Liu Jin-Qiao, Chen Wen-Juan, Zhou Meng-Jie, Li Wen-Feng, Tang Ju, Zhou Qi-Chang
Department of Ultrasound, The Second Xiangya Hospital of Central South University, Changsha, China.
Department of Ultrasound, Hunan Children's Hospital, Changsha, China.
Front Pediatr. 2021 Feb 24;9:641318. doi: 10.3389/fped.2021.641318. eCollection 2021.
Although Kasai portoenterostomy (KPE) is performed timely for most children with biliary atresia (BA), the native liver survival (NLS) is still poor due to the progressive liver fibrosis. Many children have to receive liver transplantation (LT) within 2 years after KPE. Early prediction of the prognosis permits the implementation of prophylactic treatments for BA children. However, studies about the prediction are limited. The purpose of this study is to establish a nomogram to predict the prognosis of BA children within 2 years after KPE. The follow-up data of 151 BA children were retrospectively reviewed, and were randomly divided into a training cohort for constructing a nomogram ( = 103) and a validation cohort ( = 48). In the training cohort, patients were divided into Group A and Group B according to whether death or LT were observed within 2 years post-KPE. Multivariate Cox regression based on the baseline characteristics, liver function indicators and LSM (liver stiffness measurement) values at KPE and 3 months after KPE was utilized for the establishment of the nomogram in predicting the prognosis of BA within 2 years after KPE. The discrimination and calibration of the nomogram were internally and externally validated. Fifty-six BA children were included in Group A and 47 were included in group B. Age at KPE, METAVIR score F4, LSM at 3 months, first onset of cholangitis within 3 months, and jaundice clearance time were the independent predictors for the prognosis of BA children within 2 years after KPE (all < 0.05). The developed nomogram based on these independent predictors showed good discrimination and calibration by the internal and external validation. Its performance was better than each predictor in predicting the prognosis (all < 0.05). The established nomogram based on the indicators from the first 3 months after KPE may be useful for predicting the prognosis of BA children within 2 years post-KPE and helpful for the consideration of LT.
尽管大多数胆道闭锁(BA)患儿都及时接受了 Kasai 肝门空肠吻合术(KPE),但由于进行性肝纤维化,自体肝存活率(NLS)仍然很低。许多患儿在 KPE 术后 2 年内不得不接受肝移植(LT)。早期预测预后有助于对 BA 患儿实施预防性治疗。然而,关于预测的研究有限。本研究的目的是建立一个列线图,以预测 KPE 术后 2 年内 BA 患儿的预后。回顾性分析了 151 例 BA 患儿的随访数据,并将其随机分为用于构建列线图的训练队列(n = 103)和验证队列(n = 48)。在训练队列中,根据 KPE 术后 2 年内是否观察到死亡或 LT,将患者分为 A 组和 B 组。基于 KPE 时及 KPE 后 3 个月的基线特征、肝功能指标和肝脏硬度测量(LSM)值,采用多因素 Cox 回归建立列线图,以预测 KPE 术后 2 年内 BA 的预后。对列线图的区分度和校准度进行了内部和外部验证。A 组纳入 56 例 BA 患儿,B 组纳入 47 例。KPE 时的年龄、METAVIR 评分 F4、3 个月时的 LSM、3 个月内首次发生胆管炎以及黄疸消退时间是 KPE 术后 2 年内 BA 患儿预后的独立预测因素(均 P < 0.05)。基于这些独立预测因素开发的列线图经内部和外部验证显示出良好的区分度和校准度。在预测预后方面,其性能优于每个预测因素(均 P < 0.05)。基于 KPE 后前 3 个月指标建立的列线图可能有助于预测 KPE 术后 2 年内 BA 患儿的预后,并有助于考虑是否进行 LT。