Molecular Diagnostics | Factor V (5) (Leiden) Gene Mutation by PCR

UWHC Lab Test Details
Test NameFactor V (5) (Leiden) Gene Mutation by PCR
Test Code(s)XFAC5, FVPCR
Approval RequiredTesting request needs faculty review. Contact the UWHC Test Referral Office at (608)262-6388 prior to collection.
CPT Code(s)81241
MethodologyReal-Time PCR followed by Melting Point Analysis
Clinical Information

Factor V (5) 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 (5) 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.

Testing SiteUniversity Hospital
Days PerformedOnce a week.
In-Lab Turnaround Time10 days.
Stat In-Lab Turnaround TimeNot available stat.
Collection Requirements
SpecimenBlood
Collection Container
Collection ContainerLavender top
Also AcceptableLight blue top (3.2% NaCitrate)
Collection Instructions

A documented prior authorization will need to be present in Health Link before testing can be performed. 

The ordering source should consult the Genetic Testing at UW Health Clinical Laboratories document on U-Connect prior to ordering testing. Contact UWHC Referral office at (608) 262-6388 for questions. 

Collection Volume4 mL
Pediatric Collection Volume2 mL
Specimen Processing Requirements
Stability
Stability Ambient

7 days

Stability Refrigerated

3 weeks

Stability Frozen

Not acceptable

Sample AnalyzedWhole Blood
Testing Volume2 mL
Pediatric Testing Volume1.2 mL
Specimen Processing

Do not centrifuge or freeze sample.

Outreach Specimen Processing

Refrigerate specimen. Do not freeze or centrifuge.

Specimen 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.

Interpretation

A written interpretive report is provided by the laboratory.

Additional Information

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.

 

 The results are not intended to be used as the sole means for clinical diagnosis or patient management decisions. The UWHC Clinical Laboratories is authorized under Clinical Laboratory Improvement Amendments (CLIA) to perform high-complexity testing.

 

A professional fee is associated with this test.(CPT Code G0452)