4.6 Article

The international normalised ratio to monitor coagulation factor production during normothermic machine perfusion of human donor livers

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THROMBOSIS RESEARCH
卷 228, 期 -, 页码 64-71

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PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.thromres.2023.05.025

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Normothermic machine perfusion; Liver transplantation; Coagulation factors; Hemostasis; International Normalized Ratio; Viability testing

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Normothermic machine perfusion (NMP) of donor livers allows for new diagnostic and therapeutic strategies. However, high concentrations of heparin and low levels of fibrinogen may affect coagulation assays such as the International Normalised Ratio (INR) performed in perfusate.
Background: Normothermic machine perfusion (NMP) of donor livers allows for new diagnostic and therapeutic strategies. As the liver produces most of the haemostatic proteins, coagulation assays such as the International Normalised Ratio (INR) performed in perfusate may be useful to assess hepatocellular function of donor livers undergoing NMP. However, high concentrations of heparin and low levels of fibrinogen may affect coagulation assays.Methods: Thirty donor livers that underwent NMP were retrospectively included in this study, of which 18 were subsequently transplanted. We measured INRs in perfusate in presence or absence of exogenously added fibrinogen and/or polybrene. Additionally, we prospectively included 14 donor livers that underwent NMP (of which 11 were transplanted) and measured INR using both a laboratory coagulation analyser and a point-of-care device.Results: In untreated perfusate samples, the INR was above the detection limit in all donor livers. Addition of both fibrinogen and polybrene was required for adequate INR assessment. INRs decreased over time and detectable perfusate INR values were found in 17/18 donor livers at the end of NMP. INR results were similar between the coagulation analyser and the point-of-care device, but did not correlate with established hepatocellular viability criteria.Conclusions: Most of the donor livers that were transplanted showed a detectable perfusate INR at the end of NMP, but samples require processing to allow for INR measurements using laboratory coagulation analysers. Point-of-care devices bypass this need for processing. The INR does not correlate with established viability criteria and might therefore have additional predictive value.

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