Patients receiving left-sided mechanical circulatory support (MCS) require systemic anticoagulation with unfractionated heparin (UFH) to prevent clotting of the circuit and reduce the risk of arterial thrombosis. With MCS, there is a very high frequency of bleeding and ischaemic complications, including stroke and systemic embolism. Monitoring of UFH can be very challenging. Whilst most centres routinely monitor the activated clotting time, prothrombin time, activated partial thromboplastin time (aPTT) and fibrinogen to assess haemostasis, there is no clear guidance available regarding the optimal test.
Additional tests, including antithrombin level, anti-factor Xa assay and thromboelastography can be used for risk stratification of patients to try and predict the risks of thrombosis and bleeding. Each has their specific role, strengths and limitations. Measurement of anti-Xa level best correlates with heparin dose, and appears predictive of circuit thrombosis, although aPTT is a better predictor of bleeding. Increased thrombin generation may have a role in predicting thrombosis. Acquired von Willebrand syndrome is frequent with MCS, contributing to bleeding risk and can be detected by assessing the von Willebrand factor activity to antigen ratio, whilst the Platelet Function Analyzer can be used in urgent situations with high negative predictive value. Tests of platelet aggregation can aid the prediction bleeding.
A selection of complementary tests to collectively assess heparin-effect, coagulation, platelet function and platelet aggregation is recommended to personalise management and thereby optimise outcomes in patients receiving MCS.