Considerations and experience driving expansion of combined heart-liver transplantation

Timothy Gong1,2,3, Shelley Hall1,2,3

  • 1Center for Advanced Heart and Lung Disease, Baylor Annette C. and Harold C. Simmons Transplant Institute, Baylor University Medical Center.

Insights

Combined heart and liver transplants offer survival benefits and reduced rejection rates. Further research is needed to understand the liver allograft's immunoprotective effects in heart transplant patients.

Area of Science:

  • Cardiology
  • Hepatology
  • Transplant Immunology

Background:

  • Combined heart and liver transplantation (CHLT) is indicated for end-stage heart failure with irreversible liver failure.
  • The immunologic benefits of the liver allograft in CHLT are not fully understood.
  • CHLT is a growing procedure, accounting for approximately 25 cases annually.

Purpose of the Study:

  • To review the current literature on the immunologic benefit of combined heart and liver transplantation (CHLT).
  • To explore the potential immunoprotective role of the liver allograft in CHLT outcomes.
  • To investigate the implications of CHLT for surgical techniques and immunosuppression.

Main Methods:

  • Literature review of combined heart and liver transplantation outcomes.
  • Analysis of registry data comparing CHLT with isolated heart transplantation.
  • Examination of reported rates of acute cardiac rejection and cardiac allograft vasculopathy (CAV).

Main Results:

  • CHLT survival rates are equivalent to or modestly improved compared to isolated heart transplantation.
  • CHLT is associated with lower rates of acute cardiac rejection.
  • CHLT demonstrates reduced incidence of cardiac allograft vasculopathy (CAV).

Conclusions:

  • CHLT is a safe and viable option for patients with combined end-stage heart and liver disease.
  • The liver allograft may confer an immunoprotective effect on the transplanted heart, warranting further investigation.
  • Future research should focus on candidacy criteria, allocation protocols, and understanding the mechanisms of tolerogenicity in CHLT.
Abstract