Hemostatic treatment of hemophilia with inhibitors

Author:

OGURA Taemi

Publisher

Japanese Society on Thrombosis and Hemostasis

Subject

General Medicine

Reference33 articles.

1. 1) Darby SC, Keeling DM, Spooner RJ, Wan Kan S, Giangrande PL, Collins PW, Hill FG, Hay CR; UK Haemophilia Centre Doctors’ Organisation: The incidence of factor VIII and factor IX inhibitors in the hemophilia population of the UK and their effect on subsequent mortality, 1977–99. J Thromb Haemost 2: 1047–1054, 2004.

2. 4) White GC 2nd, Rosendaal F, Aledort LM, Lusher JM, Rothschild C, Ingerslev J; Factor VIII and Factor IX Subcommittee: Definitions in hemophilia. Recommendation of the scientific subcommittee on factor VIII and factor IX of the scientific and standardization committee of the International Society on Thrombosis and Haemostasis.Thromb Haemost 85: 560, 2001.

3. 6) Inoue T, Shima M, Takeyama M, Matsumoto T, Nishiya K, Tanaka I, Sakurai Y, Giddings JC, Yoshioka A: Higher recovery of factor VIII (FVIII) with intermediate FVIII/von Willebrand factor concentrate than with recombinant FVIII in a haemophilia A patient with an inhibitor. Haemophilia 12: 110–113, 2006.

4. 7) Kyrle PA, Minar E, Hirschl M, Bialonczyk C, Stain M, Schneider B, Weltermann A, Speiser W, Lechner K, Eichinger S: High plasma levels of factor VIII and the risk of recurrent venous thromboembolism. N Engl J Med 343: 457–462, 2000.

5. 8) Yoshioka A, Kamisue S, Tanaka I, Kato M, Kohmura I, Shima M, Fukui H: Anamnestic response following infusion of prothrombin complex concentrates (PCC) and activated prothrombin complex concentrates (aPCC) in haemophilia A Patients with inhibitors. Blood coagul Fibrinolysis 2: 51–58, 1991.

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