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Von Willebrand's disease is a hereditary deficiency of von Willebrand's factor (VWF), which causes platelet dysfunction. Bleeding tendency is usually mild. Screening tests show a normal platelet count and, possibly, a slightly prolonged PTT. Diagnosis is based on low levels of VWF antigen and abnormal ristocetin cofactor activity. Treatment involves control of bleeding with replacement therapy (cryoprecipitate or pasteurized intermediate-purity factor VIII concentrate) or desmopressin.

Von Willebrand's factor (VWF) is synthesized and secreted by vascular endothelium to form part of the perivascular matrix. VWF promotes the platelet adhesion phase of hemostasis by binding with a receptor on the platelet surface membrane (glycoprotein Ib-IX), which connects the platelets to the vessel wall. VWF is also required to maintain normal plasma factor VIII levels. Levels of VWF can temporarily increase in response to stress, exercise, pregnancy, inflammation, or infection.

Von Willebrand's disease (VWD) is classified into 3 types:

• Type 1: a quantitative deficiency of VWF, which is the most common form and is an autosomal dominant disorder
• Type 2: a qualitative impairment in synthesis of VWF that can result from various genetic abnormalities and is an autosomal dominant disorder
• Type 3: a rare autosomal recessive disorder in which homozygotes have no detectable VWF

Although VWD, like hemophilia A, is a hereditary disorder that may, when severe, cause factor VIII deficiency, the deficiency is usually only moderate.

Symptoms and Signs

Bleeding manifestations are mild to moderate and include easy bruising, mucosal bleeding, bleeding from small skin cuts that may stop and start over hours, sometimes, increased menstrual bleeding; and abnormal bleeding after surgical procedures (eg, tooth extraction, tonsillectomy). Platelets function well enough that petechiae and purpura do not occur.

Diagnosis

• Total plasma VWF antigen, VWF function, and plasma factor VIII level

VWD is suspected in patients with bleeding disorders, particularly those with a family history of the disorder. Screening coagulation tests reveal a normal platelet count; normal INR; and, sometimes, a slightly prolonged PTT. Bleeding time may be prolonged, but this test has poor reproducibility and is of limited value. Diagnosis requires measuring total plasma VWF antigen; VWF function, as determined by the ability of the plasma to support agglutination of normal platelets by ristocetin (ristocetin cofactor activity); and plasma factor VIII level. Stimuli that temporarily increase VWF levels can cause false-negative results in mild VWD; tests may need to be repeated.

In the common (type 1) form of VWD, results are concordant; ie, VWF antigen, VWF function, and plasma factor VIII level are equally depressed. The degree of depression varies from about 15 to 60% of normal and determines the severity of a patient's abnormal bleeding. Levels of VWF antigen can also be as low as 40% of normal in healthy people with type O blood.

Type 2 variants are suspected if tests are discordant, ie, VWF antigen is higher than expected for the degree of abnormality in ristocetin cofactor activity. (VWF antigen is higher than expected because the VWF defect in type 2 is qualitative, not quantitative.) Diagnosis is confirmed by demonstrating a reduced concentration of large VWF multimers on agarose gel electrophoresis. Four different type 2 variants are recognized, distinguished by different functional abnormalities of the VWF molecule.

Patients with type 3 VWD have no detectable VWF and a marked deficiency of factor VIII.

Treatment

• VWF replacement when necessary

Patients are treated only if they are actively bleeding or are undergoing an invasive procedure (eg, surgery, dental extraction). Treatment involves replacement of VWF by infusion of pasteurized intermediate-purity factor VIII concentrates, which contain components of VWF. These concentrates are virally inactivated and therefore do not transmit HIV infection or hepatitis. Because they do not cause transfusion-transmitted infections, these concentrates are preferred to the previously used cryoprecipitate. High-purity factor VIII concentrates are prepared by immunoaffinity chromatography and contain no VWF.

Desmopressin Some Trade Names
DDAVP
STIMATE
Click for Drug Monograph
is an analog of antidiuretic hormone ( vasopressin Some Trade Names
PITRESSIN
Click for Drug Monograph
) that stimulates release of VWF into the plasma and may increase levels of factor VIII. Desmopressin Some Trade Names
DDAVP
STIMATE
Click for Drug Monograph
can be helpful for type 1 VWD but is usually of no value in other types and may even be harmful in some. To ensure adequate response to the drug, physicians give patients a test dose and measure the response of VWF antigen. Desmopressin Some Trade Names
DDAVP
STIMATE
Click for Drug Monograph
0.3μg/kg given in 50 mL 0.9% saline solution IV over 15 to 30 min may enable patients to undergo minor procedures (eg, tooth extraction, minor surgery) without needing replacement therapy. If a replacement product is needed, desmopressin Some Trade Names
DDAVP
STIMATE
Click for Drug Monograph
may reduce the required dose. One dose of desmopressin Some Trade Names
DDAVP
STIMATE
Click for Drug Monograph
is effective for about 8 to 10 h. About 48 h must elapse for new stores of VWF to accumulate, permitting a second injection of desmopressin Some Trade Names
DDAVP
STIMATE
Click for Drug Monograph
to be as effective as the initial dose.

Last full review/revision May 2009 by James N. George, MD

Content last modified May 2009