Have a personal or library account? Click to login
Diagnostic and therapeutic status of haemophilia in Latin America Cover

Diagnostic and therapeutic status of haemophilia in Latin America

Open Access
|Apr 2018

References

  1. 1. Shapiro AD. A global view on prophylaxis: possibilities and consequences. Haemophilia 2003; 9 Suppl 1: 10V7.10.1046/j.1365-2516.9.s1.2.x12709032
  2. 2. Stonebraker JS, Brooker M, Amand RE, et al. A study of reported factor VIII use around the world. Haemophilia 2010; 16W1X: 33V46.10.1111/j.1365-2516.2009.02131.x19845774
  3. 3. MancoVJohnson MJ, Abshire TC, Shapiro AD, et al. Prophylaxis versus episodic treatment to prevent joint disease in boys with severe hemophilia. N Engl J Med 2007; 357W6X: 535V44.
  4. 4. National Hemophilia Foundation Medical Bulletin 1994, 193.
  5. 5. World Health Organization. Report of a joint WHO and WFH Meeting on the control of hemophilia: Modern treatment of hemophilia. WHO; Geneva, 1994.
  6. 6. KruseVJarres R. Inhibitors: our greatest challenge. Can we minimize the incidence? Haemophilia 2013; 19 Suppl 1: 2V7.10.1111/hae.1204923278993
  7. 7. Iorio A, Halimeh S, Holzhauer S, et al. Rate of inhibitor development in previously untreated hemophilia A patients treated with plasmaVderived or recombinant factor VIII concentrates: a systematic review. J Thromb Haemost 2010; 8W6X: 1256V65.10.1111/j.1538-7836.2010.03823.x20345722
  8. 8. Santagostino E, Morfini M, Auerswald GK, et al. Paediatric haemophilia with inhibitors: existing management options, treatment gaps and unmet needs. Haemophilia 2009; 15W5X: 983V9.10.1111/j.1365-2516.2009.01999.x19712172
  9. 9. Rothschild C, Gill J, Scharrer I, Bray G. Transient inhibitors in the Recombinate PUP study. Thromb Haemost 2000; 84W1X: 145V6.10.1055/s-0037-1613988
  10. 10. Lenk H; ITT Study Group. The German Registry of immune tolerance treatment in hemophiliaVV1999 update. Haematologica 2000; 85W10 SupplX: 45V7.
  11. 11. Ettingshausen CE, Kreuz W. The immune tolerance induction WITIX dose debate: does the International ITI Study provide a clearer picture? Haemophilia 2013; 19 Suppl 1: 12V7.10.1111/hae.1205123278995
  12. 12. Brackmann HH, Schwaab R, Effenberger W, et al. Antibodies to factor VIII in hemophilia A patients. Vox Sang 2000; 78 Suppl 2: 187V90.
  13. 13. Ettingshausen CE, Kreuz W. Role of von Willebrand factor in immune tolerance induction. Blood Coagul Fibrinolysis 2005; 16 Suppl 1: S27V31.10.1097/01.mbc.0000167660.30886.e915849524
  14. 14. Kallas A, Talpsep T. von Willebrand factor in factor VIII concentrates protects against neutralization by factor VIII antibodies of haemophilia A patients. Haemophilia 2001; 7W4X: 375V80.10.1046/j.1365-2516.2001.00530.x11442642
  15. 15. Berntorp E. Variation in factor VIII inhibitor reactivity with different commercial factor VIII preparations: is it of clinical importance? Haematologica 2003; 88W6X: EREP03.
  16. 16. Suzuki T, Arai M, Amano K, et al. Factor VIII inhibitor antibodies with C2 domain specificity are less inhibitory to factor VIII complexed with von Willebrand factor. Thromb Haemost 1996;76W5X: 749V54.10.1055/s-0038-1650655
  17. 17. Gensana M, Altisent C, Aznar JA, et al. Influence of von Willebrand factor on the reactivity of human factor VIII inhibitors with factor VIII. Haemophilia 2001; 7W4X: 369V74.10.1046/j.1365-2516.2001.00526.x11442641
  18. 18. Astermark J, Voorberg J, Lenk H, et al. Impact of inhibitor epitope profile on the neutralizing effect against plasmaVderived and recombinant factor VIII concentrates in vitro. Haemophilia 2003; 9W5X: 567V72.10.1046/j.1365-2516.2003.00802.x14511295
  19. 19. Inoue T, Shima M, Takeyama M, et al. Higher recovery of factor VIII WFVIIIX with intermediate FVIII/von Willebrand factor concentrate than with recombinant FVIII in a haemophilia A patient with an inhibitor. Haemophilia 2006; 12W1X: 110V3.10.1111/j.1365-2516.2006.01182.x16409188
  20. 20. Kreuz W, EscuriolaVEttingshausen C, Auerswald G, et al. Immune tolerance induction WITIX in haemophilia A V patients with inhibitors V the choice of concentrate affecting success. Haematologica 2001; 86WS4X: 16V22.
  21. 21. Auerswald G, Spranger T, Brackmann HH. The role of plasmaVderived factor VIII/von Willebrand factor concentrates in the treatment of hemophilia A patients. Haematologica 2003; 88W6X: EREP05.
  22. 22. Colowick AB, Bohn RL, Avorn J, Ewenstein BM. Immune tolerance induction in hemophilia patients with inhibitors: costly can be cheaper. Blood 2000; 96W5X: 1698V702.10.1182/blood.V96.5.1698
  23. 23. Teitel JM, Barnard D, Israels S, et al. Home management of haemophilia. Haemophilia 2004; 10W2X: 118V33.10.1046/j.1365-2516.2003.00853.x14962201
  24. 24. Soucie JM, Symons J 4th, Evatt B, et al. HomeVbased factor infusion therapy and hospitalization for bleeding complications among males with haemophilia. Haemophilia 2001; 7W2X: 198V206.10.1046/j.1365-2516.2001.00484.x11260280
  25. 25. Kurth MA, Dimichele D, Sexauer C, et al. Immune tolerance therapy utilizing factor VIII/von Willebrand factor concentrate in haemophilia A patients with high titre factor VIII inhibitors. Haemophilia 2008; 14W1X: 50V5.
DOI: https://doi.org/10.17225/jhp.00022 | Journal eISSN: 2055-3390
Language: English
Page range: 30 - 34
Published on: Apr 21, 2018
Published by: Haemnet Ltd
In partnership with: Paradigm Publishing Services
Publication frequency: 1 issue per year

© 2018 Cesar Alberto Montaño, Maria Sol Cruz, Felipe Lemos, Alfredo Quiroz, Gerardo Rojas, published by Haemnet Ltd
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 License.