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LEVETIRACETAM (KEPPRA) LEVEL, SERUM

test app

 
 
TEST NAME: LEVETIRACETAM (KEPPRA™), SERUM
LAB DEPT: Core Lab Sendouts
 
SPECIMEN REQUIREMENTS
Specimen Type:
Blood
Container/Tube
 
Preferred:
Gold/Red SST Vacutainer®.
 
Acceptable:
Plain, red-top Vacutainer®.
 
Collection Volume:
2.0 mL (minimum 1.0 mL)
 
Patient Preparation:
None
 
Sample Rejection:
Mislabeled or unlabeled specimens.
 
Special Instructions:
Collect specimen immediately before next scheduled dose.
For sustained-release formulations ONLY, collect specimen a minimum of 12 hours after last dose.
Send to lab promptly.
 
LOGISTICS
Test Availability:
Daily
Turnaround Time:
2-4 days
Test set-up:
Monday-Sunday
Lab Testing Section:
Send-outs
Referred to:
Mayo Medical Laboratories (MMLI) / Test ID: LEVE
 
INTERPRETIVE
Therapeutic Range:
10.0-40.0 mcg/mL
Therapeutic ranges are based on specimen collected at trough (ie, immediately before the next dose)
Critical Values:
Toxic levels have not been well established
Limitations:
NA
Methodology:
Liquid Chromatography-Tandem Mass Spectrometry (LC-MS/MS)
Test Classification:
This test was developed and its performance characteristics determined by Mayo Clinic in a manner consistent with CLIA requirements. This test has not been cleared or approved by the U.S. Food and Drug Administration.
 
ADDITIONAL INFORMATION
For SLCH Laboratory use only
Lab Processing instructions:
Centrifuge specimen to separate within 2 hours of collection. Aliquot serum into a 5-mL screw-capped plastic vial for transport.
 
Processed Volume:
1.0 mL (minimum 0.5 mL) serum
 
Transport Temperature:
Refrigerated
 
Analyte Stability:
PROCESSED:
Ambient: 28 days
Refrigerated: 28 days
Frozen: 28 days
 
Notes:
None
 
GENERAL INFORMATION
EPIC order name:
Levetiracetam Level  (EPIC Test# LAB477)
Cerner order name:
Levetiracetam
CPT Codes:
80177
LOINC Value:
30471-7
Synonyms:
Keppra
Last Updated: 12/20
Last Reviewed: 12/23