Test Code 13ACT Coagulation Factor XIII (13) Activity Assay, Plasma
Ordering Guidance
Coagulation testing is highly complex, often requiring the performance and correlation of factor XIII activity with multiple assays and correlation with clinical information. For that reason, if indicated, consider ordering ALBLD / Bleeding Diathesis Profile, Limited, Plasma.
Specimen Required
Patient Preparation:
1. Fasting: 8 hours, preferred but not required
2. It is best to perform this study pre-plasma transfusion if possible. If patient has been recently transfused, wait at least 48 hours after transfusion before collecting the specimen.
3. Specimen should be collected prior to factor replacement therapy.
Collection Container/Tube: Light-blue top (3.2% sodium citrate)
Submission Container/Tube: Plastic vial
Specimen Volume: 1 mL Platelet-poor plasma
Collection Instructions:
1. For complete instructions, see Coagulation Guidelines for Specimen Handling and Processing.
2. Centrifuge, transfer all plasma into a plastic vial, and centrifuge plasma again.
3. Aliquot plasma into a plastic vial, leaving 0.25 mL in the bottom of centrifuged vial.
4. Freeze plasma immediately (no longer than 4 hours after collection) at -20° C or, ideally, -40° C or below.
Additional Information:
1. Double-centrifuged specimen is critical for accurate results.
2. Each coagulation assay requested should have its own vial.
Useful For
Measuring factor XIII activity
Special Instructions
Method Name
Fluorescence-Based Enzyme Activity
Reporting Name
Factor XIII(13) Activity, PSpecimen Type
Plasma Na CitSpecimen Minimum Volume
Platelet-poor plasma: 0.5 mL
Specimen Stability Information
| Specimen Type | Temperature | Time |
|---|---|---|
| Plasma Na Cit | Frozen | 180 days |
Reference Values
≥55%
Day(s) Performed
Monday through Friday
Report Available
1 to 8 daysPerforming Laboratory
Mayo Clinic Laboratories in Rochester
Test Classification
This test was developed and its performance characteristics determined by Mayo Clinic in a manner consistent with CLIA requirements. It has not been cleared or approved by the US Food and Drug Administration.CPT Code Information
85290
LOINC Code Information
| Test ID | Test Order Name | Order LOINC Value |
|---|---|---|
| 13ACT | Factor XIII(13) Activity, P | In Process |
| Result ID | Test Result Name | Result LOINC Value |
|---|---|---|
| 623415 | Factor XIII (13) Activity, P | In Process |
Forms
If not ordering electronically, complete, print, and send an Coagulation Test Request (T753) with the specimen.