Haemostatic Markers in Cardiopulmonary Bypass

Von Willebrand factor (VWF) is a large plasma glycoprotein involved in thrombosis, haemostasis and vascular biology. Its principal role is to capture platelets at sites of blood vessel endothelial injury allowing the formation of an unstable platelet plug, an initial step in haemorrhage control. Following this, blood coagulation at the site of injury, results in the formation of fibrin strands, which enmesh and stabilise the platelet plug, until vessel repair is complete.

Following endothelial cell (EC) injury or activation, VWF becomes tethered, either to EC or to the now exposed subendothelial matrix (SEM). The shear stress generated by blood flow causes the tethered VWF to unravel, exposing its multiple platelet binding sites, resulting in platelet capture.

One of the most important domains of VWF is the A1 domain, which contains binding sites for the platelet receptor glycoprotein Ib (GPIb) as well as for collagen and heparin.

Heparin is the major component of mast cell secretory granules. Its precise physiological role is unknown but it has been proposed that it plays a role in host defense mechanisms. The anticoagulant properties of heparin, however, have been exploited pharmaceutically and exogenous heparin has been a clinically useful anticoagulant since 1935.4 It is known to potentiate the effects of antithrombin in the inactivation of Factor Xa and thrombin. Unfractionated heparin therapy can be monitored using the plasma activated partial thromboplastin time (APTT), anti -factor Xa activity or, if very high doses are used, the activated clotting time (ACT). The APTT is most commonly used to monitor UFH therapy as it is cost effective and readily available. However, it is subject to several pre-analytical and analytical variables and therefore may not provide an accurate measure of the anticoagulant effect of UFH. The anti-factor Xa activity is less susceptible to confounding factors and makes this the assay of choice but it is less widely available.

Studies have shown that heparin also competitively inhibits the binding of VWF to platelet receptor GPIb, an anti-thrombotic effect distinct from its anticoagulant role via Antithrombin. This may in part explain why the bleeding complications that occur during heparin therapy are unpredictable, despite using current techniques for monitoring its anticoagulant effect. This additional activity of heparin is likely to be of particular importance during CPB when very high concentrations of heparin are used to maintain the extracorporeal circuit and which have to be reversed to restore haemostasis at the end of the procedure. The currently available literature remains incomplete in the characterisation of the changes that occur in VWF-dependent platelet function and do not explain the observed recovery of VWF function above baseline levels, after reversal of heparin with protamine sulphate. The aim of this study is to fully characterise the changes in VWF concentration, function and platelet interaction, that occur in patients undergoing cardiac surgery and receiving intravenous unfractionated heparin, intra- and post-operatively. This is a prospective, single centre cohort study involving the analysis of haemostatic assays in patients receiving IV heparin during cardiopulmonary bypass surgery. The study aims to recruit 30 eligible adult patients (>18 years) undergoing first time cardiac surgery for the correction of atrial septal defects or undergoing tissue mitral valve replacement and receiving IV unfractionated heparin intra-operatively at Royal Brompton Hospital. The study aims to recruit a uniform population of 30 patients which should be achieved within 6 months.