Epilepsy Symposia Flashcards

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1
Q

What is epilepsy

A

Recurring, unprovoked, spontaneous seizures

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2
Q

What does a generalised onset mean?

A

Electrical discharges appear to start over the whole brain at the same time

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3
Q

What does partial/facial onset mean?

A

Electrical discharges appear to start in one cortical region and then may remain localised or spread over the whole brain

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4
Q

Describe frontal lobe seizures

A

Forced head and eye deviation to contralateral side
Difficulty speaking, unresponsiveness
Repetitive movements
Pt can be fully aware whilst it is happening

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5
Q

Epileptogenesis

A

Process where parts of normal brain converted to hyperexcitable brain

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6
Q

Epileptic seizure

A

Explosion of synchronous activity

Rhythmic firing of AP by neurons

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7
Q

What are febrile convulsions/seziures

A

Fever-induced

Can be due to point mutation in Na+ channel causing abnormally slow inactivation

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8
Q

Describe temporal lobe seizures

  • physical
  • cognitive
  • affective
A
Preceded by warnings of deja vu, rising epigastric sensation, followed by lip-smacking and speech arrest 
Hallucinations 
Pallor/flushing 
Can mimic panic attacks 
Changes in smell
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10
Q

Parietal lobe seizures

A

Positive sensory symptoms
Tingling, pain
Distortion of body shape
Sensory Jacksonian March

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11
Q

Describe the tonic phase in a tonic clonic seizure

A
Continuous muscle spasms 
Will fall 
May have cyanosis due to thorax muscle contracting 
Tongue biting 
Incontinence
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12
Q

Describe the clonic phase in a tonic clonic seizure

A

Rhythmic jerking slows & gets larger in amplitude as the seizure ends

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13
Q

Describe the postictal phase in a tonic-clonic seizure

A
Coma 
Drowsiness
Headache 
Confusion 
Muscle aching
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14
Q

Jacksonian march

A

Simple, partial seizures
Patient aware- localised discharge

Symptoms

  • Lip smacking
  • sudden muscle contraction
  • sudden head and eye deviation
  • lasts very briefly
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15
Q

Describe occipital lobe seizures

A

Visual hallucinations
Amaurosis on onset
-blackout

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16
Q

perampanel

A

AMPA receptor antagonist

non-competitive inhibitor

reduce spread / generalisation of seizure

well tolerated with improved alertness

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17
Q

Carbamazepine, oxcarbazepine and eslicarbazepine

A

Anticonvulsant
competitively inhibit the voltage gated sodium channel by binding with the receptor in its inactive state, prolonging the period between successive firings (prevents burst firing)

18
Q

First line treatment for primary generalized epilepsy

A

sodium valproate

lamotrigine

19
Q

First line treatment for partial (focal onset) epilepsy

A

carbamezapine

lamotrigine

20
Q

Name drugs that can exacerbate generalized seizure types such as myoclonus and absences

A
  • phenytoin
  • carbamazepine
  • gabapentin/pregabalin
21
Q

Benzodiazepines

-side effects
acute/long term

A
Acute:
Drowsiness
Ataxia		
Hyperactivity
Personality Change
Cognitive impairment

Long Term:
tolerance/dependence

22
Q

Phenytoin

-side effects
acute/long term

A

Acute:

Ataxia, Diplopia, Nystagmus

Long Term:

Gingival hyperplasia
Osteomalacia
Cerebellar atrophy

23
Q

Sodium Valproate

-side effects
acute/long term

A

Acute:

sedation
nausea and vomiting
tremor

Long Term:

Hair thinning
Weight gain
Menstrual irregularities
Encephalopathy

24
Q

difference between provoked seizures versus epilepsy

A

provoked caused by acute insults such as metabolic disturbance, withdrawal, stroke, alcohol

25
Q

Causes of epilepsy

A
CVS 
Alcohol
Tumour 
Post-traumatic
Idiopathic
26
Q

Idiopathic (Primary) Generalized Seizures

A
  • tonic clonic
  • absences
  • myoclonic

> onset in childhood or adolescence
usually no focal symptoms/signs
often a number of seizure types cluster
a polygenic cause is presumed with no identifiable structural lesion on imaging
generalized (all leads) spike and wave discharges on EEG, photosensitivity may be present

27
Q

Juvenile Myoclonic Epilepsy

A
>commonest form of primary generalized epilepsy 		
>3-12% all epilepsy
>juvenile onset, probably lifelong
>early morning myoclonic jerks (ask)
>photosensitive, sleep deprivation triggers
>+/- absences 
>generalized tonic clonic seizures –
>occur without warning
28
Q

Tonic clonic seizures “grand mal”

A

-occurs without warning –risk of injury

-tonic phase
continuous muscle spasm, fall, cyanosis, tongue biting, incontinence

-clonic phase
rhythmic jerking slows and gets larger in amplitude as attack ends

-post-ictal (post-seizure) phase
coma, drowsiness, confusion, headache
muscle aching

29
Q

Absences - “petit mal”

A
  • abrupt
  • short, 5-20 seconds
  • multiple times/day, can lead to learning difficulties
  • unresponsive, amnesia for the gap, rapid recovery
  • tone preserved (or mildly reduced)
  • eyelid flickering
  • absences only, tend to remit in adulthood (childhood absence epilepsy)
30
Q

simple partial seizure (SPS)

A

patient aware - aura

31
Q

complex partial seizure (CPS)

A

aura/warning with a level of reduced awareness

32
Q

Secondary Generalized Tonic Clonic Seizures – (GTCS)

A

warning/aura –eg epigastric rising sensation, altered smell, déjà vu, fear
cannot abort attack
onset sudden
duration 1-3 minutes
then falls , loses consciousness as seizure generalizes
rigidity/ convulsive jerks/ excess salivation
incontinence/tongue bite common
red/blue, wakes in ambulance/A&E

33
Q

First line treatment for absent seizures

A

Ethosuximide