A simplified approach to identification of risk status in patients with atherosclerotic cardiovascular disease

医学 推车 心肌梗塞 指南 内科学 疾病 急性冠脉综合征 冲程(发动机) 冠状动脉疾病 人口 病史 弗雷明翰风险评分 病历 回顾性队列研究 急诊医学 心脏病学 病理 工程类 环境卫生 机械工程
作者
Aparna Sajja,Hsin-Fang Li,Kateri J. Spinelli,Amir Ali,Salim S. Virani,Seth S. Martin,Ty J. Gluckman
出处
期刊:American journal of preventive cardiology [Elsevier BV]
卷期号:7: 100187-100187 被引量:1
标识
DOI:10.1016/j.ajpc.2021.100187
摘要

The 2018 American Heart Association/American College of Cardiology (AHA/ACC) Blood Cholesterol Guideline recommendation to classify patients with atherosclerotic cardiovascular disease (ASCVD) as very high-risk (VHR) vs not-VHR (NVHR) has important implications for escalation of medical therapy. We aimed to define the prevalence and clinical characteristics of these two groups within a large multi-state healthcare system and develop a simpler means to assist clinicians in identifying VHR patients using classification and regression tree (CART) analysis.We performed a retrospective analysis of all patients in a 28-hospital US healthcare system in 2018. ICD-10 codes were used to define the ASCVD population. Per the AHA/ACC Guideline, VHR status was defined by ≥2 major ASCVD events or 1 major ASCVD event and ≥2 high-risk conditions. CART analysis was performed on training and validation datasets. A random forest model was used to verify results.Of 180,669 ASCVD patients identified, 58% were VHR. Among patients with a history of myocardial infarction (MI) or recent acute coronary syndrome (ACS), 99% and 96% were classified as VHR, respectively. Both CART and random forest models identified recent ACS, ischemic stroke, hypertension, peripheral artery disease, history of MI, and age as the most important predictors of VHR status. Using five rules identified by CART analysis, fewer than 50% of risk factors were required to assign VHR status.CART analysis helped to streamline the identification of VHR patients based on a limited number of rules and risk factors. This approach may help improve clinical decision making by simplifying ASCVD risk assessment at the point of care. Further validation is needed, however, in more diverse populations.
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