Circulation, Vol 52, 685-690, Copyright © 1975 by American Heart Association
III Kyger ER, GJ Reul Jr, FM Sandiford, DC Wukasch, GL Hallman and DA Cooley
In the 20-year period ending December 31, 1973 we operated on 105 patients
for palliation of tricuspid atresia (TA) with reduced pulmonary blood flow.
Pott's anastomosis (85), Blalock-Taussig anastomosis (19), intrapericardial
aorta (Ao)-to-right pulmonary artery (RPA) (18), Glenn procedure (3) and
miscellaneous shunts (2) have been used. Of patients undergoing operation
more than 15 years ago, 45% (9/20) are still alive. The over-all operative
mortality was 9%. It was highest in patients less than one month of age
(7/23, 30%). There were no operative deaths in patients older than 12
months. The median age at first operation for the entire series was five
months. Our results indicate the Pott's anastomosis and Ao-to-RPA
anastomosis are superior to the Blalock-Taussig anastomosis (BT) for
palliation of TA. Of patients surviving BT, 69% (11/16) required
reoperation, compared to 22% (17/78) surviving Pott's anastomosis and 13%
(2/16) surviving Ao-to- RPA shunts. All three patients undergoing Glenn
procedures (superior vena cava-to-RPA anastomosis) required reoperation or
died without significant benefit. Ballon atrial septosomy and Pott's
anastomosis appear to be indicated for infants less than six months of age,
and Ao- to-RPA shunt with simultaneous atrial septectomy (if indicated) for
older children.
ARTICLES
Surgical palliation of tricuspid atresia
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