Heparin, Anti‑Xa
Also known as: Heparin Anti-Xa (LMWH)
Use
This assay measures heparin levels by detecting inhibition of factor Xa via the heparin‑antithrombin III complex using a chromogenic substrate. It is calibrated to both unfractionated heparin (UFH) and low molecular weight heparin (LMWH), allowing monitoring of either therapy. Peak anti‑Xa levels for LMWH dosing (e.g., enoxaparin 1 mg/kg q12h) are typically 0.5–1 IU/mL; for q24h dosing of LMWHs (e.g., enoxaparin 1.5 mg/kg q24h), levels are 1–2 IU/mL, sampled approximately 4 hours post‑dose after steady state. UFH monitoring timing depends on local hospital protocols, often ~6 hours after dosage change, recognizing potential delays when samples are sent to Quest laboratories.
Special Instructions
Not provided.
Limitations
Any medication with anti‑Xa activity—such as fondaparinux, rivaroxaban, apixaban, or edoxaban—can interfere with the assay. Additionally, routine LMWH monitoring is generally not recommended, and UFH testing may be delayed due to shipping and processing timelines.
Methodology
Other
Biomarkers
LOINC Codes
- 3271-4
Result Turnaround Time
1 day
Related Documents
For more information, please review the documents below
Specimen
Plasma
Volume
2 mL
Minimum Volume
1 mL
Container
3.2% sodium citrate (light blue‑top) tube
Collection Instructions
Collect platelet‑poor plasma: centrifuge light blue‑top tube 15 minutes at approximately 1500 g within 60 minutes of collection; remove plasma avoiding buffy layer; centrifuge again; transfer platelet‑poor plasma (<10 000 platelets/µL) into plastic vial; freeze immediately and ship on dry ice.
Storage Instructions
Frozen; maintain cold chain, ship on dry ice.
Causes for Rejection
Hemolysis; specimen received at room temperature or refrigerated
Stability Requirements
| Temperature | Period |
|---|---|
| Room Temperature | Unacceptable |
| Refrigerated | Unacceptable |
| Frozen | 30 days |
