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Published on: July 12, 2011
[Eisenmenger syndrome. Pathophysiology]
1Institut de Puériculture de Paris, Hôpital Necker Enfants Malades, France. marilyne.levy@nck.ap-haphp.fr
Summary
Eisenmenger syndrome, a severe complication of congenital heart defects with left-to-right shunts, is now rare in developed nations due to improved patient care. The presence of circulating endothelial cells indicates a poor prognosis.
Area of Science:
- Cardiology
- Vascular Biology
- Congenital Heart Disease
Context:
- Eisenmenger syndrome is a feared complication in patients with congenital heart disorders involving a left-to-right shunt.
- Historically, this condition posed significant risks, but advancements have made it less common in industrialized countries.
- Optimized perinatal care and early shunt elimination have contributed to its decreased incidence.
Purpose:
- To summarize the current understanding of Eisenmenger syndrome as a complication of congenital heart disease.
- To highlight the reduced prevalence in developed nations.
- To identify prognostic factors associated with Eisenmenger syndrome.
Summary:
- Eisenmenger syndrome, a severe outcome of congenital heart defects with left-to-right shunts, is now infrequent in industrialized nations.
- This decline is attributed to enhanced perinatal management and timely surgical or interventional closure of shunts.
- The identification of circulating endothelial cells serves as a critical indicator of a poor prognosis in affected patients.
Impact:
- Improved patient outcomes for congenital heart defects with left-to-right shunts.
- Reduced incidence of Eisenmenger syndrome in developed healthcare systems.
- Enhanced risk stratification for patients through the identification of poor prognostic markers like circulating endothelial cells.
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