Barbiturates




Test Mnemonic

BARBS

CPT Codes

  • 80345 - QTY (1)
  • G0480 - QTY (1)

Includes

  • Butalbital
  • Pentobarbital
  • Phenobarbital

Performing Laboratory

ARUP

FDA Category

Laboratory Developed Test


Specimen Requirements

Volume Type Container Collect Temperature Transport Temperature Special Instructions
3.5 mLPlasmaPotassium oxalate/sodium fluoride (Gray) RefrigeratedDo not use separator tubes. Separate plasma from cells ASAP or within 2 hours of collection and transfer into standard aliquot tube.

Alternate Specimen Requirements

Volume Type Container Collect Temperature Transport Temperature Special Instructions
3.5 mLPlasmaEDTA (Lavender) RefrigeratedDo not use separator tubes. Separate plasma from cells ASAP or within 2 hours of collection and transfer into standard aliquot tube.
3.5 mLSerumNo additive (Red) RefrigeratedDo not use separator tubes. Separate serum from cells ASAP or withing 2 hours of collection and transfer into standard aliquot tube.
3.5 mLPlasmaSodium heparin (Green) RefrigeratedDo not use separator tubes. Separate plasma from cells ASAP or within 2 hours of collection and transfer into standard aliquot tube.

Minimum Specimen Requirements

Volume Type Container Collect Temperature Transport Temperature Special Instructions
1.5 mL     

Stability

Environmental Condition Description
AmbientAfter separation from cells: 1 week
RefrigeratedAfter separation from cells: 2 weeks
FrozenAfter separation from cells: 3 years (Avoid repeated freeze/thaw cycles)

Days Performed

Tue, Thu, Sat

Turnaround Time

2 - 8 days

Methodology

Name Description
Gas Chromatography Mass Spectrometry (GCMS) 
Quantitative Liquid Chromatography - Tandem Mass Spectrometry 

Reference Range

Butalbital
Sex Age From Age To Type Range Range Unit
       Cut off: 50 ng/mL 
Pentobarbital
Sex Age From Age To Type Range Range Unit
       Cut off: 50 ng/mL 
Phenobarbital
Sex Age From Age To Type Range Range Unit
       Cut off: 50 ng/mL 

Special Info

All drugs will be quantified if positive. Positive cutoff for all drugs: 50 ng/mL. Separator tubes will be rejected. Hemolyzed specimens will be rejected. Specimens exposed to repeated freeze/thaw cycles are unacceptable. Plasma or whole blood collected in sodium citrate (light blue) tubes will be rejected. This test is a reflex from Drug Screen 9 Panel, Serum or Plasma (DRGSC9). This test is New York DOH approved.

Clinical Info

This test can be useful to optimize drug therapy, monitor patient adherence, or rule out barbiturate exposure. 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.

Clinical Limitation

For medical purposes only; not valid for forensic use.