Abstract

Sudden cardiac death (SCD) is a rare clinical encounter in pediatrics, but its social impact is immense because of its unpredicted and catastrophic nature in previously healthy individuals. Unlike in adults where the primary cause of SCD is related to ischemic heart disease, the etiology is diverse in young SCD victims. Although certain structural heart diseases may be identified during autopsy in some SCD victims, autopsy-negative SCD is more common in pediatrics, which warrants the diagnosis of sudden arrhythmic death syndrome (SADS) based upon the assumption that the usual heart rhythm is abruptly replaced by lethal ventricular arrhythmia. Despite current advances in molecular genetics, the causes of more than half of SADS cases remain unanswered even after postmortem genetic testing. Moreover, the majority of these deaths occur at rest or during sleep even in the young. Recently, sudden unexpected death in epilepsy (SUDEP) has emerged as another etiology of SCD in children and adults, suggesting critical involvement of the central nervous system (CNS) in SCD. Primary cardiac disorders may not be solely responsible for SCD; abnormal CNS function may also contribute to the unexpected lethal event. In this review article, we provide an overview of the complex pathogenesis of SADS and its diverse clinical presentation in the young and postulate that SADS is, in part, induced by unfortunate miscommunication between the heart and CNS via the autonomic nervous system.

Highlights

  • Sudden cardiac death (SCD) is a rare clinical encounter in pediatrics, but its social impact is immense because of its unpredicted and catastrophic nature in previously healthy individuals

  • Certain structural heart diseases may be identified during autopsy in some SCD victims, autopsy-negative SCD is more common in pediatrics, which warrants the diagnosis of sudden arrhythmic death syndrome (SADS) based upon the assumption that the usual heart rhythm is abruptly replaced by lethal ventricular arrhythmia

  • We provide an overview of the complex pathogenesis of SADS and its diverse clinical presentation in the young and postulate that SADS is, in part, induced by unfortunate miscommunication between the heart and central nervous system (CNS) via the autonomic nervous system

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Summary

Sudden cardiac death without identifiable structural heart disease

A substantial number of young SCD victims are previously healthy individuals who have no known history of underlying cardiac disease and who unexpectedly present with SCD as their first manifestation (Behr et al, 2007; Corrado et al, 2001). Seizure occurred in 22%, but no previous medical history was recorded in 45% (Glinge et al, 2015) Nonspecific symptoms, such as dizziness and palpitation, and transient loss of consciousness, including syncope and seizure-like activity, are common preceding events in potentially lethal congenital ion channelopathies (MacCormick et al, 2011). The pathophysiology of these antecedent symptoms is poorly understood but may represent aborted SCD. The reasons why more people die at rest or during sleep than induced by vigorous exercise are poorly understood

Electrophysiology of SCA
Substrates and triggers that cause VF
Genetic ion channelopathies
Clinically borderline cardiomyopathies responsible for SCD
Heart-CNS Axis in SCD
Dysregulation of ANS may induce lethal ventricular arrhythmias and SCD
Findings
Conclusion
Full Text
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