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1.
Pacing Clin Electrophysiol ; 47(2): 253-255, 2024 02.
Artigo em Inglês | MEDLINE | ID: mdl-37221934

RESUMO

Heart block is rare in pediatrics with many possible causes. An association between complete heart block (CHB) and pathogenic titin (TTN) mutations have not been previously described. We report a 9-year-old female with history of leukodystrophy and family history of atrial fibrillation who presented with syncope and conduction abnormalities, including CHB. She underwent pacemaker implantation and genetic testing demonstrated a pathogenic TTN mutation likely responsible for her cardiac findings. Our case suggests an association between TTN mutations and conduction disease and emphasizes broadening gene testing in assessing these patients, especially when a family history is present.


Assuntos
Arritmias Cardíacas , Bloqueio Cardíaco , Humanos , Criança , Feminino , Conectina/genética , Doença do Sistema de Condução Cardíaco , Mutação/genética
4.
Pediatr Cardiol ; 44(2): 479-486, 2023 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-36495348

RESUMO

Although ectopic atrial tachycardia (EAT) is common following surgery for congenital heart disease (CHD), there are limited data regarding this arrhythmia. This study assessed risk factors and outcomes for patients less than one year of age with post-operative EAT. This was a retrospective analysis of infants undergoing CHD surgery from 2007 to 2020. Patients and surgeries with EAT were compared to controls without EAT. Out of 5372 infant CHD surgeries, EAT developed in 129 (2.5%). Compared to controls, the EAT cohort was younger (median 7 vs 85 days, p < 0.01), weighed less at time of surgery (3.3 vs 4.2 kg, p < 0.01), and was more likely to have DiGeorge syndrome (7.7% vs 3.0%, p < 0.01). Multivariate analysis revealed total anomalous venous connection (TAPVC) repair (odds ratio [OR] 2.8; 95% confidence interval 1.5-5.2), DiGeorge syndrome (OR 2.4; 1.1-5.2), Society of Thoracic Surgeons-European Association for Cardio-Thoracic surgery (STAT) category ≥ 4 (OR 2.1; 1.0-4.4), and longer cardiopulmonary bypass times (OR 1.1; 1.0-1.2) as independent risk factors for EAT. The onset of EAT occurred a median of 9 days (IQR 5-14 days) after CHD surgery. Antiarrhythmic treatment was initiated in 109/129 patients (84%) with propranolol (71%) and amiodarone (24%) the most commonly used medications. Although 15 (11.6%) patients did not survive to hospital discharge, EAT was not directly implicated in any deaths. EAT occurred after 2.5% of infant CHD surgeries. In addition to TAPVC repair, longer and more complex surgeries were associated with an increased the risk for the development of post-operative EAT.


Assuntos
Síndrome de DiGeorge , Cardiopatias Congênitas , Taquicardia Atrial Ectópica , Taquicardia Supraventricular , Lactente , Humanos , Taquicardia Atrial Ectópica/etiologia , Estudos Retrospectivos , Síndrome de DiGeorge/complicações , Taquicardia Supraventricular/tratamento farmacológico , Cardiopatias Congênitas/cirurgia , Cardiopatias Congênitas/complicações
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