人工智能分析单导联心电图预测长期临床结果。

IF 4.4 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS
European heart journal. Digital health Pub Date : 2025-06-09 eCollection Date: 2025-07-01 DOI:10.1093/ehjdh/ztaf057
Abdullah Alrumayh, Patrik Bächtiger, Arunashis Sau, Josephine Mansell, Melanie T Almonte, Karanjot Chhatwal, Fu Siong Ng, Mihir A Kelshiker, Nicholas S Peters
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引用次数: 0

摘要

目的:人工智能(AI)应用于单导联心电图(AI- ecg)可以检测出受损的左心室收缩功能障碍[LVSD:左心室射血分数(LVEF)≤40%]。本研究旨在确定AI-ECG是否也可以预测两年主要不良心血管事件(MACE)风险和独立于LVSD的全因死亡率。方法与结果:对接受常规超声心动图检查并同时接受单导联心电图记录进行AI-ECG分析的患者进行2年随访后的临床结果。通过Cox回归比较MACE和全因死亡率,以LVEF >或≤40%的分级来衡量。超声心动图LVEF≥50%的患者进行亚组分析。根据先前建立的阈值,“阳性”AI-ECG定义为lvef预测值≤40%,阴性AI-ECG表示lvef预测值≤40%;1007例患者纳入分析(平均年龄62.3岁;52.4%的男性)。339例(33.7%)患者ai - ecg预测LVEF≤40%,MACE率较高(LVEF≤40% vs. bb0 40%: 34.2% vs.11.9%;调整风险比(aHR) 1.93;95% ci, 1.39-2.69;P < 0.001),主要是由于死亡率增加(23% vs. 9.6%;P < 0.001;aHR 1.56;95% ci, 1.06-2.29;P = 0.0239)。在超声心动图LVEF≥50%的患者中,AI-ECG“假阳性”预测LVEF≤40%的患者MACE发生率更高(27.2% vs.11.9%;P < 0.001;aHR 1.71, 95% CI 1.11-2.47)和全因死亡率(20.4% vs. 9.6%;P < 0.001;aHR为1.59,95% CI为1.09-2.42)。结论:设计用于检测LVEF≤40%的AI-ECG算法也可以识别单导联心电图记录的MACE和全因死亡风险患者,而不依赖于超声显示的实际LVEF。这需要进一步的评估,作为护理点风险分层工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Artificial intelligence analysis of the single-lead ECG predicts long-term clinical outcomes.

Artificial intelligence analysis of the single-lead ECG predicts long-term clinical outcomes.

Artificial intelligence analysis of the single-lead ECG predicts long-term clinical outcomes.

Aims: Artificial intelligence (AI) applied to a single-lead electrocardiogram (AI-ECG) can detect impaired left ventricular systolic dysfunction [LVSD: left ventricular ejection fraction (LVEF) ≤ 40%]. This study aimed to determine if AI-ECG can also predict the two-year risk of major adverse cardiovascular events (MACE) and all-cause mortality independent of LVSD.

Methods and results: Clinical outcomes after two-year follow-up were collected on patients who attended for routine echocardiography and received simultaneous single-lead-ECG recording for AI-ECG analysis. MACE and all-cause mortality were compared by Cox regression, measured against the classification of LVEF > or ≤40%. A subgroup analysis was performed on patients with echocardiographic LVEF ≥ 50%. With previously established thresholds, 'positive' AI-ECG was defined as an LVEF-predicted ≤40%, and negative AI-ECG signified an LVEF-predicted >40%; 1007 patients were included for analysis (mean age, 62.3 years; 52.4% male). 339 (33.7%) had an AI-ECG-predicted LVEF ≤ 40% and had a higher MACE rate (LVEF ≤ 40% vs. >40%: 34.2% vs.11.9%; adjusted hazard ratio (aHR) 1.93; 95% CI, 1.39-2.69; P < 0.001), primarily driven by increased mortality (23% vs. 9.6%; P < 0.001; aHR 1.56; 95% CI, 1.06-2.29; P = 0.0239). In patients with echocardiographic LVEF ≥ 50%, there was a higher incidence of MACE in those with an AI-ECG 'false positive' prediction of LVEF ≤ 40% (27.2% vs.11.9%; P < 0.001; aHR 1.71 and 95% CI, 1.11-2.47) and all-cause mortality (20.4% vs. 9.6%; P < 0.001; aHR 1.59, 95% CI, 1.09-2.42).

Conclusion: An AI-ECG algorithm designed to detect LVEF ≤ 40% can also identify patients at risk of MACE and all-cause mortality from single-lead ECG recording-independent of actual LVEF on echo. This requires further evaluation as a point-of-care risk stratification tool.

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