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Primidone, Serum or Plasma

CPT 80184; 80188
Synonyms
  • Mysoline®

Test Details

Methodology

Immunoassay

Result Turnaround Time

2 - 3 days

Turnaround time is defined as the usual number of days from the date of pickup of a specimen for testing to when the result is released to the ordering provider. In some cases, additional time should be allowed for additional confirmatory or additional reflex tests. Testing schedules may vary.

Use

This deoxybarbiturate is closely related chemically to the barbiturates. It is converted to two active metabolites, phenobarbital and phenylethylmalonamide (PEMA). Primidone is used principally in generalized tonic-clonic and complex and simple partial seizures; some clinicians believe that the drug has specific usefulness for complex partial seizures. It is as effective as carbamazepine or phenytoin in controlling partial or generalized tonic-clonic seizures, although a greater incidence of adverse reactions, especially during initial therapy, limits patient acceptance. Primidone is commonly given with phenytoin but monotherapy is preferred. The conversion of primidone to phenobarbital is significantly increased when this drug is used with other antiepileptic medication. It is not effective in absence seizures.

Footnotes

1. Bourgeois BF. Pharmacokinetic properties of current antiepileptic drugs. What improvements are needed? Neurology. 2000; 55(Suppl 3):S11-S16. 11147563

References

American Medical Association, Division of Drugs and Toxicology. Drug Evaluations Subscription. Chicago, Ill: AMA; Fall 1992.

Custom Additional Information

Plasma half-life of primidone usually ranges from six to eight hours with rapid elimination (24 to 40 hours). Since phenobarbital requires a longer interval (48 hours) to achieve therapeutic blood levels, checking both levels can be used to determine chronic compliance. The phenobarbital:primidone ratio normally is 2.5, can be higher (4.3 mean) in patients on other anticonvulsants (phenytoin, carbamazepine) and lower than normal among patients discontinued from those medicines or who are chronically noncompliant. Primidone decreases the effects of oral anticoagulants, carbamazepine, valproate, ethosuximide, felbamate, lamotrigine, topiramate, and oxcarbazepine.1

Specimen Requirements

Specimen

Serum or plasma

Volume

1 mL

Minimum Volume

0.3 mL

Container

Red-top tube or green-top (heparin) tube. Do not use a gel-barrier tube. The use of gel-barrier tubes is not recommended due to slow absorption of the drug by the gel. Depending on the specimen volume and storage time, the decrease in drug level due to absorption may be clinically significant.

Collection Instructions

Transfer separated serum or plasma to a plastic transport tube. Collect specimen immediately prior to next dose.

Stability Requirements

Temperature

Period

Room temperature

14 days

Refrigerated

14 days

Frozen

14 days

Freeze/thaw cycles

Stable x3

Reference Range

Therapeutic: primidone: 5.0−12.0 μg/mL, phenobarbital: 15−40 μg/mL

Storage Instructions

Room temperature

Causes for Rejection

Gel-barrier tube; severe hemolysis; lipemia; icteric specimen

LOINC® Map

Order Code Order Code Name Order Loinc Result Code Result Code Name UofM Result LOINC
007856 Primidone (Mysoline(R)), Serum 3978-4 018713 Primidone, Serum ug/mL 3978-4
007856 Primidone (Mysoline(R)), Serum 3978-4 007830 Phenobarbital, Serum ug/mL 3948-7
Order Code007856
Order Code NamePrimidone (Mysoline(R)), Serum
Order Loinc3978-4
Result Code018713
Result Code NamePrimidone, Serum
UofMug/mL
Result LOINC3978-4
Order Code007856
Order Code NamePrimidone (Mysoline(R)), Serum
Order Loinc3978-4
Result Code007830
Result Code NamePhenobarbital, Serum
UofMug/mL
Result LOINC3948-7