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Definition
- continuous seizure activity lasting >30 mins
- has been suggested that the duration be reduced to 5 mins on the
basis that typical fits rarely last 5 mins and that spontaneous
termination is less likely in fits lasting >5 mins. In children
spontaneously remitting fits may last longer - up to 12 mins
- two or more seizures with recovery of baseline consciousness
Types
- Repeated generalized tonic and/or clonic convulsive seizures where the
patient does not fully recover neurological function between attacks
- Non-convulsive status: prolonged “twilight” state
- Continuous focal epileptic activity
without alteration of consciousness
Aetiology
| Patients without past history of epilepsy |
Patients with past history of epilepsy |
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Generalized convulsive status epilepticus
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Most common and dangerous form of SE
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Wide range of presentations from repeated overt
generalized seizures to very subtle focal twitches of a localized part of
the bocy
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If patient inadequately treated generalized convulsions
may stop despite continued ictal EEG discharges
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Pseudoseizures are most important differential
Complications
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Hypoxia
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Lactic acidosis
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Hypercarbia
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Rhabdomyolysis, hyperkalaemia, ARF
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Hyperpyrexia
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Hypoglycaemia
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Hyper/hypotension
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Cardiac arrhythmias
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Pulmonary oedema
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Aspiration pneumonitis
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Intracranial hypertension
Investigations
| Initial |
Subsequent |
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Glucose, urea, creatinine, sodium, potassium,
calcium
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Anti-convulsant levels
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Complete blood count
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Arterial blood gases or oximetry
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Urinalysis
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Treatment

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If hypoglycaemic or blood glucose unknown give glucose
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first line agent of choice is lorazepam. Not only is it
more effective than diazepam but its longer duration of anti-epileptic
action (>6 h compared with 20 mins) means that recurrence of fits is less
likely
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if first line therapy is ineffective the probability of
either phenytoin or phenobarbitone terminating the status epilepticus is not
high and therefore some authorities recommend treating these patients for
refractory status epilepticus. Others recommend trying phenytoin (if this
has not already been done) before deciding the patient has refractory SE
Refractory status epilepticus
- intubate the patient
- if the patient is hyperkalaemic or the potassium is unknown use
rocuronium instead of suxamethonium as muscle relaxant. Disadvantage of
rocuronium is that seizures are masked for a prolonged period of time.
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treatment options for refractory SE are:
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midazolam infusion
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propofol infusion
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thiopentone infusion
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treatment should be titrated to abolish electrical
seizure activity rather than a specific EEG pattern. Seizures may still
occur despite burst-suppression and may be abolished when EEG only shows
slow waves.
Non convulsive status epilepticus
- Incidence in comatose patients in ICU varies in incidence from 8% of
medical ICU patients to 30-40% of patients in neuro-intensive care units.
Occurs in significant proportion of patients with another cause for coma eg
subarachnoid haemorrhage, traumatic brain injury
- Two types:
- Absence SE
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Prolonged confusional state
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Characteristic EEG pattern
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Almost never causes coma
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Patients rarely require ICU admission
- Complex partial SE
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Diagnosis may be difficult
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Variable presentation
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Characteristic manifestation is altered mentation with
variable responsiveness and amnesia
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May demonstrate automatism, complex motor activity,
bizarre behaviour, lateralizing or localizing neurological deficits (eg
aphasia or paresis)
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Duration usually minutes to hours
Further reading
Alldredge BK et
al. A comparison of lorazepam, diazepam, and placebo for the treatment of
out-of-hospital status epilepticus. N Engl J Med 2001; 345:631-7
Marik PE and Varon J. The management of status epilepticus. Chest 2004;
126:582-591
Treiman DM et
al. A comparison of four treatments for generalized convulsive status
epilepticus. N Engl J Med 1998; 339:792-8
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