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Updated: Feb 19, 2026

Establishment of a Novel Ex Vivo Lung Perfusion System for Rat Lungs After Circulatory Death
Published on: October 18, 2024
A Whole-body Cooling Strategy in Uncontrolled Donation After Circulatory Death: Insights From a Porcine Ex Vivo Lung
Hiromichi Niikawa1,2, Daisuke Sakota3, Ryo Kosaka3
1Department of Thoracic Surgery, Institute of Development, Aging and Cancer, Tohoku University, Miyagi, Japan.
Background:
Prolonged warm ischemia in uncontrolled donation after circulatory death (uDCD) potentially increases the risk of graft dysfunction in lung transplantation. To address this concern, a noninvasive, whole-body cooling approach was developed using a specialized liquid refrigerant at -21 °C. The aim of this study was to investigate whether this method reduces lung temperature and improves lung function in uDCD donors.
Methods:
Fifteen pigs were randomly assigned to 3 groups. In the study group (n = 5), the entire donor body was submerged in a basin containing a coolant of -21 °C, and chest compression was performed during 90 min of warm ischemia. In the sham group (n = 5), neither body cooling nor chest compression was performed during 90 min of warm ischemia. Lungs were evaluated by cellular ex vivo lung perfusion (EVLP) after 5 h of additional cold ischemia. Lungs in the donation after brain death (DBD) group (n = 5) were perfused after 1 h of cold ischemia.
Results:
Tracheal temperature decreased to 28.5 °C in the study group and remained at 38.1 °C in the sham group. Lungs in the study group showed higher transplant suitability with significantly higher PaO2/FiO2, and lower peak inspiratory pressure during EVLP than those in the sham group (all P < 0.05). The study group had a significantly higher ATP level, a relatively lower hypoxia-inducible factor-1α level, and lower percentage of apoptotic cells than the sham group.
Conclusions:
This novel cooling approach effectively reduced lung temperature during warm ischemia, resulting in improved lung function during EVLP. These data suggest that this method could mitigate ischemia-reperfusion injury in uDCD donors, expanding the donor lung pool.
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