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Test Code MEPHS Mephobarbital and Phenobarbital, Serum

Reporting Name

Mephobarbital and Phenobarbital, S

Useful For

Monitoring of mephobarbital and phenobarbital therapy

Profile Information

Test ID Reporting Name Available Separately Always Performed
MBARS Mephobarbital, S No Yes
PHBRS Phenobarbital, S No Yes

Method Name

Gas Chromatography Mass Spectrometry (GC-MS)

Performing Laboratory

Mayo Clinic Laboratories in Rochester

Specimen Type

Serum Red


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: 2.0 mL

Collection Instructions:

1. Collect specimen immediately before next scheduled dose.

2. Centrifuge and aliquot serum into plastic vial within 2 hours of collection.


Specimen Minimum Volume

0.7 mL

Reject Due To

Gross hemolysis Reject
Gross lipemia OK
Gross icterus OK

Specimen Stability Information

Specimen Type Temperature Time Special Container
Serum Red Refrigerated (preferred) 14 days
  Ambient  14 days
  Frozen  14 days

Reference Values

MEPHOBARBITAL

Therapeutic range: 1.0-7.0 mcg/mL

Toxic concentration: ≥15.0 mcg/mL

 

PHENOBARBITAL

Therapeutic range

Children: 15.0-30.0 mcg/mL

Adults: 20.0-40.0 mcg/mL

Toxic concentration: ≥60.0 mcg/mL

Day(s) Performed

Thursday

CPT Code Information

80184

LOINC Code Information

Test ID Test Order Name Order LOINC Value
MEPHS Mephobarbital and Phenobarbital, S 97183-8

 

Result ID Test Result Name Result LOINC Value
89706 Mephobarbital, S 3750-7
84582 Phenobarbital, S 3948-7

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

3 to 9 days

Forms

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