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European Journal of Cardio-Thoracic Surgery, Vol 6, 366-371, Copyright © 1992 by European Association for Cardio-thoracic Surgery
P Horvath, B Hucin, J Hruda, J Sulc, P Brezovsky, S Tuma, J Liesler and J Skovranek
Since 1979, a total of 69 infants and children aged 0.1 to 11.9 (median
0.7) years required surgical intervention for: double aortic arch (26),
anomalous origin of innominate artery (26), right aortic arch with left
ligamentum arteriosum (9), pulmonary artery sling (5), retroesophageal
right subclavian artery (3). Before operation, the morbidity was high: 84%
of children were symptomatic in the first trimester of life with 24
patients requiring mechanical ventilation. Seven children had an
accompanying heart defect. Left thoracotomy was the preferred approach.
There were 2 early (asphyxic brain damage, postoperative pneumonia) and 2
late (tracheomalacia, complex heart defect) deaths. Five patients (2
originally operated elsewhere) needed reoperation for persistent symptoms.
All 65 survivors are well 1 month to 11.9 (mean 3.9 +/- 3.62) years after
surgery. Tracheobronchoscopy, magnetic resonance imaging, and lung function
testing were helpful for postoperative evaluation. Minor tracheal
compression was revealed in 4 patients despite their good clinical
condition.
ARTICLES
Intermediate to late results of surgical relief of vascular tracheobronchial compression
Kardiocentrum University Hospital Motol, Prague, Czechoslovakia.
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