Hemophilia is primarily treated with recombinant or plasma-derived products to replace missing clotting factors and prevent or treat bleeding. Patients with severe forms of von Willebrand's disease or those requiring major surgery may need replacement therapy with plasma-derived factor VIII concentrate containing von Willebrand factor. Recessively inherited coagulation disorders are typically treated with single-donor fresh frozen plasma containing all clotting factors. Treatment of disseminated intravascular coagulation focuses on the underlying cause, with supportive measures used depending on symptoms of bleeding or clotting.
Hemophilia is primarily treated with recombinant or plasma-derived products to replace missing clotting factors and prevent or treat bleeding. Patients with severe forms of von Willebrand's disease or those requiring major surgery may need replacement therapy with plasma-derived factor VIII concentrate containing von Willebrand factor. Recessively inherited coagulation disorders are typically treated with single-donor fresh frozen plasma containing all clotting factors. Treatment of disseminated intravascular coagulation focuses on the underlying cause, with supportive measures used depending on symptoms of bleeding or clotting.
Hemophilia is primarily treated with recombinant or plasma-derived products to replace missing clotting factors and prevent or treat bleeding. Patients with severe forms of von Willebrand's disease or those requiring major surgery may need replacement therapy with plasma-derived factor VIII concentrate containing von Willebrand factor. Recessively inherited coagulation disorders are typically treated with single-donor fresh frozen plasma containing all clotting factors. Treatment of disseminated intravascular coagulation focuses on the underlying cause, with supportive measures used depending on symptoms of bleeding or clotting.
1 IV replacement with recombinant or plasma-derived
products to treat or prevent bleeding is the primary treatment of hemophilia. 2 Patients with type 1 von Willebrands disease (vWD) unresponsive to desmopressin, patients with types 2 and 3 vWD, and major surgery patients require replacement therapy with plasma-derived intermediate- and high-purity factor VIII, virus-inactivated factor VIII concentrate containing von Willebrands factor (vWF). 3 The primary treatment of recessively inherited coagulation disorders (RICDs) is single-donor freshfrozen plasma (FFP) that contains all coagulation factors. 4 The cornerstone of the management of disseminated intravascular coagulation (DIC) is aggressive treatment of the underlying primary illness. Supportive measures may be used as necessary; however, owing to the heterogeneity of the DIC etiology, treatment should be guided by predominant symptoms (bleeding or clotting).