Rapid assessment of coagulation activity in whole blood

• US 20030064414A1
• Filed: 03/28/2002
• Published: 04/03/2003
• Est. Priority Date: 03/30/2001
• Status: Abandoned Application

• Current Assignee: Coagulation Diagnostics, Inc.
• Original Assignee: Coagulation Diagnostics, Inc.
• Inventors: Moskowitz, Keith A., Post, Diane R., Benecky, Michael J.
• Application Number:
  US10/107,409
• Publication Number:
  US 20030064414A1
• Time in Patent Office: Days
• US Class Current: 435/7.21
• CPC Class Codes: C12Q 1/56 involving blood clotting factors, e.g. involving thrombin, thromboplastin, fibrinogen
• CPC Class Codes: G01N 2333/96433 Serine endopeptidases (3.4.21)
• CPC Class Codes: G01N 2333/96441 with definite EC number
• CPC Class Codes: G01N 2800/52 Predicting or monitoring the response to treatment, e.g. for selection of therapy based on assay results in personalised medicine; Prognosis
• CPC Class Codes: G01N 33/86 involving blood coagulating time or factors, or their receptors

Abstract

The present invention is directed to methods to rapidly assess the overall coagulant properties of a patient'"'"'s blood sample by inhibiting the activation of the intrinsic contact activation pathway of coagulation and activating the extrinsic pathway of coagulation. When the sample is whole blood, the resulting clotting time represents the overall coagulant activity of the plasma and cellular components of the blood, which is indicative of existing or impending pathology arising from abnormal coagulability. The invention also provides a method for measuring the risk of a patient for a thrombotic event and for monitoring the effectiveness of procoagulant/anticoagulant therapy. A blood collection apparatus suitable for use in for performing the methods of the invention is also provided.

Claims

1. A method for measuring coagulation of blood, comprising

obtaining blood from a mammal;

inhibiting in vitro activation of the intrinsic contact activation pathway of coagulation in the blood;

initiating activation of the extrinsic activation pathway of coagulation by contacting the blood with at least one procoagulant; and

measuring coagulation of the blood.

2. The method according to claim 1, wherein the blood is contacted with a surface of low thrombogenic activity.

3. The method according to claim 2, wherein the low thrombogenic activity surface is plastic or siliconized glass.

4. The method according to claim 1, wherein inhibiting activation of the intrinsic contact activation pathway of coagulation comprises contacting the blood with at least one contact activation pathway inhibitor.

5. The method according to claim 4, wherein the contact activation pathway inhibitor is a Factor XIIa inhibitor, a Factor XIa inhibitor, or a kallikrein inhibitor.

6. The method according to claim 5, wherein the Factor XIIa inhibitor is corn trypsin inhibitor, an antibody to Factor XIIa, CI-esterase inhibitor, or a XIIa-binding peptide.

7. The method according to claim 5, Wherein the kallikrein inhibitor is aprotinin, an antibody to kallikrein, CI-esterase inhibitor, or a kallikrein-binding peptide.

8. The method according to claim 1, wherein the procoagulant is Factor VIIa, Factor IXa, Factor Xa, Factor XIa, viper venom, lipidated tissue factor, apo-tissue factor, or recombinant soluble tissue factor.

9. The method according to claim 8, wherein the Factor VIIa is added at a final concentration ranging from about 5 nanomoles/L to 100 nanomoles/L in the blood.

10. The method according to claim 8, wherein the Factor VIIa is recombinant Factor VIIa, natural Factor VIIa, or lipidated Factor VIIa.

11. The method according to claim 1, wherein inhibiting activation of the intrinsic contact activation pathway of coagulation comprises contacting the blood with a surface having a low thrombogenic activity, and wherein initiating activation of the extrinsic activation pathway of coagulation comprises contacting the blood with Factor VIIa, Factor IXa, Factor Xa, Factor XIa, viper venom, lipidated tissue factor, apo-tissue factor, or recombinant soluble tissue factor.

12. The method according to claim 1, wherein inhibiting activation of the intrinsic contact activation pathway of coagulation comprises contacting the blood with corn trypsin inhibitor and wherein initiating activation of the extrinsic activation pathway of coagulation comprises contacting the blood with Factor VIIa, Factor IXa, Factor Xa, Factor XIa, viper venom, lipidated tissue factor, apo-tissue factor, or recombinant soluble tissue factor.

