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Test Directory

Leflunomide Metabolite

Test Summary

Leflunomide is an immunosuppressant medication used in the treatment of rheumatoid arthritis. Leflunomide is rapidly and extensively metabolized to teriflunomide, which is the active form of the medication. Steady state plasma concentrations in patients receiving recommended daily dosages: up to 63,000 ng/mL. It is recommended that all women of childbearing potential who discontinue leflunomide and women receiving treatment who wish to become pregnant undergo the cholestyramine drug elimination procedure. This procedure includes verification that plasma levels of teriflunomide are less than 20 ng/mL by two separate tests at least 14 days apart.

Aliases

  • N/A

Specimen Collection

Special Instructions

N/A

Preferred Specimen

1 mL serum collected in a red-top tube (no gel)

Minimum Volume

0.5 mL

Instructions

N/A

Patient Preparation

N/A

Storage

N/A

Transport Temperature

Room temperature

Specimen Stability

  • Room temperature: 5 days
  • Refrigerated: 14 days
  • Frozen: 30 days

Limitations

N/A

Other Acceptable Specimens

Plasma collected in: Sodium heparin (green-top) or lithium heparin (green-top)

Unacceptable Specimens

Serum separator tubes (SST)

Order Code

LEFMET

EPIC (Premier) Code

LAB5161

Includes

N/A

CPT Code

  • 80193

Billing Code

  • 700000

CPT Statement

Methodology

Chromatography/Mass Spectrometry

FDA Status

This test was developed and its analytical performance characteristics have been determined by Quest Diagnostics. It has not been cleared or approved by the U.S. Food and Drug Administration. This assay has been validated pursuant to the CLIA regulations and is used for clinical purposes.

Physician Attestation of Informed Consent

N/A

Testing Laboratory

Quest Diagnostics Nichols Institute Valencia
27027 Tourney Road
Valencia CA, 91355

Reference Range

See Laboratory Report

Setup Schedule / Expected Turnaround Time

Tuesday, Thursday, Saturday; Report available: 3 - 5 days

Specimen Collection

Special Instructions

N/A

Preferred Specimen

1 mL serum collected in a red-top tube (no gel)

Minimum Volume

0.5 mL

Instructions

N/A

Patient Preparation

N/A

Storage

N/A

Transport Temperature

Room temperature

Specimen Stability

  • Room temperature: 5 days
  • Refrigerated: 14 days
  • Frozen: 30 days

Limitations

N/A

Other Acceptable Specimens

Plasma collected in: Sodium heparin (green-top) or lithium heparin (green-top)

Unacceptable Specimens

Serum separator tubes (SST)

Billing

CPT Code

  • 80193

Billing Code

  • 700000

CPT Statement

Result Information

Methodology

Chromatography/Mass Spectrometry

Testing Laboratory

N/A

Reference Range

See Laboratory Report

Setup Schedule / Expected Turnaround Time

Tuesday, Thursday, Saturday; Report available: 3 - 5 days