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Status epilepticus (SE) is associated with high Fever is a common cause of SE.
morbidity and mortality in children. Fever is
a common cause of SE and may precipitate
seizures in children who have underlying
epilepsy risk factors or may signal intracranial
infection. Metabolic abnormalities, such
as hypoglycemia, can also cause SE. Early
termination of SE is the goal of therapy.
Non-intravenous benzodiazepines can be
initiated at home or en route to the hospital.
Use of anticonvulsants depends on the
progression of the seizure. Children with SE
need to be hospitalized for a comprehensive
evaluation of the seizure etiology done in
consultation with a paediatric neurologist.
When counselling parents, address the social
and academic repercussions of epilepsy and
emphasize first aid measures and use of
medications, such as rectal benzodiazepines.
• P artial seizures begin in one portion of Table 1. Causes and mortality rate of paediatric status epilepticus
the brain and have symptoms related to
that region’s function. These seizures may Cause Cases, % Mortality rate
remain restricted to one location without
Infection 52 5
affecting alertness (simple partial seizure);
they may spread to adjacent regions and Remote 38 0
affect consciousness (complex partial Lowered antiepileptic drug levels 21 0
seizures); or they may spread across the Cerebral stroke 10 0
entire cortex (secondary generalization).
Metabolic abnormality 7 0
Seizures are often isolated events that
Hypoxia 5 0
terminate spontaneously within several
minutes. However, they can present as recur- CNS infection 2 0
rent episodes in close proximity, with recov- Drug overdose 2 0
ery between episodes (repetitive seizures);
Adapted from Shorvon SD et al. In: Engel J Jr, Pedley T, eds. Epilepsy: A Comprehensive Textbook. 2008.7
or they may be continuous, or frequent,
without recovery between episodes (SE).
Status epilepticus. SE can be divided Table 2. Suggested doses for management of metabolic seizures and
status epilepticus in children
into 2 types:
• Non-convulsive SE consists of continuous
Metabolic abnormality Treatment
abnormal electroencephalographic (EEG)
activity without convulsive activity in the Hypoglycaemia 2–4 mL/kg IV bolus of 25% glucose
presence of altered sensorium.
Hyponatraemia 4–6 mL/kg IV bolus of 3% saline
• Convulsive SE is typically tonic-clonic in
nature and can be generalized or partial Hypocalcaemia 0.3 mL/kg of 10% IV calcium gluconate over 5 min
with secondary generalization. Convul- Hypomagnesaemia 50 mg/kg of IV magnesium sulfate over 1 h
sive SE is defined as either two or more
convulsions without complete recovery
of consciousness or a single prolonged initially divided into symptomatic and idio- factors, such as cerebral palsy. Intracranial
seizure episode that lasts for at least 30 pathic types and then further classified as infections, such as meningitis and encephali-
minutes. 2,4
generalized and localized on the basis of the tis, can also present with fever and seizures.
Because of the high morbidity and clinical presentation along with EEG findings. Children may also have seizures because of
mortality associated with SE and the recog- the presence of metabolic abnormalities,
nition that anti-seizure medications are less Causes such as hypoglycaemia, hyponatraemia,
effective in terminating prolonged seizures, hypocalcaemia, and hypomagnesaemia. For
some experts have recommended shorten- Fever is a common cause of seizures and SE a list of the more common causes of SE in
ing the minimum seizure duration in the SE in children. Some children will present in SE children, see Table 1.
