Coarctation of the aorta in infancy

M J Levy1, L Levinsky, E Deviri

  • 1Thoracic and Cardiovascular Surgery Department, Beilinson Medical Center, Tel Aviv University Medical School, Tel Aviv, Israel.

Insights

Surgical repair of coarctation of the aorta in infants showed a high survival rate. Most deaths and late complications in survivors were linked to associated intracardiac anomalies.

Area of Science:

  • Cardiology
  • Pediatric Surgery
  • Congenital Heart Disease

Background:

  • Coarctation of the aorta is a critical congenital heart defect.
  • Infants with coarctation often have associated intracardiac anomalies, complicating surgical outcomes.

Purpose of the Study:

  • To evaluate the surgical outcomes and long-term follow-up of infants undergoing coarctation of the aorta repair.
  • To identify factors influencing survival and late complications in this pediatric population.

Main Methods:

  • Retrospective review of 25 infants (<1 year) undergoing coarctation of the aorta repair between 1965-1982.
  • Analysis of surgical techniques, associated anomalies, operative mortality, and long-term follow-up data.

Main Results:

  • Twenty-one of 25 infants survived the initial operation.
  • All operative deaths and three late deaths were associated with intracardiac anomalies.
  • Two of 18 long-term survivors developed mild hypertension with residual gradients; others were in good health.

Conclusions:

  • Surgical repair of coarctation of the aorta in infants can achieve good survival rates.
  • Associated intracardiac anomalies are a significant determinant of both early and late outcomes.
  • Long-term follow-up is crucial for managing potential complications like re-coarctation and hypertension.

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