Skip Ribbon Commands
Skip to main content
Sign In

25571 Factor X Chromogenic Activity Assay, Plasma (FXCH)

Factor X Chromogenic Activity Assay, Plasma (FXCH)
Test Code: FXCHSO
Useful For
Monitoring oral anticoagulant therapy, especially in patients whose plasma contains lupus anticoagulants and in patients receiving the drug Argatroban
Specimen Requirements
Fasting Required Specimen Type Preferred Container/Tube Acceptable Container/Tube Specimen Volume
​No ​Platelet-poor Plasma ​Citrate Blue Top Tube (BTT) ​1 mL
Collection Processing Instructions

Spin down, remove plasma, and spin plasma again.
Freeze specimen immediately at < or =-40 degrees C, if possible. 
Double-centrifuged specimen is critical for accurate results as platelet contamination may cause spurious results.
Each coagulation assay requested should have its own vial.

Specimen Stability Information
Specimen Type Temperature Time
​Plasma ​Frozen ​14 days
Interference
Liver disease and vitamin K deficiency may lower factor X levels. If factor X deficiency is suspected, order F_10/9066 Coagulation Factor X Activity Assay, Plasma.
Performing Laboratory Information
Performing Location Day(s) Test Performed Analytical Time Methodology/Instrumentation
​Mayo Medical Laboratories ​Monday through Friday ​7 days ​Chromogenic Coagulation Study
Reference Lab
Test Information

The antithrombotic effect of oral vitamin K antagonists (eg, warfarin) is mediated by reduction in the plasma activity of vitamin K-dependent procoagulant factors II (prothrombin) and X. The intensity of oral anticoagulation therapy with vitamin K antagonists must be monitored and adjusted to a narrow therapeutic range; undermedicating increases the risk of thrombosis, while overmedicating increases the risk of bleeding. Such therapy typically is monitored with the prothrombin time/international normalized ratio (INR) system.

Lupus anticoagulants (LAC) are autoantibodies that interfere with phospholipid-dependent clotting tests and most commonly cause prolongation of the activated partial thromboplastin time (APTT). LAC can be associated with a prothrombotic disorder termed the antiphospholipid syndrome. LAC occasionally may cause prolongation of the baseline prothrombin time, rendering the INR system inaccurate for monitoring the intensity of oral anticoagulant therapy. LAC-induced prolongation of the prothrombin time is most commonly seen with recombinant human tissue factor thromboplastins (ie, prothrombin time reagents) with a low international sensitivity index (ISI) such as Innovin (ISI = 1.0). The chromogenic factor X activity is an alternative assay for monitoring oral anticoagulant therapy. This assay is unaffected by LAC because the assay end point is not a phospholipid-dependent clotting time.

Argatroban is a parenteral direct thrombin inhibitor that is approved for treatment of heparin-induced thrombocytopenia (HIT), an antibody-mediated prothrombotic disorder. Argatroban therapy prolongs the prothrombin time, which also renders the INR inaccurate for monitoring the warfarin effect while transitioning from Argatroban to oral anticoagulant therapy. The chromogenic coagulation factor X activity assay may be used as an alternative to the INR for monitoring and adjusting the warfarin dose during this transition.

Reference Range Information
60-140%
Interpretation
A chromogenic factor X activity of approximately 20% to 35% corresponds to the usual warfarin therapeutic INR range (ie, INR = 2.0-3.0).
Outreach CPTs
CPT Modifier
(if needed)
Quantity Description Comments
​85260
Ordering Applications
Ordering Application Description
If the ordering application you are looking for is not listed, contact your local laboratory for assistance.
Specimen Requirements
Fasting Required Specimen Type Preferred Container/Tube Acceptable Container/Tube Specimen Volume
​No ​Platelet-poor Plasma ​Citrate Blue Top Tube (BTT) ​1 mL
Collection Processing

Spin down, remove plasma, and spin plasma again.
Freeze specimen immediately at < or =-40 degrees C, if possible. 
Double-centrifuged specimen is critical for accurate results as platelet contamination may cause spurious results.
Each coagulation assay requested should have its own vial.

Specimen Stability Information
Specimen Type Temperature Time
​Plasma ​Frozen ​14 days
Interference
Liver disease and vitamin K deficiency may lower factor X levels. If factor X deficiency is suspected, order F_10/9066 Coagulation Factor X Activity Assay, Plasma.
Useful For
Monitoring oral anticoagulant therapy, especially in patients whose plasma contains lupus anticoagulants and in patients receiving the drug Argatroban
Reference Range Information
60-140%
Interpretation
A chromogenic factor X activity of approximately 20% to 35% corresponds to the usual warfarin therapeutic INR range (ie, INR = 2.0-3.0).
For more information visit:
Performing Laboratory Information
Performing Location Day(s) Test Performed Analytical Time Methodology/Instrumentation
​Mayo Medical Laboratories ​Monday through Friday ​7 days ​Chromogenic Coagulation Study
Reference Lab
For billing questions, see Contacts
Outreach CPTs
CPT Modifier
(if needed)
Quantity Description Comments
​85260
For most current information refer to the Marshfield Laboratory online reference manual.