Methotrexate Level

Test Code
MTRX


CPT Codes
80299

Preferred Specimen
PST GREEN


Minimum Volume
2. mL plasma


Other Acceptable Specimens
Serum or plasma is the recomended specimen. Whole blood cannot be used. The anticoagulants heparin, EDTA, and oxalate may be used with this assay.
Plasma and serum should be separated from the cells by centrifugation within 2 hours of collection. Specimens are stable in capped tubes at room temperature (15-25oC) for 3 days


Instructions
Store the serum or plasma refrigerated at 2-8°C and protected from light (methotrexate in solution is light sensitive) for up to 7 days. For transporting, maintain the sample temperature at 2-8°C and protect from light. Methotrexate is stable for 3 days at room temperature (15-25°C) and up to 6 months in the dark frozen at ≤-20°C.


Methodology
The Emit® Methotrexate is a homogeneous enzyme immunoassay intended for use in vitro diagnostic use in the quantitative determination of methotrexate in human serum or plasma (heparin, EDTA, or oxalate).

Setup Schedule
24x7


Limitations
Analytical Range:  0.02-26000 umol/L


Reference Range
Reference Range:
       <10.00 umol/L at 24 hours
       <1.00  umol/L at 48 hours
       <0.20  umol/L at 72 hours
Information is for high dose methotrexate in the setting of Leucovorin rescue with normal methotrexate elimination. Specific treatment protocols may call for differing target drug levels. Reference range is from Methotrexate FDA Safety Information (updated 2016).


Clinical Significance
Methotrexate is an anti-metabolite and folate antagonist drug used in the treatment of certain neoplastic diseases, severe psoriasis, and adult rheumatoid arthritis. High-dose Methotrexate is used for central nervous system prophylaxis in patients with leukemia (such as acute lymphoblastic leukemia) and high-risk lymphoma to help maintain remission, and for the treatment of leptomeningeal metasases, primary CNS lymphoma and osteosarcoma.
 


Performing Laboratory
CRMC Core Laboratory



The CPT Codes provided in this document are based on AMA guidelines and are for informational purposes only. CPT coding is the sole responsibility of the billing party. Please direct any questions regarding coding to the payor being billed. Any Profile/panel component may be ordered separately. Reflex tests are performed at an additional charge.