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The Journal of Thoracic and Cardiovascular Surgery, Vol 88, 76-81, Copyright © 1984 by The American Association for Thoracic Surgery and The Western Thoracic Surgical Association
JJ Lamberti, J Carlisle, JD Waldman, FA Lodge, SE Kirkpatrick, L George, JW Mathewson, SW Turner and SJ Pappelbaum
From September, 1978, to January, 1983, 44 cyanotic infants and children
underwent a systemic-pulmonary artery shunt for the treatment of reduced
pulmonary blood flow. Age ranged from 18 hours to 4 years (mean age = 0.49
years). Weight ranged from 1.7 kg to 13.2 kg (mean weight = 4.9 kg). There
were 12 classic Blalock-Taussig shunts, five central
polytetrafluoroethylene shunts, six interposition modified Blalock-Taussig
shunts, and 21 Great Ormond Street type of modified Blalock-Taussig shunts.
No direct aorta-pulmonary artery anastomoses were performed. There was one
postoperative death (1/44 = 2.3%) in a 1,700 gm neonate born with pulmonary
atresia and intact ventricular septum (shunt patent). Four shunts required
early revision: one thrombosed central shunt, a kinked patent interposition
Blalock-Taussig shunt, a small but patent Blalock-Taussig shunt, and one
excessive Great Ormond Street type of Blalock-Taussig shunt. Two late
deaths were probably shunt-related: one Blalock-Taussig and one central.
All four types of shunts provided good palliation, but the Great Ormond
Street type of Blalock-Taussig shunt is our preferred shunt because of (1)
low operative risk, (2) predictable patency (100% in our series), (3) lack
of distortion of pulmonary arterial anatomy, and (4) technical ease of
insertion as well as takedown.
ARTICLES
Systemic-pulmonary shunts in infants and children. Early and late results
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