scholarly journals Vomiting, electrolyte disturbance, and medications; the perfect storm for acquired long QT syndrome and cardiac arrest: a case report

2022 ◽  
Vol 16 (1) ◽  
Author(s):  
K. D. Tiver ◽  
D. Dharmaprani ◽  
J. X. Quah ◽  
A. Lahiri ◽  
K. E. Waddell-Smith ◽  
...  

Abstract Background Acquired long QT syndrome is an important and preventable cause of cardiac arrest. Certain medications and electrolyte disturbance are common contributors, and often coexist. In this case, we report five contributors to cardiac arrest. Case presentation This case is of a 51-year-old Caucasian female patient who presented with vomiting associated with hypokalemia and hypomagnesemia. She subsequently received ondansetron and metoclopramide, on the background of chronic treatment with fluoxetine. She then suffered an in-hospital monitored cardiac arrest, with features of long QT and torsades de pointes retrospectively noted on her prearrest electrocardiogram. She was diagnosed with acquired long QT syndrome, and her QT interval later normalized after removal of offending causes. Conclusions This case highlights the importance of proper consideration prior to prescribing QT prolonging medications, especially in patients who have other risk factors for prolonged QT, such as electrolyte disturbances and pretreatment with QT prolonging medications.

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


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.


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

2016 ◽  
Vol 2 (2) ◽  
pp. 81-84
Author(s):  
Dániel Czuriga ◽  
Andrea Szegedi ◽  
Ferenc Győry ◽  
Attila Szilágyi ◽  
Sándor Sipka ◽  
...  

Abstract QT interval prolongation on the electrocardiogram is considered a precursory sign for imminent, potentially lethal ventricular arrhythmias. Beside the inherited condition of long QT syndrome, numerous drugs, certain electrolyte disturbances and early transmural ischemia have been identified to induce reversible prolongation of the QT interval, collectively called as acquired long QT syndrome. Herein we describe a case of a patient with transient QT prolongation and Takotsubo cardiomyopathy, a rather infrequent cause of long QT development. Serial changes of the repolarization pattern were documented to demonstrate progression and resolution of the abnormal QT interval.


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 ◽  
...  

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 ◽  
...  

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