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用于治疗胆道闭锁的葛西手术。

The Kasai procedure in the treatment of biliary atresia.

作者信息

Oh M, Hobeldin M, Chen T, Thomas D W, Atkinson J B

机构信息

Division of Surgery, Children's Hospital Los Angeles, CA, USA.

出版信息

J Pediatr Surg. 1995 Jul;30(7):1077-80; discussion 1080-1. doi: 10.1016/0022-3468(95)90345-3.

Abstract

From 1978 to 1992, 62 patients were diagnosed as having extrahepatic biliary atresia (EHBA) at Childrens Hospital Los Angeles. The patients presented with either persistent jaundice, alcoholic stools, and/or hepatomegaly. Hepatobiliary IDA scans were performed in 47 of the patients; 46 had results typical of EHBA. Fifty-nine of the 62 patients underwent a Kasai portoenterostomy; three patients were more than 4 months of age at initial presentation and were referred directly for liver transplantation. The preoperative total bilirubin level for all patients averaged 8.6 mg/dL (range, 4.1 to 18.1). All patients underwent a standardized Kasai procedure using a 40-cm Roux-en-Y intestinal segment performed in the end-to-side fashion. Postoperative management included oral antibiotics and fat-soluble vitamins for at least 9 months. Long-term complications included cholangitis in 20 cases and portal hypertension in 25, which led to variceal hemorrhage in 12 cases. Growth rates were at or above the 50th percentile for age in 59% of the Kasai patients. Forty-one of the 59 Kasai patients survived (69.5%); six deaths occurred within 2 years after the Kasai procedure. Twelve patients were lost to follow-up within 2 years after surgery, and for calculation of mortality were presumed dead. Seventeen patients had follow-up for 5 or more years, 13 had follow-up for 2 to 5 years, and 29 had follow-up for less than 2 years. The average total bilirubin level for the patients with less than 2 years of follow-up was 7.9 mg/dL (0.3 to 20.8), and that for the patients with more than 2 years of follow-up was 1.6 mg/dL (0.3 to 18.1). Orthotopic liver transplantation was performed in 11 Kasai patients, in whom chronic liver failure eventually developed. Rejection occurred in one of these patients, which required retransplantation. Based on these results, the Kasai portoenterostomy procedure continues to offer palliation, if not long-term success, in a large percentage of patients with EHBA.

摘要

1978年至1992年期间,洛杉矶儿童医院诊断出62例肝外胆管闭锁(EHBA)患者。这些患者表现为持续性黄疸、陶土样便和/或肝肿大。47例患者进行了肝胆显像扫描;46例结果典型为EHBA。62例患者中有59例行Kasai肝门肠吻合术;3例初诊时年龄超过4个月,直接被转诊进行肝移植。所有患者术前总胆红素水平平均为8.6mg/dL(范围4.1至18.1)。所有患者均采用40cm的Roux-en-Y肠段,以端侧方式进行标准化Kasai手术。术后管理包括口服抗生素和脂溶性维生素至少9个月。长期并发症包括20例胆管炎和25例门静脉高压,其中12例导致静脉曲张出血。59%接受Kasai手术的患者生长速率达到或高于同龄人的第50百分位数。59例接受Kasai手术的患者中有41例存活(69.5%);6例在Kasai手术后2年内死亡。12例患者在术后2年内失访,计算死亡率时假定已死亡。17例患者随访5年或更长时间,13例随访2至5年,29例随访时间不足2年。随访时间不足2年的患者平均总胆红素水平为7.9mg/dL(0.3至20.8),随访时间超过2年的患者为1.6mg/dL(0.3至18.1)。11例接受Kasai手术且最终发展为慢性肝衰竭的患者接受了原位肝移植。其中1例发生排斥反应,需要再次移植。基于这些结果,Kasai肝门肠吻合术在很大比例的EHBA患者中继续提供缓解,即使不是长期成功。

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