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Association between bleeding time and platelet adherence to artery subendothelium
Thrombosis and Haemostasis
|October 31, 1984
Summary
This study evaluated factor VIII-von Willebrand factor (FVIII-VWF) preparations for platelet adherence. High-purity FVIII-VWF and cryoprecipitate normalized platelet adherence and bleeding time in von Willebrand
Area of Science:
- Hematology
- Vascular Biology
- Biochemistry
Background:
- Von Willebrand factor (VWF) is crucial for platelet adhesion to damaged blood vessels.
- Deficiencies in VWF cause von Willebrand's disease (VWD), leading to bleeding disorders.
- Effective VWF replacement therapy requires preparations that restore normal platelet function.
Purpose of the Study:
- To assess the efficacy of different factor VIII-von Willebrand factor (FVIII-VWF) preparations in promoting platelet adherence.
- To evaluate FVIII-VWF preparations as potential treatments for von Willebrand's disease (VWD).
- To validate an in vitro platelet adherence assay for testing FVIII-VWF preparation efficacy.
Main Methods:
- Utilized an annular perfusion chamber with human arteries and reconstituted blood to test FVIII-VWF preparations.
- Compared purified FVIII-VWF, cryoprecipitate, a commercial concentrate (Hemofil), and a high-purity concentrate (Concentrate II).
- Assessed platelet adherence and bleeding times in plasma from normal subjects and VWD patients.
Main Results:
- Purified FVIII-VWF, cryoprecipitate, and Concentrate II effectively mediated platelet adherence.
- Commercial Hemofil concentrate showed impaired platelet adherence compared to normal levels.
- Concentrate II normalized platelet adherence and bleeding time in VWD patient plasma.
Conclusions:
- High-purity FVIII-VWF preparations (like Concentrate II) and cryoprecipitate are effective in restoring platelet adherence.
- The developed platelet adherence assay is an efficient in vitro tool for evaluating FVIII-VWF preparations for VWD.
- Commercial FVIII-VWF concentrates may not be as effective as purer preparations in restoring normal hemostasis.