13. The method according to claim 1, wherein inhibiting activation of the intrinsic contact activation pathway of coagulation comprises contacting the blood with aprotinin and wherein initiating activation of the extrinsic activation pathway of coagulation comprises contacting the blood with plasma or recombinant Factor VIIa, Factor IXa, Factor Xa, Factor XIa, viper venom, thrombin, lipidated tissue factor, apo-tissue factor, or soluble recombinant tissue factor.

14. The method according to claim 1, wherein inhibiting activation of the intrinsic contact activation pathway of coagulation comprises contacting the blood with CI-esterase inhibitor and wherein initiating activation of the extrinsic activation pathway of coagulation comprises contacting the blood with plasma or recombinant Factor VIIa, Factor IXa, Factor Xa, Factor XIa, viper venom, thrombin, lipidated tissue factor, apo-tissue factor, or soluble recombinant tissue factor.

15. The method according to claim 12, wherein inhibiting activation of the intrinsic contact activation pathway of coagulation comprises contacting the blood with aprotinin, and wherein initiating activation of the extrinsic activation pathway of coagulation comprises contacting the blood with Factor VIIa, wherein the Factor VIIa is natural, recombinant, or lipidated.

16. The method according to any one of claims 11 to 14, and wherein initiating activation of the extrinsic activation pathway of coagulation comprises contacting the blood with Factor Xa.

17. The method according to any of claims 11 to 14, wherein initiating activation of the extrinsic activation pathway of coagulation comprises contacting the blood with recombinant tissue factor.

18. The method according to any of claims 11 to 14, wherein initiating activation of the extrinsic activation pathway of coagulation comprises contacting the blood with lipidated tissue factor.

19. The method according to any of claims 11 to 14, wherein initiating activation of the extrinsic activation pathway of coagulation comprises contacting the blood with Factor VIIa.

20. The method according to claim 1, further comprising adding at least one anti-platelet agent to the blood.

21. The method according to claim 20, wherein the anti-platelet agent is aspirin, NSAIDs, dipyridamole, ticlopidine, clopidogrel, adenosine, theophylline, or a glycoprotein IIb/IIIa antagonist.

22. The method according to claim 1, further comprising the step of comparing coagulation of the blood to reference data defining a range of normal coagulation.

23. The method according to claim 1, further comprising the step of comparing coagulation of the blood to coagulation of a control sample, wherein the control sample has been treated with a known amount of a coagulation factor or inhibitor.

24. The method according to claim 1, wherein the blood has not been treated to prevent clotting, or has been citrated and recalcified.

25. The method according to claim 1, wherein inhibition of the intrinsic contact activation pathway occurs concurrently with activation of the extrinsic activation pathway.

26. The method according to claim 25, wherein the blood has not been treated to prevent clotting, or has been citrated and recalcified.

27. The method according to claim 5, wherein the Factor XIa inhibitor is an antibody to factor XI, CI-esterase inhibitor, or a Factor XIa-binding peptide.

28. The method according to claim 27, wherein the antibody is a monoclonal antibody.

29. The method according to claim 21, wherein the glycoprotein IIb/IIIa antagonist is abciximab, eptifibatide, or tirofiban.

30. The method according to claim 1, wherein the blood has been treated with low molecular weight heparin, UFH, pentasaccharide, a direct thrombin inhibitor, a direct factor Xa inhibitor, a tissue factor pathway inhibitor, a Factor IX inhibitor, activated protein C, or ATIII.

31. The method according to claim 21, wherein a coagulation inhibitor is administered to the mammal before the blood is obtained.

32. The method according to claim 30, wherein the coagulation inhibitor is low molecular weight heparin, UFH, pentasaccharide, a direct thrombin inhibitor, a direct factor Xa inhibitor, a tissue factor pathway inhibitor, a Factor IX inhibitor, activated protein C, or ATIII.

40. The method according to claim 4, wherein the procoagulant is lipidated tissue factor and the contact activation pathway inhibitor is aprotinin.

