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Recommendations when to order or not order the test. May include related or preferred tests.
Monitor treatment efficacy of low molecular weight heparin.
Methodology
Process(es) used to perform the test.
Chromogenic Assay
Performed
Days of the week the test is performed.
Sun-Sat
Reported
Expected turnaround time for a result, beginning when ARUP has received the specimen.
1-2 days
New York DOH Approval Status
Indicates test has been approved by the New York State Department of Health.
This test is New York DOH approved.
Specimen Required
Patient Preparation
Collect
Lt. blue (sodium citrate). Refer to Specimen Handling at aruplab.com for hemostasis/thrombosis specimen handling guidelines.
Specimen Preparation
Centrifuge specimen within one hour of collection. Transport 2 mL platelet-poor plasma. (Min: 1.5 mL)
Storage/Transport Temperature
Frozen.
Unacceptable Conditions
Serum. EDTA, oxalate, heparin, or plasma separator tubes. Specimens refrigerated more than eight hours. Hemolyzed specimens.
Remarks
This test cannot be used to quantitate anticoagulants other than low molecular weight heparin. This includes, but is not limited to, direct oral anticoagulants and Fondaparinux (Arixtra).
Stability
After separation from cells: Ambient: Unacceptable; Refrigerated: Unacceptable; Frozen: 1 month University of Utah Clients: After separation from cells: Ambient: 4 hours; Refrigerated: 8 hours; Frozen: 2 weeks
Reference Interval
Normal range/expected value(s) for a specific disease state. May also include abnormal ranges.
0.50-1.10 U/mL
Interpretive Data
Background information for test. May include disease information, patient result explanation, recommendations, details of testing, associated diseases, explanation of possible patient results.
Therapeutic range based on enoxaparin brand low molecular weight heparin.
Compliance Category
FDA
Note
Additional information related to the test.
Hotline History
N/A
CPT Codes
The American Medical Association Current Procedural Terminology (CPT) codes published in ARUP's Laboratory Test Directory are provided for informational purposes only. The codes reflect our interpretation of CPT coding requirements based upon AMA guidelines published annually. CPT codes are provided only as guidance to assist clients with billing. ARUP strongly recommends that clients confirm CPT codes with their Medicare administrative contractor, as requirements may differ. CPT coding is the sole responsibility of the billing party. ARUP Laboratories assumes no responsibility for billing errors due to reliance on the CPT codes published.
* Component test codes cannot be used to order tests. The information provided here is not sufficient for interface builds; for a complete test mix, please click the sidebar link to access the Interface Map.
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