[Surgical treatment of coarctation and interrupted aortic arch complex in infants]

J Murakami1, H Kado

  • 1Department of Cardiovascular Surgery, Fukuoka Children's Hospital, Fukuoka, Japan.

Nihon Geka Gakkai Zasshi
|August 30, 2001
PubMed

Insights

One-stage biventricular repair offers good outcomes for neonates with coarctation and interrupted aortic arch complex. This approach minimizes mortality and recoarctation rates, with catheter intervention proving effective for recoarctation.

Area of Science:

  • Pediatric Cardiac Surgery
  • Congenital Heart Disease
  • Aortic Arch Anomalies

Context:

  • Review of 142 neonates and infants with coarctation and interrupted aortic arch complex.
  • Surgical repair outcomes at Fukuoka Children's Hospital (1991-2000).
  • Comparison of one-stage versus two-stage biventricular repair strategies.

Purpose:

  • To evaluate the effectiveness of one-stage biventricular repair for complex aortic arch anomalies.
  • To compare mortality and recoarctation rates between one-stage and two-stage repair methods.
  • To assess the utility of descending aorta cannulation and cerebral perfusion techniques.

Summary:

  • One-stage repair showed favorable outcomes for coarctation and interrupted aortic arch complex, with lower mortality rates compared to two-stage repairs.
  • Recoarctation rates were low (5.3% and 2.1%) and successfully managed with catheter intervention, avoiding reoperation.
  • The anterior approach with descending aorta cannulation and cerebral perfusion is effective, but two-stage repair remains viable for critically ill patients.

Impact:

  • Demonstrates the efficacy of one-stage biventricular repair in improving outcomes for complex congenital heart defects.
  • Highlights the importance of surgical technique, including cerebral perfusion, in minimizing complications.
  • Provides evidence supporting tailored surgical approaches based on patient condition and anomaly severity.

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