Halff G, Todo S, Tzakis A G, Gordon R D, Starzl T E
Department of Surgery, University Health Center of Pittsburgh, University of Pittsburgh, Pennsylvania.
Ann Surg. 1990 Jan;211(1):43-9. doi: 10.1097/00000658-199001000-00007.
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.
进行了一项回顾性研究,分析了23例因布加综合征合并终末期肝病接受原位肝移植的患者。患者随访时间长达14年。讨论了与布加综合征相关的技术要点。术后抗凝未出现严重并发症。3例患者均死亡,出现了布加综合征复发。术后肝活检未发现其他患者有布加综合征复发的证据。1年、3年和5年的精算生存率分别为68.8%、44.7%和44.7%。得出的结论是,原位肝移植是布加综合征合并终末期肝病患者最有效的治疗方法。