25.0 mL urine in a sterile container, no preservative.
Specimen Required
5.0 mL. urine
Specimen Min Vol
3.0 mL urine
Specimen Preparation
None
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
80365
Synonyms
Oxycontin
Methodology
Gas Chromatography-Mass Spectrometry (GCMS)
Performing Location
Chemistry (Toxicology)
Reported STAT
Not available
Reported Routine
6 days
Additional Information
Cutoff Concentration: 200 ng/mL
This test was developed and its performance characteristics determined by 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
Twice a week
Reference Interval
Negative
Additional Information
Cutoff Concentration: 200 ng/mL
This test was developed and its performance characteristics determined by 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
25.0 mL urine in a sterile container, no preservative.
Specimen Required
5.0 mL. urine
Specimen Min Vol
3.0 mL urine
Specimen Preparation
None
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
80365
Synonyms
Oxycontin
Methodology
Gas Chromatography-Mass Spectrometry (GCMS)
Performing Location
Chemistry (Toxicology)
Reported STAT
Not available
Reported Routine
6 days
Additional Information
Cutoff Concentration: 200 ng/mL
This test was developed and its performance characteristics determined by 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
Twice a week
Result Interpretation
Reference Interval
Negative
Additional Information
Cutoff Concentration: 200 ng/mL
This test was developed and its performance characteristics determined by 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.
