scholarly journals TRICUSPID VALVE RECONFIGURATION FOLLOWING PULMONARY ARTERY BANDING IN PATIENTS WITH CONGENITALLY CORRECTED TRANSPOSITION OF THE GREAT ARTERIES AS SEEN ON ECHOCARDIOGRAPHY

2016 ◽  
Vol 67 (13) ◽  
pp. 977 ◽  
Author(s):  
Dan Gil Halpern ◽  
Meena Nathan ◽  
Or Yaacov ◽  
Gerald Marx
2019 ◽  
Vol 11 (4) ◽  
pp. NP247-NP250
Author(s):  
Yuka Takeda ◽  
Nobuo Momoi ◽  
Mariko Hayashi ◽  
Kisei Endo ◽  
Yoshimichi Aoyagi ◽  
...  

At 32 weeks of gestation, a male fetus with congenitally corrected transposition of the great arteries developed hydrops fetalis caused by a combination of mitral valve regurgitation and tricuspid valve regurgitation (TR). We performed a pulmonary artery banding (PAB) at 108 days old for gradually progressing TR, after confirming that a balloon dilatation test in the main pulmonary artery reduced TR. As the patient grew, the PAB became tighter and systolic blood pressure in the morphological left ventricle increased. At present, the patient is waiting for a double switch operation.


2016 ◽  
Vol 27 (3) ◽  
pp. 597-599
Author(s):  
Dai Asada ◽  
Kazuyuki Ikeda ◽  
Masaaki Yamagishi

AbstractThere are a few reports of successful replacement of the left-sided systemic tricuspid valve with a mechanical valve in small infants with congenitally corrected transposition of the great arteries having Ebstein’s anomaly. Tricuspid valve replacement is the preferred option when pulmonary artery banding, performed as a prelude to performing the double-switch operation, is not feasible because of severe heart failure caused by tricuspid regurgitation.


2010 ◽  
Vol 38 (6) ◽  
pp. 728-734 ◽  
Author(s):  
Olivier Metton ◽  
Régis Gaudin ◽  
Phalla Ou ◽  
Sébastien Gerelli ◽  
Shafi Mussa ◽  
...  

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