A von Willebrand factor (vWF) activity – ristocetin cofactor test lets doctors evaluate the functioning of the protein vWF, which helps blood to clot. A clot is a lump of blood that the body produces to prevent excessive bleeding by sealing leaks from blood vessels caused by wounds, cuts, scratches, or other conditions.
The blood's ability to clot is a complex process involving platelets (also called thrombocytes) and proteins called clotting factors. Platelets are oval-shaped cells made in the bone marrow. Most clotting factors are made in the liver. Some, like vWF, are made in blood vessel walls.
When a blood vessel breaks, platelets are first to the area to help seal the leak and temporarily stop or slow bleeding. But for the clot to become strong and stable, the action of clotting factors is required.
The body's clotting factors are numbered using the Roman numerals I through XII. They work together in a specialized sequence, almost like pieces of a puzzle. When the last piece is in place, the clot develops, but if even one piece is missing or defective, the puzzle can't come together.
Von Willebrand factor is involved in the early stages of blood clotting. As the platelets gather at the injury site, vWF acts like glue, helping them stick together to stop the bleeding. Sometimes, though, children are born with an abnormal gene that causes them to produce too little vWF, or a defective version of it. The result is a bleeding disorder called von Willebrand disease.
Variations of von Willebrand disease range from mild to severe. In most cases, the genetic mutation that causes the disease is hereditary, but it may occur spontaneously as well.
Why It's Done
Doctors order the vWF activity – ristocetin cofactor test to help diagnose or monitor the treatment of von Willebrand disease. Symptoms of von Willebrand disease can include easy bruising, frequent nosebleeds, excessive bleeding after a mouth injury or dental work, abnormal menstrual bleeding, or, in infant boys, prolonged bleeding after circumcision. Von Willebrand disease may also be suspected when a child has a family member with a bleeding disorder.
This test is frequently performed along with other tests that give doctors a fuller picture of clotting ability. These may include:
clotting time tests, such as prothrombin time (PT) and partial thromboplastin time (PTT)
the vWF antigen test (which checks blood levels of vWF)
the factor VIII activity test (which checks the amount and functioning of factor VIII, the factor that's missing or defective in the bleeding disorder hemophilia A)
Because factor VIII circulates in the body attached to vWF, a decreased amount of factor VIII can also mean a decreased amount of vWF.
No special preparations are needed for this test. Tell the doctor if your child takes any blood-thinning medications because these may affect the results.
On the day of the test, having your child wear a T-shirt or short-sleeved shirt can make things easier for your child and the technician who will be drawing the blood.
A health professional will usually draw the blood from a vein. If the blood is being drawn from a vein, the skin surface is cleaned with antiseptic, and an elastic band (tourniquet) is placed around the upper arm to apply pressure and cause the veins to swell with blood. A needle is inserted into a vein (usually in the arm inside of the elbow or on the back of the hand) and blood is withdrawn and collected in a vial. A chemical in the vial keeps the blood from clotting before the test begins.
After the procedure, the elastic band is removed. Once the blood has been collected, the needle is removed and the area is covered with cotton or a bandage to stop the bleeding. Collecting blood for this test will only take a few minutes.
What to Expect
Collecting a sample of blood is only temporarily uncomfortable and can feel like a quick pinprick. Afterward, there may be some mild bruising, which should go away in a day or so.
At the lab, the blood cells are separated from the plasma (the liquid part of the blood). Ristocetin, an antibiotic that causes vWF and platelets to stick together, is then added to the plasma. In the presence of ristocetin, blood with adequate vWF clots normally. Blood that's deficient in vWF or has defective vWF won't clot.
Tests results, which are usually available after a few days, are reported as a percentage of what occurs in normal plasma. A low percentage is generally an indication of von Willebrand disease, though further testing may be required.
The vWF activity - ristocetin cofactor test is considered a safe procedure. However, as with many medical tests, some problems can occur with having blood drawn, such as:
fainting or feeling lightheaded
hematoma (blood accumulating under the skin causing a lump or bruise)
pain associated with multiple punctures to locate a vein
Helping Your Child
Having a blood test is relatively painless. Still, many children are afraid of needles. Explaining the test in terms your child can understand might help ease some of the fear.
Allow your child to ask the technician any questions he or she might have. Tell your child to try to relax and stay still during the procedure, as tensing muscles and moving can make it harder and more painful to draw blood. It also may help for your child to look away when the needle is being inserted into the skin.
If You Have Questions
If you have questions about the vWF activity – ristocetin cofactor test, speak with your doctor. You can also talk to the technician before the procedure.