Ignite Creation Date:
2024-05-06 @ 12:51 PM
Last Modification Date:
2024-10-26 @ 1:05 PM
Study NCT ID:
NCT03861286
Status:
COMPLETED
Last Update Posted:
2019-09-25
First Post:
2019-03-01
Brief Title:
Haemostatic Markers in Cardiopulmonary Bypass
Sponsor:
Imperial College London
Organization:
Imperial College London
Study Overview
Official Title:
Characterisation of the Haemostatic Changes In Patients Receiving Intravenous Heparin for Cardiopulmonary Bypass Surgery
Status:
COMPLETED
Status Verified Date:
2019-09
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
This study is to understand the changes occurring in a blood clotting protein von Willebrand factor VWF in patients undergoing cardiac surgery who receive the blood thinner called Heparin These patients are given Heparin through their veins to prevent blood clot formation as it passes through the heart bypass machine At the end of the operation the effect of Heparin is reversed by another drug Protamine Sulphate
Heparin prevents blood clots forming mainly by inactivating thrombin a crucial protein needed for blood clotting This effect of Heparin is monitored through blood tests called the Anti Factor-Xa and the APTT
Heparin has another effect on clotting it can block the attachment of special blood cell fragments called platelets to damaged blood vessels but this effect is not usually measured
Following blood vessel injury the large VWF sticks to the damaged surface and captures platelets to form a plug which stops bleeding The platelet plug is then stabilised by other clotting proteins This stops blood loss and allows vessel repair underneath
Heparin blocks the ability of VWF to capture platelets at the site of blood vessel injury The higher the dose of Heparin the greater this blocking effect is This secondary effect of Heparin cannot be readily monitored and may explain why bleeding complications occur in patients receiving Heparin despite the monitoring with blood tests used
This study will look at the blood levels of Heparin VWF and platelets before during and after surgery and how well VWF functions in the presence of heparin including its ability to attach to platelets
The investigators will determine if all of the heparin related changes in blood clotting can be detected using a method that looks at all of the different steps in forming a blood clot
Heparin prevents blood clots forming mainly by inactivating thrombin a crucial protein needed for blood clotting This effect of Heparin is monitored through blood tests called the Anti Factor-Xa and the APTT
Heparin has another effect on clotting it can block the attachment of special blood cell fragments called platelets to damaged blood vessels but this effect is not usually measured
Following blood vessel injury the large VWF sticks to the damaged surface and captures platelets to form a plug which stops bleeding The platelet plug is then stabilised by other clotting proteins This stops blood loss and allows vessel repair underneath
Heparin blocks the ability of VWF to capture platelets at the site of blood vessel injury The higher the dose of Heparin the greater this blocking effect is This secondary effect of Heparin cannot be readily monitored and may explain why bleeding complications occur in patients receiving Heparin despite the monitoring with blood tests used
This study will look at the blood levels of Heparin VWF and platelets before during and after surgery and how well VWF functions in the presence of heparin including its ability to attach to platelets
The investigators will determine if all of the heparin related changes in blood clotting can be detected using a method that looks at all of the different steps in forming a blood clot
Detailed Description:
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 19354 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
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 19354 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
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None