Preoperative diagnosis of long QT syndrome in an infant with tetralogy of Fallot.

Published

Journal Article

Long QT syndrome is a well-described entity in infants. Its presentation in the context of congenital heart disease is rare and is almost exclusively diagnosed postoperatively. For patients undergoing surgical intervention, preoperative knowledge of the diagnosis and appropriate perioperative management can be life-saving. We present the rare case of an infant with tetralogy of Fallot who was preoperatively diagnosed with long QT syndrome and discuss the implications of this diagnosis for his perioperative management.

Full Text

Duke Authors

Cited Authors

  • Hornik, CP; Campbell, MJ; Carboni, MP; Lodge, AJ; Rhodes, JF; Kanter, RJ

Published Date

  • August 2011

Published In

Volume / Issue

  • 32 / 6

Start / End Page

  • 834 - 838

PubMed ID

  • 21448618

Pubmed Central ID

  • 21448618

Electronic International Standard Serial Number (EISSN)

  • 1432-1971

Digital Object Identifier (DOI)

  • 10.1007/s00246-011-9957-0

Language

  • eng

Conference Location

  • United States