Early Assessment of Cardiac Allograft Vasculopathy Risk Among Recipients of Hepatitis C Virus-infected Donors in the

Kaushik Amancherla1, Irene D Feurer2, Scott A Rega3

  • 1Division of Cardiovascular Medicine, Vanderbilt University Medical Center, Nashville, Tennessee.

PubMed

Insights

Heart transplants from hepatitis C virus (HCV)-positive donors did not show increased cardiac allograft vasculopathy (CAV) risk in the direct-acting antiviral era. Further studies are needed to confirm these findings and guide post-transplant care.

Area of Science:

  • Cardiology
  • Transplantation Immunology
  • Infectious Diseases

Background:

  • Direct-acting antiviral (DAA) therapies have revolutionized hepatitis C virus (HCV) treatment, leading to increased use of HCV-positive donor organs for transplantation.
  • Historically, HCV-positive donors were associated with accelerated cardiac allograft vasculopathy (CAV).
  • The impact of HCV nucleic acid test-positive (NAT+) donors on CAV in the DAA era is not well understood.

Purpose of the Study:

  • To investigate the association between HCV NAT+ donor heart transplantation and the development of CAV in the DAA era.
  • To compare CAV outcomes between recipients of HCV NAT+ and HCV NAT- donor hearts within the first year post-transplant.

Main Methods:

  • Retrospective, single-center observational study.
  • Compared 84 recipients of HCV NAT+ donor hearts with 231 recipients of HCV NAT- donor hearts.
  • Utilized coronary angiography and intravascular ultrasound to assess CAV development, including rapidly progressive CAV.

Main Results:

  • Unadjusted analysis showed reduced survival free of CAV in recipients of HCV NAT+ hearts.
  • After adjusting for known CAV risk factors, no significant difference in CAV development was observed between the HCV NAT+ and NAT- cohorts.
  • No significant difference in the development of rapidly progressive CAV was found between the groups.

Conclusions:

  • Transplantation of hearts from HCV NAT+ donors does not appear to increase CAV risk in the DAA era.
  • Larger, longer-term studies are recommended to confirm these findings.
  • Further research will inform post-transplant management strategies for recipients of HCV NAT+ donor hearts.
Abstract