Clinical and laboratory evaluation of the treatment of von Willebrand's disease patients with heat-treated factor VIII concentrate (BPL 8Y)
- 1 June 1990
- journal article
- research article
- Published by Wiley in British Journal of Haematology
- Vol. 75 (2) , 228-233
- https://doi.org/10.1111/j.1365-2141.1990.tb02654.x
Abstract
Adequate rises of vWF:activity and satisfactory haemostasis have been obtained in six von Willebrand patients treated with heated 8Y factor VIII concentrate, despite multimeric analysis showing the concentrate to have an alteration in the proportions of the different vWF:Ag multimers including slight loss of the highest molecular weight multimers and an abnormal triplet. As heat-treated concentrates reduce the risk of transmitting blood borne viruses 8Y concentrate should be considered as a possible first line treatment of vWD patients in the U.K. if they do not have mild forms of type I von Willebrand''s disease which can be treated with desmopressim (DDAVP) infusions.This publication has 16 references indexed in Scilit:
- Safety trial of heated factor VIII concentrate (8Y).Archives of Disease in Childhood, 1989
- Desmopressin: a nontransfusional form of treatment for congenital and acquired bleeding disorders [see comments]Blood, 1988
- Hemostatic effect of a heat-treated factor VIII concentrate (Haemate P) in von Willebrand's diseaseAnnals of Hematology, 1988
- Correction of the bleeding time in treated patients with severe von willebrand disease is not solely dependent on the normal multimeric structure of plasma von willebrand factorAmerican Journal of Hematology, 1987
- The use of heat-treated factor VIII-concentrates in von willebrand's diseaseAnnals of Hematology, 1985
- Analysis of the complexity of the multimeric structure of factor VIII related antigen/von Willebrand protein using a modified electrophoretic technique.Journal of Clinical Pathology, 1983
- Characteristics of Various Factor VIII Concentrates used in Treatment of Haemophilia ABritish Journal of Haematology, 1977
- Antihemophilic factor concentrate therapy in von Willebrand disease. Dissociation of bleeding-time factor and ristocetin-cofactor activitiesPublished by American Medical Association (AMA) ,1976
- Failure of AHF concentrate to control bleeding in von Willebrand's diseaseThe American Journal of Medicine, 1976
- Brief Report: Correction of the Hemostatic Defects in Von Willebrand’s DiseaseBlood, 1967