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Normothermic Ex Situ Heart Perfusion in Working Mode: Assessment of Cardiac Function and Metabolism
Published on: January 12, 2019
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.
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.
Background:
This study investigated oxygen handling of human hearts donated after circulatory death (DCD) on normothermic ex-situ heart perfusion (ESHP) and evaluated oxygen handling markers as adjuncts to cardiac viability assessment.
Methods:
This single-center retrospective study included human DCD heart transplantation procedures using ESHP. Lactate concentrations, blood gas, myocardial oxygen consumption (MVO2), delivery (MDO2), and extraction (MEO2), coronary blood flow (CBF), coronary vascular resistance (CVR), and adenosine infusion were reported over time. Correlation between parameters was assessed, and statistical testing compared patients who did and did not require extracorporeal membrane oxygenation (ECMO) support after transplantation.
Results:
Lactate concentrations decreased during ESHP in all transplanted hearts (n = 25) and increased in 1 rejected heart. Arterial partial pressure of oxygen (PO2) was 75.2 ± 2.9 kPa, with an arteriovenous ΔPO2 of 44.8 ± 10.4 kPa. Oxygen saturation was 100% in most arterial and venous samples. Average MVO2 was 2.7 ± 0.6 ml/min/100 g myocardium, MDO2 98.5 ± 20.4 ml/min, and MEO2 8.6 ± 1.8%. Average CVR was 0.025 ± 0.006 mm Hg min/ml/100 g and increased over time. ΔPO2 correlated strongly with MVO2 (R = 0.797, p < 0.001) and lactate trend (R = 0.799, p < 0.001) in transplanted hearts, without differences compared to the rejected heart with increasing lactate. Adenosine infusion on ESHP was significantly higher in patients requiring ECMO post-transplantation vs non-ECMO cases (11.7 (4.5-21.0) vs 2.2 (1.5-6.7) ml/h, p = 0.039).
Conclusions:
Hearts on normothermic ESHP receive excessive MDO2, due to high PO2 and CBF, while the MVO2 is relatively low. Thus, CBF and PO2 can potentially be lowered. Furthermore, ΔPO2 could serve as additional marker of metabolic function under these hyperoxic circumstances. The adenosine infusion rate might predict post-transplantation ECMO requirement.
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