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September 1949, Vol 59, No. 3 >
ARTICLE | September 1949

SURGICAL TREATMENT OF TRICUSPID ATRESIA

EGBERT H. FELL, M.D.; BENJAMIN M. GASUL, M.D.; CARL B. DAVIS, M.D.; RAUL CASAS, M.D.
Arch Surg. 1949;59(3):445-453. doi:10.1001/archsurg.1949.01240040453008.
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WILLIS POTTS and Sidney Smith1 added an important chapter in the treatment of tetralogy of Fallot to that which Blalock and Taussig2 so well began. The Potts-Smith operation, a lateral anastomosis of the pulmonary artery to the aorta, establishes an artificial ductus arteriosus, thus utilizing vessels that are accessible and large enough so that the infant under the age of 2 years who heretofore died of severe oxygen want now has a chance to live. It has been stated that there is a greater mortality in the group awaiting operation than in the operative and postoperative group.

The favorable results we have had with the Potts-Smith procedure in the age group from 4 to 12 months encouraged us to attempt this operation on 3 very small, cyanotic infants with diagnoses of congenital tricuspid atresia, or nonfunctioning right ventricle. There have been other cases of tricuspid atresia reported but

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Country-Specific Mortality and Growth Failure in Infancy and Yound Children and Association With Material Stature

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AAM 2010;304:1493-1495.
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BMJ 2010;341:c5893-c1494.
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