Test Code AMPAS Amphetamine Panel, Serum
Ordering Guidance
This test should only be ordered by healthcare professionals to monitor patients who have been prescribed amphetamines or identify misuse/abuse.
Specimen Required
Supplies: Sarstedt Aliquot Tube, 5 mL (T914)
Collection Container/Tube: Red top (Serum gel/SST are not acceptable)
Submission Container/Tube: Plastic vial
Specimen Volume: 1 mL Serum
Collection Instructions: Within 2 hours of collection, centrifuge and aliquot serum into a plastic vial.
Useful For
Confirming drug exposure involving amphetamine-like stimulants such as methamphetamine, amphetamine, 3,4-methylenedioxymethamphetamine (MDMA), 3,4-methylenedioxyamphetamine (MDA), and 3,4-methylenedioxyethylamphetamine (MDEA)
Special Instructions
Method Name
Liquid Chromatography Tandem Mass Spectrometry (LC-MS/MS)
Reporting Name
Amphetamine Panel, SSpecimen Type
Serum RedSpecimen Minimum Volume
Serum: 0.5 mL
Specimen Stability Information
| Specimen Type | Temperature | Time |
|---|---|---|
| Serum Red | Refrigerated (preferred) | 28 days |
| Ambient | 28 days | |
| Frozen | 15 days |
Reference Values
Therapeutic range and metabolite information (as applicable):
Methamphetamine: 10-50 ng/mL
Amphetamine: 20-30 ng/mL
Amphetamine is a separate prescribable drug as well as the metabolite of methamphetamine.
3,4-methylenedioxymethamphetamine (MDMA): Not Applicable
3,4-methylenedioxyamphetamine (MDA): Not Applicable
3,4-methylenedioxyethylamphetamine (MDEA): Not Applicable
MDA is a separate drug and also a metabolite of MDEA and MDMA.
Cutoff concentrations:
Methamphetamine: 5.0 ng/mL
Amphetamine: 5.0 ng/mL
MDMA: 5.0 ng/mL
MDA: 5.0 ng/mL
MDEA: 5.0 ng/mL
Interpretation
Clinically, the presence of amphetamines in serum can be used to verify adherence or compliance and discourage drug misuse, abuse, and diversion.
Clinical Reference
1. Jannetto PJ, Bratanow NC, Clark WA, et al. Executive Summary: American Association of Clinical Chemistry Laboratory Medicine Practice Guideline-Using Clinical Laboratory Tests to Monitor Drug Therapy in Pain Management Patients. J Appl Lab Med. 2018;2(4):489-526. doi:10.1373/jalm.2017.023341
2. Langman LJ, Bechtel LK, Holstege CP. Chapter 43: Clinical toxicology. In: Rifai N, Chiu RWK, Young I, Burnham C-AD, Wittwer CT, eds. Tietz Textbook of Laboratory Medicine. 7th ed. Elsevier; 2023:chap 43
3. Baselt RC. Disposition of Toxic Drugs and Chemical in Man. 12th ed. Biomedical Publications; 2020
4. Milone MC, Shaw LM. Chapter 42: Therapeutic Drugs and Their Management. In: Rifai N, Chiu RWK, Young I, Burnham C-AD, Wittwer CT, eds. Tietz Textbook of Laboratory Medicine. 7th ed. Elsevier; 2023:chap 42
Day(s) Performed
Tuesday
Report Available
2 to 9 daysPerforming Laboratory
Mayo Clinic Laboratories in Rochester
Test Classification
This test was developed and its performance characteristics determined by Mayo Clinic in a manner consistent with CLIA requirements. It has not been cleared or approved by the US Food and Drug Administration.CPT Code Information
G0480
80324 (if appropriate for select payers)
80359 (if appropriate for select payers)
LOINC Code Information
| Test ID | Test Order Name | Order LOINC Value |
|---|---|---|
| AMPAS | Amphetamine Panel, S | In Process |
| Result ID | Test Result Name | Result LOINC Value |
|---|---|---|
| 623599 | Methamphetamine | 3778-8 |
| 623600 | Amphetamine | 30112-7 |
| 623601 | Methylenedioxymethamphetamine-MDMA | 18356-6 |
| 623602 | Methylenedioxyamphetamine-MDA | 59837-5 |
| 623603 | Methylenedioxyethylamphetamine-MDEA | 33016-7 |