Liver transplantation for the Budd-Chiari syndrome

Ann Surg. 1990 Jan;211(1):43-9. doi: 10.1097/00000658-199001000-00007.

Abstract

A retrospective study was performed that analyzed 23 patients who had an orthotopic liver transplantation for the Budd-Chiari syndrome with end-stage liver disease. Patient follow-up was as long as 14 years. The technical considerations relevant to the Budd-Chiari syndrome were discussed. There have been no serious complications of postoperative anticoagulation. Three patients, all of whom died, had recurrence of the Budd-Chiari syndrome. No other patient has had evidence of recurrent Budd-Chiari syndrome on postoperative liver biopsies. One-, 3-, and 5-year actuarial survival was 68.8%, 44.7%, and 44.7%, respectively. It was concluded that orthotopic liver transplantation is the most effective treatment for patients with the Budd-Chiari syndrome and end-stage liver disease.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adolescent
  • Adult
  • Budd-Chiari Syndrome / mortality
  • Budd-Chiari Syndrome / pathology
  • Budd-Chiari Syndrome / surgery*
  • Cause of Death
  • Female
  • Hepatic Artery
  • Humans
  • Liver / pathology
  • Liver Transplantation*
  • Male
  • Middle Aged
  • Postoperative Complications / epidemiology
  • Prothrombin Time
  • Recurrence
  • Retrospective Studies
  • Splenic Vein
  • Thrombosis / epidemiology