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Pediatric Seizures
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Published on Nov 18, 2015
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PRESENTATION OUTLINE
1.
PEDIATRIC SEIZURES
PEDIATRICS IN REVIEW, AUGUST 2013
Photo by
thinker thing
2.
TAKING A SEIZURE HISTORY: SEMIOLOGY
Response to tactile stimulation
Eye (fluttering, deviation)
Head (forced flexion)
Mouth (chewing, lip smacking)
Facial (twitching)
3.
TAKING A SEIZURE HISTORY: SEMIOLOGY
Hand (repetitive reaching)
Limbs (arm/leg freezing)
Incontinence
Color change
Length, post-ictal phase
4.
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
5.
FEBRILE SEIZURES
6.
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
7.
SIMPLE VS. COMPLEX
Simple: Generalized,
Complex: Focal, >15min, multiple seizures in 24hrs
8.
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
9.
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
10.
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
11.
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.
12.
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
13.
EPILEPSY
CLASSIFICATION AND MANAGEMENT
Photo by
thinker thing
14.
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)
15.
SEIZURE TYPES: 2 BROAD CATEGORIES
Partial (most common type of seizure in childhood)
Generalized
16.
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
17.
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
18.
TYPES OF GENERALIZED SEIZURES
Tonic clonic (GTC)
Absence
Atypical absence
Myoclonic tonic
Atonic, Tonic
19.
GENERALIZED TONIC CLONIC
Generalized epileptiform activity on EEG
DOC: Lamotrigine, Valproic Acid, Topirimate
a.k.a. Grand Mal
20.
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
21.
ATYPICAL ABSENCE SEIZURES
Similar presentation as CAE, but duration is longer (15-60sec)
Onset and cessation is less clear
DOC: Valproic Acid
22.
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
23.
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
24.
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
25.
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
26.
EPILEPSIES TO BE FAMILIAR WITH
Benign Rolandic Epilepsy
Infantile Spasms
Juvenile Myoclonic Epilepsy
Lennox-Gastaut
Pediatric Pseudoseizures
27.
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
28.
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
29.
PEDIATRIC PSEUDOSEIZURES
Psychogenic, often due to stressors
Accounts for 5% of events in Pediatric epilepsy monitoring
No changes on EEG
30.
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
31.
JUVENILE MYOCLONIC EPILEPSY
Begins at age 5-15
Myoclonic jerks upon waking
May develop GTCs, Absence
32.
BEHAVIORAL ISSUES IN EPILEPSY
Children with new onset seizures have high rates of:
Anxiety disorders (35%)
Depressive disorders (22%)
ADHD (26%)
33.
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
34.
Untitled Slide
Jonathan Strysko
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