冠状动脉计算机断层血管造影预测风险与实际存在冠状动脉粥样硬化的比较。

IF 1.3 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS
Emma Playford, Simon Stewart, Gerard Hoyne, Geoff Strange, Girish Dwivedi, Christian Hamilton-Craig, Gemma Figtree, David Playford
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引用次数: 0

摘要

背景:有有限的数据显示,传统心血管风险评分(CVRS)预测无症状冠状动脉疾病(CAD)的准确性是由冠状动脉计算机断层扫描血管造影(CCTA)确定的。方法:回顾性提取没有已知CAD的无症状个体,进行筛查CCTA,并提供足够的数据来计算其CVRS。使用自然语言处理CCTA报告提取动脉粥样硬化,包括冠状动脉钙评分(CACS)和CAD的程度和严重程度。无动脉粥样硬化被定义为零斑块和零CACS,根据斑块负担的位置和程度,动脉粥样硬化被定义为低、中度或广泛。结果:828例(中位年龄58.6岁,IQR = 52.0, 65.3岁,57%男性)符合纳入标准,其中13例、483例、113例和219例(男性分别占8%、49%、74%和66%)CVRS为零、低、中、高。548次扫描中主要检测到低斑块负荷动脉粥样硬化(67%为男性)。然而,在广泛动脉粥样硬化的137名男性和68名女性中,分别有47名(34%)和38名(56%)的CVRS分级较低。总体而言,23%的男性和31%的女性有CVRS预测的CAD (Monte Carlo:女性,p = 0.024;男性,p κ = 0.149;雌性,κ = 0.096)。结论:在没有已知CAD的无症状个体中,低CVRS并不排除广泛的CAD。包含额外标记的新工具可能有助于这些个体的风险预测。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparing predictive risk to actual presence of coronary atherosclerosis on coronary computed tomography angiography.

Background: There is limited data showing the predictive accuracy of traditional cardiovascular risk scores (CVRS) to predict asymptomatic coronary artery disease (CAD) determined by coronary computed tomography angiography (CCTA).

Methods: Asymptomatic individuals without known CAD undergoing a screening CCTA and sufficient data to calculate their CVRS, were extracted retrospectively. Atherosclerosis was extracted using natural language processing of the CCTA report, including the coronary artery calcium score (CACS) and the extent and severity of CAD. Absence of atherosclerosis was defined as both zero plaque and zero CACS, and atherosclerosis was defined as low, moderate, or extensive by location and extent of plaque-burden. CVRS was categorized as high (>15 %), moderate (10-15 %), low (1-9 %) and "zero" (<1 %) risk.

Results: 828 individuals (median age 58.6, IQR = 52.0, 65.3 years, 57 % male) met inclusion criteria, and a zero, low, moderate, and high CVRS was identified in 13, 483, 113 and 219 individuals (8 %, 49 %, 74 %, 66 % male), respectively. Predominantly low plaque-burden atherosclerosis was detected in 548 scans (67 % male). However, of the 137 males and 68 females with extensive atherosclerosis, 47 (34 %) and 38 (56 %) respectively had low CVRS classification. Overall, 23 % of males and 31 % of females had CAD predicted by CVRS (Monte Carlo: females, p = 0.024; males, p < 0.001), but there was little to no agreement between CVRS and atherosclerosis burden (Cohen's kappa: males, κ = 0.149; females, κ = 0.096).

Conclusions: In asymptomatic individuals without known CAD, a low CVRS does not exclude extensive CAD. Newer tools incorporating additional markers may be helpful in risk prediction in such individuals.

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