Acquired long QT syndrome: Risperidone-facilitated triggered activity and Torsades de Pointes during complete AV block. I

2007 ◽  
Vol 116 (3) ◽  
pp. 416-420 ◽  
Author(s):  
Tomas Raviña ◽  
Paula Raviña ◽  
Javier Gutierrez
2014 ◽  
Vol 2 (1) ◽  
pp. 44-45
Author(s):  
Ahmad Mursel Anam ◽  
Raihan Rabbani ◽  
Farzana Shumy ◽  
M Mufizul Islam Polash ◽  
M Motiul Islam ◽  
...  

We report a case of drug induced torsades de pointes, following acquired long QT syndrome. The patient got admitted for shock with acute abdomen. The initial prolonged QT-interval was missed, and a torsadogenic drug was introduced post-operatively. Patient developed torsades de pointes followed by cardiac arrest. She was managed well and discharged without complications. The clinical manifestations of long QT syndromes, syncope or cardiac arrest, result from torsades de pointes. As syncope or cardiac arrest have more common differential diagnoses, even the symptomatic long QT syndrome are commonly missed or misdiagnosed. In acquired long QT syndrome with no prior suggestive feature, it is not impossible to miss the prolonged QT-interval on the ECG tracing. We share our experience so that the clinicians, especially the junior doctors, will be more alert on checking the QT-interval even in asymptomatic patients. DOI: http://dx.doi.org/10.3329/bccj.v2i1.19970 Bangladesh Crit Care J March 2014; 2 (1): 44-45


2015 ◽  
Vol 1 (4) ◽  
pp. 315-322 ◽  
Author(s):  
Marwan Badri ◽  
Aashay Patel ◽  
Chinmay Patel ◽  
Guizhi Liu ◽  
Matthew Goldstein ◽  
...  

2018 ◽  
Vol 71 (11) ◽  
pp. A2612 ◽  
Author(s):  
Hetavi Mahida ◽  
Obiora Maludum ◽  
Nene Ugoeke ◽  
Bharatsinh Gharia ◽  
Dawn Calderon ◽  
...  

Heart Rhythm ◽  
2011 ◽  
Vol 8 (4) ◽  
pp. 555-561 ◽  
Author(s):  
Christopher Madias ◽  
Timothy P. Fitzgibbons ◽  
Alawi A. Alsheikh-Ali ◽  
Joseph L. Bouchard ◽  
Benjamin Kalsmith ◽  
...  

2020 ◽  
Vol 47 (2) ◽  
pp. 163-164
Author(s):  
Samuel S. Gordon ◽  
John Hollowed ◽  
Justin Hayase ◽  
Carlos Macias ◽  
Jessica Wang ◽  
...  

Acquired long QT syndrome is typically caused by medications, electrolyte disturbances, bradycardia, or catastrophic central nervous system events. We report a case of myocardial infarction–related acquired long QT syndrome in a 58-year-old woman that had no clear cause and progressed to torsades de pointes requiring treatment with isoproterenol and magnesium. Despite negative results of DNA testing against a known panel of genetic mutations and polymorphisms associated with long QT syndrome, the patient's family history of fatal cardiac disease suggests a predisposing genetic component. This report serves to remind clinicians of this potentially fatal ventricular arrhythmia after myocardial infarction.


Heart Rhythm ◽  
2010 ◽  
Vol 7 (12) ◽  
pp. 1808-1814 ◽  
Author(s):  
Kayo Haraoka ◽  
Hiroshi Morita ◽  
Yukihiro Saito ◽  
Norihisa Toh ◽  
Toru Miyoshi ◽  
...  

2016 ◽  
Vol 21 (6) ◽  
pp. 572-579
Author(s):  
Piotr Kukla ◽  
Marek Jastrzębski ◽  
Kamil Fijorek ◽  
Sebastian Stec ◽  
Leszek Bryniarski ◽  
...  

2013 ◽  
Vol 43 (5) ◽  
pp. 340 ◽  
Author(s):  
Dae Gil Kang ◽  
Sung Eun Kim ◽  
Myoung Soo Park ◽  
Eun Jung Kim ◽  
Jun Hee Lee ◽  
...  

2011 ◽  
Vol 4 (1) ◽  
pp. 103-111 ◽  
Author(s):  
Mitsunori Maruyama ◽  
Shien-Fong Lin ◽  
Yuanfang Xie ◽  
Su-Kiat Chua ◽  
Boyoung Joung ◽  
...  

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