Seizure Disorders in Children
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Transcript Seizure Disorders in Children
Seizure Disorders in
Children
By Paula Peterson, APRN, FNC, PNP
LPN2007, November/December 2007
2.0 ANCC/AACN contact hours
Online: www.nursingcenter.com
© 2007 by Lippincott Williams & Wilkins. All world rights reserved.
Seizures and Epilepsy
A seizure is defined as a transitory disturbance in
consciousness or in motor, sensory, or autonomic
function caused by uncontrolled electrical discharges in
the brain
Epilepsy refers to disorders characterized by recurrent
seizures rather than a single seizure
- Categorized by causes and types of seizures
Causes of Seizures
brain injury
trauma
infection
metabolic and neurodegenerative diseases
cortical malformation
Classification of Seizures
Symptomatic - symptom of underlying disease
Idiopathic - caused by genetically inherited trait
Cryptogenic - unknown cause
Partial - uncontrolled electrical activity in area of brain
Generalized - affects both hemispheres of brain at once
Types of Partial Seizures
Simple - person remains alert
Complex - person experiences aura, with altered
consciousness during seizure and confusion following
the seizure
More Seizure Types
Absence seizures - “staring episodes,” also called
petit mal seizures
Atonic seizures - sudden loss in muscle strength, often
resulting in a fall
Infantile spasms - brief flexion/extension of the upper
body, usually not seen after 18 to 24 months of age
More Seizure Types
Tonic seizures - usually occur during sleep involving
most of the brain, causing increased muscle tone
Clonic seizures - rhythmic jerking movements of the
entire body
Tonic-clonic seizures - also known as “grand mal”
seizures, whole-body jerking movements with loss of
bowel, bladder, and consciousness
Seizure Syndromes
Juvenile myoclonic epilepsy - inherited, myoclonic
seizures late in childhood, responds to medication but
rarely resolves
Benign rolandic epilepsy - common seizure syndrome
with good prognosis for the child to outgrow
Lennox-Gastaut syndrome - early childhood onset, no
cure, treated with medications
Causes of Lennox-Gastaut
brain malformations
perinatal asphyxia
severe head injury
central nervous system infection
inherited genetic or metabolic conditions
unknown in 30% to 35% of cases
Febrile Seizures
Brought on by fever in infants and children
Classified as typical or atypical
Typical febrile seizure- occurs in 2% to 5% of children
ages 6 months to 5 years of age, usually during first day
of acute infection
Atypical Febrile Seizure
Febrile seizure that recurs in a 24-hour period
Risk of epilepsy after is associated with risk factors for
seizure disorders
Often accompanied with Todd’s paralysis (transient
paralysis of a limb)
Diagnostic Tools
History and physical - emphasis on seizure event is
most valuable tool
Lab tests - complete blood cell count, metabolic panel
Brain imaging studies - Computed tomography scan,
magnetic resonance imaging
Diagnostic Tools
Electroencephalogram - to correlate with seizure
activity and electrical discharges in the brain
Possibly a spinal tap for spinal fluid specimen
Managing Seizure Disorders
Medication is mainstay
Goals:
- freedom from seizures and adverse events
- avoid drug interactions
- adherence to therapy
- minimal interference with daily life
Challenge to the health care provider is to meet these
goals with monotherapy
Other Management Options
When medications have limited success:
ketogenic diet
vagal nerve stimulation
surgery
Ketogenic Diet
rigid food plan
high fat, essential proteins, low carbohydrates
requires high level of family commitment
mixed results of decrease in seizures with medication
small number of children seizure-free
Vagal Nerve Stimulation
Surgical implantation (usually in patient’s neck) of a
device delivering electrical stimulation to the vagus nerve
Decrease in seizures reported with quicker recovery, not
seizure-free
Caring for Your Patient
Education of family and/or support system is key
Education about what to do during seizure
Education about medications and treatments
Referrals for family support