2017
DOI: 10.7759/cureus.1581
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Long QT Syndrome Unveiled by a Fatal Combination of Medications and Electrolyte Abnormalities

Abstract: Long QT syndrome (LQTS) can present with syncope and seizure-like activity in the setting of torsades de pointes (TdP) with hemodynamic instability. Electrolyte abnormalities and medications can predispose to TdP in the setting of latent LQTS. An implantable cardioverter defibrillator (ICD) is needed if patients with TdP continue to be symptomatic despite medical treatment. We report a case of a patient who presented with seizures and was found to have prolonged corrected QT interval (QTc). During her admissio… Show more

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Cited by 1 publication
(3 citation statements)
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“…The long QT syndrome (LQTS) is a type of cardiac arrhythmia syndrome characterized with impaired ventricular repolarization manifest as prolongation of QT interval on the ECG [1,2]. This predisposes to the development risk of syncope, ventricular arrhythmias, seizure, and cardiac death to the patient [1,3,4].…”
Section: Discussionmentioning
confidence: 99%
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“…The long QT syndrome (LQTS) is a type of cardiac arrhythmia syndrome characterized with impaired ventricular repolarization manifest as prolongation of QT interval on the ECG [1,2]. This predisposes to the development risk of syncope, ventricular arrhythmias, seizure, and cardiac death to the patient [1,3,4].…”
Section: Discussionmentioning
confidence: 99%
“…Long QT syndrome incidences is approximately about 1 in 10.000 to 15.000 peoples and female is more prevalent [5]. Although there are many patients asymptomatic, the first clinical signs of this disease might be sudden cardiac death [1,2]. The following is a case report of 46-year-old women who came to the cardiology clinic with chief complaint of dizziness and diagnose with acquired LQTS secondary to electrolyte imbalance.…”
Section: Introductionmentioning
confidence: 99%
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