Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 1 de 1
Filtrar
Mais filtros








Base de dados
Intervalo de ano de publicação
1.
Heart Rhythm ; 7(6): 781-5, 2010 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-20197117

RESUMO

BACKGROUND: Previous studies of patients with long QT syndrome (LQTS) and 2:1 atrioventricular block (AVB) have reported a mortality rate greater than 50% during infancy. OBJECTIVE: The purpose of this study was to determine the outcome of this high-risk population in the current era. METHODS: A retrospective study from four tertiary care pediatric centers assessed patients with congenital LQTS and 2:1 AVB from January 2000 to January 2009. All neonates who presented with 2:1 AVB and prolonged QTc unrelated to medication were included in the study. Statistical analysis was performed using a paired t-test. Medical records were reviewed for ECG findings, genotype, medications, and device therapy. RESULTS: Twelve patients that met the inclusion criteria were identified. All patients underwent diagnostic ECG in the first 24 hours of life. The average QTc interval prior to therapy was 616 +/- 99 ms (range 531-840 ms). Over a follow-up period of 71 +/- 45 months (range 15-158 months), 11 of 12 patients received devices (8 permanent pacemaker, 3 implantable cardioverter-defibrillator). Average age of device placement was 48 months (median 2 months, range 3 days to 10.5 years). All patients were treated with beta-blockers; mexiletine was added in three patients, and mexiletine and flecainide were added in one patient. Three (25%) patients experienced torsades de pointes while receiving beta-blockers, one of which was refractory to medical therapy. This patient underwent left cardiac sympathetic denervation and implantable cardioverter-defibrillator placement. Genotyping was available for 6 (50%) patients (2 SCN5A mutation, 4 KCNH2 mutation). At last follow-up, no mortality was observed. Follow-up QTc intervals had decreased (mean 480 +/- 20 ms, range 450-507 ms, P <.002). CONCLUSION: Management of patients with LQTS and 2:1 AVB presents unique challenges. Despite historical data indicating poor prognosis, our study represents a cohort of high-risk LQTS patients with a relatively optimistic outcome. This finding reflects early diagnosis and intervention, coupled with improved management strategies, in the current era.


Assuntos
Bloqueio Atrioventricular/patologia , Desfibriladores Implantáveis , Síndrome do QT Longo/patologia , Torsades de Pointes/patologia , Antagonistas Adrenérgicos beta/uso terapêutico , Antiarrítmicos/uso terapêutico , Bloqueio Atrioventricular/congênito , Bloqueio Atrioventricular/tratamento farmacológico , Bloqueio Atrioventricular/terapia , Criança , Pré-Escolar , Estudos de Coortes , Feminino , Flecainida/uso terapêutico , Genótipo , Humanos , Lactente , Recém-Nascido , Síndrome do QT Longo/congênito , Síndrome do QT Longo/tratamento farmacológico , Síndrome do QT Longo/terapia , Masculino , Mexiletina/uso terapêutico , Análise Multivariada , Prognóstico , Propanolaminas/uso terapêutico , Propranolol/uso terapêutico , Estudos Retrospectivos , Medição de Risco , Fatores de Risco , Torsades de Pointes/congênito , Torsades de Pointes/tratamento farmacológico , Torsades de Pointes/terapia , Resultado do Tratamento
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA