1.Complete Atrioventricular Block-Induced Torsade de Pointes, Manifested by Epilepsy.
Jun Han JEON ; Sung Ho HER ; Jung Yeon CHIN ; Ki Hoon PARK ; Hee Jeong YOON ; Jong Min LEE ; Seung Won JIN
The Korean Journal of Internal Medicine 2011;26(1):99-102
Complete atrioventricular (AV) block is frequently regarded as a cause of informed syncopal attacks, even though the escape rhythm is maintained. Torsade de pointes (TdP) may be a significant complication of AV block associated with QT prolongation. Here, we report the case of a 42-year-old female who was referred to our hospital due to recurrent seizure-like attacks while taking anti-convulsant drugs at a psychiatric hospital. TdP with a long QT interval (corrected QT = 0.591 seconds) was observed on an electrocardiogram (ECG) taken in the emergency department. The patient's drug history revealed olanzapine as the suspicious agent. Even after the medication was stopped, however, the QT interval remained within an abnormal range and multiple episodes of TdP and related seizure-like symptoms were found via ECG monitoring. A permanent pacemaker was thus implanted, and the ventricular rate was set at over 80 beats/min. There was no recurrence of tachyarrhythmia or other symptoms.
Adult
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Atrioventricular Block/*complications
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Benzodiazepines/adverse effects
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Electrocardiography
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Epilepsy/*etiology
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Female
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Humans
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Pacemaker, Artificial
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Torsades de Pointes/*etiology/therapy
2.A Case of Torsade de Pointes Associated with Hypopituitarism due to Hemorrhagic Fever with Renal Syndrome.
Nam Ho KIM ; Jeong Gwan CHO ; Young Keun AHN ; Seung Uk LEE ; Kun Hyung KIM ; Jang Hyun CHO ; Han Gyun KIM ; Wan KIM ; Myung Ho JEONG ; Jong Chun PARK ; Jung Chaee KANG
Journal of Korean Medical Science 2001;16(3):355-359
We describe a 51-yr-old man presenting with syncope due to torsade de pointes. The torsade de pointes was refractory to conventional medical therapy, including infusion of isoproterenol, MgSO4, potassium, lidocaine, and amiodarone. His past history, physical findings, and hormone study confirmed that QT prolongation was caused by anterior hypopituitarism that developed as a sequela of hemorrhagic fever with renal syndrome. The long QT interval with deep inverted T wave was completely normalized 4 weeks after starting steroid and thyroid hormone replacement. Hormonal disorders should be considered as a cause of torsade de pointes, because this life-threatening arrhythmia can be treated by replacing the missing hormone.
Hemorrhagic Fever with Renal Syndrome/*complications/physiopathology
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Hormone Replacement Therapy
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Human
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Hypopituitarism/drug therapy/*etiology/physiopathology
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Male
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Middle Age
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Tachycardia, Ventricular
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Torsades de Pointes/drug therapy/*etiology/physiopathology
3.Long QT Syndrome and Torsade de Pointes Associated with Takotsubo Cardiomyopathy.
Ji Hun AHN ; Sang Ho PARK ; Won Yong SHIN ; Se Whan LEE ; Seung Jin LEE ; Dong Kyu JIN ; Han Min LEE ; Jun Young EUN
Journal of Korean Medical Science 2011;26(7):959-961
Prolongation of QTc interval associated with Takotsubo cardiomyopathy (TC) has previously been reported in published case series. We report an unusual case of a patient who presented with TC associated with long-QT syndrome and developed cardiac arrest secondary to torsade de pointes. Since QT prolongation and bradycardia persisted after the resolution of TC, the patient received permanent pacemaker. Since then additional event did not occur. QT prolongation and bradycardia could be persistent even after recovery of TC, and permanent pacemaker insertion may be a treatment option of long QT syndrome related with TC.
Aged
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Bradycardia/diagnosis/therapy
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Cardiac Pacing, Artificial
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Coronary Angiography
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Diagnosis, Differential
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Electrocardiography
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Female
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Heart Arrest/diagnosis/etiology
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Humans
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Long QT Syndrome/*diagnosis/etiology
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Takotsubo Cardiomyopathy/complications/*diagnosis/ultrasonography
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Torsades de Pointes/*diagnosis/etiology