Antiepileptic drug | Dose | Therapeutic drug level to treat epilepsy (μg/mL) | Monitoring | TDM clinical pearls |
---|---|---|---|---|
Phenytoin | Load: 15–20 mg/kg Maintenance: 4–6 mg/kg/day | 10–20 | 1 h postload or ~ 7–10 days after initiation of maintenance dose (may check earlier within 2–3 days in seizing patients to ensure their metabolism is not significantly different from average patient population) | At total concentrations > 20 μg/mL, nystagmus may occur. In concentrations > 30 μg/mL, ataxia, slurred speech, and incoordination can be observed. If total concentrations are above 40 μg/mL, coma is possible. At concentrations > 50–60 μg/m drug induced seizures may occur |
Valproic acid | Load: 20–40 mg/kg Maintenance: 10–15 mg/kg/day | 50–100 (levels as high as 175 are used in RSE) | 1 h postload or 2–4 days after initiation of maintenance dose | At total concentrations > 75 μg/mL lethargy and ataxia may occur. In concentrations > 100 μg/mL tremor is observed. Coma may occur if total serum concentrations are above 175 μg/mL. Thrombocytopenia is a dose-related side effect that can be limited by reducing the dose |
Phenobarbital | Load: 20 mg/kg Maintenance: 1.5–2 mg/kg/day (dose adjustment may be required in liver impairment due to reduced clearance) | 15–40 (higher levels may be utilized in RSE) | 1 h postload or 4–7 days after initiation of maintenance dose | CNS depression is a dose-related side effect. In concentrations > 60 μg/mL respiratory depression may occur |
Pentobarbital | Load: 5–15 mg/kg Maintenance: 0.5–5 mg/kg/h | 1–5 (rarely used to assess clinical efficacy or toxicity) | May be used after discontinuation to monitor the residual effects of the drug | Drug levels have not been correlated with electroencephalography CNS depression, respiratory depression, and hemodynamic instability are dose-related side effects |