Right ventricular function late after total repair of tetralogy of Fallot.

Abstract:

:Over the past decades, life expectancy in patients with congenital heart disease has increased dramatically. However, serious complications may develop late after total repair in infancy. These complications are usually the result of longstanding pulmonary regurgitation, which leads to dilatation of the right ventricle and an increased risk for severe arrhythmias. Therefore lifelong follow-up in these patients is required. Cardiac magnetic resonance imaging is the current imaging tool of choice because it offers superior imaging quality and enables accurate quantification of functional parameters such as flow volumes and systolic and diastolic performance.

journal_name

Eur Radiol

journal_title

European radiology

authors

van Straten A,Vliegen HW,Hazekamp MG,de Roos A

doi

10.1007/s00330-004-2574-z

subject

Has Abstract

pub_date

2005-04-01 00:00:00

pages

702-7

issue

4

eissn

0938-7994

issn

1432-1084

journal_volume

15

pub_type

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