Epic Test Code LAB310 Coagulation Factor XII Activity Assay, Plasma
Additional Codes
MML Code: F_12
NY State Approved
YesPerforming Laboratory
Mayo Clinic Laboratories in RochesterReporting Name
Coag Factor XII Assay, PMethod Name
Optical Clot-Based
Specimen Stability Information
Specimen Type | Temperature | Time | Special Container |
---|---|---|---|
Plasma Na Cit | Frozen | 14 days |
Ordering Guidance
Coagulation testing is highly complex, often requiring the performance of multiple assays and correlation with clinical information. For that reason, consider ordering a Coagulation Consultation.
Necessary Information
If priority specimen, mark request form, give reason, and request a call-back.
Specimen Required
Specimen Type: Platelet-poor plasma
Patient Preparation: Patient must not be receiving Coumadin (warfarin) or heparin therapy.
Collection Container/Tube: Light-blue top (3.2% sodium citrate)
Submission Container/Tube: Plastic vial
Specimen Volume: 1 mL
Collection Instructions:
1. Specimen must be collected prior to factor replacement therapy
2. For complete instructions, see Coagulation Guidelines for Specimen Handling and Processing.
3. Centrifuge, transfer all plasma into a plastic vial, and centrifuge plasma again.
4. Aliquot plasma into a plastic vial, leaving 0.25 mL in the bottom of centrifuged vial.
5. Freeze plasma immediately (no longer than 4 hours after collection) at -20° C or ideally, at or below -40° C.
Additional Information:
1. Double-centrifuged specimen is critical for accurate results as platelet contamination may cause spurious results.
2. Each coagulation assay requested should have its own vial.
Blood Tube Draw Volume
Min 90% draw volume
Specimen Type
Plasma Na CitSpecimen Minimum Volume
0.5 mL
Reference Values
Adults: 55-180%
Normal, full-term newborn infants or healthy premature infants may have decreased levels (≥15% to 20%), which may not reach adult levels for 180 or more days postnatal.*
*See Pediatric Hemostasis References section in Coagulation Guidelines for Specimen Handling and Processing.
Report Available
1 to 3 daysDay(s) Performed
Monday through Saturday
CPT Code Information
85280
Reject Due To
Gross hemolysis | Reject |
Gross lipemia | Reject |
Gross icterus | Reject |
Useful For
Diagnosing deficiency of coagulation factor XII
Determining cause of prolonged activated partial thromboplastin time
Special Instructions
Clinical Information
Factor XII is synthesized in the liver. Its biological half-life is 40 to 50 hours. Factor XII is a component of the contact activation system and is involved in both intrinsic pathway and fibrinolytic system.
Factor XII deficiency is often discovered when activated partial thromboplastin time is found to be unexpectedly long. The deficiency does not cause a known bleeding disorder.
An association between severe factor XII deficiency and thrombosis risk has been proposed but not proven.
Interpretation
Acquired deficiency is associated with liver disease, nephritic syndrome, and chronic granulocytic leukemia.
Congenital homozygous deficiency: 20% activity
Congenital heterozygous deficiency: 20% to 50% activity
Cautions
Deficiencies of other contact activator proteins (prekallikrein, high molecular weight kininogen) can also cause prolonged activated partial thromboplastin time but do not cause clinical bleeding.
Specimen Retention Time
7 daysForms
If not ordering electronically, complete, print, and send a Coagulation Test Request (T753) with the specimen.