European Heart Rhythm Association (EHRA)/Heart Rhythm Society (HRS)/Asia Pacific Heart Rhythm Society (APHRS)/Latin American Heart Rhythm Society (LAHRS) …

JC Nielsen, YJ Lin, MJ de Oliveira Figueiredo… - Ep …, 2020 - academic.oup.com
Patients with cardiac diseases or conditions with high risk of developing cardiac diseases
undergo risk assessment by cardiologists, primary care physicians, and scientists based on …

[HTML][HTML] Artificial intelligence in diagnosis of long QT syndrome: a review of current state, challenges, and future perspectives

NR Dehkordi, NR Dehkordi, KK Toudeshki… - Mayo Clinic …, 2024 - Elsevier
Long QT syndrome (LQTS) is a potentially life-threatening cardiac repolarization disorder
characterized by an increased risk of fatal arrhythmias. Accurate and timely diagnosis is …

JCS/JHRS 2022 guideline on diagnosis and risk assessment of arrhythmia

B Takase, T Ikeda, W Shimizu, H Abe, T Aiba… - Circulation …, 2024 - jstage.jst.go.jp
Sinus node dysfunction may be either transient (reversible/physiological) due to the
involvement of the autonomic nervous system or pharmaceuticals, or chronic due to …

Deep learning analysis of electrocardiogram for risk prediction of drug-induced arrhythmias and diagnosis of long QT syndrome

E Prifti, A Fall, G Davogustto, A Pulini… - European Heart …, 2021 - academic.oup.com
Aims Congenital long-QT syndromes (cLQTS) or drug-induced long-QT syndromes (diLQTS)
can cause torsade de pointes (TdP), a life-threatening ventricular arrhythmia. The current …

Territory-wide Chinese cohort of long QT syndrome: random survival forest and Cox analyses

G Tse, S Lee, J Zhou, T Liu, ICK Wong… - Frontiers in …, 2021 - pmc.ncbi.nlm.nih.gov
Introduction: Congenital long QT syndrome (LQTS) is a cardiac ion channelopathy that
predisposes affected individuals to spontaneous ventricular tachycardia/fibrillation (VT/VF) …

Phenotypes of overdiagnosed long QT syndrome

S Bains, R Neves, JM Bos, JR Giudicessi… - Journal of the American …, 2023 - jacc.org
Abstract Background Long QT syndrome (LQTS) predisposes individuals to arrhythmic
syncope or seizure, sudden cardiac arrest, or sudden cardiac death (SCD). Increased …

Improving long QT syndrome diagnosis by a polynomial-based T-wave morphology characterization

BJM Hermans, FC Bennis, AS Vink, T Koopsen, A Lyon… - Heart Rhythm, 2020 - Elsevier
Background Diagnosing long QT syndrome (LQTS) remains challenging because of a
considerable overlap in QT interval between patients with LQTS and healthy subjects …

Long QT syndrome and perioperative torsades de pointes: what the anesthesiologist should know

N Niimi, K Yuki, K Zaleski - Journal of Cardiothoracic and Vascular …, 2022 - jcvaonline.com
TORSADES DE pointes (TdP or “twisting of the points”) is a rare but potentially fatal
polymorphic ventricular tachycardia characterized by rapid, wide QRS complexes of …

A phenotype-enhanced variant classification framework to decrease the burden of missense variants of uncertain significance in type 1 long QT syndrome

S Bains, SM Dotzler, C Krijger, JR Giudicessi, D Ye… - Heart Rhythm, 2022 - Elsevier
Background Pathogenic/likely pathogenic (P/LP) variants in the KCNQ1-encoded Kv7. 1
potassium channel cause type 1 long QT syndrome (LQT1). Despite the revamped 2015 …

Modeling genetic cardiac channelopathies using induced pluripotent stem cells–Status quo from an electrophysiological perspective

MVK Kamga, M Reppel, J Hescheler… - Biochemical …, 2021 - Elsevier
Abstract Long QT syndrome (LQTS), Brugada syndrome (BrS), and catecholaminergic
polymorphic ventricular tachycardia (CPVT) are genetic diseases of the heart caused by …