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HBV and HCV infections in heart transplant recipients

S Fagiuoli1, F Minniti, S Pevere

  • 1Department of Surgical and Gastroenterological Sciences,University of Padova, Padova, Italy. fagiuoli@ux1.unipd.it

Insights

Hepatotropic viral infections like hepatitis B virus (HBV) and hepatitis C virus (HCV) pose risks to heart transplant (HTx) recipients. While prevalence is similar to the general population, these infections can lead to chronic liver disease and cirrhosis in HTx patients.

Area of Science:

  • Hepatology
  • Transplant Medicine
  • Infectious Diseases

Background:

  • Heart transplant (HTx) recipients are susceptible to hepatotropic viral infections, including hepatitis B virus (HBV) and hepatitis C virus (HCV).
  • The impact of these viral infections on long-term survival after HTx is not well understood.
  • This study aimed to investigate the prevalence, clinical characteristics, and natural history of HBV and HCV in HTx recipients.

Purpose of the Study:

  • To determine the prevalence of HBV and HCV infections in a cohort of heart transplant recipients.
  • To describe the clinical features and outcomes of these viral infections post-transplant.
  • To assess the natural history and impact of HBV and HCV on HTx patient survival.

Main Methods:

  • Retrospective analysis of 360 consecutive heart transplant recipients.
  • Monitoring of clinical status, liver injury markers, and viral serology (HBV and HCV) post-transplantation.
  • Follow-up duration averaged 8 years.

Main Results:

  • 16.5% of HTx recipients tested positive for HBV or HCV (3.1% HBV, 12% HCV, 0.5% co-infection).
  • HCV prevalence was significantly lower in recipients transplanted after 1990 (4.2%) compared to before (28%).
  • All HBV-positive and 58% of HCV-positive recipients developed chronic liver disease; 16% developed cirrhosis, and 8% died from end-stage liver disease.

Conclusions:

  • The prevalence of HBV and HCV in HTx recipients is comparable to the general population.
  • HBV and HCV infections exhibit active viral replication and aggressive natural history in HTx recipients.
  • Improved screening and vaccination policies likely contribute to the lower prevalence of HBV and HCV in recent HTx cohorts.
Abstract

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