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European Journal of Cardio-Thoracic Surgery, Vol 5, 283-286, Copyright © 1991 by European Association for Cardio-thoracic Surgery
MG Hazekamp, JM Quaegebeur, S Singh, R Hardjowijono, AJ Bogers, J Ottenkamp, J Rohmer, M Witsenburg, J Hess and E Bos
Between August 1985 and May 1990, 27 neonates and infants underwent
combined correction of intracardiac and aortic arch anomalies through a
median sternotomy. Coarctation (CoA) was combined with VSD (6), AVSD (2),
Taussig-Bing (TB) heart (5), transposition of the great arteries (TGA) (1),
TGA + VSD (2), congenitally corrected TGA + VSD (1) and VSD + myxoid
stenotic outlet valves (1). Interrupted aortic arch (IAA) was combined with
VSD (10) and TB heart (1). Two patients had IAA type B as well as CoA. Age
at operation varied from 2 to 243 days with a mean age of 51 days. Twenty
patients (70%) were younger than 30 days. One TGA + VSD and all TB hearts
had maligned outlet septum and right ventricular outflow tract obstruction
(RVOTO). Posterior outlet septum deviation and left ventricular outflow
tract obstruction (LVOTO) occurred in 8 patients with malalignment VSD and
IAA (7) or CoA (1). Aortic arch reconstruction was performed using extended
end-to-end anastomoses. In 3 patients, arch hypoplasia necessitated patch
implantation. VSDs were closed through the right atrium unless the anatomy
dictated otherwise. One TB heart was reconstructed with a Kawashima
procedure. All other TB hearts and all TGAs were corrected with arterial
switch operation. Obstructing outlet septum was resected whenever
necessary. Follow-up was complete and included echo-Doppler control. Eleven
patients had postoperative heart catheterisation. Early mortality was 18.5%
(5 patients). Persisting LVOTO or RVOTO was responsible. There was no late
mortality. Five patients were reoperated upon: 3 for stenotic anastomoses
and 2 for a subaortic membranous stenosis. Successful balloon dilatation of
recoarctation was performed four times.(ABSTRACT TRUNCATED AT 250 WORDS)
ARTICLES
One stage repair of aortic arch anomalies and intracardiac defects
Department of Cardiothoracic Surgery, University Hospital Rotterdam, The Netherlands.
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