CHILDREN AND INFANT WITH SEIZURE
I. INTRODUCTION
Seizures
are
a common occurrence in
children. About 8% will have at
least one
seizure by 15
years
of age.
Many
underlying conditions and neurological challenges
may
provoke seizures. In over
50% of children
seizures are isolated events associated with a high
fever
or minor head
injury in young children. Most seizures
in children are brief,
terminate spontaneously and
do not need any treatment.
Seizures
that persist beyond
five minutes may not stop
spontaneously, so it is
usual practice to institute anti-convulsive
treatment.
II. DEFINITION
A seizure may be defined as a sudden
attack of altered behavior,
consciousness,
sensation or
function produced
by
a transient disruption of
brain
function.
Generalized
convulsion (tonic-clonic)
status epilepticus is
defined as a generalized convulsion
lasting 30
minutes or longer or when successive convulsions
occur frequently over a
30 minute period and
the patient
does not recover consciousness between them.
III. EPIDEMIOLOGY
Of all children, 3 to 5 percent will
have a single febrile seizure in
the
first five years
of life; 30
percent will
have
additional febrile seizures, and 3 to 6 percent of those with febrile seizures will
develop afebrile seizures
or epilepsy.
IV. ETIOLOGY
1- Febrile convulsion (6 months to less than 6 years)
• Febrile convulsions
are
common in children 6 months
to less than 6 years old.
• The convulsion
is usually short and generalized.
The child may sleep
following the convulsion, but can
be aroused and there are no localized
neurological signs.
The generally accepted criteria
for
febrile seizures include:
· A convulsion
associated with an elevated
temperature greater than 38°C per axilla
· A child younger than
six years of
age
· No central nervous system
infection or inflammation
· No acute
systemic metabolic abnormality that
may
produce convulsions
· No history of previous
afebrile seizures
2- Convulsion due to infectious causes (other than febrile convulsion)
- Severe malaria
- Meningitis (including tuberculosis)
- Encephalitis
3-
Afebrile convulsion
- Hypoglycemia
convulsion may occur in malnutrition, malaria and other severe
infection. Always confirm the diagnosis
by
using a gluocometer
or taking venous blood.
- Hyponatraemic convulsion
- Hypocalcaemia convulsion may occur
with severe malnutrition including Rickets. It
can
occur also after repeated
blood transfusion.
- Convulsion due to
intoxication or poisoning (see Intoxication CPG)
- Convulsion due to epilepsy
(see Epilepsy CPG)
- Head trauma
including
child abuse
V. APPROACH TO
DIAGNOSIS History:
· Gestation, birth, general
health, growth and development
· Current
medication; allergies
· Previous history of convulsion
· Precipitating factors:
o Fever
o Preceding illness
o Sleep
deprivation
o Recent
head trauma
o Ingestion/poisoning
o Change in antiepileptic medication
Physical
examination:
· Vital
signs: temperature, respiratory rate,
heart
rate,
blood pressure
· Complete
Neurological examination: pupillary asymmetry, altered
mental status, signs
of meningism, fixed
eye deviation,
focal motor weakness
· Signs
of head trauma or child abuse:
retimal
hemorrhages, evidence of increase
intracranial
pressure
· Head circumference:
microcephaly or
hydrocephalus
· Complete
general examination looking for infectious
causes and other diseases
· Skin
examination: café au
lait spots, facial hemangioma,
purpura
· Convulsions: focal or generalized
Investigations
· bedside glucose
· malaria smear (if
in malaria area)
· FBC
· Where possible
o Electrolytes
o sepsis screening (e.g.
blood culture, CSF, urine
etc)
o calcium
VI. TREATMENT
The priorities
are:
1. Initial resuscitation
2. Stop
convulsion
3. Find
and treat the cause of convulsion
1 Initial resuscitation:
The first step
in the management
of the patient who is having a seizure is to
assess
|
and
support airway, breathing and circulation.
This will ensure that the seizure does not compromise supply of oxygenated
blood to the brain and is not secondary to
hypoxia and/or
ischemia.
· Open
and maintain airway with
simple maneuver (see basic life
support CPG)
· Secretion
clearance
with gentle suction
· Put the child
in recovery position
(left lateral decubitus) to minimize the
risk
of aspiration once the child is breathing satisfactorily.
Breathing:
· High flow
oxygen via face mask
with
reservoir as soon
as the airway is
opened
adequately
· Support
respiration with bag-valve
mask ventilation and consider intubation if the child is hypoventilating.
