Anatomy, echocardiography, and surgical approach to double outlet right ventricle

2008 ◽  
Vol 18 (S3) ◽  
pp. 39-51 ◽  
Author(s):  
William T. Mahle ◽  
Richard Martinez ◽  
Norman Silverman ◽  
Meryl S. Cohen ◽  
Robert H. Anderson
2005 ◽  
Vol 15 (S1) ◽  
pp. 106-110
Author(s):  
Christo I. Tchervenkov

The presence of an obstructed aortic arch in patients with transposition, or the Taussig-Bing variant of double outlet right ventricle, presents a formidable surgical challenge. Over the years, there have been several controversies with respect to primary versus staged repair, the best technique for reconstruction of the aortic arch, and whether to use circulatory arrest or antegrade regional cerebral perfusion. In this review, I will address all these issues and describe my favoured surgical approach at The Montreal Children's Hospital, namely the single-stage arterial switch operation with concomitant repair of the aortic arch with a patch fashioned from a pulmonary homograft, all conducted using antegrade regional cerebral perfusion.


2017 ◽  
Vol 44 (4) ◽  
pp. 245-251 ◽  
Author(s):  
Kun-Jing Pang ◽  
Hong Meng ◽  
Sheng-Shou Hu ◽  
Hao Wang ◽  
David Hsi ◽  
...  

Selecting an appropriate surgical approach for double-outlet right ventricle (DORV), a complex congenital cardiac malformation with many anatomic variations, is difficult. Therefore, we determined the feasibility of using an echocardiographic classification system, which describes the anatomic variations in more precise terms than the current system does, to determine whether it could help direct surgical plans. Our system includes 8 DORV subtypes, categorized according to 3 factors: the relative positions of the great arteries (normal or abnormal), the relationship between the great arteries and the ventricular septal defect (committed or noncommitted), and the presence or absence of right ventricular outflow tract obstruction (RVOTO). Surgical approaches in 407 patients were based on their DORV subtype, as determined by echocardiography. We found that the optimal surgical management of patients classified as normal/committed/no RVOTO, normal/committed/RVOTO, and abnormal/committed/no RVOTO was, respectively, like that for patients with large ventricular septal defects, tetralogy of Fallot, and transposition of the great arteries without RVOTO. Patients with abnormal/committed/RVOTO anatomy and those with abnormal/noncommitted/RVOTO anatomy underwent intraventricular repair and double-root translocation. For patients with other types of DORV, choosing the appropriate surgical approach and biventricular repair techniques was more complex. We think that our classification system accurately groups DORV patients and enables surgeons to select the best approach for each patient's cardiac anatomy.


2015 ◽  
Vol 26 (1) ◽  
pp. 172-174 ◽  
Author(s):  
Robert D. Tunks ◽  
R. Dennis Steed ◽  
Andrew J. Lodge

AbstractAlthough the spectrum of physiology seen in infants and children with double-outlet right ventricle is broad, this anatomy in combination with an aortopulmonary window is extremely rare. We present an interesting case of an infant prenatally diagnosed with this rare CHD. To our knowledge, this is the first report of complete repair in the neonatal period for such a combination of defects.


Circulation ◽  
1969 ◽  
Vol 39 (5s1) ◽  
Author(s):  
BILLY M. HIGHTOWER ◽  
ALBERTO BARCIA ◽  
LIONEL M. BARGERON ◽  
JOHN W. KIRKLIN

Circulation ◽  
1997 ◽  
Vol 96 (4) ◽  
pp. 1233-1239 ◽  
Author(s):  
S. Kleinert ◽  
T. Sano ◽  
R.G. Weintraub ◽  
R.B.B. Mee ◽  
T.R. Karl ◽  
...  

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