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Pediatric Seizures

Published on Nov 18, 2015

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PRESENTATION OUTLINE

PEDIATRIC SEIZURES

PEDIATRICS IN REVIEW, AUGUST 2013
Photo by thinker thing

TAKING A SEIZURE HISTORY: SEMIOLOGY

  • Response to tactile stimulation
  • Eye (fluttering, deviation)
  • Head (forced flexion)
  • Mouth (chewing, lip smacking)
  • Facial (twitching)

TAKING A SEIZURE HISTORY: SEMIOLOGY

  • Hand (repetitive reaching)
  • Limbs (arm/leg freezing)
  • Incontinence
  • Color change
  • Length, post-ictal phase

OTHER IMPORTANT PARTS OF A SEIZURE HX

  • Mimics: GERD, ADHD, Sleep Disorders
  • Family Hx of Epilepsy
  • Diarrhea, Rickets (electrolyte disturbances)
  • Medications (Buspirone)
  • Presence of fever

FEBRILE SEIZURES

FEBRILE SEIZURES

  • Seizure in >1mo febrile pt, not d/t CNS infection
  • Usually occur 6-60 months, peak at 18months
  • Incidence 3-8% in kids
  • 25-40% have + family hx
  • 9-22% have +sibling hx

SIMPLE VS. COMPLEX

  • Simple: Generalized,
  • Complex: Focal, >15min, multiple seizures in 24hrs

FEBRILE SEIZURES: RISK FACTORS

  • Febrile seizure in 1st degree relative
  • Neurodevelopmental delays
  • Increased exposure to HHV6
  • Recent Vaccination: MMR, DTaP, Flu
  • *High incidence of sodium channelopathies

MANAGEMENT OF FEBRILE SEIZURES

  • LP:
  • CT: Complex, neuro deficits, prolonged post-ictal, high ICP
  • EEG: Febrile Status Epilepticus
  • Rectal Diazepam: Prolonged, Risk factors for recurrence
  • AEDs Lowers risk of FS recurrence but not development of epilepsy

FEBRILE SEIZURES: RECURRENCE RISK

  • Younger age of onset
  • Low temperature threshold
  • First degree relative
  • Brief duration between fever onset & seizure
  • Risk of recurrence is 60% after initial FS

FEBRILE SEIZURES: RISK OF EPILEPSY

  • 2-7% risk of developing epilepsy
  • Family Hx of Epilepsy
  • Complex FS
  • Neurodevelopmental abnormalities
  • 40% w/ complex & status develop mesial temp lobe epil.

FEBRILE SEIZURES: ANTICIPATORY GUIDANCE

  • Recurrence risk
  • Epilepsy development risk
  • No assoc. with later developmental delay
  • No assoc. with SIDS
  • Antipyretics do not reduce risk of recurrence

EPILEPSY

CLASSIFICATION AND MANAGEMENT
Photo by thinker thing

EPILEPSY DEFINED

  • 2 or more unprovoked afebrile seizures
  • AEDs are recommended after 2nd episode
  • Chances of recurrence after single, unprovoked seizure: 60%
  • AEDs prescribed based on: Semiology (clinical findings) and EEG findings
  • Also consider: Mood stability, Abx use, comorbidities (obesity)

SEIZURE TYPES: 2 BROAD CATEGORIES

  • Partial (most common type of seizure in childhood)
  • Generalized

TYPES OF PARTIAL SEIZURES

  • Simple (no LOC, focal jerking or sensory loss)
  • Complex (+LOC, +/-aura) aka "Psychomotor Seizures"
  • Partial complex may develop secondary generalization
  • Focal slowing or epileptiform activity on EEG
  • DOC: Levitiracetam or Oxcarbazepine

SEIZURES IN ADOLESCENCE

  • As children get older, seizures usually become:
  • Generalized (GTCs), although teens may have partial seizures
  • Epileptiform discharges originate from frontal or centrofrontal lobe

TYPES OF GENERALIZED SEIZURES

  • Tonic clonic (GTC)
  • Absence
  • Atypical absence
  • Myoclonic tonic
  • Atonic, Tonic

