Skip to main content

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

CPT 80362

Test Details

Methodology

Mass spectrometry

Result Turnaround Time

4 - 7 days

Turnaround time is defined as the usual number of days from the date of pickup of a specimen for testing to when the result is released to the ordering provider. In some cases, additional time should be allowed for additional confirmatory or additional reflex tests. Testing schedules may vary.

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.

Specimen Requirements

Specimen

Urine

Volume

30 mL

Minimum Volume

15 mL

Container

Urine bottle

Collection Instructions

Random urine

Stability Requirements

• Room temperature: 5 days

Storage Instructions

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

Causes for Rejection

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

LOINC® Map

Order Code Order Code Name Order Loinc Result Code Result Code Name UofM Result LOINC
702518 Naltrexone, MS, Ur, MAT 18334-3 702542 OPIATE ANTAGONIST 3879-4
702518 Naltrexone, MS, Ur, MAT 18334-3 702543 Naltrexone 18334-3
Order Code702518
Order Code NameNaltrexone, MS, Ur, MAT
Order Loinc18334-3
Result Code702542
Result Code NameOPIATE ANTAGONIST
UofM
Result LOINC3879-4
Order Code702518
Order Code NameNaltrexone, MS, Ur, MAT
Order Loinc18334-3
Result Code702543
Result Code NameNaltrexone
UofM
Result LOINC18334-3