Catecholaminergic Polymorphic Ventricular Tachycardia in a 16-year-old: Case Report

Introduction: Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a rare, inheritable cardiac disorder associated with stress- or exercise-induced syncope or cardiac arrest in children and young adults. Diagnosis of CPVT is often missed or delayed due to variable presentation and normal...

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Main Authors: John Wahhab, Ani Oganesyan, Krishi Korrapati
Format: Article
Language:English
Published: eScholarship Publishing, University of California 2025-04-01
Series:Clinical Practice and Cases in Emergency Medicine
Online Access:https://escholarship.org/uc/item/5hf8811c
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author John Wahhab
Ani Oganesyan
Krishi Korrapati
author_facet John Wahhab
Ani Oganesyan
Krishi Korrapati
author_sort John Wahhab
collection DOAJ
description Introduction: Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a rare, inheritable cardiac disorder associated with stress- or exercise-induced syncope or cardiac arrest in children and young adults. Diagnosis of CPVT is often missed or delayed due to variable presentation and normal cardiac imaging and electrocardiogram results, with about 40% of patients dying within 10 years of diagnosis. This case underscores the importance of cross-departmental communication when managing complex pediatric cases, especially when using an interpreter. Case Report: A 16-year-old male presented to the hospital with cardiac arrest in ventricular fibrillation following collapse despite a history of treatment with flecainide and nadolol. He was resuscitated, stabilized with antiarrhythmic drips, received an implantable cardioverter defibrillator, and was discharged neurologically intact nine days later. It is vital for physicians to consider CPVT in young patients with syncope to prevent errors in diagnosis of this highly fatal disease. Conclusion: Catecholaminergic polymorphic ventricular tachycardia is a rare genetic disease with significant morbidity and mortality. Treatment decisions for acute CPVT often occur without prior knowledge of the disease; so, in patients diagnosed with CPVT, physicians should implement appropriate therapeutic options to prevent future cardiac events. For patients who remain symptomatic despite compliance with beta blockers and/or other antiarrhythmic therapy, interventions such as placement of an implantable cardioverter defibrillator or sympathetic denervation may be necessary to prevent life-threatening arrhythmias. This case also underscores the importance of obtaining a detailed family history and coordinating care with other physicians in cases where history is limited.
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spelling doaj-art-4639e681ced3472889d5dc00c459c0eb2025-08-20T02:25:47ZengeScholarship Publishing, University of CaliforniaClinical Practice and Cases in Emergency Medicine2474-252X2025-04-019222022210.5811/cpcem.34847cpcem-9-220Catecholaminergic Polymorphic Ventricular Tachycardia in a 16-year-old: Case ReportJohn Wahhab0Ani Oganesyan1Krishi Korrapati2Chicago Medical School at Rosalind Franklin University of Medicine and Science, North Chicago, IllinoisChicago Medical School at Rosalind Franklin University of Medicine and Science, North Chicago, IllinoisChicago Medical School at Rosalind Franklin University of Medicine and Science, North Chicago, IllinoisIntroduction: Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a rare, inheritable cardiac disorder associated with stress- or exercise-induced syncope or cardiac arrest in children and young adults. Diagnosis of CPVT is often missed or delayed due to variable presentation and normal cardiac imaging and electrocardiogram results, with about 40% of patients dying within 10 years of diagnosis. This case underscores the importance of cross-departmental communication when managing complex pediatric cases, especially when using an interpreter. Case Report: A 16-year-old male presented to the hospital with cardiac arrest in ventricular fibrillation following collapse despite a history of treatment with flecainide and nadolol. He was resuscitated, stabilized with antiarrhythmic drips, received an implantable cardioverter defibrillator, and was discharged neurologically intact nine days later. It is vital for physicians to consider CPVT in young patients with syncope to prevent errors in diagnosis of this highly fatal disease. Conclusion: Catecholaminergic polymorphic ventricular tachycardia is a rare genetic disease with significant morbidity and mortality. Treatment decisions for acute CPVT often occur without prior knowledge of the disease; so, in patients diagnosed with CPVT, physicians should implement appropriate therapeutic options to prevent future cardiac events. For patients who remain symptomatic despite compliance with beta blockers and/or other antiarrhythmic therapy, interventions such as placement of an implantable cardioverter defibrillator or sympathetic denervation may be necessary to prevent life-threatening arrhythmias. This case also underscores the importance of obtaining a detailed family history and coordinating care with other physicians in cases where history is limited.https://escholarship.org/uc/item/5hf8811c
spellingShingle John Wahhab
Ani Oganesyan
Krishi Korrapati
Catecholaminergic Polymorphic Ventricular Tachycardia in a 16-year-old: Case Report
Clinical Practice and Cases in Emergency Medicine
title Catecholaminergic Polymorphic Ventricular Tachycardia in a 16-year-old: Case Report
title_full Catecholaminergic Polymorphic Ventricular Tachycardia in a 16-year-old: Case Report
title_fullStr Catecholaminergic Polymorphic Ventricular Tachycardia in a 16-year-old: Case Report
title_full_unstemmed Catecholaminergic Polymorphic Ventricular Tachycardia in a 16-year-old: Case Report
title_short Catecholaminergic Polymorphic Ventricular Tachycardia in a 16-year-old: Case Report
title_sort catecholaminergic polymorphic ventricular tachycardia in a 16 year old case report
url https://escholarship.org/uc/item/5hf8811c
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AT anioganesyan catecholaminergicpolymorphicventriculartachycardiaina16yearoldcasereport
AT krishikorrapati catecholaminergicpolymorphicventriculartachycardiaina16yearoldcasereport