Portal and Arterial Flushing with HTK and Tacrolimus Can Attenuate the Incidence of Early Liver Allograft Dysfunction

A. Shcherba, S. Korotkov, D. Efimov, A. Minou, O. Lebedz, Alla Karytka, D. Fedaruk, Eugeny Santotsky, A. Dzyadzko, O. Rummo
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Abstract

It was shown that Tacrolimus (TAC) can suppress inflammation and immune response involved in liver ischemic reperfusion injury (IRI) (Kristo I., Transpl Int. 2011). The aim: We hypothesize that back-table arterial and portal liver perfusion with TAC can influence the incidence and severity of EAD. A prospective randomized study was conducted (ClinicalTrials.gov Identifier: NCT01887171). Materials and methods: Including criteria: 1 liver transplantation from DBD donor with sequential portal-arterial reperfusion. At back-table portal vein and hepatic artery were perfused each by 500 ml of HTK solution containing 20 ng/ml TAC during 10-15 min followed by portal flushing with 200 ml 5% solution of Albumin containing 20 ng/ml TAC and by resting of liver in effluent. No Tac was added in the control group. Primary Outcome: EAD (Olthoff KM, et al. Liver Transpl. 2010) and severe EAD (P.R. Salvalaggio, et al. Transpl.
HTK和他克莫司联合冲洗门静脉和动脉可减轻早期同种异体肝移植功能障碍的发生率
研究表明他克莫司(TAC)可以抑制肝脏缺血再灌注损伤(IRI)的炎症和免疫反应(Kristo I., Transpl Int. 2011)。目的:我们假设TAC可影响EAD的发生率和严重程度。进行了一项前瞻性随机研究(ClinicalTrials.gov识别码:NCT01887171)。材料和方法:包括标准:1例DBD供体肝移植伴序贯门动脉再灌注。用含20 ng/ml TAC的HTK溶液500 ml分别灌注门静脉和肝动脉10-15 min,然后用含20 ng/ml TAC的5%白蛋白溶液200 ml冲洗门静脉,并将肝脏置于排出液中静置。对照组不添加Tac。主要结局:EAD (Olthoff KM, et al.)。肝脏转运,2010)和严重EAD (P.R. Salvalaggio等)。Transpl。
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