Pharmacodynamic monitoring of factor VIII replacement therapy in hemophilia A: Combining thrombin and plasmin generation.
Lars L F G ValkeLaura H BukkemsWideke BartelingBritta A P Laros-van GorkomNicole M A BlijlevensRon A A MathôtWaander L van HeerdeSaskia E M ScholsPublished in: Journal of thrombosis and haemostasis : JTH (2020)
HA patients showed clear differences in baseline TG and PG despite having comparable FVIII activity levels. These results reveal a discrepancy between FVIII activity level and TG, in which the latter may be a better parameter to monitor individualized treatment in HA patients.