Stetson Alyssa, Bondoc Alexander, Tiao Greg
Cincinnati Children's Hospital Medical Center, United States.
Cincinnati Children's Hospital Medical Center, United States.
Semin Pediatr Surg. 2024 Dec;33(6):151476. doi: 10.1016/j.sempedsurg.2025.151476. Epub 2025 Jan 16.
The Kasai portoenterostomy (KPE) can provide a surgical cure for children with biliary atresia (BA), without the need for a liver transplant (OLTxp). Revision KPE can be attempted following a failed initial KPE where biliary clearance is not achieved. The most common indications for revision KPE are recurrent jaundice or recurrent cholangitis, although it has also been performed for persistent jaundice or bile lakes. Outcomes are heterogenous but the best results appear to be with recurrent jaundice or limited episodes of recurrent cholangitis. In the setting of a failed KPE, providers must make a patient-specific decision about whether to attempt revision KPE versus proceed with OLTxp. While the choice is multifactorial, patients who undergo revision KPE likely do not have worse long-term outcomes than patients who undergo a single KPE.
肝门空肠吻合术(KPE)可为患有胆道闭锁(BA)的儿童提供手术治愈方法,而无需进行肝移植(OLTxp)。在初次KPE失败且未实现胆汁清除的情况下,可以尝试进行KPE翻修术。KPE翻修术最常见的指征是复发性黄疸或复发性胆管炎,不过也有因持续性黄疸或胆汁湖而进行该手术的情况。结果各异,但似乎复发性黄疸或复发性胆管炎发作次数有限时效果最佳。在KPE失败的情况下,医疗人员必须根据患者的具体情况决定是尝试进行KPE翻修术还是继续进行OLTxp。虽然选择是多因素的,但接受KPE翻修术的患者的长期预后可能并不比接受单次KPE的患者差。