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胆管闭锁肝门空肠吻合术(Kasai手术)的多变量危险因素分析:来自两个中心的25年经验

A multivariable risk factor analysis of the portoenterostomy (Kasai) procedure for biliary atresia: twenty-five years of experience from two centers.

作者信息

Altman R P, Lilly J R, Greenfeld J, Weinberg A, van Leeuwen K, Flanigan L

机构信息

Department of Surgery, College of Physicians & Surgeons, Columbia University, Babies & Children's Hospital of New York, NY 10032, USA.

出版信息

Ann Surg. 1997 Sep;226(3):348-53; discussion 353-5. doi: 10.1097/00000658-199709000-00014.

Abstract

OBJECTIVE

The authors investigated risk factors for failure after portoenterostomy for biliary atresia using univariate and multivariable methods.

SUMMARY BACKGROUND DATA

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.

METHODS

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.

RESULTS

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.

CONCLUSIONS

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%.

摘要

目的

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。

总结背景资料

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。

方法

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。

结果

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。

结论

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%。

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本文引用的文献

1
Biliary atresia: the King's College Hospital experience (1974-1995).
J Pediatr Surg. 1997 Mar;32(3):479-85. doi: 10.1016/s0022-3468(97)90611-4.
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Biliary atresia: should all patients undergo a portoenterostomy?胆道闭锁:所有患者都应接受肝门空肠吻合术吗?
J Pediatr Surg. 1997 Feb;32(2):168-72; discussion 172-4. doi: 10.1016/s0022-3468(97)90173-1.
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Surgical limitation for biliary atresia: indication for liver transplantation.
J Pediatr Surg. 1989 Sep;24(9):851-4. doi: 10.1016/s0022-3468(89)80580-9.
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Optimal therapy for patients with biliary atresia: portoenterostomy ("Kasai" procedures) versus primary transplantation.
J Pediatr Surg. 1990 Jan;25(1):153-60; discussion 160-2. doi: 10.1016/s0022-3468(05)80183-6.

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