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

共 50 条

[21] Fetal Atrioventricular Block and Postpartum Augmentative QT Prolongation in a Patient With Long-QT Syndrome With KCNQ1 Mutation
Furushima, Hiroshi
Chinushi, Masaomi
Sato, Akinori
Aizawa, Yoshifusa
Kikuchi, Akira
Takakuwa, Koichi
Tanaka, Kenichi
JOURNAL OF CARDIOVASCULAR ELECTROPHYSIOLOGY, 2010, 21 (10) : 1170 - 1173
[22] Rare cause of long QT and torsade de pointes tachycardia
Kriatselis, C
Helbig, S
Göhl, K
Richter, P
Höher, M
Gottwik, M
INTERNIST, 2005, 46 (01): : 92 - 96
[23] Arrhythmias in the congenital long QT syndrome: how often is torsade de pointes pause dependent?
Viskin, S
Fish, R
Zeltser, D
Belhassen, B
Heller, K
Brosh, D
Laniado, S
Barron, HV
HEART, 2000, 83 (06) : 661 - 666
[24] Recurrent torsades de pointes after catheter ablation of incessant ventricular bigeminy in combination with QT prolongation
Reithmann, Christopher
Fiek, Michael
Beckmann, Britt-Maria
Kaeaeb, Stefan
EUROPACE, 2012, 14 (02): : 299 - 300
[25] Donepezil-Induced Adverse Side Effects of Cardiac Rhythm: 2 Cases Report of Atrioventricular Block and Torsade de Pointes
Tanaka, Atsushi
Koga, Shoichi
Hiramatsu, Yoshihiro
INTERNAL MEDICINE, 2009, 48 (14) : 1219 - 1223
[26] Fetal Long QT Syndrome Manifested as Atrioventricular Block and Ventricular Tachycardia: A Case Report and a Review of the Literature
Anuwutnavin, Sanitra
Wanitpongpan, Prapat
Chungsomprasong, Paweena
Soongswang, Jarupim
Srisantiroj, Nattinee
Wataganara, Tuangsit
PEDIATRIC CARDIOLOGY, 2013, 34 (08) : 1955 - 1962
[27] Fetal Long QT Syndrome Manifested as Atrioventricular Block and Ventricular Tachycardia: A Case Report and a Review of the Literature
Sanitra Anuwutnavin
Prapat Wanitpongpan
Paweena Chungsomprasong
Jarupim Soongswang
Nattinee Srisantiroj
Tuangsit Wataganara
Pediatric Cardiology, 2013, 34 : 1955 - 1962
[28] Complete AV Block and Torsades de Pointes in a Case of Primary Cardiac T-Cell Lymphoma
Wang, Tzu-Lin
Lai, Chih-Hung
Liou, Jer-Young
Lo, Huey-Ming
Shyu, Kou-Gi
ACTA CARDIOLOGICA SINICA, 2015, 31 (03) : 245 - 248
[29] Preventing and Treating Torsades de Pointes in the Mother, Fetus and Newborn in the Highest Risk Pregnancies with Inherited Arrhythmia Syndromes
Wacker-Gussmann, Annette
Eckstein, Gretchen K.
Strasburger, Janette F.
JOURNAL OF CLINICAL MEDICINE, 2023, 12 (10)
[30] Optimal location of the QT interval evaluation in patients with drug-induced QT prolongation and torsades de pointes: Limb leads, chest leads, or both?
Lakkis, Bachir
Refaat, Marwan M.
JOURNAL OF CARDIOVASCULAR ELECTROPHYSIOLOGY, 2020, 31 (10) : 2702 - 2703

← 1 2 3 4 5 →