Mayourian Joshua, El-Bokl Amr, Lukyanenko Platon, La Cava William G, Geva Tal, Valente Anne Marie, Triedman John K, Ghelani Sunil J
Department of Cardiology, Boston Children's Hospital, Boston, MA, USA.
Department of Pediatrics, Harvard Medical School, Boston, MA, USA.
Eur Heart J. 2025 Mar 3;46(9):856-868. doi: 10.1093/eurheartj/ehae651.
Robust and convenient risk stratification of patients with paediatric and adult congenital heart disease (CHD) is lacking. This study aims to address this gap with an artificial intelligence-enhanced electrocardiogram (ECG) tool across the lifespan of a large, diverse cohort with CHD.
A convolutional neural network was trained (50%) and tested (50%) on ECGs obtained in cardiology clinic at the Boston Children's Hospital to detect 5-year mortality. Temporal validation on a contemporary cohort was performed. Model performance was evaluated using the area under the receiver operating characteristic and precision-recall curves.
The training and test cohorts composed of 112 804 ECGs (39 784 patients; ECG age range 0-85 years; 4.9% 5-year mortality) and 112 575 ECGs (39 784 patients; ECG age range 0-92 years; 4.6% 5-year mortality from ECG), respectively. Model performance (area under the receiver operating characteristic curve 0.79, 95% confidence interval 0.77-0.81; area under the precision-recall curve 0.17, 95% confidence interval 0.15-0.19) outperformed age at ECG, QRS duration, and left ventricular ejection fraction and was similar during temporal validation. In subgroup analysis, artificial intelligence-enhanced ECG outperformed left ventricular ejection fraction across a wide range of CHD lesions. Kaplan-Meier analysis demonstrates predictive value for longer-term mortality in the overall cohort and for lesion subgroups. In the overall cohort, precordial lead QRS complexes were most salient with high-risk features including wide and low-amplitude QRS complexes. Lesion-specific high-risk features such as QRS fragmentation in tetralogy of Fallot were identified.
This temporally validated model shows promise to inexpensively risk-stratify individuals with CHD across the lifespan, which may inform the timing of imaging/interventions and facilitate improved access to care.
目前缺乏针对小儿及成人先天性心脏病(CHD)患者的强大且便捷的风险分层方法。本研究旨在通过一种人工智能增强的心电图(ECG)工具,对一个大型、多样化的CHD队列的整个生命周期进行风险分层,以填补这一空白。
在波士顿儿童医院心脏病诊所获取的心电图上对卷积神经网络进行训练(50%)和测试(50%),以检测5年死亡率。对当代队列进行了时间验证。使用受试者操作特征曲线下面积和精确召回率曲线评估模型性能。
训练队列和测试队列分别由112804份心电图(39784例患者;心电图年龄范围0 - 85岁;5年死亡率4.9%)和112575份心电图(39784例患者;心电图年龄范围0 - 92岁;心电图5年死亡率4.6%)组成。模型性能(受试者操作特征曲线下面积0.79,95%置信区间0.77 - 0.81;精确召回率曲线下面积0.17,95%置信区间0.15 - 0.19)优于心电图年龄、QRS时限和左心室射血分数,且在时间验证期间表现相似。在亚组分析中,人工智能增强的心电图在广泛的CHD病变中优于左心室射血分数。Kaplan - Meier分析表明该模型对整个队列和病变亚组的长期死亡率具有预测价值。在整个队列中,胸前导联QRS波群具有最显著的高危特征,包括宽而低振幅的QRS波群。还识别出了特定病变的高危特征,如法洛四联症中的QRS波破碎。
这个经过时间验证的模型有望以低成本对CHD患者进行全生命周期的风险分层,这可能为成像/干预的时机提供参考,并有助于改善医疗服务的可及性。