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   <subfield code="a">Use of a Cardioselective Beta-Blocker for Pediatric Patients With Prolonged QT Syndrome</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Jose Moltedo, Jeffrey Kim, Richard Friedman, Naomi Kertesz, Bryan Cannon]</subfield>
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   <subfield code="a">The data on the efficacy of atenolol for long-QT syndrome (LQTS) are controversial. This study aimed to evaluate the efficacy of atenolol for pediatric patients with LQTS. A retrospective observational study investigating all patients who had LQTS treated with atenolol at two institutions was performed. The study identified 57 patients (23 boys and 34 girls) with a mean QT corrected for heart rate (QTc) of 521±54 ms. The mean age of these patients at diagnosis was 9 ± 6 years. Their clinical manifestations included no symptoms (n=33, 58%), ventricular tachycardia (n=10, 18%), syncope (n=6, 10%), resuscitated sudden cardiac death (n=4, 7%), atrioventricular block (n=2, 4%), and bradycardia or presyncope (n=2, 3%). Of the 57 patients, 13 (22%) had a family history of sudden death. The follow-up period was 5.4±4.5 years. Atenolol at a mean dose of 1.4±0.5 mg/kg/day was administered twice a day for all the patients. The mean maximum heart rate was 132±27 bpm on Holter monitors and 155±16bpm on exercise treadmill tests, with medication doses titrated up to achieve a maximum heart rate lower than 150 bpm on both tests. During the follow-up period, one patient died (noncompliant with atenolol at the time of death), and the remaining patients had no sudden cardiac death events. Four patients (8%) had recurrent ventricular arrhythmias, three of whom received an implantable cardioverter defibrillator (all symptomatic at the time of diagnosis). For three patients (6%), it was necessary to rotate to a different beta-blocker because of side effects or inadequate heart rate control. Atenolol administered twice daily constitutes a valid and effective alternative for the treatment of pediatric patients with LQTS.</subfield>
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