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Test ID: PAIN
Pain Clinic Survey 10, Urine

NY State Approved Indicates the status of NY State approval and if the test is orderable for NY State clients.

Yes

Useful For Suggests clinical disorders or settings where the test may be helpful

Detecting drug use involving amphetamines, barbiturates, benzodiazepines, cocaine, methadone, opiates, phencyclidine, propoxyphene, and tetrahydrocannabinol

 

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

Profile Information A profile is a group of laboratory tests that are ordered and performed together under a single Mayo Test ID. Profile information lists the test performed, inclusive of the test fee, when a profile is ordered and includes reporting names and individual availability.

Test IDReporting NameAvailable SeparatelyAlways Performed
PN_10Pain Clinic Survey 10NoYes
OPATUOpiates, UYesYes

Reflex Tests Lists test(s) that may or may not be performed, at an additional charge, depending on the result and interpretation of the initial test(s)

Test IDReporting NameAvailable SeparatelyAlways Performed
AMPHUAmphetamines, UYesNo
COKEUCocaine Confirmation, UYesNo
BENZUBenzodiazepine Confirmation, UYesNo
BARBUBarbiturate Confirmation, UYesNo
MSPRDrug of Abuse, Propoxyphene Conf, UYesNo
MTDNUMethadone Confirmation, UYesNo
PCPUPhencyclidine Confirmation, UYesNo
THCUTetrahydrocannabinol Conf, UYesNo

Additional Tests Lists test(s) that are always performed, at an additional charge, with the initial test(s)

Test IDReporting NameAvailable SeparatelyAlways Performed
ADULTAdulterants Survey, UNoYes

Testing Algorithm Delineates situation(s) when tests are added to the initial order. This includes reflex and additional tests.

If immunoassay screen is positive, then gas chromatography-mass spectrometry (GC-MS) confirmation is performed. GC-MS confirmation with quantification of positives for amphetamines, barbiturates, benzodiazepines, cocaine and metabolites, methadone, phencyclidine, propoxyphene, and tetrahydrocannabinol metabolite will be performed at an additional charge.

 

An evaluation to detect the presence of adulterants will be performed and reported at no additional charge. See Adulterant Survey Algorithm in Special Instructions.

Special Instructions and Forms Describes specimen collection and preparation information, test algorithms, and other information pertinent to test. Also includes pertinent information and consent forms to be used when requesting a particular test

Method Name A short description of the method used to perform the test

PN_10/26320, OPATU/8473: Screened by Immunoassay and Confirmed by Gas Chromatography-Mass Spectrometry (GC-MS)

ADULT/29345: Spectrophotometry (SP)

AMPHU/8257, BARBU/80372, BENZU/80370, COKEU/9286, MTDNU/83129, MSPR/500373, PCPU/80371, THCU/8898: Gas Chromatography-Mass Spectrometry (GC-MS)

Reporting Name A shorter/abbreviated version of the Published Name for a test; an abbreviated test name

Pain Clinic Survey 10, U

Aliases Lists additional common names for a test, as an aid in searching

"J" (Jane) Tetrahydrocannabinol)
7-Amino Flunitrazepam (Metabolite of Flunitrazepam (Rohypnol)
Alprazolam (Xanax)
Amobarbital (Amytal)
Amphetamines
Amytal (Amobarbital)
Ativan (Lorazepam)
Barbita (Phenobarbital)
Barbiturates
Benzodiazepines
Benzoylecgonine (Cocaine Metabolite)
Butabarbital (Butisol)
Butalbital (Fiorinal)
Butisol (Butabarbital)
Cannabinoids (Tetrahydrocannabinol)
Chlordiazepoxide (Librium)
Clorazepate (Tranxene)
Cocaine
Codeine
Dalmane (Flurazepam)
Darvon (Propoxyphene)
Date Rape Drug (Rohypnol [Flunitrazepam])
Desalkyl Flurazepam (Metabolite)
Desoxyn (Methamphetamines)
Diazepam (Valium)
Dilaudid (Hydromorphone)
Dolophine (Methadone)
Drugs of Abuse
Ecstasy
Fiorinal (Butalbital)
Flunitrazepam (Rohypnol)
Flurazepam (Dalmane)
Halcion (Triazolam)
Heroin
Hycodan (Hydrocodone)
Hydrocodone (Hycodan, Vicodin)
Hydromorphone (Dilaudid, Vicodin)
Hydroxy-Ethyl Flurazepam (Metabolite of Flurazepam) (Dalmane)
Killer Weed (Phencyclidine)
Lorazepam (Ativan)
Lortab (Hydromorphone)
Luminal (Phenobarbital)
Marijuana (Tetrahydrocannabinol)
MDA (Methylenedioxyamphetamine) Metabolite for Methylenedioxyethylamphetamine (MDEA) and Methylenedioxymethamphetamine (MDMA)
MDMA (Methylenedioxymethamphetamine)
Mebaral (Mephobarbital)
Mephobarbital (Mebaral)
Methadone (Dolophine)
Methamphetamines (Desoxyn)
Methylenedioxyamphetamine (MDA) Metabolite for Methylenedioxyethylamphetamine (MDEA) and Methylenedioxymethamphetamine (MDMA)
Methylenedioxymethamphetamine (MDMA)
Nembutal (Pentobarbital)
Nordiazepam (Tranxene)
Norpropoxyphene (Metabolite of Propoxyphene) (Darvon)
Opiates
Oxazepam (Serax)
Oxycodone (Oxycontin, Percodan)
Oxycontin (Oxycodone)
PCP (Phencyclidine)
Pentobarbital (Nembutal)
Pentothal (Thiopental)
Percodan (Oxycodone)
Phencyclidine (PCP)
Phenobarbital
Propoxyphene (Darvon)
Restoril (Temazepam)
Rocket Fuel (Phencyclidine)
Rohypnol (Flunitrazepam)
Secobarbital (Seconal)
Seconal (Secobarbital)
Serax (Oxazepam)
Solfoton (Phenobarbital)
Speed (Amphetamines)
TCP (Phencyclidine)
Temazepam (Restoril)
Tetrahydrocannabinol (THC)
THC (Tetrahydrocannabinol)
Thiopental (Pentothal)
Toxicology Screen, Drugs
Tranxene (Clorazepate)
Triazolam (Halcion)
Tuinal (Amobarbital and Secobarbital)
Valium (Diazepam)
Vicodin (Hydrocodone)
Xanax (Alprazolam)
Librium (Chlordiazepoxide)
Crack (Cocaine)
Coke (Cocaine)

