Altman R P, Lilly J R, Greenfeld J, Weinberg A, van Leeuwen K, Flanigan L
Department of Surgery, College of Physicians & Surgeons, Columbia University, Babies & Children's Hospital of New York, NY 10032, USA.
Ann Surg. 1997 Sep;226(3):348-53; discussion 353-5. doi: 10.1097/00000658-199709000-00014.
The authors investigated risk factors for failure after portoenterostomy for biliary atresia using univariate and multivariable methods.
Kasai's portoenterostomy has gained worldwide acceptance as the initial surgical therapy for infants with biliary atresia. Although extended survival has been achieved for many patients, factors influencing outcome have not been defined clearly.
The authors analyzed risks for failure in 266 patients treated from 1972 to 1996 by the Kaplan-Meier product limit estimate and Cox proportional hazards model. Failure was defined as death or transplant.
Age at surgery, surgical decade, and anatomy of atretic bile ducts were identified as independent risk factors. Five-year survival was 49% and median survival was 15 years when bile drainage was achieved. Sixty-five patients had liver transplants. Mean age at transplant was 5.4 years.
The outcome after portoenterostomy for biliary atresia is determined by age at surgery and anatomy of the atretic extrahepatic bile ducts. Liver transplant will salvage patients with failed Kasai with 10-year posttransplant survival of 71%.
作者采用单变量和多变量方法研究了胆道闭锁行肝门空肠吻合术后失败的危险因素。
对于患有胆道闭锁的婴儿,Kasai肝门空肠吻合术已作为初始手术治疗方法获得了全球认可。尽管许多患者实现了延长生存期,但影响预后的因素尚未明确界定。
作者通过Kaplan-Meier乘积限估计法和Cox比例风险模型分析了1972年至1996年期间接受治疗的266例患者的失败风险。失败定义为死亡或移植。
手术时年龄、手术年代以及闭锁胆管的解剖结构被确定为独立危险因素。实现胆汁引流时,5年生存率为49%,中位生存期为15年。65例患者接受了肝移植。移植时的平均年龄为5.4岁。
胆道闭锁行肝门空肠吻合术后的预后取决于手术时年龄和肝外闭锁胆管的解剖结构。肝移植可挽救Kasai手术失败的患者,移植后10年生存率为71%。