Objective. To determine the yield of screening echocardiography in the eval
uation of pediatric syncope.
Design. All patients diagnosed with syncope from January 1993 to January 19
99 were identified and their records were reviewed for age, weight, sex, ye
ar of presentation, personal and family history, physical examination, and
cardiac diagnostic testing. Cardiac defects were identified by reviewing ec
hocardiograms and reports.
Results. The 480 patients (268 females) ranged in age from 1.5 to 18.0 year
s old and ranged in weight from 10.3 to 113.6 kg. Final diagnoses included
noncardiac causes in 458, long QT syndrome in 14, arrhythmias in 6, and car
diomyopathy in 2. An abnormal history, physical examination, or electrocard
iogram identified 21 of the 22 patients with a cardiac cause of syncope. Of
the 322 (67%) echocardiograms performed, abnormalities were detected in 37
. These abnormalities included 26 minor valve anomalies, 7 hemodynamically
insignificant shunt lesions, 2 mildly decreased left ventricular shortening
fractions, and 2 cardiomyopathies. Only the 2 cardiomyopathies were consid
ered to be potential causes of syncope, and in both cases, the electrocardi
ogram was markedly abnormal. A similar percentage of echocardiograms were o
rdered during the first and last 3 years of the study (61% vs 71%).
Conclusion. History, physical examination, and electrocardiography provide
a screening protocol that allows the identification of a cardiac cause of s
yncope in the overwhelming majority of pediatric patients. In the absence o
f a positive screen result, the echocardiogram does not contribute to the e
valuation of syncope in children. We speculate that primary care providers
and pediatric cardiologists continue to use echocardiography because of the
paucity of data regarding its value in pediatric syncope. However, this st
udy shows little benefit of screening echocardiography and should discourag
e its routine use.