Percutaneous coronary artery revascularization procedures in pediatric heart transplant recipients: A large single

Mariel E Turner1, Linda J Addonizio1, Marc E Richmond1

  • 1Division of Pediatric Cardiology, Columbia University College of Physicians and Surgeons, New York, New York.

Insights

Percutaneous coronary interventions (PCI) are safe for pediatric heart transplant recipients with cardiac allograft vasculopathy (CAV). However, long-term outcomes remain challenging, with high rates of disease progression and graft failure.

Area of Science:

  • Cardiology
  • Pediatric Cardiology
  • Transplant Cardiology

Background:

  • Cardiac allograft vasculopathy (CAV) is a primary cause of graft failure, mortality, and re-transplantation in pediatric heart transplant (HTx) recipients.
  • Limited data exist on the efficacy of percutaneous coronary interventions (PCI) for CAV in pediatric patients, contrasting with adult studies showing short-term benefits but no long-term outcome improvements.

Purpose of the Study:

  • To report the largest single-center experience with PCI for CAV in pediatric heart transplant recipients.
  • To evaluate the safety and effectiveness of PCI in this population.

Main Methods:

  • Retrospective chart review of pediatric HTx recipients who underwent PCI for CAV between 2005 and 2014.
  • Analysis of procedural success, complications, and long-term graft survival outcomes.

Main Results:

  • Twenty-three PCI procedures were performed in 13 pediatric patients, with a median age of 16.4 years.
  • Acute procedural success was achieved in all but one case, with a single procedure-related complication.
  • During follow-up, 7/13 patients required repeat PCI, two died, and five underwent re-transplantation, with 1-year freedom from death or re-transplant at 54%.

Conclusions:

  • PCI can be safely and effectively performed in pediatric HTx recipients diagnosed with CAV.
  • Despite procedural success, outcomes mirror adult experiences, indicating a persistent high rate of disease progression and graft failure.
Abstract

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