Drug Abuse Survey with Confirmation, Panel 9, Random, Urine

Test Code
CDAU7


Alias/See Also
Epic: LAB13446
Mayo: CDAU7


CPT Codes
80307

Includes

 

REFLEX TESTS 
 
Test Id Reporting Name Available Separately Always Performed
OPATU Opiate Confirmation, U Yes No
AMPHU Amphetamines Confirmation, U Yes No
BARBU Barbiturates Confirmation, U Yes No
COKEU Cocaine and metabolite Conf, U Yes No
ETOH Ethanol, U No No
MTDNU Methadone Confirmation, U Yes No
PCPU Phencyclidine Confirmation, U Yes No
THCU Carboxy-THC Confirmation, U Yes No
BNZU Benzodiazepines Confirmation, U Yes No


Preferred Specimen

Specimen Type: Urine
Collection Container: Sterile container
Specimen Volume: 30 mL




Minimum Volume
15 mL


Instructions
Collection Instructions:
  1. Collect a random urine specimen.
  2. Submit 30 mL in 1 plastic bottle.
  3. No preservative.

Additional Information:
  1. No specimen substitutions.
  2. Additional drug panels and specific requests are available. Call 800-533-1710 or 507-266-5700.
  3. Submitting less than 30 mL will compromise our ability to perform all necessary testing.


Transport Container
Plastic, 60-mL urine bottle


Specimen Stability
Specimen Type Temperature Time Special Container
Urine Refrigerated (preferred) 7 days  
  Frozen 14 days
 


Reject Criteria (Eg, hemolysis? Lipemia? Thaw/Other?)
All specimens will be evaluated at Mayo Clinic Laboratories for test suitability.


Methodology
CDAU7: Alcohol Screened by an Enzymatic Assay/All Others Screened by Immunoassay

ETOH: Gas Chromatography-Flame Ionization Detector (GC-FID)



Setup Schedule
Monday through Saturday


Report Available
Same day/1 to 2 days


Limitations
CAUTIONS 
Not intended for use in employment-related testing.

The test does not screen for drug classes other than those listed above. More comprehensive screening is available using the serum or urine drug screens (DSS / Drug Screen, Prescription/OTC, Serum or PDSU / Drug Screen, Prescription/OTC, Urine).


Reference Range
REFERENCE VALUES 
Negative
Screening cutoff concentrations
Amphetamines: 500 ng/mL
Barbiturates: 200 ng/mL
Benzodiazepines: 100 ng/mL
Cocaine (benzoylecgonine-cocaine metabolite): 150 ng/mL
Ethanol: 10 mg/dL
Methadone metabolite: 300 ng/mL
Opiates: 300 ng/mL
Phencyclidine: 25 ng/mL
Tetrahydrocannabinol carboxylic acid: 50 ng/mL

This report is intended for use in clinical monitoring or management of patients. It is not intended for use in employment-related testing.


INTERPRETATION 
A positive result indicates that the patient has used the drugs detected in the recent past. See individual tests (eg, AMPHU / Amphetamines Confirmation, Urine) for more information.

For information about drug testing, including estimated detection times, see Drugs of Abuse Testing at 
https://www.mayocliniclabs.com/test-info/drug-book/index.html


Clinical Significance
USEFUL FOR 
Detecting drug abuse involving, amphetamines, barbiturates, benzodiazepines, cocaine, ethanol, methadone, opiates, phencyclidine, and tetrahydrocannabinol

This test is intended to be used in a setting where the test results can be used definitively to make a diagnosis.

TESTING ALGORITHM 
Testing begins with screening tests for alcohol and drugs of abuse. Positives are confirmed and quantitated by definitive methods (gas chromatography-flame ionization detector for ethanol; gas chromatography-mass spectrometry for barbiturates, benzodiazepines, cocaine and metabolites, methadone, phencyclidine, and tetrahydrocannabinol metabolite) at an additional charge. Amphetamines and opiates that screen positive will be quantified with liquid chromatography-tandem mass spectrometry at an additional charge.

CLINICAL INFORMATION 
This assay was designed to screen by immunoassay and confirm by gas chromatography-mass spectrometry (GC-MS), gas chromatography-flame ionization detection (GC-FID), or liquid chromatography-tandem mass spectrometry (LC-MS/MS) for the following drugs:
-Amphetamines
-Barbiturates
-Benzodiazepines
-Cocaine
-Ethanol
-Opiates
-Methadone
-Phencyclidine
-Tetrahydrocannabinol

This test represents the coupling of an immunoassay screen with an automatic confirmation of all positive results by the definitive assay available and described in each individual reflex test (eg, AMPHU / Amphetamines Confirmation, Urine). All positive screening results are confirmed by GC-MS, GC-FID, or LC-MS/MS and quantitated before a positive result is reported.


Performing Laboratory
Mayo Clinic Laboratories - Rochester
3050 Superior Drive NW
Rochester, MN 55901


Additional Information
Drug Abuse Survey with Confirmation, Panel 9, Random, Urine

Last Updated: July 20, 2023
Last Review: N. Wolford, July 20, 2023


The CPT Codes provided in this document are based on AMA guidelines and are for informational purposes only. CPT coding is the sole responsibility of the billing party. Please direct any questions regarding coding to the payor being billed. Any Profile/panel component may be ordered separately. Reflex tests are performed at an additional charge.