Methods in molecular biology · 2013 · 54 citations · 21 references
MedicineHematologyMolecular BiologyHemostasisMolecular DiagnosticsCoagulation AbnormalitiesCoagulation Factor DeficienciesEnzyme-linked Immunosorbent AssayHemostatic AgentsVon Willebrand DiseaseFactor ViiaFactor Viii ActivationFactor Viii PhysiologyFactor Viiia ComplexVon Willebrand Factor Activity Assays
Hemophilia A is an inherited bleeding disorder caused by a deficiency of factor VIII coagulant activity (FVIII:C). Patients are treated with infusions of either plasma-derived or recombinant factor VIII. However, some patients develop inhibitory antibodies (inhibitors) to infused factor VIII which render it ineffective. The original Bethesda method was developed to standardize measurement of inhibitors in a factor VIII neutralization assay. One Bethesda unit is defined as that amount of inhibitor that results in 50% residual FVIII:C activity of a defined test mixture. In the Nijmegen modification of the original Bethesda method, the pH and the protein concentration of the test mixture is further standardized. As a result, the FVIII:C in the test mixture is less prone to artifactual deterioration and the test has improved specificity. Even with a standardized procedure a number of factors can affect the performance of the test and it is important for laboratory staff to be aware of their impact on the result outcome.
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Incidence of development of factor VIII and factor IX inhibitors in haemophiliacs
S. Ehrenforth, W. Kreuz, R. Linde et al. · The Lancet · 1992 · 608 citations
Medicine, Hematology, Hemostasis +11
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
Bert Verbruggen, Georges E. Rivard, Jerome Teitel et al. · Thrombosis and Haemostasis · 1998 · 143 citations