Our mission is to become a worldwide reference for education in the field for all professionals involved in the process to disseminate knowledge & skills of Acute Cardiovascular Care.
Our mission is to promote excellence in clinical diagnosis, research, technical development, and education in cardiovascular imaging in Europe.
Our mission is to promote excellence in research, practice, education and policy in cardiovascular health, primary and secondary prevention.
Our mission is to reduce the burden of cardiovascular disease in Europe through percutaneous cardiovascular interventions.
Our mission is to improve the quality of life of the population by reducing the impact of cardiac rhythm disturbances and reduce sudden cardiac death.
Our mission is to improve quality of life and longevity, through better prevention, diagnosis and treatment of heart failure, including the establishment of networks for its management, education and research.
The ESC Working Groups' goal is to stimulate and disseminate scientific knowledge in different fields of cardiology.
The ESC Councils' goal is to share knowledge among medical professionals practising in specific cardiology domains.
OUR MISSION: TO REDUCE THE BURDEN OF CARDIOVASCULAR DISEASE
Prof. harald Kaemmerer,
Harald Kaemmerer, Annalisa Angelini, Pedro Trigo-Trindade, Christian Schreiber, Juan V. Comas, Jörg Stein
Ebstein anomaly (EA) is a rare congenital abnormality affecting the tricuspid valve (TV) and the right ventricle. It is characterized by downward displacement of the functional tricuspid annulus, atrialization of a portion of the right ventricle with dilatation of the right atrioventricular junction, thinning of the affected wall and plastering of the leaflets to the underlying ventricular myocardium (lack of leaflet delamination) with fenestration, redundancy and tethering of the anterior leaflet. Functionally the valve is usually incompetent. Accessory conduction pathways are frequently found. Several classifications to describe the TV anomaly have been proposed, for surgical decision-making the Carpentier classification (Types A-D) is widely used. In asymptomatic patients conservative treatment is recommended. In symptomatic patients, interventional or surgical treatment has to be evaluated. According to the native anatomy of the TV, different surgical options (TV repair or TV replacement, +/- other options) may apply. To avoid TV replacement several repair techniques have been developed, including annuloplasty, closure of commissures, and creation of a “monocusp” valve. More recently, da Silva proposed the “cone reconstruction” of the TV leaflet tissue. Furthermore, patients with right ventricular failure may benefit from a cavo-bipulmonary anastomosis. In the current era, results of surgery in adults have low early mortality in experienced centres, and long-term survival is satisfactory. Prognosis after surgical repair depends on post-operative improvement and lower age at surgery. Apart from the residual hemodynamic problems, arrhythmia management remains challenging. In any case, the management of patients with EA is complex and has to be individualized. Close collaboration with a cardiologist experienced in congenital heart disease is mandatory.
Ebstein's malformation: recent advances
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