, 3.3%) was patients who underwent liver transplantation; and group E (28 patients, 46.7%) was the group of patients who died at time of review. Group A and group C1 were interpreted as success after Kasai operation; hence, the potential success rate in this series was 38.3% (23 patients). They were long-term survivers, and most of them performed normal activities appropriate for their ages. We concluded that approximately one third of patients with biliary atresia would benefit from or be curred by this operation, which should be the first attempt in the treatment of this disease entity.

Original languageEnglish
Pages (from-to)704-706
Number of pages3
JournalJournal of Pediatric Surgery
Volume27
Issue number6
DOIs
StatePublished - 06 1992

Keywords

  • Biliary atresia
  • Kasai operation
  • hepaticoportoenterostomy
  • liver transplantation

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