Epilepsy Symposia Flashcards

(32 cards)

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
Idiopathic (Primary) Generalized Seizures
- 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
Juvenile Myoclonic Epilepsy
``` >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
Tonic clonic seizures “grand mal”
-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
Absences - “petit mal”
- 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
simple partial seizure (SPS)
patient aware - aura
31
complex partial seizure (CPS)
aura/warning with a level of reduced awareness
32
Secondary Generalized Tonic Clonic Seizures – (GTCS)
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
First line treatment for absent seizures
Ethosuximide