Figure 1.
Figure 1. Model for the relationship of von Willebrand factor (VWF) level to risk of bleeding, thrombosis, and VWF mutations. The thick solid line indicates the frequency distribution of VWF levels (IU/dL) for the population, and 95% of values lie between 50 IU/dL and 200 IU/dL. Also shown are estimates of the relative risk of bleeding (short-dashed line, magenta shading), thrombosis (long-dashed line, green shading), and mutation within the VWF gene (thin solid line, orange shading) as a function of VWF level; the relative risk is defined as 1.0 at the population mean VWF level of 100 IU/dL. As indicated at the top, VWF levels < 20 IU/dL are generally consistent with a diagnosis of VWD type 1, low VWF levels (30 to 50 IU/dL) confer a modest risk of bleeding, and high VWF levels (> 200 IU/dL) confer a modest risk of thrombosis.

Model for the relationship of von Willebrand factor (VWF) level to risk of bleeding, thrombosis, andVWFmutations. The thick solid line indicates the frequency distribution of VWF levels (IU/dL) for the population, and 95% of values lie between 50 IU/dL and 200 IU/dL. Also shown are estimates of the relative risk of bleeding (short-dashed line, magenta shading), thrombosis (long-dashed line, green shading), and mutation within the VWF gene (thin solid line, orange shading) as a function of VWF level; the relative risk is defined as 1.0 at the population mean VWF level of 100 IU/dL. As indicated at the top, VWF levels < 20 IU/dL are generally consistent with a diagnosis of VWD type 1, low VWF levels (30 to 50 IU/dL) confer a modest risk of bleeding, and high VWF levels (> 200 IU/dL) confer a modest risk of thrombosis.

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