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基于电子健康记录的小儿急性呼吸窘迫综合征亚表型分类模型的开发与验证

Development and Validation of an Electronic Health Record-Based, Pediatric Acute Respiratory Distress Syndrome Subphenotype Classifier Model.

作者信息

Balcarcel Daniel R, Mai Mark V, Mehta Sanjiv D, Chiotos Kathleen, Sanchez-Pinto L Nelson, Himes Blanca E, Yehya Nadir

机构信息

Department of Anesthesiology and Critical Care Medicine, Children's Hospital of Philadelphia and University of Pennsylvania, Philadelphia, PA.

Department of Pediatrics (Critical Care Medicine), Children's Healthcare of Atlanta and Emory University School of Medicine, Atlanta, GA.

出版信息

Pediatr Crit Care Med. 2025 May 1;26(5):e611-e621. doi: 10.1097/PCC.0000000000003709. Epub 2025 Mar 6.

Abstract

OBJECTIVE

To determine if hyperinflammatory and hypoinflammatory pediatric acute respiratory distress syndrome (PARDS) subphenotypes defined using serum biomarkers can be determined solely from electronic health record (EHR) data using machine learning.

DESIGN

Retrospective, exploratory analysis using data from 2014 to 2022.

SETTING

Single-center quaternary care PICU.

PATIENTS

Two temporally distinct cohorts of PARDS patients, 2014-2019 and 2019-2022.

INTERVENTIONS

None.

MEASUREMENTS AND MAIN RESULTS

Patients in the derivation cohort ( n = 333) were assigned to hyperinflammatory or hypoinflammatory subphenotypes using biomarkers and latent class analysis. A machine learning model was trained on 165 EHR-derived variables to identify subphenotypes. The most important variables were selected for inclusion in a parsimonious model. The model was validated in a separate cohort ( n = 114). The EHR-based classifier achieved an area under the receiver operating characteristic curve (AUC) of 0.93 (95% CI, 0.87-0.98), with a sensitivity of 88% and specificity of 83% for determining hyperinflammatory PARDS. The parsimonious model, using only five laboratory values, achieved an AUC of 0.92 (95% CI, 0.86-0.98) with a sensitivity of 76% and specificity of 87% in the validation cohort.

CONCLUSIONS

This proof-of-concept study demonstrates that biomarker-based PARDS subphenotypes can be identified using EHR data at 24 hours of PARDS diagnosis. Further validation in larger, multicenter cohorts is needed to confirm the clinical utility of this approach.

摘要

目的

确定使用血清生物标志物定义的高炎症和低炎症小儿急性呼吸窘迫综合征(PARDS)亚表型是否可以仅通过机器学习从电子健康记录(EHR)数据中确定。

设计

使用2014年至2022年的数据进行回顾性探索性分析。

设置

单中心四级医疗重症监护病房。

患者

两个时间上不同的PARDS患者队列,2014 - 2019年和2019 - 2022年。

干预措施

无。

测量和主要结果

使用生物标志物和潜在类别分析将推导队列中的患者(n = 333)分为高炎症或低炎症亚表型。基于165个EHR衍生变量训练机器学习模型以识别亚表型。选择最重要的变量纳入简约模型。该模型在一个单独的队列(n = 114)中进行验证。基于EHR的分类器在确定高炎症PARDS时,受试者操作特征曲线(AUC)下面积为0.93(95%CI,0.87 - 0.98),灵敏度为88%,特异度为83%。仅使用五个实验室值的简约模型在验证队列中的AUC为0.92(95%CI,0.86 - 0.98),灵敏度为76%,特异度为87%。

结论

这项概念验证研究表明,可以在PARDS诊断24小时时使用EHR数据识别基于生物标志物的PARDS亚表型。需要在更大的多中心队列中进行进一步验证以确认这种方法的临床实用性。

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