seizure disorders in children
TRANSCRIPT
Contents
What is a seizure?
Seizure types
Etiology of seizures
Febrile convulsions
Epilepsies of childhood
Epilepsy syndromes
Status epilepticus
2
What is a Seizure ?
Paroxysmal, involuntary & sudden
disturbance of neurological function caused
by an abnormal or excessive neuronal
discharge.
With or without LOC.
If manifests as motor act – “convulsions”
3
Etiology of seizures
Idiopathic (70-80%) – cause unknown but
presumed genetic
Secondary
Cerebral malformations
Cerebral vascular occlusion
Cerebral damage (ex; congenital infections,
hypoxic-ischaemic encephalopathy…)
Causes for Epileptic seizures
5
Cerebral tumour
Neurodegenerative disorders
Neurocutaneous syndromes
Neurofibromatosis
Tuberous sclerosis
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Causes for Non-epileptic seizures
Febrile seizures
Metabolic
Hypoglycaemia
Hypocalcaemia
Hypomagnesaemia
Hypo/hyper natraemia
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Definition
A seizure accompanied by a fever in the
absence of intracranial infection due to
bacterial meningitis or viral encephalitis.
10
Incidence
Affects 3% of children
Positive family Hx in 10%-20%
Autosomal dominant inheritance (thus family hx
important)
Recurrent febrile seizures in 30%-40%
1%-2% of subsequent epilepsy after a simple febrile
seizure
4%-12% in complex febrile seizure
Boys > Girls11
Diagnostic criteria
Age
6 months – 60 months (5yrs)
Peak 14 – 24 months
Temperature
Usually >= 38C with rapidly rising temp.,
within 24hrs of onset of fever
12
Should not last >10min
Generalized, not focal
No residual weakness of limb or disability
except a brief period of drowsiness
No evidence of CNS infections. (meningitis,
encephalitis, abscess….)
13
Extra cranial infection may be there. ( URTI,
tonsillitis, otitis media…)
No Hx of previous afebrile seizure
No acute systemic metabolic abnormality
14
Classification
SIMPLE COMPLEX
Most common Uncommon
Lasts less than 15min Lasts more than 15min
One fit only in the same
illness
Recurring during same
illness within 24hrs
Generalized tonic-clonic Focal
15
Risk factors for recurrent febrile
seizures
Younger than 18 months (younger the child, higher
the risk...)
Shorter duration of fever before the seizure
Height of fever (lower the peak, higher the risk…)
Positive family Hx
Complex febrile seizure at onset
16
Pathogenesis
Not well known
Due to temporary impairment of the
balance between convulsant and
anticonvulsant system of brain
17
Studies done in children suggest that the
cytokine network is activated and may
have a role in the pathogenesis of febrile
seizures
Threshold level of anticonvulsant system in
these genetically predisposed children is
lower
18
Other suggestions
Endogenous pyrogens such as IL-1
increase neuronal excitability & cause
seizures
Hyperthermia induced alkalosis
19
Investigations
Usually not needed in simple febrile
convulsion
Complex form may need,
Blood glucose, serum electrolytes
LP and CSF analysis
Neuro-imaging (CT, MRI)
EEG
20
Lumbar puncture is strongly
recommended ,
Hx of irritability, reduced feeding or lethargy
Clinical signs of meningitis/encephalitis
Systemically ill
21
Prolonged post-ictal altered consciousness
After a complex convulsion
After pretreatment with antibiotics
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Neuroimaging is considered If,
Micro/ macrocephaly
Neurocutaneous syndrome
Pre-existing neurological defect
Recurrent complex febrile seizures
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Management
Fever
Find the cause (usually viral illness)
Must exclude meningitis
○ Infection screen blood culture
urine culture
LP for CSF culture
26
Treating fever promote comfort.
Not important in preventing seizures.
