Management of acquired haemophilia A
Scharf, R.-E.; Dobbelstein, C.; Werwitzke, S.; Tiede, A. · Zeitschrift für Orthopädie und Unfallchirurgie · 2015 · Heft 04 · S. 311 bis 318
Bibliografische Angaben
Zusammenfassung
SummaryAcquired haemophilia A (AHA) is caused by autoantibody inhibitors of coagulation factor VIII (FVIII : C). Recent onset of bleeds and isolated prolongation of the activated partial thromboplastin time (aPTT) are characteristic features of the disorder. Reduced FVIII : C activity and a detectable FVIII : C inhibitor in the Bethesda assay confirm the diagnosis. Patients should be referred to expert centres, whenever possible, and invasive procedures with a high risk of bleeding must be avoided, until haemostasis has been secured by adequate therapy.Bypassing agents capable of inducing sufficient thrombin for…