Index
Module 10 • Neurology
Neurocritical Care
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Data Tables
Neurocritical Care
Keaton S. Smetana ~2 min read Module 10 of 20
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Neurocritical Care

I.

Monitoring

1

Continuous EEG monitoring is necessary for status epilepticus and RSE.

2Proactively monitor serum concentrations for agents such as (fos)phenytoin and valproic acid to ensure

adequate concentrations and mitigate the risk of toxicity. Because of altered protein binding, obtaining

a free level of highly bound medications is preferred.

Table 6. Characteristics of Agents for Status Epilepticus

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

15–30 min)

Dizziness,

bradyarrhythmia, P-R

interval prolongation

Limited drug-drug interactions

Topiramate

PO/enteral loading dose of

300–800 mg, followed by a

daily dose of 400–1000 mg in

2–3 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

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