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Ristocetin Cofactor
MessageMust be collected only at the following locations:
Duke Street Lab Testing
Suburban Pavilion Lab Testing
Women and Babies' Hospital Lab Testing
Duke Street Lab Testing
Suburban Pavilion Lab Testing
Women and Babies' Hospital Lab Testing
Test Code
4459
Alias/See Also
RISTO
LAB3020606
LAB3020606
CPT Codes
85245
Preferred Specimen
1 mL frozen platelet-poor plasma collected in a 3.2% sodium citrate (light blue-top) tube
Minimum Volume
0.5 mL
Instructions
Platelet poor plasma: Centrifuge light blue-top tube for 15 minutes at approximately 1500 g within 60 minutes of collection. Using a plastic pipette, remove plasma, taking care to avoid the WBC/platelet buffy layer and place into a plastic vial. Centrifuge a second time and transfer platelet-poor plasma into a new plastic vial. Plasma must be free of platelets (<10,000/mcL). Freeze immediately and ship on dry ice.
Note: Storage of whole blood at refrigerated temperatures prior to processing may lead to cryoprecipitate formation and falsely low Factor VIII and von Willebrand Factor studies.
Note: Storage of whole blood at refrigerated temperatures prior to processing may lead to cryoprecipitate formation and falsely low Factor VIII and von Willebrand Factor studies.
Transport Temperature
Frozen
Specimen Stability
Room temperature: Unacceptable
Refrigerated: Unacceptable
Frozen: 30 days
Refrigerated: Unacceptable
Frozen: 30 days
Reject Criteria (Eg, hemolysis? Lipemia? Thaw/Other?)
Thawed plasma • Received at room temperature or refrigerated • Hemolysis • Lipemia
Methodology
Platelet Agglutination
Setup Schedule
Set up: Mon-Fri; Report available: 2-5 days
Reference Range
42-200 % normal
Clinical Significance
von Willebrand disease is the most common hereditary bleeding disorder. von Willebrand Factor is necessary for platelet adhesion to injured endothelium. Ristocetin cofactor is useful in assessing binding of von Willebrand Factor to platelet factor GP1b. When combined with other tests, results are useful in categorizing the type of von Willebrand disease.