4.6 Article

A Deep Learning-Enabled Electrocardiogram Model for the Identification of a Rare Inherited Arrhythmia: Brugada Syndrome

Journal

CANADIAN JOURNAL OF CARDIOLOGY
Volume 38, Issue 2, Pages 152-159

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.cjca.2021.08.014

Keywords

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Funding

  1. Taipei Veterans General Hospital [VN109-03, V109C-070, V110C-039, V110B-043]
  2. Ministry of Science and Technology [109-2628-E-009-009-MY3, 109-2628-B-075-017, 110-2628-B-075-015, 110-2314-B-075-063-MY3, 110-2321-B-075-002]
  3. National Health Research Institutes [NHRI-EX108-10513SC, NHRI-109BCC0-MF-202014-02]
  4. Academia Sinica [AS-TM-109-01-05, AS-TM-110-01-01]

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In this study, a deep learning ECG model was developed for automatic screening of Brugada syndrome, showing higher consistency and better diagnostic performance compared to cardiologists. The deep learning model also demonstrated satisfactory diagnostic performance in an independent validation ECG dataset.
Background: Brugada syndrome is a major cause of sudden cardiac death in young people and has distinctive electrocardiographic (ECG) features. We aimed to develop a deep learningeenabled ECG model for automatic screening for Brugada syndrome to identify these patients at an early point in time, thus allowing for life-saving therapy. Methods: A total of 276 ECGs with a type 1 Brugada ECG pattern (276 type 1 Brugada ECGs and another randomly retrieved 276 nonBrugada type ECGs for 1:1 allocation) were extracted from the hospital-based ECG database for a 2-stage analysis with a deep learning model. After trained network for identifying right bundle branch block pattern, we transferred the first-stage learning to the second task to diagnose the type 1 Brugada ECG pattern. The diagnostic performance of the deep learning model was compared with that of board-certified practicing cardiologists. The model was further validated in an independent ECG data set collected from hospitals in Taiwan and Japan. Results: The diagnoses by the deep learning model (area under the receiver operating characteristic curve [AUC] 0.96, sensitivity 88.4%, specificity 89.1%) were highly consistent with the standard diagnoses (kappa coefficient 0.78). However, the diagnoses by the cardiologists were significantly different from the standard diagnoses, with only moderate consistency (kappa coefficient 0.63). In the independent ECG cohort, the deep learning model still reached a satisfactory diagnostic performance (AUC 0.89, sensitivity 86.0%, specificity 90.0%). Conclusions: We present the first deep learningeenabled ECG model for diagnosing Brugada syndrome, which appears to be a robust screening tool with a diagnostic potential rivalling trained physicians.

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