Detection of Patients with Congenital and Often Concealed Long-QT Syndrome by Novel Deep Learning Models.

ECG artificial intelligence deep learning models electrophysiology long-QT syndrome

Journal

Journal of personalized medicine
ISSN: 2075-4426
Titre abrégé: J Pers Med
Pays: Switzerland
ID NLM: 101602269

Informations de publication

Date de publication:
13 Jul 2022
Historique:
received: 23 06 2022
revised: 10 07 2022
accepted: 12 07 2022
entrez: 27 7 2022
pubmed: 28 7 2022
medline: 28 7 2022
Statut: epublish

Résumé

The long-QT syndrome (LQTS) is the most common ion channelopathy, typically presenting with a prolonged QT interval and clinical symptoms such as syncope or sudden cardiac death. Patients may present with a concealed phenotype making the diagnosis challenging. Correctly diagnosing at-risk patients is pivotal to starting early preventive treatment. Identification of congenital and often concealed LQTS by utilizing novel deep learning network architectures, which are specifically designed for multichannel time series and therefore particularly suitable for ECG data. A retrospective artificial intelligence (AI)-based analysis was performed using a 12-lead ECG of genetically confirmed LQTS ( In this study, the XceptionTime model outperformed the FCN model for LQTS patients with even better results than in prior studies. Even when a patient cohort with cardiovascular comorbidities is used. AI-based ECG analysis is a promising step for correct LQTS patient identification, especially if common diagnostic measures might be misleading.

Identifiants

pubmed: 35887632
pii: jpm12071135
doi: 10.3390/jpm12071135
pmc: PMC9323528
pii:
doi:

Types de publication

Journal Article

Langues

eng

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Auteurs

Florian Doldi (F)

Department for Cardiology II-Electrophysiology, University Hospital Münster, 48149 Münster, Germany.

Lucas Plagwitz (L)

Institute of Medical Informatics, University of Münster, 48149 Münster, Germany.

Lea Philine Hoffmann (LP)

Department for Cardiology II-Electrophysiology, University Hospital Münster, 48149 Münster, Germany.

Benjamin Rath (B)

Department for Cardiology II-Electrophysiology, University Hospital Münster, 48149 Münster, Germany.

Gerrit Frommeyer (G)

Department for Cardiology II-Electrophysiology, University Hospital Münster, 48149 Münster, Germany.

Florian Reinke (F)

Department for Cardiology II-Electrophysiology, University Hospital Münster, 48149 Münster, Germany.

Patrick Leitz (P)

Department for Cardiology II-Electrophysiology, University Hospital Münster, 48149 Münster, Germany.

Antonius Büscher (A)

Department for Cardiology II-Electrophysiology, University Hospital Münster, 48149 Münster, Germany.

Fatih Güner (F)

Department for Cardiology II-Electrophysiology, University Hospital Münster, 48149 Münster, Germany.

Tobias Brix (T)

Institute of Medical Informatics, University of Münster, 48149 Münster, Germany.

Felix Konrad Wegner (FK)

Department for Cardiology II-Electrophysiology, University Hospital Münster, 48149 Münster, Germany.

Kevin Willy (K)

Department for Cardiology II-Electrophysiology, University Hospital Münster, 48149 Münster, Germany.

Yvonne Hanel (Y)

Institute for Genetics of Heart Diseases (IfGH), University Hospital Münster, 48149 Münster, Germany.

Sven Dittmann (S)

Institute for Genetics of Heart Diseases (IfGH), University Hospital Münster, 48149 Münster, Germany.

Wilhelm Haverkamp (W)

Department of Internal Medicine and Cardiology, Charité University Medicine, 10117 Berlin, Germany.

Eric Schulze-Bahr (E)

Institute for Genetics of Heart Diseases (IfGH), University Hospital Münster, 48149 Münster, Germany.

Julian Varghese (J)

Institute of Medical Informatics, University of Münster, 48149 Münster, Germany.

Lars Eckardt (L)

Department for Cardiology II-Electrophysiology, University Hospital Münster, 48149 Münster, Germany.

Classifications MeSH