• D Perry, E Berntorp, C Tait, G Dolan, P A Holme, M Laffan, R Lassila, A Mumford, J Pasi, J Wilde, A Will, and T T Yee.
• Haematology Department, Addenbrooke's Hospital, Hills Road, Cambridge, UK. david.perry@addenbrookes.nhs.uk
• Haemophilia. 2010 Jan 1; 16 (1): 80-9.

AbstractIn patients with severe haemophilia and inhibitors, regular factor VIII inhibitor bypassing activity (FEIBA) prophylaxis has been shown to reduce the frequency of bleeding by up to 85% and to improve patient quality of life. FEIBA is well tolerated; the incidence of thrombotic events and of allergic reactions is extremely low. The concept of prophylaxis in haemophilia patients with inhibitors is relatively new and some clinicians may be unsure of how to use FEIBA in this context. These treatment recommendations, based on published evidence plus the collective experience of a group of haematologists (with practical knowledge of managing inhibitor patients with FEIBA prophylaxis), are intended to provide guidance to clinicians considering initiating and maintaining patients on FEIBA prophylaxis with specific focus on practical aspects of patient selection, dosing, monitoring and stop criteria.

23 keywords...

hide…