Best Practice & Research Clinical Haematology
Volume 19, Issue 1 , Pages 35-49, March 2006

Clinical uses of plasma and plasma fractions: plasma-derived products for hemophilias A and B, and for von Willebrand disease

  • Cassandra D. Josephson, MD (Assistant Director, Children's Healthcare of Atlanta Blood Banks and Transfusion Services; Assistant Professor, Pathology and Laboratory Medicine and Pediatrics)

      Affiliations

    • Corresponding Author InformationCorresponding author. Tel.: +1 404 785 4553; Fax: +1 404 785 1370.
  • Thomas C. Abshire, MD (Professor of Pediatrics and Director, Comprehensive Hemophilia Program)

Division of Hematology/Oncology/Bone Marrow Transplant, Pathology; Laboratory Medicine; Pediatrics, Emory University School of Medicine, 2015 Uppergate Dr. NE, Atlanta, GA 30322, USA

AFLAC Cancer Center and Blood Disorders Service, Emory University School of Medicine, Atlanta, USA

The use of plasma-derived factor products to treat hemophilia A, hemophilia B, and von Willebrand disease (vWD) has changed since the start of the human immunodeficiency virus (HIV) epidemic. The use of plasma-derived factor concentrates for hemophilias A and B has decreased in developed countries because of the availability of recombinant products. However, in developing countries, which encompass most of the world's hemophilia community, plasma-product-based therapy remains the backbone of treatment because of economic constraints. Viral attenuation strategies have resulted in a much safer product profile. vWD product selection is less complicated than for hemophilas A and B because plasma-derived products are the only choice for patients who are unresponsive or who cannot receive pharmacologic therapy. As the majority of patients in the world with hemophilias A, B and vWD are treated with plasma-derived clotting factors, the need for these safe and efficacious therapies will continue in the future. This chapter discusses safety strategies for plasma-derived clotting factor, its availability, economics, efficacy, and inhibitor formation.

Key words: hemophilia treatment, plasma-derived factor products, viral attenuation

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PII: S1521-6926(05)00032-0

doi:10.1016/j.beha.2005.01.031

Best Practice & Research Clinical Haematology
Volume 19, Issue 1 , Pages 35-49, March 2006