scholarly journals 315 * FATE OF RIGHT VENTRICLE TO PULMONARY ATRESIA CONDUITS FOLLOWING COMPLETE REPAIR OF PULMONARY ATRESIA WITH MAJOR AORTOPULMONARY COLLATERALS

2014 ◽  
Vol 19 (suppl 1) ◽  
pp. S93-S94
Author(s):  
R. Mainwaring ◽  
J. Schaffer ◽  
V. M. Reddy ◽  
F. L. Hanley
2015 ◽  
Vol 99 (5) ◽  
pp. 1685-1691 ◽  
Author(s):  
Richard D. Mainwaring ◽  
William L. Patrick ◽  
Rajesh Punn ◽  
Michal Palmon ◽  
V. Mohan Reddy ◽  
...  

2013 ◽  
Vol 95 (4) ◽  
pp. 1397-1402 ◽  
Author(s):  
Richard D. Mainwaring ◽  
V. Mohan Reddy ◽  
Lynn Peng ◽  
Calvin Kuan ◽  
Michal Palmon ◽  
...  

2014 ◽  
Vol 97 (3) ◽  
pp. 909-915 ◽  
Author(s):  
Naruhito Watanabe ◽  
Richard D. Mainwaring ◽  
V. Mohan Reddy ◽  
Michal Palmon ◽  
Frank L. Hanley

2020 ◽  
Vol 2020 ◽  
pp. 1-3
Author(s):  
Katia Bravo-Jaimes ◽  
Brian Walton ◽  
Poyee Tung ◽  
Richard W. Smalling

The association of pulmonary atresia, ventricular septal defect (VSD) and major aortopulmonary collaterals (MAPCA) is an extreme form of tetralogy of Fallot (TOF). It carries a high mortality risk if not intervened on during infancy with only 20% of unoperated patients surviving into adulthood. We present the case of a 40-year-old man who presented for evaluation prior to retinal surgery and was found to have hypoxia and a loud murmur. Cardiac catheterization was performed in the general catheterization laboratory, demonstrating a membranous VSD, pulmonary atresia, and MAPCA. We highlight the challenges and limitations that an adult interventional cardiologist may have when encountering these patients.


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