Abstract
Most cardiac arrhythmias may occur in the fetus, infant, child, and adolescent as a result of congenital arrhythmia substrates or in response to hemodynamic perturbations related to structural defects or subsequent surgical treatments. Unrelated to surgery, arrhythmias are especially prevalent in persons having Ebstein anomaly of the tricuspid valve, congenitally corrected transposition, or heterotaxy. Atrial arrhythmias are important following the older atrial redirection operations for d-transposition of the great arteries and following the Fontan operation for single ventricle physiology. Catheter ablation of these substrates is now possible using electroanatomic mapping systems and high output radiofrequency generators. Ventricular tachycardia and sudden death are of concern in some patients following surgical repair of tetralogy of Fallot and left ventricular outflow tract obstruction. Among children having structurally normal hearts, atrioventricular reciprocating tachycardia and atrioventricular nodal reentrant tachycardia comprise the majority of tachyarrhythmias in infants and teenagers, respectively. Catheter ablation has largely supplanted pharmacological therapy for supraventricular tachycardias in children older than about 5 years, with results comparable to those in adults. Risk of collateral damage to structures in the growing heart makes catheter ablation less attractive as primary therapy in smaller children. Indications for device implantation are being established for the young and may be applied down to newborns (pacemakers) and older infants (implantable cardioverter-defibrillators). Planning such implantations in children and in patients having congenital heart disease requires careful consideration of somatic growth, cardiac anatomy, and venous caliber.
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Trivedi, B., Kanter, R. (2011). Arrhythmias in Children. In: Yan, GX., Kowey, P. (eds) Management of Cardiac Arrhythmias. Contemporary Cardiology. Humana Press, Totowa, NJ. https://doi.org/10.1007/978-1-60761-161-5_17
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