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HelpTest Code HEPTP Heparin Anti-Xa, Plasma
Useful For
Measuring heparin concentration:
-In patients treated with low-molecular-weight heparin preparations
-In the presence of prolonged baseline activated partial thromboplastin time (APTT) (eg, lupus anticoagulant, "contact factor" deficiency, etc)
-When unfractionated heparin dose needed to achieve desired APTT prolongation is unexpectedly higher (>50%) than expected
This test is not useful for monitoring therapy with the heparinoid "danaparoid."
Method Name
Chromogenic Method
Reporting Name
Heparin Anti-Xa, PSpecimen Type
Plasma Na CitOrdering Guidance
To test for the presence of inhibitors directed against factor X (FX), order 10INE / Factor X Inhibitor Evaluation, Plasma.
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, aliquot plasma, and centrifuge plasma again.
4. Aliquot plasma into a plastic vial leaving 0.25 mL in the bottom of centrifuged vial.
Additional Information: Double-centrifuged specimen is critical for accurate results as platelet contamination may cause spurious results.
Specimen Minimum Volume
0.5 mL
Specimen Stability Information
| Specimen Type | Temperature | Time | Special Container |
|---|---|---|---|
| Plasma Na Cit | Frozen (preferred) | 14 days | |
| Ambient | 2 hours |
Reject Due To
| Gross hemolysis | Reject |
| Gross lipemia | OK |
| Gross icterus | OK |
Clinical Information
Heparins are sulphated glycosaminoglycans that inactivate thrombin, factor Xa, and several other coagulation factors; act by enhancing activity of the plasma coagulation inhibitor, antithrombin III; and prolong the activated partial thromboplastin time (APTT). The anti-Xa assay is the preferred method for monitoring low-molecular-weight heparin (LMWH) therapy because of reduced sensitivity of APTT. Heparin is absent in normal plasma. The heparin level obtained must be analyzed in the context of the treatment given to the patient (type of heparin, dosage, administration mode, time of sampling, etc) and the desired therapeutic effect. It is clinically recommended that platelet counts be monitored frequently in patients receiving unfractionated heparin or LMWH in order to detect heparin-induced thrombocytopenia.
Reference Values
Adult Therapeutic Range
UFH therapeutic range: 0.30-0.70 IU/mL
(6 hours following initiation or dose adjustment)
LMWH therapeutic range: 0.50-1.00 IU/mL for twice daily dosing*
LMWH therapeutic range: 1.00-2.00 IU/mL for once daily dosing*
LMWH prophylactic range: 0.10-0.30 IU/mL
*Sample obtained 4 to 6 hours following subcutaneous injection
Interpretation
Results above the therapeutic range may be supratherapeutic suggesting that the heparin dose may need to be decreased.
Results below the therapeutic range may be subtherapeutic suggesting that the heparin dose may need to be increased.
Day(s) Performed
Monday through Sunday
Report Available
Same day/1 daySpecimen Retention Time
1 dayPerforming Laboratory
Mayo Clinic Laboratories in Rochester
Test Classification
This test has been cleared, approved, or is exempt by the US Food and Drug Administration and is used per manufacturer's instructions. Performance characteristics were verified by Mayo Clinic in a manner consistent with CLIA requirements.CPT Code Information
85520
LOINC Code Information
| Test ID | Test Order Name | Order LOINC Value |
|---|---|---|
| HEPTP | Heparin Anti-Xa, P | 3274-8 |
| Result ID | Test Result Name | Result LOINC Value |
|---|---|---|
| HEPTP | Heparin Anti-Xa, P | 3274-8 |