Publications by authors named "Brugada J"

Purpose: COVID-19 is an independent risk factor for cardiovascular disease. The aim of this study is to determine the burden, characteristics, and causes of sudden death in sport (SrSD) before and after the COVID-19 pandemic in the general population.

Methods: Retrospective observational study.

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  • * AAs were the first symptom of IAS in 52% of patients, and nearly a quarter had multiple AAs documented.
  • * The study found a moderate incidence of severe outcomes, including a yearly primary endpoint rate of 1.4%, with younger patients experiencing higher risks and other complications affecting some patients as well.
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  • Genetic testing is crucial for diagnosing short QT syndrome, a rare inherited condition that leads to dangerous heart rhythms and is marked by short QT intervals on an ECG.
  • Researchers reviewed and updated knowledge about 34 rare genetic variants linked to short QT syndrome, identifying only nine that definitively cause the condition.
  • The variants were found in four main genes (KCNQ1, KCNH2, KCNJ2, SLC4A3), highlighting the importance of reanalyzing genetic data to improve patient care and early identification of at-risk individuals.
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  • Risk stratification for patients with drug-induced type-1 Brugada syndrome is difficult, and the usefulness of electrophysiological studies (EPS) is unclear.
  • A systematic literature search categorized patients into three groups based on EPS results: positive, negative, and no EPS conducted.
  • The study found no significant differences in the rates of arrhythmia events among these groups over an average follow-up of 5.1 years, suggesting EPS may not enhance long-term prognosis in these patients.
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Background: Young (<18 years of age) patients with Brugada syndrome (BrS) are often under-represented in BrS studies and their management, especially related to syncopal episodes, remains unclear.

Objectives: This study sought to describe the arrhythmia prevalence among young patients with BrS undergoing continuous rhythm monitoring by implantable loop recorder (ILR) and to assess the etiology behind syncope of undetermined origin.

Methods: A total of 147 patients with BrS with ILR were enrolled in 12 international centers and divided into pediatric (age <12 years; n = 77, 52%) and adolescents (age 13-18 years; n = 70, 48%).

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Background: Chronic diseases have a negative impact on quality of life (QOL) and psychological health. There are limited related data regarding this topic in Brugada syndrome (BrS). We evaluated the effects of the diagnosis of BrS on health-related QOL and psychological status among patients and their relatives.

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  • Left bundle branch pacing (LBBP) is a potential alternative to cardiac resynchronization therapy (CRT) but is not suitable for all heart failure patients.
  • A study analyzed 187 CRT candidates, finding a success rate of 81.2% for LBBP implantation, with failed cases primarily due to poor QRS morphology and technical issues.
  • Key predictors for unsuccessful implantation included left ventricular end-diastolic diameter (LVEDD) and non-left bundle branch block (non-LBBB) morphology, with non-LBBB significantly increasing the risk of failure.
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Background: A partial delineation of targets for ablation of ventricular tachycardia (VT) during a stable rhythm is likely responsible for a suboptimal success rate. The abnormal low-voltage near-field functional components may be hidden within the high-amplitude far-field signal.

Objectives: The aim of this study was to evaluate the benefit and feasibility of functional substrate mapping using a full-ventricle S3 protocol and to assess its colocalization with arrhythmogenic conducting channels (CCs) on late gadolinium enhancement cardiac magnetic resonance.

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  • * Right ventricle outflow tract fibrosis has been observed in some Brugada syndrome patients, indicating structural issues in the heart.
  • * A case is reported of a 4-year-old boy with pulmonary atresia showing a Brugada pattern after testing, suggesting that certain genetic variants may cause both conditions to develop similarly.
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Aims: Longitudinal dyssynchrony correction and 'strain' improvement by comparable cardiac resynchronization therapy (CRT) techniques is unreported. Our purpose was to compare echocardiographic dyssynchrony correction and 'strain' improvement by conduction system pacing (CSP) vs. biventricular pacing (BiVP) as a marker of contractility improvement during 1-year follow-up.

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Background: Voltage mapping could identify the conducting channels potentially responsible for ventricular tachycardia (VT). Standard thresholds (0.5-1.

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Background: Atrial arrhythmogenic substrate is a key determinant of atrial fibrillation (AF) recurrence after pulmonary vein isolation (PVI), and reduced conduction velocities have been linked to adverse outcome. However, a noninvasive method to assess such electrophysiologic substrate is not available to date.

Objective: This study aimed to noninvasively assess regional conduction velocities and their association with arrhythmia-free survival after PVI.