Physical methods
Fanning
Tepid sponging (now not recommended)
Light clothing
Drugs
PCM
ibuprofen
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Management at home
Move danger away
Left lateral position
Do not try to stop fitting
Do not put anything in mouth
28
If seizure lasting >5-10 min,
Seek medical advice
Diazepam
0.5mg/kg rectal
Midazolam
0.5mg/kg buccal
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Prognosis
Generally excellent
Risk of further febrile seizures – 30%
Risk of epilepsy after single febrile seizure – 3%
No increased risk of death
31
No evidence of deaths
What to do when fitting
If lasting >10 min & not stopping
Rectal diazepam
-OR-
Take to the hospital
Information & advice sheets
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Definition
Chronic neurological disorder
characterized by recurrent unprovoked
seizures, associated with abnormal,
excessive or synchronous neuronal activity
in brain
35
Pathogenesis
Sudden, excessive, disorderly
discharging neurons
Increased GLUTAMATE levels &
decreased GABA levels
36
Classification
Generalized
Discharges from both hemispheres
○ Absence
○ Myoclonic
○ Tonic
○ Tonic-clonic
○ Atonic
37
Focal
Arise from one or part of one hemisphere
○ Frontal seizures
○ Temporal lobe seizures
○ Occipital seizures
○ Parietal lobe seizures
38
Generalized seizures
There is,
Always LOC
No warning
Symmetrical
B/L synchronous discharge on EEG
39
AbsenceTransient LOC
Abrupt onset & termination
Typical(petit mal) or atypical
Often due to hyperventilation
MyoclonicBrief, repetitive, jerky movements
Limbs, neck or trunk
Physiologically in hiccoughs
Tonic Generalized increased tone
Tonic – clonic
Rhythmic contractions of muscle
groups
Become cyanosed
Jerking of limbs
Tongue biting & incontinence
Atonic Combined with myoclonic jerk
Followed by transient loss of muscle
tone
Sudden fall or drop of head40
Focal seizures
Begin in one hemisphere
May herald by an aura
May or may not have change in
consciousness
41
Frontal Motor phenomena
Temporal Auditory or sensory (smell
or taste) phenomena
Occipital Positive or negative visual
phenomena
Parietal Contra lateral altered
sensation
43
Diagnosis
Primarily by detailed Hx
Child & eye witnesses
Video if available
Skin markers of Neurocutaneous syn.
Or neurological abnormalities
44
Investigations
EEG Indicated whenever suspected
To detect structural abnormalities
Neuronal hyperexcitability
○ Sharp waves
○ Spike-wave complexes
45
Many children with epilepsy
Many children never had epilepsy
Normal initial EEG
Abnormal initial EEG
46
Additional techniques
Sleep deprived record
24h ambulatory EEG
Video – telemetry
Subdural electrodes (prior to surgery)
47
Imaging studies
Structural scans
MRI
CT brain
Can identify
Tumours
Vascular lesions
Sclerotic areas
48
Functional scans
Structural lesions not always possible to see
Can see areas of abnormal metabolism
Suggestive of focal seizures
Ex :- PET, SPECT
49
West syndrome
Age of onset 4-6 months
Violent flexor spasms of head, trunk &
limbs
Extension of arms
“salaam spasms”
EEG shows hypsarrhythmia
51
Childhood absence epilepsy
Age of onset 4-12 y
Suddenly stop moving & stare
Lasts only few seconds
Has no recall
May look puzzled
Induced by hyperventilation
53
Benign epilepsy with
centrotemporal spikes (BECTS)
Age of onset 4-10 y
Tonic clonic seizures in sleep
Abnormal feelings in tongue & face
Focal sharp waves in EEG
Benign so important to recognize
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A seizure lasting >30min or repeated
seizures for 30min without recovery of
consciousness in between
57
Management
Diazepam 0.5mg/kg PR
Lorazepam 0.1mg/kg IV Midazolam 0.5mg/kg buccal
Check blood glucose
If <3mmol/L give IV glucose & recheck
AirwayBreathing Circulation
58
Rapid-sequence induction with Thiopental
Mechanical ventilation Transfer to PICU
Phenytoin 18mg/kg IV over 20min or
Phenobarbital 15mg/kg if on oral phenytoin
Paraldehyde 0.4ml/kg PR
(If no response in 10min)
59
Summary
60
Febrile convulsions
Affect 3% of children
Usually tonic-clonic with
rapid rise in fever
Must exclude CNS infection
Family advice about
management
Does not affect intellect
Reassure the parents
Epilepsy
Affects 1 in 200 children
Underlying etiology important
If suspected EEG is indicated
Need psychological help
Parents & teachers need to be
aware of the management
Avoid injurious situations