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Abstract
Background
Primary graft dysfunction (PGD) remains a major obstacle after lung transplantation. Ischemia–reperfusion injury is a known contributor to the development of PGD following lung transplantation. We developed a novel approach to assess the impact of increased pulmonary blood flow in a large porcine single-left lung transplantation model.
Materials
Twelve porcine left lung transplants were divided in two groups (n = 6, in low- (LF) and high-flow (HF) group). Donor lungs were stored for 24 h on ice, followed by left lung transplantation. In the HF group, recipient animals were observed for 6 h after reperfusion with partially clamping right pulmonary artery to achieve a higher flow (target flow 40–60% of total cardiac output) to the transplanted lung compared to the LF group, where the right pulmonary artery was not clamped.
Results
Survival at 6 h was 100% in both groups. Histological, functional and biological assessment did not significantly differ between both groups during the first 6 h of reperfusion. injury was also present in the right native lung and showed signs compatible with the pathophysiological hallmarks of ischemia–reperfusion injury.
Conclusions
Partial clamping native pulmonary artery in large animal lung transplantation setting to study the impact of low versus high pulmonary flow on the development of ischemia reperfusion is feasible. In our study, differential blood flow had no effect on IRI. However, our findings might impact future studies with extracorporeal devices and represent a specific intra-operative problem during bilateral sequential single-lung transplantation.
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Details

1 KU Leuven, Department of Cardiovascular Sciences, Leuven, Belgium (GRID:grid.5596.f) (ISNI:0000 0001 0668 7884)
2 Leuven Lung Transplant Unit, KU Leuven, BREATHE, Department of Chronic Diseases, Metabolism and Ageing (Chrometa), Leuven, Belgium (GRID:grid.5596.f) (ISNI:0000 0001 0668 7884)
3 Rega Institute for Medical Research, KU Leuven, Laboratory of Virology and Chemotherapy, Department of Microbiology and Immunology, Leuven, Belgium (GRID:grid.5596.f) (ISNI:0000 0001 0668 7884)
4 Leuven Lung Transplant Unit, KU Leuven, BREATHE, Department of Chronic Diseases, Metabolism and Ageing (Chrometa), Leuven, Belgium (GRID:grid.5596.f) (ISNI:0000 0001 0668 7884); Hospital Universitari Vall D’Hebron, Lung Transplant Unit, Barcelona, Spain (GRID:grid.411083.f) (ISNI:0000 0001 0675 8654)
5 Leuven Lung Transplant Unit, KU Leuven, BREATHE, Department of Chronic Diseases, Metabolism and Ageing (Chrometa), Leuven, Belgium (GRID:grid.5596.f) (ISNI:0000 0001 0668 7884); University Hospitals Leuven, Department of Respiratory Diseases, Leuven, Belgium (GRID:grid.410569.f) (ISNI:0000 0004 0626 3338)
6 Leuven Lung Transplant Unit, KU Leuven, BREATHE, Department of Chronic Diseases, Metabolism and Ageing (Chrometa), Leuven, Belgium (GRID:grid.5596.f) (ISNI:0000 0001 0668 7884); University Hospitals Leuven, Department of Thoracic Surgery, Leuven, Belgium (GRID:grid.410569.f) (ISNI:0000 0004 0626 3338)
7 KU Leuven, Department of Cardiovascular Sciences, Leuven, Belgium (GRID:grid.5596.f) (ISNI:0000 0001 0668 7884); University Hospitals Leuven, Department of Anesthesiology, Leuven, Belgium (GRID:grid.410569.f) (ISNI:0000 0004 0626 3338)