Although isolated premature ventricular contractions may be seen in as many
as 15% of normal newborns, one third of normal adolescents, and two thirds
of adolescents and adults with repaired heart disease, sustained ventricul
ar arrhythmias are relatively rare in young normal hearts. Sudden cardiac h
ealth is rare in young normal hearts, although there is an increased incide
nce in dilated cardiomyopathies and following repair of particular congenit
al heart lesions. Noninvasive and invasive techniques imperfectly stratify
these patients. Patients with cardiomyopathy often have ventricular arrhyth
mias, although the risk of mortality is more closely linked to ventricular
function. There are many infants and pediatric patients with apparently nor
mal hearts who have combinations of asymptomatic nonsustained ventricular t
achycardia and potentially serious symptoms. The clinical concern is to ide
ntify diagnoses such as long QT syndrome associated with recurrent cardiac
syncope and premature mortality so that appropriate choices can be made reg
arding drug and device therapy. Although this broad range of disease places
a premium on careful evaluation, selective therapy, and continued research
, serious symptoms, even in the absence of ectopy, are concerning in any pa
tient.