Survival of a Newborn with 2:1 Atrioventricular Block, Long QT Syndrome, and Torsades de Pointes

被引：0

作者：

Sarkar, Shubho ^{[1
]}

Brumund, Michael ^{[2
]}

Darling, Rani ^{[1
]}

Snyder, Christopher S. ^{[1
]}

机构：

[1] Ochsner Clin Fdn, Dept Pediat, Pediat Cardiol Sect, New Orleans, LA USA

[2] Pediat Cardiol Associates, Baton Rouge, LA USA

来源：

OCHSNER JOURNAL | 2007年 / 7卷 / 04期

关键词：

Atrioventricular block; long QT;

D O I：

暂无

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

Long QT syndrome is a rare disorder that can manifest as syncope, Torsades de Pointes, or sudden cardiac death. We report a newborn with asymptomatic bradycardia, 2:1 atrioventricular block, long QT syndrome, and episodes of Torsades de Pointes. The patient was managed with mexiletine and propranolol and continued to have episodes of Torsades de Pointes, so she underwent epicardial pacemaker implantation. No further episodes of Torsades de Pointes were noted prior to discharge.

引用

页码：181 / 184

页数：4

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