Table 1.
Pt | Age (yrs) | Medical History | Presentation | Load Dose (mg/kg) | Serum Level (μg/mL) | Effect | Short-Term Outcome |
---|---|---|---|---|---|---|---|
1 | 14 | Cardiac transplantation on immunosuppressant medication. Renal and liver dysfunction. Hypotension requiring vasopressors. Intubated. Comatose | Generalized convulsion followed by multifocal malignant NCSE refractory to phenobarbital (level 52) and phenytoin (level 14) | 13 | 16 | Temporary termination of sz. No adverse effects | Care withdrawn. Fungal sepsis and meningitis |
2 | 9 | Previously healthy. Presumed encephalitis of unknown etiology. Intubated. Comatose | Single seizure followed by malignant NCSE refractory to phenytoin (level 24) and phenobarbital (level 51) | 26 | 19 | Temporary termination of sz. No adverse effects | Care withdrawn |
3 | 2 | Previously healthy. Presumed encephalitis of unknown etiology. Intubated. Comatose | Malignant NCSE refractory to phenytoin (level 22) | 20 | 26 | Temporary termination of sz. No adverse effects | Developed progressive cerebral edema. Care withdrawn |
4 | 5 | Previously healthy. Cardiac arrest due to anaphylaxis treated with therapeutic hypothermia protocol. Hypotension requiring vasopressors. Intubated. Comatose | NCSE during rewarming period. LEV used as first-line anticonvulsant | 20 | 8 | Termination of NCSE. No adverse effect | Moderate neuropsychological impairment (able to talk and ambulate) |
5 | 13 | Previously healthy. Cardiac arrest treated of unknown etiology treated with therapeutic hypothermia protocol. Hypotension requiring vasopressors. Intubated Comatose | NCSE during rewarming period. LEV used as first-line anticonvulsant | 22 | 8 | Termination of NCSE. No adverse effects | Moderate neuropsychological impairment (able to talk and ambulate) |
6 | 5 | DiGeorge syndrome with truncus arteriosus repair at birth admitted for truncal aortic valve replacement. Intubated. Obtunded | Postoperative 4 clinical repetitive focal seizures with secondary generalization LEV used as first-line anticonvulsant | 21 | 32 | No sz occurred after LEV. No adverse effects | Unknown |
7 | 0.08 | Nonaccidental traumatic brain injury with subdural hematoma status postevacuation and parenchymal hemorrhage. Lethargic | Persistently altered mental status. Frequent subclinical focal seizures. LEV used as first-line anticonvulsant | 31 | 37 | No sz occurred after LEV. No adverse effects | Severe neurologic impairment |
8 | 0.25 | Desmoplastic infantile ganglioglioma resection. Lethargic | Postoperative 4 clinical focal seizures. LEV used as first-line anticonvulsant | 30 | 40 | No sz occurred after LEV. No adverse effects | Normal infant |
9 | 4 | Previously healthy. Asystolic cardiac arrest of unclear etiology. Intubated. Comatose | Persistently altered mental status. Frequent subclinical focal seizures. LEV used as first-line anticonvulsant | 30 | 41 | LEV reduced sz by 75%. Another 30 mg/kg intravenous loaded 1.5 hrs later and seizures terminated. No adverse effects | Severe neurologic impairment |
10 | 7 | Previously healthy. Enterovirus encephalitis. Obtunded | Persistently altered mental status and abnormal eye blinks associated with Bi-PEDS and burst suppression. LEV employed as first line anticonvulsant | 15 | 27 | Reduction of Bi-PEDS by 75%. No adverse effect | Moderate neuropsychological impairment (able to talk and ambulate) |
LEV, levetiracetam; NCSE, nonconvulsive status epilepticus; PED, periodic epileptiform discharges; sz, seizure.
“Temporary termination of sz” = 12–24 hrs.