Neurocritical Care
Monitoring
Continuous EEG monitoring is necessary for status epilepticus and RSE.
adequate concentrations and mitigate the risk of toxicity. Because of altered protein binding, obtaining
a free level of highly bound medications is preferred.
Antiepileptic
Drug
Dosing
Common
Adverse Effects
Considerations
Lorazepam
0.1 mg/kg IV (slow IV push)
(maximum 4 mg/dose); up to 8
mg total
Sedation, hypotension
IV formulation contains propylene
glycol
Midazolam
(intermittent)
0.2 mg/kg IM (maximum 10
mg/dose)
Sedation, hypotension
Short duration with IV bolus
Diazepam
0.15 mg/kg IV (slow IV push);
typically up to 10 mg total
0.2 mg/kg rectally (20 mg
maximum)
Sedation, hypotension
IV formulation contains propylene
glycol; rectal administration may be
considered
Fosphenytoin
20 mg PE/kg IV (not to exceed
150 mg PE/min);
may also give IM
Hypotension,
arrhythmia,
hepatotoxicity
Several drug-drug interactions
Phenytoin
20 mg/kg IV (not to exceed 50
mg/min)
Hypotension,
arrhythmia,
phlebitis, purple
glove syndrome,
hepatotoxicity
Several drug-drug interactions,
IV formulation contains propylene
glycol and ethanol. Addition of
parenteral phenytoin to dextrose
and dextrose-containing solutions
should be avoided because of lack of
solubility and resultant precipitation
Valproic acid
40 mg/kg IV (not to exceed 6
mg/kg/min)
Hyperammonemia,
thrombocytopenia,
hepatotoxicity
Many drug-drug interactions, avoid
in patients with a TBI
Levetiracetam
60 mg/kg IV (maximum 4.5 g)
Sedation/paradoxical
excitation, irritability
Renally eliminated, limited drug-
drug interactions
Lacosamide
400 mg IV (typically over
15β30 min)
Dizziness,
bradyarrhythmia, P-R
interval prolongation
Limited drug-drug interactions
Topiramate
PO/enteral loading dose of
300β800 mg, followed by a
daily dose of 400β1000 mg in
2β3 doses
Metabolic acidosis,
nephrolithiasis
No IV formulation available
Phenobarbital
20 mg/kg (not to exceed 100
mg/min)
Sedation,
hypotension,
respiratory depression
IV formulation contains propylene
glycol