One stage repair of aortic arch anomalies and intracardiac defects

J. M. Quaegebeur, S. Singh, A. J.J.C. Bogers, E. Bos, R. Hardjowijono, M. G. Hazekamp, H. A. Huysmans, J. Ottenkamp, J. Rohmer, M. Witsenburg, J. Hess

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29 Scopus citations

Abstract

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 malaligned 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. Two patients with malaligned septum remain with significant LVOTO. Final results are good in the other 20 patients. One stage repair gives good results and will benefit the patient in the immediate postoperative course as well as in its further development. RVOTO in TB anomaly or TGA must be carefully corrected. Persisting LVOTO continues to be a major problem in patients with malalignment VSD.

Original languageEnglish
Pages (from-to)283-287
Number of pages5
JournalEuropean Journal of Cardio-thoracic Surgery
Volume5
Issue number6
DOIs
StatePublished - Jun 1991
Externally publishedYes

Keywords

  • Cardiac surgery
  • Coarctation
  • Congenital heart disease
  • Interrupted aortic arch
  • One stage repair

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