Ordering Recommendation
Optimize drug therapy and monitor patient adherence.
Mnemonic
VAN
Methodology
Fluorescence Polarization Immunoassay
Performed
Sun-Sat
Reported
Within 24 hours
New York DOH Approval Status
This test is New York DOH approved.
Specimen Required
Patient Preparation
Collect
Plain red. Also acceptable: Green (sodium or lithium heparin).
Specimen Preparation
Transfer 1 mL serum or plasma to an ARUP Standard Transport Tube. (Min: 0.2 mL)
Storage/Transport Temperature
Frozen.
Unacceptable Conditions
Gray (sodium fluoride/potassium oxalate), Lavender (EDTA), lt. blue (sodium citrate), or separator tubes. Grossly hemolyzed, icteric, or lipemic specimens.
Remarks
Stability
After separation from cells: Ambient: 8 hours; Refrigerated: 1 week; Frozen: 2 weeks
Reference Interval
Effective November 18, 2013
Trough Level | Optimal: 10.0-20.0 µg/mL |
Peak Level | Optimal: 30.0-40.0 µg/mL |
Interpretive Data
Compliance Category
FDA
Note
Hotline History
N/A
CPT Codes
80202
Components
Component Test Code* | Component Chart Name | LOINC |
---|---|---|
0090285 | Vancomycin, Random | 20578-1 |
* 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
- Vancocin
- Vancomycin Hydrochloride
- Vancomycin, Random Level, Serum
- Vancor
Vancomycin, Random Level