European Heart Journal Advance Access originally published online on June 22, 2006
European Heart Journal 2006 27(14):1644-1645; doi:10.1093/eurheartj/ehi823
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© The European Society of Cardiology 2006. All rights reserved. For Permissions, please e-mail: journals.permissions@oxfordjournals.org
Eisenmenger syndrome: towards identifying the risk factors for death
Department of Paediatric Cardiology, University Hospital of Cologne, Kerpenerstrasse 62, 50937 Cologne, Germany
* Corresponding author. Tel: +49 221 478 86301; Fax: +49 221 478 86302. E-mail address: n.sreeram@uni-koeln.de
This editorial refers to Presentation, survival prospects and predictors of death in Eisenmenger syndrome: a combined retrospective and casecontrol study
by G.-P. Diller et al., on page 1737
| The first 10% of the full text of this article appears below. |
The first description of Eisenmenger syndrome was provided over a 100 years ago, and the concept of Eisenmenger reaction, with progressive pulmonary vascular disease and reversal of shunt as representing a final pathway for several morphological cardiac defects, is well understood.1 Given the improved awareness of congenital heart disease among paediatricians and cardiologists, the advances in imaging, surgery and intensive care facilities, and that early definitive therapy for the majority of lesions associated with a risk of developing Eisenmenger syndrome is available, a progressive decrease in the prevalence of this disease may be expected. This does not detract from the fact that a significant population of (young) adults is currently under follow-up at various centres throughout the world with this syndrome. Data from several studies suggest that their survival prospects appear to be improving (although
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Related articles in EHJ:
- Presentation, survival prospects, and predictors of death in Eisenmenger syndrome: a combined retrospective and casecontrol study
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EHJ 2006 27: 1737-1742.[Abstract] [FREE Full Text]
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