American Journal of Hematology · 2007 · 19 citations · 10 references
MedicineHematologyHematopathologyHemostasisPharmacodynamicsCoagulation AbnormalitiesCoagulation Factor DeficienciesHemostatic AgentsHemostatic DisordersVon Willebrand DiseaseAntigenicity ReductionCoagulation Factor ConcentratesCoagulation Factor Replacement TherapyFactor Viii ReplacementReactivityVon Willebrand Factor AntigenVon Willebrand Factor FunctionVon Willebrand Factor Replacement Therapy
A relevant aspect in the treatment of patients with hemophilia A (HA) presenting inhibitor against factor VIII (FVIII) is the different antigenicity of FVIII used for replacement therapy. The aim of the study was to assess the effect of different products, with variable von Willebrand factor (vWF) concentration, in preventing the binding of inhibitor to FVIII. The reactivity of inhibitors from plasma of 18 patients with HA versus three commercial concentrates containing different amounts of vWF was compared. The results show that increasing amounts of vWF might have a protective effect on the transfused FVIII inactivation.
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A More Uniform Measurement of Factor VIII Inhibitors
Carol K. Kasper, Louis M. Aledort, David L. Aronson et al. · Thrombosis and Haemostasis · 1975 · 587 citations
A More Uniform Measurement of Factor VIII Inhibitors
Carol K. Kasper, Louis M. Aledort, Richard B Counts et al. · Thrombosis and Haemostasis · 1975 · 320 citations