阻塞性睡眠呼吸暂停患者的社会风险因素和心血管风险:社区卫生中心临床预测因素的系统评估

Q2 Computer Science
Diego R Mazzotti, Ryan Urbanowicz, Marta Jankowska
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引用次数: 0

摘要

我们利用来自全国社区卫生中心网络(ADVANCE)临床研究网络(CRN)加速数据价值的电子健康记录(EHR)数据来识别社会风险因素集群,评估其与阻塞性睡眠呼吸暂停(OSA)的关联,并确定OSA患者心血管(CV)结局的相关临床预测因素。通过潜在类别分析,使用地理信息社会指标来定义社会风险因素集群。使用流程化(一种端到端严格且可解释的自动化机器学习管道),将ehr全范围诊断用作5年主要不良CV事件(MACE)发生率的预测因子。对140多万人的分析显示,社会负担最低(35.7%)、平均(43.6%)和最高(22.7%)是三个主要的社会风险因素集群。在调整分析中,与社会负担最低的患者相比,社会负担最重的患者被诊断为OSA的可能性更小(OR [95%CI]=0.85[0.82-0.88])。在患有OSA且无既往CV疾病的患者中(N=4,405),预测MACE事件的ROC-AUC总体达到0.70[0.03],但在每个社会风险因素集群内评估时存在差异。特征重要性也揭示了不同的临床因素可能解释每个集群之间的预测。结果表明,在OSA患者中,OSA的诊断和心血管疾病的临床预测指标存在相关的健康差异,这表明有必要采取针对性的干预措施,以尽量减少这些差异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Social risk factors and cardiovascular risk in obstructive sleep apnea: a systematic assessment of clinical predictors in community health centers.

We leveraged electronic health record (EHR) data from the Accelerating Data Value Across a National Community Health Center Network (ADVANCE) Clinical Research Network (CRN) to identify social risk factor clusters, assess their association with obstructive sleep apnea (OSA), and determine relevant clinical predictors of cardiovascular (CV) outcomes among those experiencing OSA. Geographically informed social indicators were used to define social risk factor clusters via latent class analysis. EHR-wide diagnoses were used as predictors of 5-year incidence of major adverse CV events (MACE) using STREAMLINE, an end-to-end rigorous and interpretable automated machine learning pipeline. Analyses among over 1.4 million individuals revealed three major social risk factor clusters: lowest (35.7%), average (43.6%) and highest (22.7%) social burden. In adjusted analyses, those experiencing highest social burden were less likely to have received a diagnosis of OSA when compared to those experiencing lowest social burden (OR [95%CI]=0.85[0.82-0.88]). Among those with OSA and free of prior CV diseases (N=4,405), performance of predicting incident MACE reached a ROC-AUC of 0.70 [0.03] overall but varied when assessed within each social risk factor cluster. Feature importance also revealed that different clinical factors might explain predictions among each cluster. Results suggest relevant health disparities in the diagnosis of OSA and across clinical predictors of CV diseases among those with OSA, across social risk factor clusters, indicating that tailored interventions geared toward minimizing these disparities are warranted.

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