Optimal ex vivo lung perfusion techniques with oxygenated perfusate
Background Accumulating evidence supports an increasing role of ex vivo lung perfusion (EVLP) in clinical lung transplantation. However, EVLP has adverse effects on the quality of lung grafts, which have rarely been discussed. Careful optimization of current EVLP protocols might improve outcomes. Th...
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Veröffentlicht in: | The Journal of heart and lung transplantation 2017-04, Vol.36 (4), p.466-474 |
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Sprache: | eng |
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Zusammenfassung: | Background Accumulating evidence supports an increasing role of ex vivo lung perfusion (EVLP) in clinical lung transplantation. However, EVLP has adverse effects on the quality of lung grafts, which have rarely been discussed. Careful optimization of current EVLP protocols might improve outcomes. This study revisited the effects of different levels of oxygenation of the perfusate circulated through the lungs during EVLP and the impact on posttransplant functional outcomes. Methods We compared the results of four different oxygenation levels in the perfusate during EVLP: 6%, 40%, 60%, and 100% O2 . We evaluated lung function, compliance, and vascular resistance and the levels of glucose and other markers in the perfusate. Following EVLP, lung grafts were transplanted, and posttransplant outcomes were compared. Results Lungs perfused with 40% O2 on EVLP had the lowest glucose consumption as compared with the other perfusates. Lungs treated with 40% O2 or 60% O2 exhibited significantly less inflammation, as indicated by reduced pro-inflammatory cytokines mRNA levels as compared with lungs perfused with 6% O2 or 100% O2 . Significantly more oxidative damage, was noted after 4 hours of EVLP perfused with 100% O2 . Following transplantation, lungs perfused with 40% O2 during EVLP had the best posttransplant functional outcomes. Conclusions Optimization of the oxygen levels in the perfusate during EVLP improved outcomes in this rat model. Importantly, deoxygenated perfusate, the current standard during EVLP, exhibited significantly more inflammation with compromised cellular metabolic activity and compromised posttransplant outcomes. |
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ISSN: | 1053-2498 1557-3117 |
DOI: | 10.1016/j.healun.2016.10.014 |