Congenital long QT syndrome and 2:1 atrioventricular block: an optimistic outcome in the current era

Peter F Aziz1, Ronn E Tanel, Ilana J Zelster

  • 1Division of Cardiology, Children's Hospital of Philadelphia, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania, USA. aziz@email.chop.edu

Heart Rhythm
|March 4, 2010
PubMed

Insights

Infants with congenital long QT syndrome (LQTS) and 2:1 atrioventricular block (AVB) have a better outlook with modern management. Early diagnosis and intervention improved outcomes in this high-risk group.

Area of Science:

  • Pediatric Cardiology
  • Clinical Electrophysiology
  • Genetics

Background:

  • Congenital long QT syndrome (LQTS) with 2:1 atrioventricular block (AVB) historically carries a >50% infant mortality.
  • This high-risk population requires updated prognostic evaluation.

Purpose of the Study:

  • To determine the current outcomes for infants diagnosed with congenital LQTS and 2:1 AVB.
  • To assess the effectiveness of contemporary management strategies.

Main Methods:

  • Retrospective analysis of 12 neonates with congenital LQTS and 2:1 AVB from 2000-2009 across four pediatric centers.
  • Review of ECG, QTc intervals, genotype, medications, and device therapies.
  • Statistical analysis including paired t-test.

Main Results:

  • No mortality observed in the cohort over a median follow-up of 71 months.
  • 11 of 12 patients received cardiac device therapy (pacemaker or ICD).
  • Significant reduction in QTc intervals post-intervention (mean 480 ms vs. 616 ms).

Conclusions:

  • Contemporary management of LQTS with 2:1 AVB offers a more optimistic prognosis than previously reported.
  • Early diagnosis, intervention, and improved therapeutic strategies contribute to favorable outcomes.
  • This study highlights the importance of proactive management in this challenging pediatric condition.
Abstract

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