scholarly journals Diagnosis and natural history of Ebstein's anomaly.

Heart ◽  
1985 ◽  
Vol 54 (5) ◽  
pp. 517-522 ◽  
Author(s):  
D J Radford ◽  
R F Graff ◽  
G H Neilson
2004 ◽  
Vol 24 (3) ◽  
pp. 223-224 ◽  
Author(s):  
M. Respondek-Liberska ◽  
K. Janiak ◽  
J. Wilczynski ◽  
A. Sysa ◽  
J. A. Moll ◽  
...  

1994 ◽  
Vol 46 (2) ◽  
pp. 113-119 ◽  
Author(s):  
Pramod.K. Jaiswal ◽  
K.G. Balakrishnan ◽  
Arabinda Saha ◽  
C.G. Venkitachalam ◽  
Jaganmohan Tharakan ◽  
...  

2015 ◽  
Vol 76 (2) ◽  
Author(s):  
Antonello D’Andrea ◽  
Giancarlo Scognamiglio ◽  
Franco Giordano ◽  
Sergio Cuomo ◽  
Maria Giovanna Russo ◽  
...  

We present the echocardiographic analysis of an 86- year-old man affected by Ebstein’s anomaly. In the natural history of this congenital disease only 5% of patients survive beyond the fifth decade. The patient presented severe right atrial dilatation and right heart failure, and he was referred to our institution for supraventricular tachycardia.


2009 ◽  
Vol 2009 ◽  
pp. 1-2 ◽  
Author(s):  
Elisabetta Palmerini ◽  
Duccio Federici ◽  
Alessia Del Pasqua ◽  
Sonia Bernazzali ◽  
Matteo Lisi ◽  
...  

We present an echocardiographic evaluation of an elderly man affected with Ebstein's anomaly. In the natural history of this congenital disease only 5% of patients survive beyond the fifth decade. The patient presented severe right heart failure and he was refered to our institution for heart transplantation.


2010 ◽  
Vol 1 (4) ◽  
pp. 12-15 ◽  
Author(s):  
A V Ardashev ◽  
E G Zhelyakov ◽  
M S Rybachenko ◽  
A V Konev

The case history of 19-year old patient with Ebstein's anomaly and WPW syndrome, which was held surgical correction of cardiac arrhythmias by radiofrequency ablation is described. 3-year observation of patient confirmed the success of the operation – absence episodes of arrhythmia


2007 ◽  
Vol 122 ◽  
pp. S45
Author(s):  
Ya-Mei Chang ◽  
Jou-Kou Wang ◽  
Ming-Tai Lin ◽  
Sheunn-Nan Chiu ◽  
En-Ting Wu ◽  
...  

2013 ◽  
Vol 24 (2) ◽  
pp. 191-200 ◽  
Author(s):  
Lianne M. Geerdink ◽  
Livia Kapusta

AbstractEbstein's anomaly is a complex congenital disorder of the tricuspid valve. Presentation in neonatal life and (early) childhood is common. Disease severity and clinical features vary widely and require a patient-tailored treatment. In this review, we describe the natural history of children and adolescents with Ebstein's anomaly, including symptoms and signs presenting at diagnosis. Current classification strategies of Ebstein's anomaly are discussed. We report on diagnostic methods for establishing the severity of disease that might enhance decision on the timing of surgical intervention. Furthermore, we describe different surgical options for severely ill neonates and multiple surgical interventions after infancy. Only with ample knowledge and understanding of the above, this complex and diverse group of patients can be correctly treated in order to improve not only duration, but also quality of life.


2017 ◽  
Vol 65 (08) ◽  
pp. 639-648 ◽  
Author(s):  
Rüdiger Lange ◽  
Melchior Burri

AbstractSurgical repair of the tricuspid valve is a milestone in the medical history of patients with Ebstein's anomaly. The timely alleviation of the insufficiency has an important impact on the prognosis. In this review, we describe features of the disease relevant to surgical correction and the evolution of surgical techniques over six decades. We compare the results of different repair and replacement techniques. Additionally, we discuss concomitant antiarrhythmic surgery and bailout strategies for postoperative right ventricular failure. Finally, we review the surgical options in symptomatic neonates with Ebstein's disease.


2020 ◽  
Vol 1 (1) ◽  
pp. 17
Author(s):  
Eliana Susilowati

There is a growing number of mothers suffering innate heart disease which could potentially risk their gestation period. Ebstein’s anomaly refers to a rare innate disease in the heart which accounts for less than 1% of most cases of innate heart disease, and only 5% of the patients surviving beyond 50 years of age. Cone reconstruction (CR) is an option for the repairment of tricuspid valve in patients with Ebstein anomaly. However, persistent arrhytmia, such as AFL, is possible to occur after CR. This case report aims to opt suitable pregnancy management of patients with persistent atrial flutter (AFL) after Cone reconstruction for Ebstein’s Anomaly. We report a 31 year-old woman who consulted for pregnancy planning due to history of Ebstein’s Anomaly, and had undergone successful cone reconstruction. No recorded history of AFL is reported. Physical examination finding was tricuspid regurgitation murmur without signs and symptoms of right ventricular failure. Electrocardiography showed counter-clockwise typical AFL. Echocardiography finding demonstrated post Cone reconstruction (CR), mild tricuspid regurgitation, and EF of 76%.


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