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The efficacy of convolutional neural network (CNN)-enhanced electrocardiography (ECG) in detecting hypertrophic cardiomyopathy (HCM) and dilated HCM (dHCM) remains uncertain in real-world applications. This retrospective study analyzed data from 19,170 patients (including 140 HCM or dHCM) in the Shinken Database (2010-2017). We evaluated the sensitivity, positive predictive rate (PPR), and F1 score of CNN-enhanced ECG in a ''basic diagnosis'' model (total disease label) and a ''comprehensive diagnosis'' model (including disease subtypes). Using all-lead ECG in the "basic diagnosis" model, we observed a sensitivity of 76%, PPR of 2.9%, and F1 score of 0.056. These metrics improved in cases with a diagnostic probability of ≥ 0.9 and left ventricular hypertrophy (LVH) on ECG: 100% sensitivity, 8.6% PPR, and 0.158 F1 score. The ''comprehensive diagnosis'' model further enhanced these figures to 100%, 13.0%, and 0.230, respectively. Performance was broadly consistent across CNN models using different lead configurations, particularly when including leads viewing the lateral walls. While the precision of CNN models in detecting HCM or dHCM in real-world settings is initially low, it improves by targeting specific patient groups and integrating disease subtype models. The use of ECGs with fewer leads, especially those involving the lateral walls, appears comparably effective.
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http://dx.doi.org/10.1007/s00380-024-02367-9 | DOI Listing |
Pacing Clin Electrophysiol
June 2025
Department of Cardiovascular Medicine, Institute of Science Tokyo, Tokyo, Japan.
Introduction: Right ventricular apex (RVA) pacing has been reported to induce pacing-induced cardiomyopathy (PICM), with biventricular pacing being the standard cardiac resynchronization therapy (CRT) for RVA-PICM. However, recent studies suggest that left bundle branch area pacing (LBBAP) may provide even better outcomes as a CRT. In this case, we observed a dynamic alteration in the left ventricular (LV) activation pattern when transitioning from RVA-PICM to LBBAP, including changes in the functional block line.
View Article and Find Full Text PDFBackground: The efficacy of artificial intelligence (AI)-enhanced electrocardiography (ECG) for detecting hypertrophic cardiomyopathy (HCM) and its dilated phase (dHCM) has been developed, though specific ECG characteristics associated with these conditions remain insufficiently characterized.
Methods: This retrospective study included 19,170 patients, with 140 HCM or dHCM cases, from the Shinken Database (2010-2017). The 140 cases (HCM-total) were categorized into basal-only HCM (HCM-basal, = 75), apical involvement (HCM-apical, = 46), and dHCM ( = 19).
ESC Heart Fail
December 2024
Institut universitaire de cardiologie et de pneumologie de Québec, Québec, Canada.
Aim: The diagnosis of hypertrophic cardiomyopathy (HCM) with moderate hypertrophy is challenging. Hypertensive heart disease (HHD) is the most common differential diagnosis that mimics the LVH of HCM. The aim of this study was to compare the QRS duration in HCM and HHD to create a novel diagnostic tool to identify primary HCM.
View Article and Find Full Text PDFSci Rep
July 2024
Department of Cardiology, Faculty of Medicine, University of Tsukuba, 1-1-1 Tennoudai, Tsukuba, Ibaraki, 305-8575, Japan.
Hypertrophic cardiomyopathy (HCM) is an inherited disorder characterized by left ventricular hypertrophy and diastolic dysfunction, and increases the risk of arrhythmias and heart failure. Some patients with HCM develop a dilated phase of hypertrophic cardiomyopathy (D-HCM) and have poor prognosis; however, its pathogenesis is unclear and few pathological models exist. This study established disease-specific human induced pluripotent stem cells (iPSCs) from a patient with D-HCM harboring a mutation in MYBPC3 (c.
View Article and Find Full Text PDFHeart Vessels
June 2024
Department of Cardiovascular Medicine, The Cardiovascular Institute, 3-2-19 Nishiazabu, Minato-Ku, Tokyo, 106-0031, Japan.