Ex Vivo Optimization of Donor Lungs with Inhaled Sevoflurane during Normothermic Ex Vivo Lung Perfusion (VITALISE): A Pilot and Feasibility Study in Sheep.

在常温体外肺灌注期间吸入七氟醚对供体肺进行体外优化(VITALISE):绵羊的试点和可行性研究

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作者:Steinkühler Timo, Yang Shuqi, Hu Michiel A, Jainandunsing Jayant S, Jager Neeltina M, Erasmus Michiel E, Struys Michel M R F, Bosch Dirk J, van Meurs Matijs, Jabaudon Matthieu, Richard Damien, Timens Wim, Leuvenink Henri G D, Nieuwenhuijs-Moeke Gertrude J
Volatile anesthetics have been shown in different studies to reduce ischemia reperfusion injury (IRI). Ex vivo lung perfusion (EVLP) facilitates graft evaluation, extends preservation time and potentially enables injury repair and improvement of lung quality. We hypothesized that ventilating lungs with sevoflurane during EVLP would reduce lung injury and improve lung function. We performed a pilot study to test this hypothesis in a slaughterhouse sheep DCD model. Lungs were harvested, flushed and stored on ice for 3 h, after which EVLP was performed for 4 h. Lungs were ventilated with either an FiO(2) of 0.4 (EVLP, n = 5) or FiO(2) of 0.4 plus sevoflurane at a 2% end-tidal concentration (C(et)) (S-EVLP, n = 5). Perfusate, tissue samples and functional measurements were collected and analyzed. A steady state of the target C(et) sevoflurane was reached with measurable concentrations in perfusate. Lungs in the S-EVLP group showed significantly better dynamic lung compliance than those in the EVLP group (p = 0.003). Oxygenation capacity was not different in treated lungs for delta partial oxygen pressure (PO(2); +3.8 (-4.9/11.1) vs. -11.7 (-12.0/-3.2) kPa, p = 0.151), but there was a trend of a better PO(2)/FiO(2) ratio (p = 0.054). Perfusate ASAT levels in S-EVLP were significantly reduced compared to the control group (198.1 ± 93.66 vs. 223.9 ± 105.7 IU/L, p = 0.02). We conclude that ventilating lungs with sevoflurane during EVLP is feasible and could be useful to improve graft function.

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