Von Willebrand disease is the most common inherited bleeding disorder. Recent studies estimate the incidence at 1-2% of the general population. Since it is inherited in an autosomal dominant fashion, males and females are equally affected. Von Willebrand disease is associated with mucous membrane bleeding, excessive bruising, and bleeding from cuts. It can result in excessive bleeding with invasive dental work, during surgical procedures, and after accident or injury. In women, excessive menstrual bleeding is often the major symptom. Women with von Willebrand disease are also at risk of postpartum hemorrhage, particularly delayed postpartum hemorrhage.
Recently developed products have changed the treatment options for individuals with von Willebrand disease. The following are current recommendations for treating bleeding in these individuals.
1. Persons with type 1 von Willebrand disease should be treated with the synthetic agent desmopressin (DDAVP Injectable or Stimate Nasal Spray for Bleeding, 1.5 mg/ml), and their response at first use should be documented for future reference (DDAVP trial). For surgery, trauma, or other serious bleeding episodes, if hemostasis is not achieved with DDAVP, a factor VIII concentrate rich in the high molecular weight multimers of von Willebrand factor should be used (see #3 below).
2. Persons with type 2A, 2M, and 2N von Willebrand disease should be treated with DDAVP if they have been shown by a DDAVP trial to be responsive.
3. Persons with type 2B and type 3 von Willebrand disease, and those with type 1, 2A, 2M, and 2N who have been shown to be nonresponsive to DDAVP, should be treated with a factor VIII concentrate that is known to contain the higher molecular weight multimers of von Willebrand factor and that has been virally attenuated to eliminate transmission of HIV and hepatitis A, B, and C. Alphanate (Grifols), Humate P (CSL-Behring), and Wilate (Octapharma) have been approved by the FDA for use in VWD. Koate DVI (Talecris) may also be effective in these patients, but it has not been approved by the FDA for use in von Willebrand disease. For further information, see MASAC Document #195, MASAC Recommendations Concerning Products Licensed for the Treatment of Hemophilia and Other Bleeding Disorders Revised April 2010.
4. Because of the increased risk of HIV and hepatitis A, B, and C transmission, cryoprecipitate should not be used except in an emergency situation where one of the above-mentioned products is not available and delay of treatment would be life- or limb-threatening.
5. Desmopressin is a potent antidiuretic agent, and fluid retention is a potential complication of this drug. Both parenterally administered DDAVP and Stimate Nasal Spray have been associated with the development of hyponatremia and seizures. To minimize this risk, the following precautions should be observed when this drug is used at home:
a. DDAVP and Stimate should be administered no more often than once every 24 hours.
b. DDAVP and Stimate should be used for no more than three consecutive days unless directed to do so by Hemophilia Treatment Center medical staff.
c. DDAVP and Stimate should not be used in children under the age of two years.
d. DDAVP and Stimate should be used with caution in the elderly and in individuals with a history of heart disease, hypertension, or stroke.
e. If a patient is treated with DDAVP before surgery, the anesthesiologist should be advised to avoid fluid overload and dilutional hyponatremia.
f. DDAVP should be used with caution in pregnant women in the peripartum and immediate postpartum period with careful attention to fluid management so as to avoid hyponatremia.
6. An adjunctive treatment for mucous membrane bleeding is the antifibrinolytic agent amino- caproic acid (Amicar). This agent can be given orally or intravenously.
7. Prior to surgery in a patient with von Willebrand disease, consultation should be obtained with a pediatric or adult hematologist who specializes in the management of individuals with inherited bleeding disorders. This consultation should cover such issues as the need for a DDAVP stimulation test; type of fluid replacement/fluid restriction; dose and duration if DDAVP is to be used; appropriate dose, timing, and duration of factor replacement therapy; and use of adjunctive medications (Amicar).
1. Mannucci PM. Desmopressin (DDAVP) for treatment of disorders of hemostasis. Prog Hemost Thromb 1986; -45.
2. Mannucci PM, Canciani MT, Rota L, Donovan BS. Response of factor VIII/von Willebrand factor to DDAVP in healthy subjects and patients with haemophilia A and von Willebrand disease. Br J Haematol 1981; 47: 283-93.
3. Mannucci PM, Lusher JM. Desmopressin and thrombosis. Lancet 1989; 2: 675-6.
4. Nilsson IM, Hethagen S. Current status of DDAVP formulations and their use. In Lusher JM, Kessler CM, eds. Hemophilia and von Willebrand disease in the 1990’s. International Congress Series/Excerpta Medica 1991; 943: 443-53.
This material is provided for your general information only. NHF does not give medical advice or engage in the practice of medicine. NHF under no circumstances recommends particular treatment for specific individuals and in all cases recommends that you consult your physician or local treatment center before pursuing any course of treatment.
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