Percutaneous coronary interventions in cardiac allograft vasculopathy: a single-center experience

P Colombo1, G Bruschi, A Sacco

  • 1A De Gasperis Cardiology and Cardiac Surgery Department, Niguarda Ca' Granda Hospital, Milan, Italy.

Insights

Percutaneous coronary intervention (PCI) with stents is safe for heart transplant recipients, achieving high success rates. Drug-eluting stents may reduce restenosis compared to bare-metal stents, though disease progression remains a concern.

Area of Science:

  • Cardiology
  • Transplantation Medicine
  • Interventional Cardiology

Background:

  • Cardiac allograft vasculopathy (CAV) is accelerated obstructive coronary disease and a leading cause of late mortality post-heart transplant.
  • Percutaneous coronary intervention (PCI) for CAV has historically shown high restenosis rates, often considered palliative.

Purpose of the Study:

  • To review the experience with percutaneous coronary interventions (PCI) using stents in cardiac transplant recipients.
  • To evaluate the safety and efficacy of PCI in managing cardiac allograft vasculopathy.

Main Methods:

  • Analysis of primary adult heart transplant patients who underwent PCI after at least 12 months post-transplant.
  • Inclusion criteria: hospital discharge post-transplant and clinical follow-up of 12 months.

Main Results:

  • Seventy patients underwent 85 procedures treating 135 lesions; mean time to intervention was 9.3 years post-transplant.
  • Primary PCI success was 96%. Recurrent stenosis occurred in 16% of patients, with 16% restenosis in drug-eluting stent (DES) treated lesions.
  • Mean follow-up was 45.2 months; 27 deaths (19 cardiac) and 1 re-transplantation occurred post-PCI.

Conclusions:

  • PCI with stents is a safe option for cardiac transplant recipients with high primary success rates.
  • Restenosis rates after PCI in transplant recipients are higher than in native arteries.
  • Drug-eluting stents may offer a benefit in reducing restenosis compared to bare-metal stents; however, overall clinical benefit may be limited by progression in untreated segments.
Abstract

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