33. A method for measuring the effectiveness of at least one coagulation factor or coagulation inhibitor on the coagulation of blood, comprising

obtaining blood from a mammal;

dividing the blood into at least two aliquots;

treating the first aliquot to steps comprising;

(a) inhibiting in vitro activation of the intrinsic contact activation pathway of coagulation;

(b) initiating activation of the extrinsic activation pathway of coagulation by contacting the first aliquot with a procoagulant; and

(c) measuring coagulation of the first aliquot;

treating the second aliquot to steps comprising;

(d) inhibiting in vitro activation of the intrinsic contact activation pathway of coagulation in vitro;

(e) contacting the second aliquot with the at least one coagulation factor or coagulation inhibitor;

(f) initiating activation of the extrinsic activation pathway of coagulation by contacting the second aliquot with at least one procoagulant; and

(g) measuring coagulation of the second aliquot; and

(h) comparing coagulation measurements of the first and second aliquots.

35. The method according to claim 33, wherein the coagulation factor or coagulation inhibitor is administered to the mammal before the second blood sample is obtained.

36. The method according to any one of claims 33 or 34, further comprising adjusting the concentration of the at least one coagulation factor or coagulation inhibitor in the mammal after the coagulation measurements are compared.

37. The method according to any one of claims 33 or 34, further comprising administering at least one second coagulation factor or coagulation inhibitor to the mammal after the coagulation measurements are compared.

38. The method according to claim 33, wherein the blood has not been treated to prevent clotting, or has been citrated and recalcified.

45. The method of claim 33, wherein the coagulation inhibitor is low molecular weight heparin, UFH, pentasaccharide, a direct thrombin inhibitor, a direct factor Xa inhibitor, a tissue factor pathway inhibitor, a Factor IX inhibitor, activated protein C, or ATIII.

46. The method of claim 45, wherein the tissue factor pathway inhibitor is TFPI, VIIai, rNAPc2, anti-tissue factor monoclonal antibody, soluble AA mutated tissue factor, or coumadin.

47. The method of claim 46, wherein the Factor IX inhibitor is an anti-Factor IX monoclonal antibody or FIXai.

34. A method for measuring the effectiveness of at least one coagulation factor or coagulation inhibitor on coagulation of a blood sample, comprising

obtaining a first blood sample from a mammal;

inhibiting activation of the intrinsic contact activation pathway of coagulation;

initiating activation of the extrinsic activation pathway of coagulation by contacting the first blood sample with a procoagulant agent;

measuring coagulation of the first blood sample;

obtaining a second blood sample from the mammal;

inhibiting activation of the intrinsic contact activation pathway of coagulation;

contacting the second blood sample with at least one coagulation factor or inhibitor;

initiating activation of the extrinsic pathway of coagulation by contacting the second blood sample with at least one procoagulant;

measuring coagulation of the second blood sample; and

comparing coagulation measurements of the first and second blood samples.

39. The method according to claim 34, wherein the blood has not been treated to prevent clotting, or has been citrated and recalcified.

48. The method of claim 34, wherein the coagulation inhibitor is low molecular weight heparin, UFH, pentasaccharide, a direct thrombin inhibitor, a direct factor Xa inhibitor, a tissue factor pathway inhibitor, a Factor IX inhibitor, activated protein C, or ATIII.

49. The method of claim 48, wherein the tissue factor pathway inhibitor is TFPI, VIIai, rNAPc2, anti-tissue factor monoclonal antibody, soluble AA mutated tissue factor, or coumadin.

50. The method of claim 49, wherein the Factor IX inhibitor is an anti-Factor IX monoclonal antibody or FIXai.

41. A blood collection apparatus comprising a vessel, wherein the vessel contains a contact activation pathway inhibitor.

42. The apparatus of claim 41, wherein the vessel is an evacuated tube.

43. The apparatus of claim 41, further comprising a Ca²⁺chelator.

44. A method for monitoring recovery of a patient from a condition related to abnormal blood coagulation, comprising:

obtaining at least two blood samples from a patient;

inhibiting activation of the intrinsic contact activation pathway of coagulation in the blood samples;

initiating activation of the extrinsic activation pathway of coagulation by contacting the blood samples with at least one procoagulant; and

measuring coagulation of the blood, wherein one of the blood samples is obtained before administration of medical treatment or a surgical procedure and the other blood samples are obtained during or after administration of the medical treatment or the surgical procedure.