Epilepsy Flashcards

1
Q

What are the two focal seizures

A

Occipital lobe/SeLEAS
SeLECTS - central-temporal part of brain

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2
Q

What are the Generalised Epilepsy Syndromes

A

Childhood Absence Epilepsy
Juvenile Absence Epilepsy
Juvenile Myoclonic Epilepsy
Epilepsy with generalised tonic clonic seizures

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3
Q

What does Myoclonic mean

A

Sudden brief muscle contractions

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4
Q

What does Tonic mean

A

Sudden stiffening

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5
Q

What does Atonic mean

A

Sudden loss of muscle tone

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6
Q

How is Epilepsy diagnosed

A

EEG and MRI
Have to have 2 or more unprovoked seizures to have epilepsy

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7
Q

What is a seizure

A

Physical manifestations of abnormal electrical activity in the brain

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8
Q

How many children grow out of epilepsy by adulthood?

A

50-60%

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9
Q

What causes epilepsy?

A

Genetic disorders, structural lesions, previous brain injury, epilepsy syndromes

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10
Q

What is epilepsy

A

The tendency to recurrent unprovoked seizures

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11
Q

Name the types of seizures

A

Focal seizure

Generalised seizure

Tonic Clonic

Absence

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12
Q

How are epilepsy syndromes charaterised?

A

By characteristic clusters or clinic and EEG features

Supported by structural, genetic, metabolic immune or infectious aetiologies

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13
Q

Give me information on SeLects

A
  • It’s FOCAL
  • Centro-temporal part of brain
  • 4-10 years
  • Often nocturnal events
  • Normal development and cognition
  • Typically involve focal clonic or tonic activity of throat/tongue and one side of the lower face
  • EEG - normal background, high activity in C-T area and activated in sleep
  • Infrequent seizures that usually stop at puberty
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14
Q

Tell me about Occipital lobe/SeLEAS

A
  • It’s FOCAL
  • Seizures further back in the brain are longer, and so it’s longer than absence seizures
  • Self limited with autonomic seizures
  • Infrequent - with 25% only having one seizure
  • Remission in a few years is typical
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15
Q

Tell me about Childhood Absence Epilepsy

A
  • GENERALISED
  • Onset is 4-10 years
  • Normal development
  • Very frequent, like 40 a day
  • 3-20 seconds
  • EEG: 3Hx spike wave
  • Seizures are brought out by hyperventilation

Treatment: Ethosuximide

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16
Q

Tell me about Juvenile Myoclonic Epilepsy

A
  • GENERALISED
  • Older children: 10-24 years
  • higher rates in ADHD
  • Myoclonic seizures on wakening, also Absence and GTCS
  • Triggered by sleep deprivation and photic stimulation
  • Generally a worse prognosis
17
Q

Tell me about Developmental Epileptic Encephalopathy –> BAD

A
  • Diseases where epilepsy itself contributes to cognitive and behavioural impairments
  • Frequent epileptiform activity
  • Many causes: Myogenetic, structural, metabolic, secondary to insult - BD before
18
Q

Tell me about Infantile spasms

A
  • Onset: 1-24 months
  • Sudden and brief - arm extension and neck flexion
  • Ass. with poor development and developmental regression
  • Ass. with T21 and Tuberous sclerosis
  • EEG: Hypsarrythmia –> slow and disorganised
  • Treatment: Steroids and Vigabatrin
19
Q

Tell me about Landau Kleffner syndrome

A
  • Rare and in school aged children
  • Acquired aphasia of childhood with seizures
  • Epileptic Aphasia
  • Verbal auditory agnosia
  • Epileptiform activity in sleep
  • Infrequent seizures; not the main issue

May lose speech they’ve developed - understanding of noise is affected

20
Q

Tell me about epileptic medication

A

Taken twice a day

Tablet/liquid

Aim for 2 years seizure free and wean off

After 2 unprovoked seizures

If it’s infrequent, like SeLEAS or SeLECT –?

21
Q

What medication is given for convulsive seizures exceeding 5 mins

A

Buccal Midazolam

22
Q

What are non pharmalogical treatments?

A
  • Keotgenic diet
  • Epileptic surgery
  • Vagus nerve stimulation
23
Q

SUDEP - tell me about it

A
  • Not in the context of a seizure
  • Nocturnal is the worry
  • Occurs in benign circumstance
    Risk factors: epilepsy not being treated, that’s symptomatic, resistant to treatment, ID/Developmental delay, Polytherapy etc…
24
Q

What is NOT epilepsy

A
  • Tics
  • Febrile seizures (6months to 6 years only, seizures only occur in high temps., generally short GTCS less than 5 mins), normal development
  • Staring in ASD
  • Syncope (fainting)
  • Functional Neurological Disorder
  • Infantile gratification
25
Q

What are some co-morbidities of Epilepsy

A
  • Mental health
  • Behavioural issues
  • IDs
  • Sleep disturbance
  • Bone health - due to drugs
26
Q

Tell me about genetics in Epilepsy

A
  • Karyotype – an individual’s complete set of chromosome
  • Microarray – is there a bit missing or a bit added to our genes
  • Single gene testing – one spelling mistake in one gene
  • Gene panel
  • Whole exome/genome sequencing
27
Q

Tell me about an EEG

A

Painless, 1 hour, electrodes placed on scalp, +/- sleep deprivation, Hyperventilation and photic stimulation to evoke a seizure

28
Q

Some facts about epilepsy

A
  • most common neurological condition in children - 1 in 200 children
  • 50-60 % out of it by adulthood
29
Q

What is the treatment for Childhood absence seizures

A

Ethosuximide

30
Q

What is the treatment for infantile spasms

A

Steroids and Vigabatrin

31
Q

Clinical features of epilepsy

A

Alterations in consciousness, motor/sensory/autonomic or cognitive event

32
Q

Describe Tonic Clonic seizures

A

Starts with a cry

Sudden fall to the ground with bilateral stiffening and jerky movements, +/- tongue biting or incontinence

33
Q

Describe Absence seizures

A

5-10 seconds staring and impaired consciousness with eye blinking and lip smacking

Generalised