scholarly journals Successful Management of Refractory Torsades De Pointes Due to Drug-Induced Long QT Syndrome Guided by Point-of-Care Monitoring of Ionized Magnesium

Cureus ◽  
2021 ◽  
Author(s):  
Chiho Matsuura ◽  
Takao Kato ◽  
Kaoru Koyama
Keyword(s):  
Long Qt Syndrome ◽  
Point Of Care ◽  
Torsades De Pointes ◽  
Successful Management ◽  
Long Qt ◽  
Drug Induced ◽  
Ionized Magnesium ◽  
Qt Syndrome

Drug-induced torsades de pointes in one patient with congenital long QT syndrome

1996 ◽  
Vol 54 (1) ◽  
pp. 85-88 ◽  
Author(s):  
Ming-Hsiung Hsieh ◽  
Shih-Ann Chen ◽  
Chern-En Chiang ◽  
Ching-Tai Tai ◽  
Shih-Huang Lee ◽  
...  
Keyword(s):  
Long Qt Syndrome ◽  
Torsades De Pointes ◽  
Long Qt ◽  
Drug Induced ◽  
Qt Syndrome ◽  
Congenital Long Qt Syndrome

Sotalol unmasks susceptibility to drug-induced long QT syndrome and torsades de pointes

2008 ◽  
Vol 124 (3) ◽  
pp. 366-367 ◽  
Author(s):  
Konstantinos P. Letsas ◽  
Michael Efremidis ◽  
Antonios Sideris
Keyword(s):  
Long Qt Syndrome ◽  
Torsades De Pointes ◽  
Long Qt ◽  
Drug Induced ◽  
Qt Syndrome

scholarly journals Elucidation of mechanisms that trigger torsades de pointes in drug-induced long QT syndrome: a simulation study

2021 ◽  
Vol 94 (0) ◽  
pp. 3-P2-02
Author(s):  
Kunichika Tsumoto ◽  
Takao Shimamoto ◽  
Akira Amano ◽  
Yuhichi Kuda ◽  
Mamoru Tanida ◽  
...  
Keyword(s):  
Simulation Study ◽  
Long Qt Syndrome ◽  
Torsades De Pointes ◽  
Long Qt ◽  
Drug Induced ◽  
Qt Syndrome

scholarly journals Elucidating the role of Cavin1 in drug-induced long QT syndrome (diLQTS)

2021 ◽  
Vol 13 (2) ◽  
pp. 228-229
Author(s):  
Z. Al Sayed ◽  
C. Pereira ◽  
C. Jouve ◽  
J. Hulot
Keyword(s):  
Long Qt Syndrome ◽  
Long Qt ◽  
Drug Induced ◽  
Qt Syndrome

A rare indication of permanent pacemaker implantation in children: congenital long QT syndrome

2020 ◽  
Vol 30 (12) ◽  
pp. 1880-1881
Author(s):  
Mehmet Taşar ◽  
Nur Dikmen Yaman ◽  
Huseyin Dursin ◽  
Murat Şimşek ◽  
Senem Özgür
Keyword(s):  
Sudden Death ◽  
Long Qt Syndrome ◽  
Pacemaker Implantation ◽  
Torsades De Pointes ◽  
Permanent Pacemaker ◽  
Long Qt ◽  
Permanent Pacemaker Implantation ◽  
Qt Syndrome ◽  
Congenital Lqts ◽  
Congenital Long Qt Syndrome

AbstractCongenital Long QT Syndrome (LQTS) is a dangerous arrhythmic disorder that can be diagnosed in children with bradycardia. It is characterised by a prolonged QT interval and torsades de pointes that may cause sudden death. Long QT syndrome is an ion channelopathy with complex molecular and physiological infrastructure. Unlike the acquired type, congenital LQTS has a genetic inheritance and it may be diagnosed by syncope, stress in activity, cardiac dysfunction, sudden death or sometimes incidentally. Permanent pacemaker implantation is required for LQTS with resistant bradycardia even in children to resolve symptoms and avoid sudden death.

scholarly journals Peripartum Cardiomyopathy Presenting with Syncope due to Torsades de Pointes: a Case of Long QT Syndrome with a Novel KCNH2 Mutation

2012 ◽  
Vol 51 (5) ◽  
pp. 461-464 ◽  
Author(s):  
Orie Nishimoto ◽  
Morihiro Matsuda ◽  
Kei Nakamoto ◽  
Hirohiko Nishiyama ◽  
Kazuya Kuraoka ◽  
...  
Keyword(s):  
Long Qt Syndrome ◽  
Torsades De Pointes ◽  
Peripartum Cardiomyopathy ◽  
Long Qt ◽  
Qt Syndrome

scholarly journals Dobutamine Infusion for Unmasking Long QT Syndrome and Torsades de Pointes

2009 ◽  
Vol 32 (6) ◽  
pp. E78-E81 ◽  
Author(s):  
Fang Quan ◽  
Gao Peng ◽  
Cheng Kangan ◽  
Hu Dayi ◽  
Li Cuilan ◽  
...  
Keyword(s):  
Long Qt Syndrome ◽  
Torsades De Pointes ◽  
Dobutamine Infusion ◽  
Long Qt ◽  
Qt Syndrome
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