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新生儿缺氧缺血性脑病后神经发育结局的预测模型。

Predictive Models of Neurodevelopmental Outcomes After Neonatal Hypoxic-Ischemic Encephalopathy.

机构信息

Department of Pediatrics, University of Nebraska Medical Center, Omaha, Nebraska;

Department of Pediatrics, School of Medicine, Washington University in St Louis, St Louis, Missouri.

出版信息

Pediatrics. 2021 Feb;147(2). doi: 10.1542/peds.2020-022962. Epub 2021 Jan 15.

DOI:10.1542/peds.2020-022962
PMID:33452064
Abstract

OBJECTIVES

To develop predictive models for death or neurodevelopmental impairment (NDI) after neonatal hypoxic-ischemic encephalopathy (HIE) from data readily available at the time of NICU admission ("early") or discharge ("cumulative").

METHODS

In this retrospective cohort analysis, we used data from the Children's Hospitals Neonatal Consortium Database (2010-2016). Infants born at ≥35 weeks' gestation and treated with therapeutic hypothermia for HIE at 11 participating sites were included; infants without Bayley Scales of Infant Development scores documented after 11 months of age were excluded. The primary outcome was death or NDI. Multivariable models were generated with 80% of the cohort; validation was performed in the remaining 20%.

RESULTS

The primary outcome occurred in 242 of 486 infants; 180 died and 62 infants surviving to follow-up had NDI. HIE severity, epinephrine administration in the delivery room, and respiratory support and fraction of inspired oxygen of 0.21 at admission were significant in the early model. Severity of EEG findings was combined with HIE severity for the cumulative model, and additional significant variables included the use of steroids for blood pressure management and significant brain injury on MRI. Discovery models revealed areas under the curve of 0.852 for the early model and of 0.861 for the cumulative model, and both models performed well in the validation cohort (goodness-of-fit χ: = .24 and .06, respectively).

CONCLUSIONS

Establishing reliable predictive models will enable clinicians to more accurately evaluate HIE severity and may allow for more targeted early therapies for those at highest risk of death or NDI.

摘要

目的

从新生儿缺氧缺血性脑病(HIE)患儿入住新生儿重症监护病房(NICU)时(“早期”)或出院时(“累积”)即可获得的数据中,开发预测死亡或神经发育障碍(NDI)的模型。

方法

在这项回顾性队列分析中,我们使用了来自儿童医院新生儿联合会数据库(2010-2016 年)的数据。纳入胎龄≥35 周且在 11 个参与地点接受治疗性低温治疗 HIE 的婴儿;排除 11 个月后未记录贝利婴幼儿发展量表评分的婴儿。主要结局是死亡或 NDI。使用队列的 80%生成多变量模型;在剩余的 20%中进行验证。

结果

主要结局发生在 486 名婴儿中的 242 名;180 名死亡,62 名存活至随访的婴儿患有 NDI。早期模型中,HIE 严重程度、产房内肾上腺素的使用、入院时的呼吸支持和吸入氧分数为 0.21 具有显著意义。累积模型中,脑电图发现的严重程度与 HIE 严重程度相结合,其他显著变量包括用于血压管理的类固醇和 MRI 上有明显的脑损伤。发现模型显示早期模型的曲线下面积为 0.852,累积模型的曲线下面积为 0.861,两个模型在验证队列中表现良好(拟合优度 χ2:分别为 0.24 和 0.06)。

结论

建立可靠的预测模型将使临床医生能够更准确地评估 HIE 严重程度,并可能为那些死亡或患有 NDI 风险最高的患者提供更有针对性的早期治疗。

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