Test Code AXAPIX Anti Xa DOAC (Apixaban)
Clinical Information
The Apixaban assay is a chromogenic assay for the determination of the activity of Apixaban (Eliquis) in plasma and for the monitoring of Apixaban therapy.
Synonym
- AXAPIX
- Eliquis
Specimen Required
Preferred Container/Tube: 3.2% Citrate Blue Top - 2.7 mL
Specimen Volume: 2.7 mL
Acceptable Container/Tube: 3.2% Citrate Blue Top - 1.8 mL
Specimen Volume: 1.8 mL
Platelet poor plasma (PPP):
Specimen Volume: 2 - 1 mL aliquots platelet poor plasma (PPP)
Specimen Minimum Volume: 1 - 1 mL aliquot platelet poor plasma (PPP)
Specimen Collection Information
For Outreach, other than OSU Patient Service Centers: Samples must be processed and received frozen/must remain frozen in transit.
For sending frozen plasma specimens, process immediately upon receipt. Centrifuge capped specimen tube in accordance with CLSI H21, at a speed and time required to consistently produce platelet-poor plasma (PPP = platelet count <10 K/uL). Transfer PPP into plastic aliquot tubes, cap and freeze. DO NOT transport until specimens are completely frozen.
Specimen Stability Information
Ambient:
Whole blood: 3 hours
Platelet poor plasma: 6 hours
Frozen:
Platelet poor plasma: PPP removed from the cells and frozen at -20°C or ideally -70°C.
Rejected Due To
- Ambient WB specimens >3 hours old
- Ambient PPP specimens >6 hours old
- Clotted specimens
- Underfilled or overfilled tube
- Hemolysis
- Icterus
- Lipemia
Interpretation
Therapeutic reference ranges have not been established. At steady state - median (5th-95th percentile) peak and trough levels have been observed in clinical trials:
VTE prevention after total hip replacement
Peak Concentration, ng/mL (a) | Trough Concentration, ng/mL (b) | |
---|---|---|
2.5 mg twice daily | 77 (41-146) | 51 (23-109) |
Stroke and systemic embolism prevention in patients with AF
Peak Concentration, ng/mL (a) | Trough Concentration, ng/mL (b) | |
---|---|---|
2.5 mg twice daily | 123 (69-221) | 79 (34-162) |
5 mg twice daily | 171 (91-321) | 103 (41-230) |
Prevention and treatment of DVT and PE
Peak Concentration, ng/mL (a) | Trough Concentration, ng/mL (b) | |
---|---|---|
2.5 mg twice daily | 67 (30-153) | 32 (11-90) |
5 mg twice daily | 132 (59-302) | 63 (22-77) |
10 mg twice daily | 251 (111-572) | 120 (41-335) |
(a) Defined as samples collected 2-4 hours after dosing
(b) Defined as samples collected 10-12 hours after dosing
AF-atrial fibrillation, CR-CL-creatinine clearance, DVT-deep vein thrombosis, VTE-venous thromboembolism
Method Description
Chromogenic measurement at 405nm
Test Classification
This test has been modified from the manufacturer's instructions. Its performance characteristics were determined by The Ohio State University in a manner consistent with CLIA requirements. This test has not been cleared or approved by the U.S. Food and Drug Administration.
Performing Lab
Clinical Lab UH
Day(s) Performed
Monday through Sunday
Report Available
Same day/1 day
Reporting Name
Anti Xa DOAC (Apixaban)
CPT Code Information
80299