Specimen Type Describes the specimen type needed for testing

Urine

Specimen Required Defines the optimal specimen. This field describes the type of specimen required to perform the test and the preferred volume to complete testing. The volume allows automated processing, fastest throughput and, when indicated, repeat or reflex testing.

Collection Container/Tube: Plastic urine container

Submission Container/Tube: Plastic, 60-mL urine bottle

Specimen Volume: 30 mL

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. No STATS are accepted for this procedure.

3. For situations where chain-of-custody is required, a Chain-of-Custody Kit (Supply T282) is available. For chain-of-custody information, see COCH/9426 Chain-of-Custody Processing.

4. Additional drug panels and specific requests are available. Call Mayo Medical Laboratories at 800-533-1710 or 507-266-5700.

Specimen Minimum Volume Defines the amount of specimen required to perform an assay once, including instrument and container dead space. Submitting the minimum specimen volume makes it impossible to repeat the test or perform confirmatory or perform reflex testing. In some situations, a minimum specimen volume may result in a QNS (quantity not sufficient) result, requiring a second specimen to be collected.

20 mL

Reject Due To Identifies specimen types and conditions that may cause the specimen to be rejected

Hemolysis

NA

Lipemia

NA

Icterus

NA

Other

NA

Specimen Stability Information Provides a description of the temperatures required to transport a specimen to the laboratory. Alternate acceptable temperature(s) are also included.

Specimen TypeTemperatureTime
UrineRefrigerated (preferred)14 days
 Frozen 14 days
 Ambient 72 hours

Clinical Information Discusses physiology, pathophysiology, and general clinical aspects, as they relate to a laboratory test

This assay was designed to test for and confirm by gas chromatography-mass spectrometry (GC-MS) the following:

-Amphetamines

-Barbiturates

-Benzodiazepines

-Cocaine

-Methadone

-Phencyclidine

-Propoxyphene

-Opiates

-Tetrahydrocannabinol

 

This test uses the simple screening technique described under IDOAU/8248 Drug Abuse Survey, Urine, which involves immunologic testing for drugs by class. Oxycodone is not detected well with the opiate screening assay; therefore, OPATU/8473 Opiates, Urine is included to detect this drug. All positive screening results are confirmed by GC-MS, and quantitated, before a positive result is reported.

Reference Values Describes reference intervals and additional information for interpretation of test results. May include intervals based on age and sex when appropriate. Intervals are Mayo-derived, unless otherwise designated. If an interpretive report is provided, the reference value field will state this.

Negative

Screening cutoff concentrations

Amphetamines: 500 ng/mL

Barbiturates: 200 ng/mL

Benzodiazepines: 200 ng/mL

Cocaine (benzoylecgonine-cocaine metabolite): 150 ng/mL

Methadone: 300 ng/mL

Opiates: 300 ng/mL

Phencyclidine: 25 ng/mL

Propoxyphene: 300 ng/mL

Tetrahydrocannabinol carboxylic acid: 20 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 Provides information to assist in interpretation of the test results

A positive result derived by this testing indicates that the patient has used 1 of the drugs detected by this technique in the recent past. See individual tests (eg, AMPHU/8257 Amphetamines, Urine) for more information.

