Test ID AATTF Antithrombin Activity, with Reflex to Antithrombin Antigen, Plasma
Ordering Guidance
Coagulation testing is highly complex, often requiring the performance of multiple assays and correlation with clinical information. For that reason, consider ordering AATHR / Thrombophilia Profile, Plasma and Whole Blood.
Specimen Required
Specimen Type: Platelet-poor plasma
Collection Container/Tube: Light-blue top (3.2% sodium citrate)
Submission Container/Tube: Plastic vial
Specimen Volume: 1 mL
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, at or below -40° C.
Additional Information:
1. A 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. Heparin treatment may lower plasma antithrombin.
Useful For
Diagnosis of antithrombin deficiency, acquired or congenital
Testing Algorithm
If the activity is abnormal low, then the summary interpretation and antigen will be performed at an additional charge.
Special Instructions
Method Name
Chromogenic Assay
Reporting Name
Antithrombin Activity, w/ Reflex, PSpecimen Type
Plasma Na CitSpecimen Minimum Volume
0.5 mL
Specimen Stability Information
Specimen Type | Temperature | Time | Special Container |
---|---|---|---|
Plasma Na Cit | Frozen | 14 days |
Reference Values
Normal values:
80%-130%
Normal, full-term newborn infants have lower levels (≥35%-40%) that reach normal values by 90 days of age. Premature infants (30-36 weeks gestation) have lower levels that reach normal values by 180 days of age.
Day(s) Performed
Monday through Saturday
Report Available
1 to 3 daysPerforming Laboratory
Mayo Clinic Laboratories in RochesterTest 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
85300 - AATTF
85301 – ATTI (if appropriate)
LOINC Code Information
Test ID | Test Order Name | Order LOINC Value |
---|---|---|
AATTF | Antithrombin Activity, w/ Reflex, P | 27811-9 |
Result ID | Test Result Name | Result LOINC Value |
---|---|---|
AATTF | Antithrombin Activity, w/ Reflex, P | 27811-9 |
NY State Approved
NoReflex Tests
Test ID | Reporting Name | Available Separately | Always Performed |
---|---|---|---|
AATTA | Antithrombin Summary Interp | No | No |
ATTI | Antithrombin Antigen, P | Yes | No |
Forms
If not ordering electronically, complete, print, and send a Coagulation Test Request (T753) with the specimen.