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The Journal of Thoracic and Cardiovascular Surgery, Vol 73, 436-442, Copyright © 1977 by The American Association for Thoracic Surgery and The Western Thoracic Surgical Association
CC Gill, DS Moodie and DC McGoon
A particular problem in treatment is presented by patients who have atresia
of the pulmonary valve and ventricular septal defect but whose pulmonary
arterial tree is extremely diminutive. The pulmonary blood flow results
from naturally occurring large bronchial collateral arteries. In the
experience reported, satisfactory palliation was provided for all 3
patients in whom right ventricle--to--pulmonary artery continuity was
constructed by placing a pericardial patch graft during open-heart
operation. The ventricular septal defect was left unrepaired. Early
evidence supports the hypothesis that, besides providing palliation of
cyanosiis, the procedure may allow progressive enlargment of the
hypoplastic pulmonary arteries. This offers hope that later second-stage
completion of total repair, involving closure of the ventricular septal
defect and ligation of any remaining large bronchial collateral arteries,
may become feasible.
ARTICLES
Staged surgical management of pulmonary atresia with diminutive pulmonary arteries
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