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The Journal of Thoracic and Cardiovascular Surgery, Vol 91, 584-589, Copyright © 1986 by The American Association for Thoracic Surgery and The Western Thoracic Surgical Association
MN Ilbawi, J Fedorchik, AJ Muster, FS Idriss, SY DeLeon, SS Gidding and MH Paul
The surgical management of severely symptomatic newborn infants with
tetralogy of Fallot and absent pulmonary valve has been controversial, and
the results of a variety of operative approaches have not been
satisfactory. We report on a technique for the treatment of these patients,
which consists of (1) ligation of the main pulmonary artery to eliminate
pulmonary regurgitation, excessive right ventricular stroke output, and
secondary pulmonary artery dilation and airway obstruction and (2)
insertion of a subclavian-pulmonary artery polytetrafluoroethylene shunt to
provide pulmonary blood flow. The procedure was used in four neonates. Two
patients operated on at 2 and 3 days of age are doing well 15 and 19 months
postoperatively. The other two, operated on at 3 and 4 weeks of age after
unsuccessful prolonged medical treatment and positive-pressure ventilation,
failed to show long-term improvement and died of sepsis and respiratory
failure 3 and 5 months after operation. This experience, though limited,
suggests that early surgical intervention to control pulmonary
regurgitation prevents progressive pulmonary artery dilatation and
secondary bronchial compression, decreases the need for prolonged
preoperative and postoperative ventilation, and improves the outcome of
these critically ill neonates.
ARTICLES
Surgical approach to severely symptomatic newborn infants with tetralogy of Fallot and absent pulmonary valve
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