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Cardiac transplantation in infants and children

M W Turrentine1, K A Kesler, R Caldwell

  • 1Department of Surgery, Riley Hospital for Children, Indiana University Medical Center, Indianapolis 46202-5125.

Insights

Pediatric cardiac transplantation offers a viable treatment for end-stage heart disease in children. Survival rates vary by condition, with idiopathic cardiomyopathy showing uniform survival.

Area of Science:

  • Pediatric Cardiology
  • Cardiovascular Surgery
  • Transplantation Medicine

Background:

  • Cardiac transplantation is an increasingly utilized therapy for pediatric heart conditions.
  • Over 30 pediatric patients have undergone orthotopic cardiac transplantation since 1986.
  • Indications span idiopathic cardiomyopathy, hypoplastic left heart syndrome, and complex congenital heart disease.

Purpose of the Study:

  • To evaluate the efficacy and outcomes of orthotopic cardiac transplantation in pediatric patients.
  • To assess survival rates based on the underlying cardiac pathology.
  • To determine the feasibility of transplantation in complex pediatric cardiac malformations.

Main Methods:

  • Retrospective analysis of 30 pediatric patients undergoing orthotopic cardiac transplantation.
  • Categorization of patients by indication: idiopathic cardiomyopathy, hypoplastic left heart syndrome, and other congenital heart diseases.
  • Follow-up to assess survival, complications, and causes of mortality.

Main Results:

  • Overall cumulative survival is 77% at a mean follow-up of 30 months.
  • Uniform survival observed in the idiopathic cardiomyopathy group.
  • Survival rates of 78% and 62% in complex congenital heart disease and hypoplastic left heart syndrome groups, respectively.
  • Operative deaths linked to pulmonary hypertension/hemorrhage; late deaths to rejection/infection.

Conclusions:

  • Orthotopic cardiac transplantation is an acceptable therapy for pediatric end-stage heart disease.
  • The procedure is technically feasible even with complex great artery or atrial malformations.
  • Further long-term data is needed, but current results are promising for select pediatric populations.

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