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The Journal of Thoracic and Cardiovascular Surgery, Vol 93, 767-774, Copyright © 1987 by The American Association for Thoracic Surgery and The Western Thoracic Surgical Association
TP Barragry, WS Ring, JW Blatchford and JE Foker
Methods of palliating critical pulmonary oligemia in neonates with complex
cyanotic congenital heart disease continue to evolve. Pulmonary artery
distortion and other complications of the use of native vessels to increase
pulmonary blood flow has led to the more frequent use of
polytetrafluoroethylene shunts either in a central position or as a
modified Blalock-Taussig shunt. Central aorta-pulmonary artery shunts have
largely fallen into disfavor because of previously reported unacceptably
high incidences of complications such as shunt thrombosis, congestive heart
failure, and pulmonary artery distortion. This report details our
experience palliating 23 neonates with pulmonary atresia or severe
pulmonary stenosis by placing central aorta-pulmonary artery shunts
utilizing a short segment (less than 1 cm) of polytetrafluoroethylene.
Although three of the 23 died postoperatively, none of the 23 patients had
evidence of shunt thrombosis. Congestive heart failure, a potential
complication of any pulmonary artery shunt, was present in eight of the 20
survivors but did not require shunt takedown and was readily controlled by
digoxin. Repeat catheterization was performed in 12 patients; pulmonary
angiography showed good growth of both pulmonary arteries and there was no
evidence of pulmonary artery hypertension. Although minor pulmonary artery
distortion was present in two patients, this distortion was centrally
located and easily remedied at the time of total correction. Thus we have
found the central aorta-pulmonary artery shunt to be an extremely effective
and reliable means of palliating pulmonary artery hypoplasia as a result of
pulmonary atresia or severe pulmonary stenosis in neonates.
ARTICLES
Central aorta-pulmonary artery shunts in neonates with complex cyanotic congenital heart disease
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