criteria from 30 minutes to 5 minutes. 5
Management Of
with their first febrile seizure. In some cases,
Epilepsy. When two or more unpro- the fever may be secondary to the convulsive Convulsive SE
voked seizures occur more than 24 hours movements. Fever may precipitate seizures
apart, epilepsy is diagnosed. Epilepsy is in children who have underlying epilepsy risk Early termination of seizures substantially
Prehospital management
Antiepileptic treatment Assessment and action
Incipient SE (seizure duration < 5 min)
• Observe patient for signs of seizure termination • Perform quick physical assessment
• Turn the patient to one side (if no neck trauma)
• Clear the area of any sharp objects
• Suction or clear vomit/saliva/food/debris from the mouth,
if possible
• Loosen clothing
If no termination of seizure within 2 to 3 min:
• A dminister a benzodiazepine if available: • Call 911 or proceed to hospital
Rectal diazepam (0.2–0.5 mg/kg) OR
Buccal midazolam (0.5 mg/kg) OR
IM midazolam (0.2 mg/kg) OR
Intranasal midazolam (0.2 mg/kg) OR
• EMTs and paramedics might consider:
IM lorazepam (0.05–0.1 mg/kg)
or other benzodiazepines
In-hospital management
Antiepileptic treatment Assessment and action
Established SE (seizure duration 5 - 10 min)
• A dminister IV lorazepam (0.05 mg/kg to a maximum of 4 mg total) • Administer oxygen; support airway; monitor breathing, circulation
• Wait 5 min before adding IV fosphenytoin (30 mg/kg) • Obtain intravenous access
• Check bedside glucose levela
• Conduct more thorough history/physical examination (reflexes,
malformations)
• Consider 2 mL/kg of 25% glucose if the seizure is prolonged;
hypoglycaemia caused by seizure may need to be treated
• Consider empiric treatment with 100 mg IV pyridoxine (if < 2 y of
age) for undetected pyridoxine deficiency, which can present with
refractory seizures
Refractory SE (no termination after 2 medications)
• A
dminister IV levetiracetam (20–30 mg/kg) OR • M easure antiepileptic blood levels; obtain metabolic profile
IV valproate (20 mg/kg) • Perform CT scan of head and other investigations as clinically
indicated
If seizure continues:
• Consult paediatric neurology, move patient to paediatric ICU, and
• Add phenobarbital (30 mg/kg)
monitor vital signs along with EEG monitoring
Prolonged refractory SE (anaesthetics fail to terminate SE)
• Induce coma with IV midazolam OR pentobarbital • Continue monitoring
If seizure continues:
• Add nasogastric topiramate OR valproate
EMTs, emergency medical technicians; EEG, electroencephalographic.
a
I n an ideal situation, if time permits and if facilities are available, one can obtain blood chemistries; however, treatment should not be delayed. If hypoglycaemia, hyponatraemia, or hypocalcaemia is
suspected, these can and should be treated empirically (see Table 2) rather than waiting for blood test results.
reduces morbidity and mortality, and is the • Minimal systemic adverse effects seizure-causing condition. It is also important
goal of therapy. The algorithm provides a • Use by nonintravenous route, if possible. to counsel parents about the adverse effects
guide to the most recent approach to the A multidisciplinary team including, but of medications and the social and academic
treatment of a child in convulsive SE. Most not limited to, paediatric emergency and criti- repercussions of epilepsy. In most instances,
important is to turn the patient on his or her cal care specialists is necessary for general restriction of physical activity is unnecessary;
side—assuming that there has been no neck supportive care. These providers attend to however, a responsible adult needs to be pres-
trauma. If in the clinic or ED, perform a rapid the airway, breathing, and circulation; treat ent when the child is bathing or swimming.
blood glucose test to determine whether underlying causes; and prevent and treat First aid measures and use of medications,
hypoglycaemia is the cause of the seizure. systemic complications. such as rectal benzodiazepines, along with
Prehospital treatment. Treatment In addition to a rapid blood glucose test fever management, should be emphasized.
that begins at home or during the prehos- to rule out hypoglycaemia, it is important to Fortunately, most children who are adherent
pital transport has been shown to be safe test for hyponatraemia, hypocalcaemia, and to medications tend to have normal IQs and
and effective. Therapy with a benzodiaz- hypomagnesaemia at the initial evaluation can be expected to lead normal lives.
epine (intramuscular midazolam, buccal and to treat these conditions appropriately
midazolam, intranasal midazolam, or rectal (Table 2). However, empiric treatment should © 2009 CMP Healthcare Media LLC. Ini-
diazepam) can be initiated in the absence of not be delayed while waiting for test results. tially published in Consultant for Paedia-
intravenous access. Rectal diazepam is often Post-seizure evaluation and tricians Dec 2009;8(12):421-424
prescribed for children with febrile seizures management. Children with SE need to be
and prolonged or repetitive seizures as a part hospitalized for a comprehensive evaluation
About the Author
of their home care. of the seizure etiology, which must be done
Dr Mahajan is Associate Professor in the departments
In-hospital treatment. Use of anticon- in consultation with a paediatric neurologist. of paediatrics and emergency medicine, and Vice Chief
vulsants depends on the progression of the Evaluation should include a detailed history, and Research Director in the department of paediatric
emergency medicine at Wayne State University School
seizures. Although most seizure episodes,
6
developmental history, family history, and of Medicine and Children’s Hospital of Michigan, both in
even in patients with poorly controlled exposure to any medications or recent travel. Detroit.
choices for convulsive SE include: of epilepsy indicated by the EEG findings. Guidelines for status epilepticus treatment. Epilepsy.
com/professionals. 2009. http://professionals.epilepsy.
• Ability to be administered rapidly Parents require support and accurate com/page/table_epilepticus_guidelines.html. Accessed
• Fast penetration of the brain information about the prognosis of the November 5, 2009.
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