Test Code LAB0204845 Coagulation Factor X Chromogenic Activity Assay, Plasma
Additional Codes
Mayo Test ID |
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FXCH |
Performing Laboratory
Mayo Clinic Laboratories in RochesterUseful For
Monitoring warfarin anticoagulant therapy, especially in patients whose plasma contains lupus anticoagulants that interfere with baseline prothrombin time/international normalized ratio and in patients receiving the drug Argatroban who are being transitioned to warfarin
This assay should not be used for monitoring heparin, or oral direct factor Xa inhibitors such as rivaroxaban (Xarelto), apixaban (Eliquis), or edoxaban (Savaysa).
Special Instructions
Method Name
Chromogenic
Reporting Name
Factor X Chromogenic Activity AssaySpecimen Type
Plasma Na CitSpecimen Required
Patient Preparation: Fasting preferred
Collection Container/Tube: Light-blue top (citrate)
Submission Container/Tube: Polypropylene vial
Specimen Volume: 1 mL
Collection Instructions:
1. For complete instructions see Coagulation Guidelines for Specimen Handling and Processing
2. Spin down, remove plasma, and spin plasma again.
3. 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.
3. If priority specimen, mark request form, give reason, and request a call-back.
Freeze plasma within 2 hours of collection and submit frozen.
Specimen Minimum Volume
0.5 mL
Specimen Stability Information
Specimen Type | Temperature | Time | Special Container |
---|---|---|---|
Plasma Na Cit | Frozen | 14 days |
Reject Due To
Gross hemolysis | Reject |
Gross lipemia | Reject |
Gross icterus | Reject |
Reference Values
≥18 years of age: 60%-140%
Chromogenic Factor X activity generally correlates with the one-stage factor X activity. In full term or premature neonates, infants, and children, the one-stage factor X activity* is lower than adult reference range and progressively rises to the adult reference range by adolescence. However, no similar data for the chromogenic factor X activity have been published.
*See Pediatric Hemostasis References section in Coagulation Guidelines for Specimen Handling and Processing.
Interpretation
A chromogenic factor X activity of approximately 20% to 40% corresponds to the usual warfarin international normalized ratio range (ie, 2.0-3.0).
Day(s) Performed
Monday through Friday
Report Available
1 to 3 daysSpecimen Retention Time
7 daysTest Classification
This test has been modified from the manufacturer's instructions. Its performance characteristics were determined by Mayo Clinic in a manner consistent with CLIA requirements. This test has not been cleared or approved by the US Food and Drug Administration.CPT Code Information
85260
LOINC Code Information
Test ID | Test Order Name | Order LOINC Value |
---|---|---|
FXCH | Factor X Chromogenic Activity Assay | 33984-6 |
Result ID | Test Result Name | Result LOINC Value |
---|---|---|
FXCH | Factor X Chromogenic Activity Assay | 33984-6 |
Forms
If not ordering electronically, complete, print, and send a Coagulation Test Request (T753) with the specimen.