Factor V Leiden Gene Mutation Analysis [FVPCR]

Factor V Leiden Gene Mutation Analysis [FVPCR]
WSLH Department: Cytogenetics
WSLH Test Code:842C90
CPT Code:81241
Price:For pricing information, please call 608-262-0402.
Includes:Test Component:
Factor V Leiden gene mutation analysis by real-time PCR amplification and melting point analysis. Factor V Leiden Gene Mutation Analysis is useful for confirming the diagnosis of resistance to APC as identified by functional coagulation testing. It can also be used to establish the diagnosis of resistance to APC in patients in whom functional coagulation testing may not be feasible, for example, patients on anticoagulant therapy (especially heparin) or positive for Lupus anticoagulants. Usually ordered with the Factor V is a test for the Prothrombin G20210A allele, which has been associated with elevated plasma prothrombin levels and moderately increased risk of first venous thrombotic events.
Methodology:**(CPT Code: 81241)** Real-Time PCR followed by Melting Point Analysis
Availability:Once a week.
Turn-around Time:10 Days
Recommended Uses:Blood
Specimen Requirements:4 mL, (2 mL pediatric)
Lavender top
Also Acceptable: Light blue top (3.2% NaCitrate)
Collection Kit/Container: 
Patient Preparation: 
Collection Instructions:Stability Ambient:
7 days,
Stability Refrigerated:
3 weeks
Specimen Handling and Transport:Transport specimen to Laboratory immediately. Refrigerate specimen if not delivered immediately. Transport specimen with coolant pack if coming from clinic location; avoid freezing. Specimen must be received within 7 days of collection date.
Unacceptable Conditions:Frozen:
Not acceptable
Requisition Form:Cytogenetics Lab Genetic Diagnosis Form #131
Required Information: 
Results include:A written interpretive report is provided by the laboratory.
Additional Tests Recommended: 
Additional Comments:This test was performed using a modification of an FDA approved method. The performance characteristics of this test were determined by the UWHC Clinical Laboratories and meet the standards for clinical testing.
Additional Tests Performed: 

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