Perfusate Enzymes and Platelets Indicate Early Allograft Dysfunction After Transplantation of Normothermically Preserved Livers

血小板 移植 医学 病理 免疫学 生物 内科学 生物化学
作者
Annemarie Weißenbacher,Christina Bogensperger,Rupert Oberhuber,András Mészáros,Silvia Gasteiger,Hanno Ulmer,Valeria Berchtold,Felix J. Krendl,Margot Fodor,Franka Messner,Theresa Hautz,Giorgi Otarashvili,Thomas Resch,Christian Margreiter,Manuel Maglione,Christian Irsara,Andrea Griesmacher,Marc Raynaud,Robert Breitkopf,Jakob Troppmair,Dietmar Öfner,Benno Cardini,Stefan Schneeberger
出处
期刊:Transplantation [Ovid Technologies (Wolters Kluwer)]
卷期号:106 (4): 792-805 被引量:25
标识
DOI:10.1097/tp.0000000000003857
摘要

Background. Normothermic machine perfusion (NMP) has become a clinically established tool to preserve livers in a near-physiological environment. However, little is known about the predictive value of perfusate parameters toward the outcomes after transplantation. Methods. Fifty-five consecutive NMP livers between 2018 and 2019 were included. All of the livers were perfused on the OrganOx metra device according to an institutional protocol. Transplant and perfusion data were collected prospectively. Results. Forty-five livers were transplanted after NMP. Five livers stem from donors after circulatory death and 31 (68.9%) from extended criteria donors. Mean (SD) cold ischemia time was 6.4 (2.3) h; mean (SD) total preservation time was 21.4 (7.1) h. Early allograft dysfunction (EAD) occurred in 13 of 45 (28.9%) patients. Perfusate aspartate aminotransferase ( P = 0.008), alanine aminotransferase ( P = 0.006), lactate dehydrogenase ( P = 0.007) and their development over time, alkaline phosphatase ( P = 0.013), and sodium ( P = 0.016) correlated with EAD. Number of perfusate platelets correlated with cold ischemia time duration and were indicative for the occurrence of EAD. Moreover, von Willebrand Factor antigen was significantly higher in perfusates of EAD livers ( P < 0.001), and Δ von Willebrand factor antigen correlated with EAD. Although perfusate lactate and glucose had no predictive value, EAD was more likely to occur in livers with lower perfusate pH ( P = 0.008). ΔPerfusate alkaline phosphatase, Δperfusate aspartate aminotransferase, Δperfusate alanine aminotransferase, and Δperfusate lactate dehydrogenase correlated closely with model for early allograft function but not liver graft assessment following transplantation risk score. Bile parameters correlated with extended criteria donor and donor risk index. Conclusions. Biomarker assessment during NMP may help to predict EAD after liver transplantation. The increase of transaminases and lactate dehydrogenase over time as well as platelets and vWF antigen are important factors indicative for EAD.
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