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The Annals of Thoracic Surgery, Vol 50, 524-528, Copyright © 1990 by The Society of Thoracic Surgeons
FW Clevenger, HB Othersen Jr and CD Smith
We have performed aortopexy in 12 children with tracheal compression. Six
infants had compression secondary to a vascular anomaly (group 1), and the
other 6 had previous repair of esophageal atresia (group 2). Eleven of the
12 children are alive after a mean follow-up of 36 months. In group 1, 1
patient died and 3 patients (50%) experienced recurrent respiratory
distress. Five infants sustained a major postoperative complication, and
the average postoperative hospital stay was 25 days. In group 2, however,
aortopexy was uniformly successful. There were no deaths, no postoperative
complications, and no cases of postoperative respiratory distress, and the
mean postoperative hospital stay was only 10 days. For children with reflex
apnea after repair of esophageal atresia, aortopexy is lifesaving and can
be performed with minimal morbidity and mortality. Great caution is
indicated in children with tracheal compression from other causes.
ARTICLES
Relief of tracheal compression by aortopexy
Department of Surgery, Medical University of South Carolina, Charleston.
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