GENERALIZED TONIC CLONIC

  • Generalized epileptiform activity on EEG
  • DOC: Lamotrigine, Valproic Acid, Topirimate
  • a.k.a. Grand Mal

ABSENCE SEIZURES (CAE)

  • 2nd most common type of epilepsy
  • Lapse in consciousness, motionless stare
  • Usually 10-15 seconds, back to baseline at 30secs
  • EEG: 3Hz generalized spike wave
  • DOC: Ethosuximide, Valproic acid, Lamotrigine

ATYPICAL ABSENCE SEIZURES

  • Similar presentation as CAE, but duration is longer (15-60sec)
  • Onset and cessation is less clear
  • DOC: Valproic Acid

MYOCLONIC TONIC

  • Rapid, rhythmic jerks in the upper ext>lower ext
  • EEG: 4-6Hz polyspikes
  • DOC: Valproic Acid, Levetiracetam
  • Relatively rare outside of Juvenile Myoclonic Epilepsy

TONIC SEIZURES

  • Tonic spasms of face, chest, trunk
  • Tonic flexion of upper ext
  • Flexion or extension of lower ext
  • May have tachycardia, cyanosis, pupillary dilatation
  • EEG: Low amplitude, very fast activity

ATONIC SEIZURES

  • Also called drop attacks
  • Sudden loss in postural tone
  • Tonic and Atonic are on a continuum, so treatment is same:
  • Lamotrigine, Topiramate, rufinamide, clobazam, felbamate
  • Corpus callostomy may be effective, some pts need permanent helmet

THINGS TO KNOW WHEN USING AEDS

  • Valproic Acid: Monitor PLTs and LFTs, avoided in
  • Lamotrigine: SJS
  • Levitiracetam can exacerbate behavioral problems, treat w/ B6
  • Oxcarbazepine (monitor CBC and BMP--leukopenia & hyponatremia)
  • AEDs continued till at least 2 yrs of seizure freedom

EPILEPSIES TO BE FAMILIAR WITH

  • Benign Rolandic Epilepsy
  • Infantile Spasms
  • Juvenile Myoclonic Epilepsy
  • Lennox-Gastaut
  • Pediatric Pseudoseizures

BENIGN ROLANDIC EPILEPSY

  • Most common epilepsy syndrome in childhood
  • Unilateral facial sensory-motor & oropharyngo-gutteral symptoms
  • Hypersalivation and speech arrest, fully aware, GTCs can occur
  • EEG: Biphasic, focal centrotemporal spikes and slow waves
  • AEDs given after 3rd episode, but usually remit by age 16

INFANTILE SPASMS (WEST SYNDROME)

  • 200 known causes (HIE, TORCH, Downs, viral, etc.)
  • Presents as spasm-like seizures in pts 3-9 months
  • DOC: Adrenocorticotropic therapy x2 weeks, w/taper
  • Neurological prognosis is poor, but Downs babies respond best
  • Vigabatrin is used in pts who have IS d/t Tuberous Sclerosis

PEDIATRIC PSEUDOSEIZURES

  • Psychogenic, often due to stressors
  • Accounts for 5% of events in Pediatric epilepsy monitoring
  • No changes on EEG

LENNOX-GASTAUT

  • Presents between age 2-6 w/ seizures & psychomotor retardation
  • Tonic seizures in 90% but can also have Myoclonic & Atonic, GTCs
  • May develop from West Syndrome
  • Lamotrigine, topiramate, rufinamide, clobazam, felbamate

JUVENILE MYOCLONIC EPILEPSY

  • Begins at age 5-15
  • Myoclonic jerks upon waking
  • May develop GTCs, Absence

BEHAVIORAL ISSUES IN EPILEPSY

  • Children with new onset seizures have high rates of:
  • Anxiety disorders (35%)
  • Depressive disorders (22%)
  • ADHD (26%)

STATUS EPILEPTICUS

  • Repeated seizures w/o return of consciousness for 30min
  • Causes: CNS infection, toxins, ingestion, drug withdrawal
  • May cause: hypoperfusion of brain, electrolyte disturb., etc.
  • Treat: Rectal diazepam till EMS arrives.
  • Ativan-Ativan-Fosphenytoin-Phenobarb, correct electrolytes
Photo by cobalt123

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