Epilepsy Flashcards

1
Q

Define epilepsy:

A

chronic disorder characterised by recurrent seizures which may vary from a brief lapse of attention or muscle jerks to severe and prolonged convulsions (spontaneous)

tendency to have spontaneous recurrent seizures

2 or more seizures without clear symptomatic provocation

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2
Q

What are the key elements to assessing a blackout?

A

clinical diagnosis is key to determining investigations/management/treatment Mis-diagnosis is common e.g. seizure/cardiac syncope can have significant consequences, or diagnosing a seizure when actually it was a faint- end up with inappropriate drug treatments, and life changing consequences (driving)

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3
Q

What are the differential diagnosis of “blackout”?

A
faint (vasovagal syncope) - very common 
seizure 
cardiac syncope 
cataplexy 
hypoglycaemic attacks (very rare but significant)
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4
Q

What are the most useful diagnostic tools for diagnosing a blackout?

A

witness account

develop clear understanding of what happens before, during and after the episode

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5
Q

What is a faint?

A

sudden impairment of consciousness with loss of tone
due to reduced blood/oxygen to the brain
frequent provoking factors - blood, pain, dehydration
Usually come round where they fell
stiffening and jerking is common
urinary and faecal incontinence may occur

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6
Q

What are presyncopal symptoms?

A

light headedness

warm, dizzy builds in intensity then may be loss of vision or hearing before loss of consicousness

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7
Q

What are the helpful features that indicate its likely to be a seizure?

A

post event confusion longer than 2 mins
deeply bitten lateral border of tongue
prolonged tonic then clonic movement lasting greater than 1 min
deep cyanosis

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8
Q

Define seizure:

A

clinical phenomenon due to abnormal, synchronous, cortical discharges
provoked seizure does not equal epilepsy

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9
Q

What are some of the aetiologies of epilepsy in adults?

A

mainly cryptogenic

trauma, idiopathic, cerebrovascular, degenerative, neoplasm

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10
Q

What is your prognosis with epilepsy?

A

70% enter spontaneous remission - therefore most it is good
poor prognosis - failure of 2 first line drugs because of efficacy- <10% of entering remission
such patients should be considered for epilepsy surgery programme

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11
Q

What is the impact in terms of QoL of epilepsy?

A
impaired QoL resulting from:
- comorbidity- cognitive and mood disturbance
- lifestyle restrictions: driving, employment, social life
- stigma and discrimination
- medication side effects
increased risk of injury
premature mortality
- underlying cause of epilepsy
- accidents
- SUDEP
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12
Q

Define drug resistant or chronic epilepsy?

A

continuous seizures despite effective trials of at least 2 appropriately selected antiepileptic drugs

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13
Q

What is the ILAE classification of seizures?

A

FOCAL

  • characterised by one or more features; aura, motor, autonomic, awareness altered
  • may evolve to bilateral convulsive response

GENERALISED

  • absence
  • myoclonic
  • atonic
  • tonic
  • tonic-clonic
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14
Q

What does it mean by “complex” partial seizures?

A
impaired consciousness or awareness
clinical manifestations vary with site of origin and degree of spread
- presence and nature of aura
- automatism 
- other motor activity
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15
Q

What are the different types of aura and which region of the brain tends to be affected?

A

somatosensory - R parietal lobe = tingling in L arm
Visual - L occipital lobe = colourful flashing lights, temporal, parietal-occipital junction = complex dream like visions
olfactory - temporal = hallucination of a familiar unpleasant smell
auditory - temporal = hearing a familiar song
autonomic - temporal mainly = rising abdominal sensation
emotional = temporal - fear, anger, sadness or sexual arousal
psychic - temporal = multisensory attacks, deja vu

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16
Q

What are absence seizures?

A

petit-mal seizures
dominant seizure type in idiopathic generalised syndromes of childhood and juvenille absence epilepsy
momentary lapse in awareness - patient may stop what they are doing, stare, blink or look vague before carrying on what you were doing
simple if just LoC and complex if also accompanied by motor activity
often don’t recollect attacks

17
Q

How can epilepsy syndromes be characterised?

A

grouping of pts that share similar:

  • seizure types
  • age of onset
  • eeg pattern
  • natural history/prognosis
  • genetics
  • response to treatment
18
Q

How are epilepsy syndromes categorised?

A

partial = cryptohenic or structural metabolic

Generalised = presumed genetic or structural metabolic

19
Q

What investigations are carried out for syncope or seizures?

A

Syncope - ECG and discharge with advice

Seizure - MRI (good at detecting subtle abnormalities) commonly, EEG maybe

20
Q

What are the DVLA rules around seizures?

A

new rules 2010 - single seizure “imaging” and EEG unsupportive of epilepsy = 6 months
Epilepsy = 12 months seizure free

21
Q

What is MOA of barbiturates and what type are they used for?

A

increases GABA

partial seizures

22
Q

What is MOA of benzodiazepine and what type are they used for?

A

increases GABA

status

23
Q

What is MOA of carbamazepine and what type are they used for?

A

inhibits Na channels

Tonic clonic

24
Q

What is MOA of phenytoin and what type are they used for?

A

inhibits Na and Ca

status

25
Q

What is MOA of valporate and what type are they used for?

A

increase GABA and inhibits Na channels

partial, TC and absence

26
Q

What is MOA of levetiracetam and what type are they used for?

A

inhibits synaptic conduction

partial

27
Q

What is MOA of lamotrigine and what type are they used for?

A

inhibits NA channels

partial, TC

28
Q

What is MOA of topiramate and what type are they used for?

A

?reduces glutamate

29
Q

How are antiepileptics chosen?

A
individual basis
- type of epilepsy
- se profile
- in women teratogencity, weight gain and interaction with oral contraceptive are important 
secondary factors - cost and ease of use
30
Q

What do the risks depend on in terms of epilepsy and teratogenesis?

A

number of AEDs
type of drug
? whether taking prophylatic high dose folic acid

31
Q

What are the high risk antiepileptics for teratogenesis?

A
valporate
phenytoin 
phenobarbitone 
topiramate
mysoline
32
Q

What effect does valporate have on neurodevelopment of infants?

A

lower IQ - dose dependent

33
Q

What is important to discuss in pre-conceptual counselling?

A

folic acid 5mg daily
monotherapy if poss
withdraw valporate, phenytoin, phenobarbitone if poss
always withdraw valporate if history of spina bifida

34
Q

What are the newer antiepileptics?

A

lamotrigine, levetiracetam, topiramate
more expensive and no more effective
improved SE / interactions- however many SE arent found for years

35
Q

Define status epilepticus

A

continuous seizures lasting at least 5 mins or 2 or more discrete seizures between which there is an incomplete recovery of consciousness

36
Q

What is the initial treatment for status (5-30mins)?

A

lorazepam better than diazepam or phenytoin - cessation and lower risk of continuation

37
Q

What are the benefits of lorazepam over diazepam?

A

smaller vol of distribution

longer therapeutic half-life

38
Q

What are the benefits of diazepam over lorazepam?

A

more lipid solube

faster onset