Hostname: page-component-745bb68f8f-b95js Total loading time: 0 Render date: 2025-02-11T14:10:57.517Z Has data issue: false hasContentIssue false

Atrioventricular block in a new born with acquired long QT syndrome

Published online by Cambridge University Press:  15 August 2006

John R. Phillips
Affiliation:
Division of Pediatric Cardiology, Cook Children's Heart Center, Fort Worth, TX, USA
Christopher L. Case
Affiliation:
Division of Pediatric Cardiology, Cook Children's Heart Center, Fort Worth, TX, USA
Paul C. Gillette
Affiliation:
Division of Pediatric Cardiology, Cook Children's Heart Center, Fort Worth, TX, USA
Rights & Permissions [Opens in a new window]

Abstract

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.

We report a case of 2:1 atrioventricular block associated with acquired long QT syndrome. A newborn presented to our neonatal intensive care unit with intermittent bradycardia due to 2:1 atrioventricular block. Initial evaluation showed QT prolongation and significant electrolytic abnormalities. After correction of the electrolytic imbalance, the QT interval normalized and atrioventricular block resolved. Compared to congenital long QT syndrome with 2:1 atrioventricular block, acquired long QT syndrome with comparable atrioventricular block has a benign prognosis, provided treatment is initiated quickly.

Type
Brief Report
Copyright
2001 Cambridge University Press