Ordering Recommendation

Optimize drug therapy and monitor patient adherence.

Mnemonic
TRAZO
Methodology

Quantitative Liquid Chromatography-Tandem Mass Spectrometry

Performed

Mon, Thu

Reported

1-5 days

New York DOH Approval Status
This test is New York DOH approved.
Specimen Required
Patient Preparation

Timing of specimen collection: Pre-dose (trough) draw - At steady state concentration.

Collect

Plain red. Also acceptable: Lavender (K2 or K3EDTA) or pink (K2EDTA ).

Specimen Preparation

Separate serum or plasma from cells within 2 hours of collection. Transfer 1 mL serum or plasma to an ARUP Standard Transport Tube. (Min: 0.5 mL)

Storage/Transport Temperature

Refrigerated.

Unacceptable Conditions

Whole blood. Gel separator tubes, light blue (citrate), or yellow (SPS or ACD solution).

Remarks
Stability

After separation from cells: Ambient: 12 hours; Refrigerated: 1 week; Frozen: 1 week

Reference Interval

Effective February 18, 2014

Therapeutic Range: 0.5-2.5 µg/mL
Toxic: Greater than 4 µg/mL

Interpretive Data

Adverse effects may include sedation, fatigue, headache, blurred vision and nausea.

Compliance Category

Laboratory Developed Test (LDT)

Note
Hotline History
N/A
CPT Codes

80338 (Alt code: G0480)

Components
Component Test Code* Component Chart Name LOINC
0090316 Trazodone 4064-2
* 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.
Aliases
  • Desyrel
  • desyrel blood level
  • Molipaxin
  • trazodone blood level
Trazodone