Naltrexone, MS Confirm, Urine, Medication Assisted Treatment (MAT)

Medication Assisted Treatment (MAT) Naltrexone, MS Confirm, Urine
Naltrexone, MS Confirm, Urine, Medication Assisted Treatment (MAT)
CPT: 80362
8036280362
8036280362
Updated on 06/20/2024
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Expected Turnaround Time

4 - 7 days


Specimen Requirements


Specimen

Urine


Volume

30 mL


Minimum Volume

15 mL


Container

Urine bottle


Collection

Random urine


Storage Instructions

Submission/transport (<3 days): Room temperature. For storage beyond three days, specimen should be refrigerated or frozen.


Stability Requirements

• Room temperature: 5 days


Causes for Rejection

Insufficient volume; no ID on container; urine from preservative tube


Test Details


Use

This test is used to confirm the presence of naltrexone. Please note this test is designed specifically for monitoring patients who are on Suboxone™/buprenorphine or naltrexone only. This testing should not be used for monitoring chronic pain patients (medical drug monitoring) or methadone medication assisted treatment.


Limitations

This test was developed and its performance characteristics determined by Labcorp. It has not been cleared or approved by the Food and Drug Administration.


Methodology

Mass spectrometry


LOINC® Map

Order Code Order Code Name Order Loinc Result Code Result Code Name UofM Result LOINC
702518 Naltrexone, MS, Ur, MAT Pending 702542 OPIATE ANTAGONIST N/A
702518 Naltrexone, MS, Ur, MAT Pending 702543 Naltrexone 18334-3

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