Test Code LAMOTM Lamotrigine, Serum
Additional Codes
EPIC EAP | Mayo |
LAB475 | LAMO |
Reporting Name
Lamotrigine, SUseful For
Monitoring serum concentration of lamotrigine
Assessing compliance
Adjusting lamotrigine dose in patients receiving other anticonvulsant drugs that interact pharmacokinetically with lamotrigine
Method Name
Liquid Chromatography-Tandem Mass Spectrometry (LC-MS/MS)
Performing Laboratory

Specimen Type
SerumSpecimen Required
Supplies: Sarstedt Aliquot Tube, 5 mL (T914)
Collection Container/Tube:
Preferred: Red top
Acceptable: Serum gel
Submission Container/Tube: Plastic vial
Specimen Volume: 1 mL
Collection Instructions:
1. Collect blood immediately before next scheduled dose.
2. Only for sustained-release formulations, collect blood a minimum of 12 hours after last dose.
3. Within 2 hours of collection, centrifuge.
4. For red-top tubes, immediately aliquot serum into a plastic vial.
5. For serum gel tubes, the serum must be aliquoted into a plastic vial within 24 hours of collection.
Specimen Minimum Volume
0.5 mL
Specimen Stability Information
Specimen Type | Temperature | Time |
---|---|---|
Serum | Refrigerated (preferred) | 28 days |
Ambient | 28 days | |
Frozen | 28 days |
Reject Due To
Gross hemolysis | OK |
Gross lipemia | OK |
Gross icterus | OK |
Reference Values
Patients receiving therapeutic doses usually have lamotrigine concentrations of 3.0-15.0 mcg/mL.
Day(s) Performed
Monday through Sunday
CPT Code Information
80175
LOINC Code Information
Test ID | Test Order Name | Order LOINC Value |
---|---|---|
LAMO | Lamotrigine, S | 6948-4 |
Result ID | Test Result Name | Result LOINC Value |
---|---|---|
80999 | Lamotrigine, S | 6948-4 |
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.Report Available
Same day/1 to 2 daysForms
If not ordering electronically, complete, print, and send 1 of the following forms with the specimen:
-Neurology Specialty Testing Client Test Request (T732)
-General Request (T239)
-Therapeutics Test Request (T831)