Myocardial oxygen handling and metabolic function of ex-situ perfused human hearts from circulatory death donors

Jorik H Amesz1,2, Sanne J J Langmuur1,2,3, Mark F A Bierhuizen1,2,4

  • 1Translational Cardiothoracic Surgery Research Lab, Department of Cardiothoracic Surgery, Erasmus University Medical Center, Rotterdam, the Netherlands.

JHLT Open
|March 27, 2025
PubMed

Insights

Human hearts donated after circulatory death (DCD) on normothermic ex-situ heart perfusion (ESHP) show high oxygen delivery but low consumption. Arteriovenous oxygen difference (ΔPO2) may indicate metabolic function and predict post-transplant ECMO needs.

Area of Science:

  • Cardiology
  • Transplantation Medicine
  • Physiology

Background:

  • Investigating oxygen handling in human DCD hearts during normothermic ex-situ heart perfusion (ESHP).
  • Evaluating oxygen handling markers for cardiac viability assessment in ESHP.
  • Utilizing DCD hearts for transplantation via ESHP.

Purpose of the Study:

  • To assess oxygen handling parameters in DCD hearts during ESHP.
  • To identify markers of cardiac viability during ESHP.
  • To correlate oxygen handling markers with post-transplantation outcomes, including ECMO support.

Main Methods:

  • Retrospective analysis of human DCD heart transplantations using ESHP.
  • Monitoring lactate, blood gas, myocardial oxygen consumption (MVO2), delivery (MDO2), extraction (MEO2), coronary blood flow (CBF), coronary vascular resistance (CVR), and adenosine infusion.
  • Assessing correlations between parameters and comparing patients with and without post-transplant ECMO.

Main Results:

  • Lactate decreased in transplanted hearts and increased in one rejected heart during ESHP.
  • High arterial partial pressure of oxygen (PO2) and arteriovenous ΔPO2 were observed.
  • ΔPO2 strongly correlated with MVO2 and lactate trends.
  • Higher adenosine infusion rates during ESHP predicted the need for post-transplantation ECMO.

Conclusions:

  • Hearts on ESHP exhibit excessive oxygen delivery (MDO2) relative to myocardial oxygen consumption (MVO2), suggesting potential for reduced PO2 and CBF.
  • Arteriovenous oxygen difference (ΔPO2) can serve as a marker of metabolic function under hyperoxic ESHP conditions.
  • Adenosine infusion rate during ESHP may predict the requirement for post-transplantation ECMO support.
Abstract

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