Drugs of Abuse Confirmation/Quantitation - Phencyclidine (PCP) - Serum or Plasma
0091571
 
Ordering Recommendation
Mnemonic
PHENCYCLID
Methodology
Quantitative Liquid Chromatography-Tandem Mass Spectrometry
Performed
Mon
Reported
1-7 days
New York DOH Approval Status
This test is New York DOH approved.
Specimen Required
Patient Preparation
 
Collect
Gray (sodium fluoride/potassium oxalate). Also acceptable: Plain red, green (sodium heparin), lavender (EDTA), or pink (K2EDTA).  
Specimen Preparation
Separate serum or plasma from cells ASAP or within 2 hours of collection. Transfer 4 mL serum or plasma to an ARUP Standard Transport Tube. (Min: 2 mL)  
Storage/Transport Temperature
Refrigerated.  
Unacceptable Conditions
Separator tubes. Plasma or whole blood collected in lt. blue (sodium citrate). Specimens exposed to repeated freeze/thaw cycles.  
Remarks
 
Stability
After separation from cells: Ambient: 1 week; Refrigerated: 2 weeks; Frozen: 3 years  
Reference Interval
Interpretive Data
Methodology: LC-MS/MS
Drugs covered:
phencyclidine (PCP).
Positive cutoff:
10 ng/mL

For medical purposes only; not valid for forensic use.

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.

See Compliance Statement B: www.aruplab.com/CS
Note
CPT Code(s)
83992
Components
Component Test Code*Component Chart Name
0092369Drug Conf, Phencyclidine, Ser/Pla
* Component test codes cannot be used to order tests. The information provided here is not sufficient for interface builds; for a complete test mix, contact interface support at interface.support@aruplab.com.
Cross References
  • Pain Management
  • PCP
  • Phencyclidine
  • Phenylcyclohexylpeperidine