Long-term follow-up of a pediatric cohort with short QT syndrome

J Am Coll Cardiol. 2013 Mar 19;61(11):1183-91. doi: 10.1016/j.jacc.2012.12.025. Epub 2013 Jan 30.

Abstract

Objectives: The purpose of this study was to define the clinical characteristics and long-term follow-up of pediatric patients with short QT syndrome (SQTS).

Background: SQTS is associated with sudden cardiac death. The clinical characteristics and long-term prognosis in young patients have not been reported.

Methods: This was an international case series involving 15 centers. Patients were analyzed for electrocardiography characteristics, genotype, clinical events, Gollob score, and efficacy of medical or defibrillator (implantable cardioverter-defibrillator [ICD]) therapy. To assess the possible prognostic value of the Gollob score, we devised a modified Gollob score that excluded clinical events from the original score.

Results: Twenty-five patients 21 years of age or younger (84% males, median age: 15 years, interquartile range: 9 to 18 years) were followed up for 5.9 years (interquartile range: 4 to 7.1 years). Median corrected QT interval for heart rate was 312 ms (range: 194 to 355 ms). Symptoms occurred in 14 (56%) of 25 patients and included aborted sudden cardiac death in 6 patients (24%) and syncope in 4 patients (16%). Arrhythmias were common and included atrial fibrillation (n = 4), ventricular fibrillation (n = 6), supraventricular tachycardia (n = 1), and polymorphic ventricular tachycardia (n = 1). Sixteen patients (84%) had a familial or personal history of cardiac arrest. A gene mutation associated with SQTS was identified in 5 (24%) of 21 probands. Symptomatic patients had a higher median modified Gollob score (excluding points for clinical events) compared with asymptomatic patients (5 vs. 4, p = 0.044). Ten patients received medical treatment, mainly with quinidine. Eleven of 25 index cases underwent ICD implantation. Two patients had appropriate ICD shocks. Inappropriate ICD shocks were observed in 64% of patients.

Conclusions: SQTS is associated with aborted sudden cardiac death among the pediatric population. Asymptomatic patients with a Gollob score of <5 remained event free, except for an isolated episode of supraventricular tachycardia, over an average 6-year follow-up. A higher modified Gollob score of 5 or more was associated with the likelihood of clinical events. Young SQTS patients have a high rate of inappropriate ICD shocks.

Publication types

  • Multicenter Study

MeSH terms

  • Adolescent
  • Arrhythmias, Cardiac* / diagnosis
  • Arrhythmias, Cardiac* / therapy
  • Child
  • Child, Preschool
  • Female
  • Follow-Up Studies
  • Heart Conduction System / abnormalities*
  • Heart Defects, Congenital* / diagnosis
  • Heart Defects, Congenital* / therapy
  • Humans
  • Infant
  • Infant, Newborn
  • Male
  • Syndrome
  • Time Factors
  • Young Adult