Monitor patient adherence.
Quantitative Liquid Chromatography/Tandem Mass Spectrometry
Tue, Thu, Sat
New York DOH Approval Status
Plain Red, Lavender (K2EDTA), Lavender (K3EDTA), Green (Sodium Heparin), Gray (Potassium Oxalate/Sodium Fluoride), or Pink (K2EDTA).
Separate from cells ASAP or within 2 hours of collection. Transfer 4 mL serum or plasma to an ARUP Standard Transport Tube. (Min: 2 mL)
Whole blood. Serum separator tubes, Light Blue (Sodium Citrate), or Plasma separator tubes. Specimens exposed to repeated freeze/thaw cycles.
Ambient: 1 week; Refrigerated: 2 weeks; Frozen: 3 years
Effective August 17, 2015
|Drugs Covered||Cutoff Concentrations|
Methodology: Quantitative Liquid Chromatography-Tandem Mass Spectrometry
Positive cutoff: 0.1 ng/mL
For medical purposes only; not valid for forensic use.
The absence of expected drug(s) and/or drug metabolite(s) may indicate non-compliance, inappropriate timing of specimen collection relative to drug administration, poor drug absorption, or limitations of testing. The concentration value must be greater than or equal to the cutoff to be reported as positive. Interpretive questions should be directed to the laboratory.
This test was developed and its performance characteristics determined by ARUP Laboratories. It has not been cleared or approved by the US Food and Drug Administration. This test was performed in a CLIA certified laboratory and is intended for clinical purposes.
Laboratory Developed Test (LDT)
80354 (Alt code: G0480)
|Component Test Code*||Component Chart Name||LOINC|
|2011777||Fentanyl, S/P, Quant||3636-8|
|2011782||Norfentanyl, S/P, Quant||11074-2|
- Fentanyl and Metabolite
- fentanyl and norfentanyl blood levels
- pain management