用于预测 90 天和 365 天内 ASCVD 短期风险的新型机器学习模型。

IF 3.2 Q1 HEALTH CARE SCIENCES & SERVICES
Frontiers in digital health Pub Date : 2024-11-01 eCollection Date: 2024-01-01 DOI:10.3389/fdgth.2024.1485508
Tomer Gazit, Hanan Mann, Shiri Gaber, Pavel Adamenko, Granit Pariente, Liron Volsky, Amir Dolev, Helena Lyson, Eyal Zimlichman, Jay A Pandit, Edo Paz
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引用次数: 0

摘要

背景:目前的动脉粥样硬化性心血管疾病(ASCVD)风险评估工具,如集合队列方程(PCEs)和 PREVENT™ 评分,可提供长期预测,但可能无法有效推动行为改变。利用移动医疗(mHealth)数据和电子健康记录(EHR)进行短期风险预测可以加强临床决策和患者参与。本研究旨在利用移动医疗和电子病历数据为高血压患者开发一个短期 ASCVD 风险预测模型,并将其性能与现有的风险评估工具进行比较:这是一项回顾性队列研究,包括51127名年龄≥18岁的高血压患者,他们在2015年1月至2024年1月期间参加了你好心脏CV风险自我管理项目。研究人员从电子病历数据以及通过家用血压计收集的移动医疗血压和心率测量数据中得出了一个机器学习(ML)模型。其性能与 PCE 和 PREVENT 进行了比较:结果:包含 291 个特征的 XgBoost 模型在两个预测期的 ASCVD 风险判别能力均优于 PCE 和 PREVENT 评分。在 90 天预测中,平均 C 统计量为 0.81(XgBoost)vs 0.74(PCE)和 0.65(PREVENT)。移动医疗测量增强了 365 天的风险预测能力(ROC-AUC 为 0.82,而无移动医疗测量时为 0.80):结论:与传统工具相比,基于电子病历和移动医疗的 ML 模型可提供更优越的短期 ASCVD 预测。这种方法支持个性化的预防策略,尤其适用于 PCE 或 PREVENT 特征不完整的人群。进一步的研究应探索这种新颖的风险预测框架,特别是更多的移动医疗数据整合,以扩大适用范围并提高预测能力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A novel, machine-learning model for prediction of short-term ASCVD risk over 90 and 365 days.

Background: Current atherosclerotic cardiovascular disease (ASCVD) risk assessment tools like the Pooled Cohort Equations (PCEs) and PREVENT™ scores offer long-term predictions but may not effectively drive behavior change. Short-term risk predictions using mobile health (mHealth) data and electronic health records (EHRs) could enhance clinical decision-making and patient engagement. The aim of this study was to develop a short-term ASCVD risk prediction model for hypertensive individuals using mHealth and EHR data and compare its performance to existing risk assessment tools.

Methods: This is a retrospective cohort study including 51,127 hypertensive participants aged ≥18 years old who enrolled in the Hello Heart CV risk self-management program between January 2015 and January 2024. A machine learning (ML) model was derived from EHR data and mHealth measurements of blood pressure (BP) and heart rate (HR) collected via at-home BP monitors. Its performance was compared to that of PCE and PREVENT.

Results: The XgBoost model incorporating 291 features outperformed the PCE and PREVENT scores in discriminating ASCVD risk for both prediction periods. For 90-day prediction, mean C-statistics were 0.81 (XgBoost) vs. 0.74 (PCE) and 0.65 (PREVENT). Similar findings were observed for 365-day prediction. mHealth measurements incrementally enhanced 365-day risk prediction (ROC-AUC 0.82 vs. 0.80 without mHealth).

Conclusion: An EHR and mHealth-based ML model offers superior short-term ASCVD prediction compared to traditional tools. This approach supports personalized preventive strategies, particularly for populations with incomplete features for PCE or PREVENT. Further research should explore this novel risk prediction framework, and particularly additional mHealth data integration for broader applicability and increased predictive power.

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