Collect

60.0 mL random urine collection in a urine specimen cup, no preservative. 15.0 mL whole blood in plain red-top tubes(s) with no gel separator or 5.0 mL serum.

Specimen Required

10.0 mL urine, 3.0 mL serum

Specimen Min Vol

6.0 mL urine, 2.0 mL serum

Specimen Preparation

Spindown and separate serum.

Storage/Transport Temperature

Refer to Specimen stability criteria as shown below

Ambient

7 days

Refrigerated

1 month

Frozen

1 year

Unacceptable Conditions

Specimens that exceed stated stability, unlabeled/mislabeled/mismatched specimens, specimens submitted in leaking containers

Special Instructions

None

CPT Codes

80307
80320
80368
80336
80342
80345

Synonyms

  • Coma Panel

Methodology

Enzyme-Multiplied Immunoassay Technique (EMIT®),  Thin Layer Chromatography, Spot Test

 

Performing Location

Chemistry (Toxicology)

Reported STAT

8 hours

Reported Routine

12 hours

Additional Information


Cutoff Concentration:
Amphetamines (500 ng/mL), Barbiturates (300 ng/mL), Benzodiazepines (200 ng/mL), Cocaine (150 ng/mL), Opiates (300 ng/mL), Phencyclidine (25 ng/mL), THC (50ng/mL), Methadone (300 ng/mL), Propoxyphene (300 ng/mL), Fentanyl (1 ng/mL), 
Buprenorphine (5 ng/mL), Oxycodone (100 ng/mL), Meperidine (500 ng/mL), Ecstasy (500 ng/mL)

TLC Method: 1000 ng/mL

This test was developed and its performance characteristics were determined by the University of California Irvine Medical Center, Department of Pathology and Laboratory Medicine. It has not been approved by the FDA, however, approval is not required for clinical use.

Test set up frequency

Daily

Reference Interval


Urine Reference Range: No Drugs Detected
Serum Reference Range: None Detected
Alchol Ethyl Reference Range: None Detected

Additional Information


Cutoff Concentration:
Amphetamines (500 ng/mL), Barbiturates (300 ng/mL), Benzodiazepines (200 ng/mL), Cocaine (150 ng/mL), Opiates (300 ng/mL), Phencyclidine (25 ng/mL), THC (50ng/mL), Methadone (300 ng/mL), Propoxyphene (300 ng/mL), Fentanyl (1 ng/mL), 
Buprenorphine (5 ng/mL), Oxycodone (100 ng/mL), Meperidine (500 ng/mL), Ecstasy (500 ng/mL)

TLC Method: 1000 ng/mL

This test was developed and its performance characteristics were determined by the University of California Irvine Medical Center, Department of Pathology and Laboratory Medicine. It has not been approved by the FDA, however, approval is not required for clinical use.
Collection

Collect

60.0 mL random urine collection in a urine specimen cup, no preservative. 15.0 mL whole blood in plain red-top tubes(s) with no gel separator or 5.0 mL serum.

Specimen Required

10.0 mL urine, 3.0 mL serum

Specimen Min Vol

6.0 mL urine, 2.0 mL serum

Specimen Preparation

Spindown and separate serum.

Storage/Transport Temperature

Refer to Specimen stability criteria as shown below

Ambient

7 days

Refrigerated

1 month

Frozen

1 year

Unacceptable Conditions

Specimens that exceed stated stability, unlabeled/mislabeled/mismatched specimens, specimens submitted in leaking containers

Special Instructions

None
Test Info

CPT Codes

80307
80320
80368
80336
80342
80345

Synonyms

  • Coma Panel

Methodology

Enzyme-Multiplied Immunoassay Technique (EMIT®),  Thin Layer Chromatography, Spot Test

 

Performing Location

Chemistry (Toxicology)

Reported STAT

8 hours

Reported Routine

12 hours

Additional Information


Cutoff Concentration:
Amphetamines (500 ng/mL), Barbiturates (300 ng/mL), Benzodiazepines (200 ng/mL), Cocaine (150 ng/mL), Opiates (300 ng/mL), Phencyclidine (25 ng/mL), THC (50ng/mL), Methadone (300 ng/mL), Propoxyphene (300 ng/mL), Fentanyl (1 ng/mL), 
Buprenorphine (5 ng/mL), Oxycodone (100 ng/mL), Meperidine (500 ng/mL), Ecstasy (500 ng/mL)

TLC Method: 1000 ng/mL

This test was developed and its performance characteristics were determined by the University of California Irvine Medical Center, Department of Pathology and Laboratory Medicine. It has not been approved by the FDA, however, approval is not required for clinical use.

Test set up frequency

Daily
Result Interpretation

Reference Interval


Urine Reference Range: No Drugs Detected
Serum Reference Range: None Detected
Alchol Ethyl Reference Range: None Detected

Additional Information


Cutoff Concentration:
Amphetamines (500 ng/mL), Barbiturates (300 ng/mL), Benzodiazepines (200 ng/mL), Cocaine (150 ng/mL), Opiates (300 ng/mL), Phencyclidine (25 ng/mL), THC (50ng/mL), Methadone (300 ng/mL), Propoxyphene (300 ng/mL), Fentanyl (1 ng/mL), 
Buprenorphine (5 ng/mL), Oxycodone (100 ng/mL), Meperidine (500 ng/mL), Ecstasy (500 ng/mL)

TLC Method: 1000 ng/mL

This test was developed and its performance characteristics were determined by the University of California Irvine Medical Center, Department of Pathology and Laboratory Medicine. It has not been approved by the FDA, however, approval is not required for clinical use.
NICU/Pediatric Info

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