Epilepsy Flashcards

1
Q

How is epilepsy defined?

A

It is defined by recurrent unprovoked (= spontaneously occurring) seizures

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2
Q

What is an epileptic seizure?

A

paroxysmal change in behaviour due to synchronised rhythmic firing of populations of CNS neurons

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3
Q

How often does epilepsy occur in the population?

A

1% of the general population has epilepsy
5% of the general population has a risk of one seizure in the lifetime

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4
Q

When is the probablity of an epileptic seizure the highest?

A

U-shaped distibution: childhood-adolescence (0-20) + older age (60-80)

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5
Q

When can a person be diagnosed with epilepsy?

A
  • 2 unprovoked seizures, > 24 hours apart
  • 1 unprovoked seizure & causative CNS disease and pathological EEG alterations
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6
Q

What is a focal seizure?

Does it originate in one hemisphere or in both?

A

initial symptoms/signs (clinical and EEG) indicate origination of seizure activity within an area of one hemisphere

Clinical data: partial onset; seizures during sleep; focal slowing or hyperexcitability; structural lesion

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7
Q

What is a generalised seizure?

Does it originate in one hemisphere or in both?

A

initial symptoms/signs indicate origination of seizure activity simultaneously in both hemispheres

Clinical data: generalized seizures; 30 minutes after awakening; positve family history; generalized hyperexcitability; negative MRI

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8
Q

What types of focal seizures are there?

A
  1. focal aware => preserved concioussness, aware of having a seizure
  2. focal impaired awareness => impaired concioussness, staring (additional symptoms of focal aware, automatic behaviors like lip smacking, fumbling, wandering)
  3. focal to bilateral tonic-clonic (secondary) => loss of concioussness, falling on the ground
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9
Q

What types of generalised seizures are there?

A
  1. Absence seizures → absent staring, non-motor, can occur in clusters
  2. Tonic seizures → stiff muscles of the back, arms, and legs
  3. Atonic seizures → “drop seizures”, loss of muscle control
  4. Clonic seizures → repeated jerking; the neck, face, and arms
  5. Myoclonic seizures → brief jerks and twitching; upper body, arms, and legs
  6. Tonic-clonic seizures → the most dramatic, stiffness and shaking, loss of consciousness
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10
Q

Where are focal aware seizures localized?

A
  1. temporal lobe (65%):
    -lateral (10%) — auditory symptoms
    -mesial (90%) — psychic or autonomic symptoms (deja vu, fear (amygdala))
  2. frontal lobe (25%) - tonic (rigility/stiff) / clonic (jerking) movements
  3. occipital lobe (5%) - visual symptoms
  4. parietal lobe (5%) - paraesthesia (tickling), vertigo

sum to 100%, no multiple localizations — very rare + a difficult case: seizure and abnormality — are there causation relations?

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11
Q

What is an epileptic syndrome in focal epilepsy?

ILAE: epileptic syndrome is “a characteristic cluster of clinical and EEG features, often supported by specific etiological findings (structural, genetic, metabolic, immune, and infectious).”

A

history/clinical data
* partial or partial onset seizures
* seizures during sleep

EEG
* focal slowing or hyperexcitability

cMRI
* structural lesion

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12
Q

What is an epileptic syndrome in generalised epilepsy?

A

history/clinical data
* generalised seizures
* 30 min after awakening
* positive family history

EEG
* generalised hyperexcitability

cMRI
* not helpful, always negative

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13
Q

What can be the etiology of epilepsy?

Structural vs. genetic epilepsy

A

Structural
1. Hippocampal sclerosis
2. Malformations of cortical development
3. Vascular malformations
4. Prenatal injuries and developmental abnormalities (oxygen deficiency, ASD, malnutrition)
4. Postnatally acquired CNS lesions
-infectious/inflammatory causes (HIV, viral encephalitis, parasitic infections)
-neoplasia
-cerebro-vascular accidents
-traumatic brain injury
-neurodegeneration

Genetic
1. ion channel mutation (Na+, K+, Cl–channels)
2. receptor mutation (GABA-receptor, acetyl-cholin-receptor)
3. ion transporter mutation (Na+-K+-ATPase)

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14
Q

What are the main differnces bertween syncope and tonic-clonic seizure?

A

syncope vs. tonic-clonic seizure
duration: < 30s vs. 1-2min
reorientation: <30s vs. 4-45 min
trigger: 50% vs. almost never
tongue biting: rare vs. frequent

Mind: convulsions (even though arrhythmic vs. rhythmic), falls and eyes open can be charasteristical of both

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15
Q

What are the features of psychogenic non-epileptic seizures?

A
  • duration: > 10 min
  • motor convulsions fluctuating
  • put on, deflectable
  • tip of the tongue biting
  • never out of sleep
  • injuries rare
  • ictal EEG unchanged
  • eyes closed
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16
Q

What is myoclonus?

A

Myoclonus is a type of muscle twitching or jerking that is caused by sudden, brief, and irregular muscle contractions. e.g. hyperventilation-induced myoclonus as a result of breathing too rapidly and deeply => decrease in carbon dioxide levels in the blood

17
Q

What is PNES?

A

Psychogenic non-epileptic seizure:
* resemble epileptic seizures but are not the result of abnormal electrical discharges in the brain
* the spike and spike pattern is not seen on EEG
* psychosomatic – physical manifestation of psychological distress

18
Q

What does the risk of reoccurence of an epileptical seizure depend on?

A

Risk for seizure reoccurence
* if you have one seizure (5%) -> 30-40% of the second seizure
* if you have two seizures (diagnosis) -> 60% of reoccurence

19
Q

Can epilepsy be modified or treated? How does it influence treatment options?

A

The chronic disorder epilepsy cannot be modified or treated. Treatment options are antiseizure medication (ASM) and secondary prophylaxis (preventing syptoms occurence)

20
Q

What is the treatment goal in chronic epilepsy

A

maintenance of normal life style = complete seizure freedom + no or minimal substance adverse effects

21
Q

What are the targets of treatment?

A

Na+ and Ca2+ channels, GABA system, glutamate receptors (AMPA & NMDA)

22
Q

How successful is treatment with antiepileptic drugs?

A

60%: good prognosis, seizure-free with 1. or 2. monotherapy, no relevant adverse effects, commonly seizure-free with AED termination
30%: pharmacoresistant with polytherapy
10%: seizure-free with polytherapy

23
Q

When is epilepsy surgery recommended? How successful it can be?

A
  • pharmacoresistance
  • identification of one epileptic focus with EEG
  • suitable MRI lesion
  • resection possible without persistent neurological/neuropsychological deficits
    • not younger than 17 years

58% of patients are seizure-free after 1 year follow up

24
Q

What are less invasive treatment options? Are they effective?

A

Laser treatment – MRI-guided borehole. Same 58% of patients seizure free

priniciple: thermal therapy

25
Q

What are most often side effects of antiepileptic drugs?

A

Side effects:
* specific for the drug
* dizziness (in the beggining => slower dosing)
* mood swings and irritability -> depression symptoms, even to suicidal attempts
* allergic reactions
* osteoporosis
* electrolyte disturbances
* loss of memory function

26
Q

What does ILAE 2017 Classification of Seizure types rely on?

A

It relies on onset region: focal vs. generalized vs. unknown