 

For information about drug testing, including estimated detection times, see Drugs of Abuse Testing at http://www.mayomedicallaboratories.com/articles/drug-book/index.html

 

Creatinine and specific gravity are measured as indicators of specimen dilution.

Cautions Discusses conditions that may cause diagnostic confusion, including improper specimen collection and handling, inappropriate test selection, and interfering substances

Not intended for use in employment-related testing.

 

For situations where chain-of-custody is required, a Chain-of-Custody Kit (Supply T282) is available. See COCH/9426 Chain-of-Custody Processing.

 

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/8421 Drug Screen, Prescription/OTC, Serum or PDSU/88760 Drug Screen, Prescription/OTC, Urine).

Clinical Reference Provides recommendations for further in-depth reading of a clinical nature

1. Physicians Desk Reference (PDR). 60th edition. Montvale, NJ, Medical Economics Company, 2006

2. Goodman and Gilman's The Pharmacological Basis of Therapeutics. 11th edition. Edited by LL Bruntman. New York, McGraw-Hill Book Company, 2006

3. Langman LJ, Bechtel L, Holstege CP: Chapter 35. Tietz Textbook of Clinical Chemistry and Molecular Diagnostics. Edited by CA Burtis, ER Ashwood, DE Bruns. WB Saunders Company, 2011, pp 1109-1188

Method Description Describes how the test is performed and provides a method-specific reference

Drug classes are detected by immunoassay technique method. All positive screening results are confirmed by gas chromatography-mass spectrometry.(Armbruster DA, Schwarzhoff RH, Hubster EC, Liserio MK: Enzyme immunoassay, kinetic microparticle immunoassay, radioimmunoassay, and fluorescence polarization immunoassay compared for drugs-of-abuse screening. Clin Chem 1993;39:2137-2146; Ellis GM Jr, Mann MA, Judson BA, et al: Excretion patterns of cannabinoid metabolites after last use in a group of chronic users. Clin Pharmacol Ther 1985;38:572-578; Foerster EH, Dempsey J, Garriott JC: A gas chromatographic screening procedure for acid and neutral drugs in blood. J Anal Toxicol 1979;3:87-91; as modified to incorporate some alkaline drugs by LE Ebnet and TP Moyer, Mayo Clinic)

Day(s) and Time(s) Test Performed Outlines the days and times the test is performed. This field reflects the day and time the sample must be in the testing laboratory to begin the testing process and includes any specimen preparation and processing time required before the test is performed. Some tests are listed as continuously performed, which means assays are performed several times during the day.

Monday through Friday; Varies

Analytic Time Defines the amount of time it takes the laboratory to setup and perform the test. This is defined in number of days. The shortest interval of time expressed is "same day/1 day," which means the results may be available the same day that the sample is received in the testing laboratory. One day means results are available 1 day after the sample is received in the laboratory.

2 days

Maximum Laboratory Time Defines the maximum time from specimen receipt at Mayo Medical Laboratories until the release of the test result

5 days

Specimen Retention Time Outlines the length of time after testing that a specimen is kept in the laboratory before it is discarded

2 weeks

Performing Laboratory Location The location of the laboratory that performs the test

Rochester

CPT Code Information Provides guidance in determining the appropriate Current Procedural Terminology (CPT) code(s) information for each test or profile. The listed CPT codes reflect Mayo Medical Laboratories interpretation of CPT coding requirements. It is the responsibility of each laboratory to determine correct CPT codes to use for billing.

80104-Drug screen, qualitative, each procedure

83925-Opiates

G0431-Drug screen, qualitative, each specimen-government payers (if appropriate)

80154-Benzodiazepines (if appropriate)

80299-Tetrahydrocannabinol carboxylic acid (if appropriate)

80299 x 2-Propoxyphene (if appropriate)

82145 x 2-Amphetamines (if appropriate)

82205-Barbiturates (if appropriate)

82520-Cocaine (if appropriate)

83840-Methadone (if appropriate)

83992-Phencyclidine (if appropriate)

LOINC® Code Information Provides guidance in determining the Logical Observation Identifiers Names and Codes (LOINC) values for the result codes returned for this test or profile.

Result IDReporting NameLOINC Code
6541Immunoassay Screen19295-5
2573Amphetamines20410-7
2574Barbiturates20411-5
6543Codeine-by GC/MS3508-9
21177Hydrocodone-by GC/MS3681-4
2575Benzodiazepines20412-3
21652Cocaine20519-5
21179Hydromorphone-by GC/MS9835-0
21178Oxycodone-by GC/MS11246-6
4435Methadone16246-1
2577Opiates17384-9
6542Morphine-by GC/MS3831-5
21180Interpretation69050-3
2578Phencyclidine16254-5
4436Propoxyphene16242-0
21181Chain of CustodyIn Process
2664Tetrahydrocannabinol3530-3
20672Chain of CustodyIn Process