Restoring Anterior Leaflet Continuity: The Spinnaker Repair of Ebstein's Anomaly

2011 ◽  
Vol 92 (2) ◽  
pp. 752-754 ◽  
Author(s):  
Nicola Viola ◽  
Joseph J. Vettukattil ◽  
Marcus P. Haw
2016 ◽  
Vol 65 (7) ◽  
pp. 404-407
Author(s):  
Sanae Yamauchi ◽  
Yasuyuki Suzuki ◽  
Kazuyuki Daitoku ◽  
Masaomi Kimura ◽  
Ken Okumura ◽  
...  

2016 ◽  
Vol 58 (8) ◽  
pp. 775-777 ◽  
Author(s):  
Nobuyuki Tsujii ◽  
Kenichi Kurosaki ◽  
Kenji Yasuda ◽  
Masanori Mizuno ◽  
Heima Sakaguchi ◽  
...  

2021 ◽  
Vol 5 (02) ◽  
pp. 147-150
Author(s):  
Ujjwal K. Chowdhury ◽  
Sukhjeet Singh ◽  
Niwin George ◽  
Lakshmi Kumari Sankhyan ◽  
Sandeep Sharan ◽  
...  

AbstractEbstein’s anomaly is a rare congenital malformation of the right ventricle and tricuspid valve which is characterized by several features that can exhibit an infinite spectrum of malformation.The abnormalities include: i) adherence of the tricuspid leaflets to the underlying myocardium (failure of delamination); ii) anterior and apical rotational displacement of the functional tricuspid annulus (septal > posterior > anterior leaflet); iii) dilatation of the right atrioventricular junction (the true tricuspid annulus) with variable degrees of hypertrophy and thinning of the wall; iv) dilatation of the “atrialized” portion of the right ventricle; and v) redundancy, fenestration, and tethering of the anterior leaflet.


Author(s):  
Sonya V Babu-Narayan

Ebstein’s anomaly of the tricuspid valve is a rare congenital anomaly (1 in 200 000 live births) and is defined by the septal insertion of the tricuspid valve leaflet being >8 mm/m2 apically displaced from the septal insertion of the mitral valve leaflet. This is due to adherence of the septal leaflet to the ventricular septum secondary to failure of delamination. The inferior–posterior, and occasionally anterior, leaflet may also be displaced and rotated. The anterior leaflet is frequently part-redundant and may be fenestrated. Leaflets may be dysplastic or tethered, altering the surgical options. Ebstein’s anomaly may result in enlargement of the native and functional right atrium, enlargement of the functional right ventricle, left ventricular compression, arrhythmia, sudden death, and heart failure. Cardiovascular magnetic resonance (CMR) enables accurate quantification of right and left ventricular volumes and function, cardiac output, and cardiac shunt from measurement of Qp:Qs. CMR is highly informative regarding the anatomy and function of the tricuspid valve, in particular when the degree of displacement and/or rotation of the tricuspid valve is more than mild to moderate.


2016 ◽  
Vol 64 (S 02) ◽  
Author(s):  
L. Geerdink ◽  
G. du Marchie Sarvaas ◽  
I. Kuipers ◽  
W. Helbing ◽  
T. Delhaas ◽  
...  

2017 ◽  
Vol 96 (1) ◽  
pp. 206-208
Author(s):  
R. R. Movsesyan ◽  
V. A. Bolsunovskiy ◽  
A. V. Bolsunovskiy ◽  
A. L. Tsytko ◽  
D. R. Yamgurov

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