Prediction of obstructive coronary artery disease and prognosis in patients with suspected stable angina

医学 内科学 心脏病学 心肌梗塞 试验前后概率 四分位数 血运重建 心绞痛 冠状动脉疾病 人口 心力衰竭 冲程(发动机) 部分流量储备 不稳定型心绞痛 冠状动脉造影 置信区间 工程类 环境卫生 机械工程
作者
Jacob Reeh,Christina Bachmann Therming,Merete Heitmann,Søren Højberg,Charlotte Sørum,Jan Bech,Dorte Husum,Helena Domínguez,Thomas Sehestedt,Thomas Hermann,Kim Wadt Hansen,Lene Simonsen,Søren Galatius,Eva Prescott
出处
期刊:European Heart Journal [Oxford University Press]
卷期号:40 (18): 1426-1435 被引量:216
标识
DOI:10.1093/eurheartj/ehy806
摘要

Abstract Aims We hypothesized that the modified Diamond–Forrester (D-F) prediction model overestimates probability of coronary artery disease (CAD). The aim of this study was to update the prediction model based on pre-test information and assess the model’s performance in predicting prognosis in an unselected, contemporary population suspected of angina. Methods and results We included 3903 consecutive patients free of CAD and heart failure and suspected of angina, who were referred to a single centre for assessment in 2012–15. Obstructive CAD was defined from invasive angiography as lesion requiring revascularization, >70% stenosis or fractional flow reserve <0.8. Patients were followed (mean follow-up 33 months) for myocardial infarction, unstable angina, heart failure, stroke, and death. The updated D-F prediction model overestimated probability considerably: mean pre-test probability was 31.4%, while only 274 (7%) were diagnosed with obstructive CAD. A basic prediction model with age, gender, and symptoms demonstrated good discrimination with C-statistics of 0.86 (95% CI 0.84–0.88), while a clinical prediction model adding diabetes, family history, and dyslipidaemia slightly improved the C-statistic to 0.88 (0.86–0.90) (P for difference between models <0.0001). Quartiles of probability of CAD from the clinical prediction model provided good diagnostic and prognostic stratification: in the lowest quartiles there were no cases of obstructive CAD and cumulative risk of the composite endpoint was less than 3% at 2 years. Conclusion The pre-test probability model recommended in current ESC guidelines substantially overestimates likelihood of CAD when applied to a contemporary, unselected, all-comer population. We provide an updated prediction model that identifies subgroups with low likelihood of obstructive CAD and good prognosis in which non-invasive testing may safely be deferred.
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