Tests:Valproic Acid: Difference between revisions
Tests:Valproic Acid
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Valpro | Valpro | ||
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| | |Availability | ||
|Monday - Sunday, testing routinely available out of hours | |Monday - Sunday, testing routinely available out of hours | ||
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== Specimen Requirements == | == Specimen Requirements == | ||
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|Specimen | |Specimen | ||
|Plasma | |Plasma | ||
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== Aliquot Requirements == | == Aliquot Requirements == | ||
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|Sample | |Sample | ||
|Plasma | |Plasma | ||
Revision as of 14:34, 20 March 2025
Overview | |
|---|---|
| Department | Biochemistry |
| Test Code | |
| Synonyms | Valproate
Sodium Valproate Epilim Valpro |
| Availability | Monday - Sunday, testing routinely available out of hours |
| Turnaround Time | 1 – 5 hrs |
| Stability – Add test | |
Specimen Requirements | |
| Specimen | Plasma
Serum |
| Preferred | 6 mL Plain Red-Top |
| Acceptable | 6 mL Li-Hep Green-Top |
| Unacceptable | |
| Specimen Transportation | |
| Paediatric Requirements | 600 μL Li-Hep Microtainer |
Aliquot Requirements | |
| Sample | Plasma
Serum |
| Preferred Volume | 1 mL |
| Minimum Volume | 0.1 mL |
| Aliquot Transportation | |
Clinical Information | |
| Reference Intervals | 350 – 700 umol/L.
Although values <300 umol/L are generally ineffective and values >700 are more likely to be toxic, the concentration does not correlate well with efficacy/toxicity. Dose adjustment should be based primarily on clinical indicators |
| Test Method | Abbott Alinity Ci, Particle-enhanced turbidimetric inhibition immunoassay (PETINIA). |
| Advanced Notice | |
| Patient Preparation | With patient at steady state, samples should be collected immediately before next dose (trough level). |
Comments | |
| With patient at steady state, samples should be collected immediately before next dose (trough level). | |