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Test Code LAB9721 FENTU Fentanyl with Metabolite Confirmation, Random, Urine

Additional Codes

FENTU

Useful For

Detection and confirmation of illicit drug use involving fentanyl

Performing Laboratory

Mayo Clinic Laboratories in Rochester

Specimen Type

Urine


Ordering Guidance


For situations where chain of custody is required, a Chain of Custody Kit (T282) is available. For chain-of-custody testing, order FENTX / Fentanyl with Metabolite Confirmation, Chain of Custody, Random, Urine.



Additional Testing Requirements


If urine creatinine is required or adulteration of the sample is suspected, the following test should also be ordered, ADULT / Adulterants Survey, Random, Urine.



Specimen Required


Supplies: Sarstedt Aliquot Tube, 5 mL (T914)

Collection Container/Tube: Clean, plastic urine collection container

Submission Container/Tube: Plastic, 5-mL tube

Specimen Volume: 5 mL

Collection Instructions:

1. Collect a random urine specimen.

2. No preservative.

Additional Information:

1. No specimen substitutions.

2. STAT requests are not accepted for this procedure.

3. Submitting less than 5 mL will compromise our ability to perform all necessary testing.


Specimen Minimum Volume

2.1 mL

Specimen Stability Information

Specimen Type Temperature Time Special Container
Urine Refrigerated (preferred) 28 days
  Frozen  28 days
  Ambient  21 days

Reference Values

Negative

Day(s) Performed

Monday through Friday

CPT Code Information

80354

G0480 (if appropriate)

LOINC Code Information

Test ID Test Order Name Order LOINC Value
FENTU Fentanyl w/metabolite Conf, U 67822-7

 

Result ID Test Result Name Result LOINC Value
45530 Fentanyl by LC-MS/MS 58381-5
45531 Norfentanyl by LC-MS/MS 58383-1
45532 Fentanyl Interpretation 69050-3

Interpretation

The presence of fentanyl above 0.20 ng/mL or norfentanyl above 1.0 ng/mL is a strong indicator that the patient has used fentanyl.

Method Description

The received urine sample is centrifuged, diluted, mixed with internal standard and ammonium hydroxide, and vortexed briefly. It is then extracted using supported liquid extraction, and the extract analyzed by an in-house developed liquid chromatography tandem mass spectrometry method.(Unpublished Mayo method)

Report Available

4 to 7 days

Specimen Retention Time

14 days

Reject Due To

Gross hemolysis OK
Gross icterus Reject

Method Name

Liquid Chromatography Tandem Mass Spectrometry (LC-MS/MS)

Forms

If not ordering electronically, complete, print, and send a Therapeutics Test Request (T831) with the specimen.