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  • Dilated cardiomyopathy is a complex heart condition linked to heart failure and arrhythmias, with about 50% of cases being inherited, highlighting the importance of genetic analysis.
  • In a study of 65 patients, researchers re-evaluated 125 previously ambiguous genetic variants, reclassifying 12% as likely benign or pathogenic, suggesting improved understanding through better population frequency data.
  • Their new algorithm indicated that 60.9% of remaining ambiguous variants had potential but unconfirmed harmful effects, while 24.5% might be benign, demonstrating the benefit of regularly updating genetic data for clearer interpretations.
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Aims: Same-day discharge (SDD) after atrial fibrillation (AF) ablation is an effective means to spare healthcare resources. However, safety remains a concern, and besides structural adaptations, SDD requires more efficient logistics and coordination. Therefore, in this study, we implement a streamlined, nurse-coordinated SDD programme following a standardized protocol.

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Background And Aims: Available data on continuous rhythm monitoring by implantable loop recorders (ILRs) in patients with Brugada syndrome (BrS) are scarce. The aim of this multi-centre study was to evaluate the diagnostic yield and clinical implication of a continuous rhythm monitoring strategy by ILRs in a large cohort of BrS patients and to assess the precise arrhythmic cause of syncopal episodes.

Methods: A total of 370 patients with BrS and ILRs (mean age 43.

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Aims: Non-invasive myocardial scar characterization with cardiac magnetic resonance (CMR) has been shown to accurately identify conduction channels and can be an important aid for ventricular tachycardia (VT) ablation. A new mapping method based on targeting deceleration zones (DZs) has become one of the most commonly used strategies for VT ablation procedures. The aim of the study was to analyse the capability of CMR to identify DZs and to find predictors of arrhythmogenicity in CMR channels.

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: Left atrial (LA) remodelling and dilatation predicts atrial fibrillation (AF) recurrences after catheter ablation. However, whether right atrial (RA) remodelling and dilatation predicts AF recurrences after ablation has not been fully evaluated. : This is an observational study of 85 consecutive patients (aged 57 ± 9 years; 70 [82%] men) who underwent cardiac magnetic resonance before first catheter ablation for AF (40 [47.

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  • The study evaluated the effectiveness of post-ablation late gadolinium enhancement cardiac magnetic resonance (LGE-CMR) imaging in assessing ventricular tachycardia (VT) lesions in patients treated for scar-related VT.
  • Out of 61 patients referred for ablation, 49 were included, revealing significant reductions in both the number and mass of conducting channels (CCs) post-ablation, with 74.4% of patients showing disappearance of arrhythmogenic CCs.
  • The presence of two or more channels or a reduction of CCs less than 55% post-ablation were identified as predictors for VT recurrence, indicating that post-ablation LGE-CMR can help gauge treatment effectiveness and risk.
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  • Brugada syndrome is a rare heart problem that can lead to sudden death, especially in young people, and it's often inherited from family members.
  • A 36-year-old man with a family history of sudden death was tested and found to have a genetic mutation linked to Brugada syndrome.
  • Doctors used special heart tests to confirm he had the syndrome and decided to implant a device to help prevent any dangerous heart issues in the future.
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Introduction: Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a cardiac inherited arrhythmogenic disease potentially leading to sudden cardiac death that is determined by electrical instability exacerbated by acute adrenergic tone.

Methods And Results: Despite its life-threatening nature, CPVT remains potentially unnoticed since diagnosis may be difficult especially in apparently healthy athletes. This review summarizes current knowledge and shortcomings of CPVT, focusing on genetics, arrhythmic mechanisms, sport preparticipation screening, and current recommendations.

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Brugada syndrome is a rare hereditary arrhythmia disorder characterized by a distinctive electrocardiogram pattern and an elevated risk of ventricular arrhythmias and sudden cardiac death in young adults. Despite recent advances, it remains a complex condition, encompassing mechanisms, genetics, diagnosis, arrhythmia risk stratification, and management. The underlying electrophysiological mechanism of Brugada syndrome requires further investigation, with current theories focusing on abnormalities in repolarization, depolarization, and current-load match.

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  • * Researchers analyzed data from 42 patients who underwent VT ablation, confirming that 93.68% of DZs correlated with CMR-determined conduction channels, with a high proportion of DZs disappearing after the initial ablation attempts.
  • * The results indicate that remapping during the procedure helps identify previously undetected areas of the heart that contribute to VT, with a one-year recurrence rate of 22.9% for VT among patients.
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