Use of a High‐Purity Factor VIII Concentrate (Hemate P) in von Willebrand's Disease1
- 1 May 1989
- journal article
- research article
- Published by Wiley in Vox Sanguinis
- Vol. 56 (4), 212-217
- https://doi.org/10.1111/j.1423-0410.1989.tb02031.x
Abstract
In previous studies, we have found Hemate P (Behring) to be the only commercial virus-inactivated high-purity factor VIII concentrate that contains native von Willebrand factor. In the present study, Hemate P was given to 7 patients with the severe recessive form of von Willebrand's disease, to 2 patients with type Ia, to 1 patient with type IIB, and to 1 patient with type IIC von Willebrand's disease. A correction of the hemostatic defect was seen in all patients. Satisfactory hemostasis was also obtained in clinical situations, 1 patient undergoing major surgery and another being delivered, both without undue loss of blood. We conclude that Hemate P is an efficacious and safe product for use in cases of von Willebrand's disease when pharmacological correction of the hemostatic defect is not possible.This publication has 25 references indexed in Scilit:
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