摘要
胆道闭锁(biliary atresia,BA)是一种严重的婴幼儿肝胆系统疾病,是儿童肝移植最常见的指征。对患儿进行预后评估及选择个性化治疗对于BA的治疗至关重要,目前尚没有规范化的BA预后预测模型对BA患儿进行有效的预后评估。本文就胆道闭锁葛西术后自体肝生存的预后危险因素及相关预测模型的研究新进展进行综述。
As a severe disease of hepatobiliary system in infants and toddlers,biliary atresia(BA)is thes most common indication for liver transplantation(LT).Prognostic assessments and individualized treatments are crucial for managing BA.Currently there is still no standardized prognostic prediction model for effectively assessing the prognosis of BA patients.This review summarized the latest advances of risk factors and predictive models for native liver survival(NLS)after Kasai procedure.
作者
陈惠芬
郑珊
Chen Huifen;Zheng Shan(Department of Pediatric Hepatobiliary Surgery,Children's Hospital of Fudan University,Shanghai 210008,China)
出处
《中华小儿外科杂志》
CSCD
北大核心
2024年第6期559-563,共5页
Chinese Journal of Pediatric Surgery
关键词
胆道闭锁
预后
预测模型
Biliary atresia
Prognosis
Predictive model