https://www.ncbi.nlm.nih.gov/pubmed/32087412

Thromb Res. 2020 Feb 13;188:65-73. doi: 10.1016/j.thromres.2020.02.008. [Epub ahead of print]

Thrombin dynamics in children with liver disease or extrahepatic portal vein obstruction or shunt.

Beattie W1, Kremers R2, Magnusson M3, Peters T2, de Laat B2, Hardikar W4, Monagle P5, Ignjatovic V6.

Abstract

INTRODUCTION:
Changes in the coagulation profile in children with liver disease and extrahepatic portal vein obstruction or shunt result in both bleeding and thrombosis. Routine coagulation tests do not accurately predict bleeding risk, as they are not sensitive to changes in anticoagulant factors. The thrombin generation assay could be suitable for describing the overall balance of coagulation in children with liver disease. This study aims to characterise the mechanism of thrombin generation in this population, focusing on prothrombin conversion and thrombin inhibition.

METHODS:
Patients were categorised as: severe (paediatric end stage liver disease score > 15) and mild disease, or portal vein obstruction or shunt. Age and gender matched healthy controls were used. The thrombin generation assay was performed in plasma samples from patients and controls with and without exogenous thrombomodulin and the results were further analysed with the computational thrombin dynamics method.

RESULTS:
A total of 42 patients (severe, n = 5; mild, n = 29, obstruction/shunt, n = 8) and 20 controls were included in this study. The total prothrombin conversion, thrombin-antithrombin formation and the thrombin decay capacity, in the presence and absence of thrombomodulin were reduced in children with severe liver disease. The rate of prothrombin conversion was increased and thrombin decay capacity was decreased in patients with portal vein obstruction or shunt compared to controls.

CONCLUSION:
This study demonstrates changes in the mechanism in thrombin generation seen in severe chronic liverdisease. The changes vary in parenchymal versus non parenchymal liver disease and further study assessing the clinical significance of these variations in mechanism is required.