A machine learning approach to predict mortality and neonatal persistent pulmonary hypertension in newborns with congenital diaphragmatic hernia. A retrospective observational cohort study.

IF 3 3区 医学 Q1 PEDIATRICS
Luana Conte, Ilaria Amodeo, Giorgio De Nunzio, Genny Raffaeli, Irene Borzani, Nicola Persico, Alice Griggio, Giuseppe Como, Mariarosa Colnaghi, Monica Fumagalli, Donato Cascio, Giacomo Cavallaro
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引用次数: 0

Abstract

Congenital diaphragmatic hernia (CDH) has high morbidity and mortality rates. This study aimed to develop a machine learning (ML) algorithm to predict outcomes based on prenatal and early postnatal data. This retrospective observational cohort study involved infants with left-sided CDH, born from 2012 to 2020. We analyzed clinical and imaging data using three classification algorithms: XGBoost, Support Vector Machine, and K-Nearest Neighbors. Medical records of 165 pregnant women with CDH fetal diagnosis were reviewed. According to inclusion criteria, 50 infants with isolated left-sided CDH were enrolled. The mean o/eLHR was 37.32%, and the average gestational age at delivery was 36.5 weeks. Among these infants, 26 (52%) had severe persistent neonatal pulmonary hypertension (PPHN), while 24 (48%) had moderate or mild form; 37 survived (74%), and 13 did not (26%). The XGBoost model achieved 88% accuracy and 95% sensitivity for predicting mortality using ten features and 82% accuracy for PPHN severity with 14 features. The area under the ROC curve was 0.87 for mortality and 0.82 for PPHN severity.

Conclusion: ML models show promise in predicting CDH outcomes and supporting clinical decisions. Future research should focus on more extensive studies to refine these algorithms and improve care management.

Clinical trial registration: NCT04609163.

What is known: • Congenital diaphragmatic hernia (CDH) is a serious condition characterized by high morbidity and mortality rates, making it critical to predict neonatal outcomes for effective clinical management accurately. • Traditional prenatal diagnostic methods often struggle to predict complications such as Neonatal Persistent Pulmonary Hypertension (PPHN) in CDH, highlighting the need for innovative predictive approaches.

What is new: • Machine learning (ML) models, particularly XGBoost, have been shown to accurately forecast mortality and the severity of PPHN in infants with CDH based on prenatal and early postnatal clinical and imaging data. • ML-based predictive models can enhance prenatal counseling, optimize birth planning, and tailor postnatal care for patients with CDH, enabling real-time risk assessment and adaptive management strategies.

先天性膈疝(CDH)的发病率和死亡率都很高。本研究旨在开发一种机器学习(ML)算法,根据产前和产后早期数据预测预后。这项回顾性观察队列研究涉及 2012 年至 2020 年出生的左侧 CDH 婴儿。我们使用三种分类算法分析了临床和成像数据:XGBoost、支持向量机和 K-近邻。我们查阅了 165 名诊断为 CDH 胎儿的孕妇的医疗记录。根据纳入标准,50 名孤立左侧 CDH 婴儿入选。平均o/eLHR为37.32%,平均胎龄为36.5周。在这些婴儿中,26 例(52%)患有重度持续性新生儿肺动脉高压(PPHN),24 例(48%)为中度或轻度;37 例存活(74%),13 例未存活(26%)。XGBoost 模型使用 10 个特征预测死亡率的准确率为 88%,灵敏度为 95%;使用 14 个特征预测 PPHN 严重程度的准确率为 82%。死亡率的 ROC 曲线下面积为 0.87,PPHN 严重程度的 ROC 曲线下面积为 0.82:ML模型有望预测CDH的预后并支持临床决策。未来的研究应侧重于更广泛的研究,以完善这些算法并改善护理管理:临床试验注册:NCT04609163:- 先天性膈疝(CDH)是一种以高发病率和高死亡率为特征的严重疾病,因此准确预测新生儿预后以进行有效的临床管理至关重要。- 传统的产前诊断方法往往难以预测 CDH 的并发症,如新生儿持续性肺动脉高压(PPHN),这凸显了对创新预测方法的需求:- 机器学习(ML)模型,尤其是 XGBoost,已被证明能根据产前和产后早期的临床和成像数据准确预测 CDH 婴儿的死亡率和 PPHN 的严重程度。- 基于 ML 的预测模型可以加强产前咨询、优化分娩计划并为 CDH 患者量身定制产后护理,从而实现实时风险评估和适应性管理策略。
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来源期刊
CiteScore
5.90
自引率
2.80%
发文量
367
审稿时长
3-6 weeks
期刊介绍: The European Journal of Pediatrics (EJPE) is a leading peer-reviewed medical journal which covers the entire field of pediatrics. The editors encourage authors to submit original articles, reviews, short communications, and correspondence on all relevant themes and topics. EJPE is particularly committed to the publication of articles on important new clinical research that will have an immediate impact on clinical pediatric practice. The editorial office very much welcomes ideas for publications, whether individual articles or article series, that fit this goal and is always willing to address inquiries from authors regarding potential submissions. Invited review articles on clinical pediatrics that provide comprehensive coverage of a subject of importance are also regularly commissioned. The short publication time reflects both the commitment of the editors and publishers and their passion for new developments in the field of pediatrics. EJPE is active on social media (@EurJPediatrics) and we invite you to participate. EJPE is the official journal of the European Academy of Paediatrics (EAP) and publishes guidelines and statements in cooperation with the EAP.
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