Circulation
· Gain iv
or intraosseous access
· Treat hypoglycemia (glycemia < 3mmol/l) with D10% 2ml/kg bolus and
D10%1/2NSS 5ml/kg/h
infusion
(without follow on infusion
there is a risk of rebound
hypoglycemia)
· Give NSS 20
ml/kg bolus to any patient with
signs
of shock (except
cardiogenic
shock, DKA, trauma and severe malnutrition –
10 ml/kg NSS bolus).(Refer to shock
CPG)
2 Stop
convulsion:
Start anticonvulsant medication (midazolam 0.2mg/kg IM or diazepam
0.25mg/kg IV or 0.5
mg/kg PR)
if the convulsion lasts more than
5 minutes. Usually if
the
convulsion started
pre hospital, then the duration
might
already be longer than
5 minutes before the arrival of the patient. In this
case, start anticonvulsant medication
immediately IM (midazolam) or
diazepam IV or rectally if cannot access IV immediately
Repeat
the
dose if the seizure continues. If
after 2 doses the child
is still seizing, treat
with Phenytoin 20mg/kg IV over
20 minutes (max 1g) or Phenobarbital 15-20mg/kg
IV over 20 minutes or
via NGT (max 1g).
Monitor
respiratory rate and have resuscitation facilities
available including
endotracheal
tube as all these drugs
cause respiratory
depression.
(see the algorithm
on management of convulsion below).
3 Find and treat
the cause:
Once the convulsion
has stopped, the effort
of management depends
on finding and treating
the causes of convulsion. If the patient
is diagnosed as
having a febrile convulsion,
then the attempt to find the cause of fever
should be made.
· Give antibiotic (Ceftriaxone if > 2 months or Ampicillin/Gentamycin
for infant < 2 months (see meningitis CPG))
to any patients thought to
have infection
leading to convulsion
are
likely.
· Treat hyponatraemia (if presenting with seizure) with IV 3% NaCl
4ml/kg over 15 minutes
· Treat confirmed hypocalcemia with 10% Calcium gluconate
0.5ml/kg, maximum
10ml over 15 minutes
Specialist
consultation or transfer
should be made in:
- Children with compromise of vital functions
- Prolonged
seizures lasting more than 30 minutes
- Seizure continuing after two
doses of a benzodiazepam
- Suspected serious
underlying cause
of seizures e.g meningitis,
encephalitis,
metabolic abnormality and head
injury.
- unable
to determine the cause
e.g. lack laboratory support to help with diagnosis
(no blood gases, cannot
check sodium, calcium level
etc)
4 Monitoring
Reassess ABC
The vital signs should
be
reassessed
frequently in addition to continuous monitoring with
ECG and oximetry:
- After each dose
of anticonvulsant medication
- Continuous
monitoring while the seizure continues
- Every 15
minutes for at least
an hour after a seizure until level
of consciousness returns to normal.
VII. COMPLICATIONS
There are many complications including:
a. obstruction of the
airway and
hypoxia b.
aspiration pneumonia
c. respiratory depression.
VIII. EDUCATION
· If the
child
has had a febrile convulsion, inform the parent convulsion can recur when
the child is less than 6 years old.
· When
fever,
reduce temperature by bath sponging
· give
paracetamol to
reduce the
fever
· Bring the child immediately to health
care facility.
· If the
child
is experiencing of tonic-clonic seizure:
o Remain
calm
o Roll on
to their side immediately if they vomit
o Protect
the
child from harm
REFERENCES
1. Samuels, M., Wieteska, S. Advanced Paediatric Life Support: The Practical Approach, Fifth Edition June
2011
2. NSW Health: Infants and
children: Acute
Management
of Seizures second edition 2009 sourced at http://www0.health.nsw.gov.au/policies/pd/2009/pdf/PD2009_065.pdf
3. Schwartz, M.W.
5-Minute Pediatric Consult 6th edtion June 2012
4. Wilfong,
A. Clinical features
and complications
of status epilepticus in children. Last
updated
Jan 2012. Available
from http://www.uptodate.com/contents/management-of-status-epilepticus-in- children?source=search_result&search=status+epilepticus&selectedTitle=3~150
5. Wilfong,
A. Management of status epilepticus in children. Last updated
Jan
2012. Available
from
http://www.uptodate.com/contents/clinical-features-and-complications-of-status-epilepticus-in- children?source=search_result&search=status+epilepticus&selectedTitle=2~150
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