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Cyanotic congenital heart defects in adult patients

  • J. Timothy Bricker and Jorge R. Alegria
Published/Copyright: November 1, 2010
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International Journal on Disability and Human Development
From the journal Volume 9 Issue 2-3

Abstract

Usually cyanotic heart defects are fatal in infancy and childhood without surgical treatment. There are rare circumstances in which a cyanotic individual can survive into adult years with reasonably good health. Prolonged survival in unop-erated cyanotic heart defect cases is dependent upon well-balanced circulation with pulmonary blood flow that is near normal but not excessive. Physicians in practice can encounter such cases in which diagnosis was missed in childhood or who had a diagnosis of a cardiac malformation but are recent immigrants from a part of the world in which surgical treatment was not possible. These unusual survivors have a different spectrum of anatomic malformations than the cyanotic defects found in newborn babies. Even with a well-balanced circulation, chronic ventricular volume overload is likely to lead to myocardial dysfunction over time. The evaluation by a cardiac team with expertise in the treatment of congenital cardiac defects in adult patients is important to long-term health and survival of the patients.


Corresponding author: J. Timothy Bricker, MD, MBA, Jacqueline A. Noonan Endowed Chair of Pediatrics, Professor and Chairman, Department of Pediatrics, University of Kentucky, Physician-in-Chief, Kentucky Children's Hospital, 800 Rose Street, MN-150, Lexington, KY 40536, USA

Received: 2010-1-7
Accepted: 2010-2-14
Published Online: 2010-11-01
Published in Print: 2010-11-01

©2010 by Walter de Gruyter Berlin New York

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