Extended Ex-Situ Heart Perfusion Maintains Cardiac Function After Orthotopic Transplantation in a Pig Model - Report - MDSpire

Extended Ex-Situ Heart Perfusion Maintains Cardiac Function After Orthotopic Transplantation in a Pig Model

  • By

  • Zhuldyz Nurmykhametova

  • Rymbay Kaliyev

  • Timur Lesbekov

  • Linar Faizov

  • Assel Medressova

  • Aiym Turarova

  • Yerik Zuparov

  • Yuriy Pya

  • April 15, 2026

  • 0 min

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Clinical Report: Extended Ex-Situ Heart Perfusion Maintains Cardiac Function

Overview

Expand on the implications of maintaining cardiac function for donor organ utilization.

Background

Heart transplantation faces significant limitations due to a shortage of viable donor organs and the constraints of static cold storage, which allows only 4-6 hours of safe ischemic time. This short window often leads to the discard of otherwise suitable grafts. Normothermic ESHP presents a promising alternative, potentially enhancing graft viability and expanding the donor pool.

Data Highlights

ParameterBaselinePost-Transplant (0h)Post-Transplant (4h)
Cardiac Output (L/min)5.94 ± 0.166.78 ± 0.127.06 ± 0.16
Oxygen Consumption (mL/min/m²)172.88 ± 7.60
Lactate LevelsLowLowLow

Key Findings

  • Hearts preserved for 24 hours on the ECMO-based ESHP system maintained adequate hemodynamic function post-transplant.
  • Cardiac output significantly increased from baseline to 4 hours post-transplantation (p = 0.017).
  • Oxygen consumption increased significantly at 4 hours post-transplantation (p = 0.0322 vs. donor).
  • No acute graft dysfunction was observed in any of the transplanted hearts.
  • Despite reductions in hemoglobin and arterial oxygen content, oxygen delivery remained adequate.

Clinical Implications

The findings suggest that prolonged normothermic preservation of donor hearts using ESHP can enhance graft viability and function, potentially reducing organ discard rates. This approach may facilitate the use of marginal grafts, including those from donation after circulatory death.

Conclusion

Highlight implications for clinical practice and suggest areas for future research.

References

  1. Basic Research in Cardiology, 2009 -- Inhibition of Acute Rejection in Mouse Heart Transplants Using STAT-1 Decoy Oligodeoxynucleotides
  2. Basic Research in Cardiology, 2024 -- Analyzing the Immune Reaction to Myocardial Infarction in Porcine Models
  3. Basic Research in Cardiology, 2010 -- Sustained Cardioprotective Effects and Mechanisms of Pacing-Induced Postconditioning
  4. Transplantation Outcomes With Donor Hearts After Circulatory Death - American College of Cardiology, 2023
  5. Frontiers, 2024 -- Extending heart preservation to 24 h with normothermic perfusion
  6. Basic Research in Cardiology — Bone marrow-derived cells play a role in the formation of seven distinct endothelial cell types within the heart
  7. 2024 ESOT/Transplant International consensus for cardiothoracic machine perfusion
  8. Transplantation Outcomes With Donor Hearts After Circulatory Death - American College of Cardiology
  9. Frontiers | Extending heart preservation to 24 h with normothermic perfusion

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