Epilepsy Flashcards

1
Q

What is a seizure?

A
  • Transient occurence of signs and/or symptoms due to abnormal excessive or synchronous neuronal activity in the brain
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2
Q

What is the definition of epilepsy?

A
  • Epilepsy is defined by any of the following:
    • At least two unprovoked seizures occurring more than 24 hours apart
    • One unprovoked seizure and a probability of further seizures similar to the general recurrence risk after two unprovoked seizures (around 60%)
    • At least two seizures in a setting of reflex epilepsy

NB - Epilepsy is considered no longer present for individuals who had age-dependent epilepsy syndrpome but are not past the applicable age for those who have remained seizure free for at least 10 years off medication.

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3
Q

What are focal (partial/localisation related) seizures?

A
  • Area of abnormality in otherwise normal brain
  • Caused by head injury, stroke, hypoxia, infection, vascular malformations and birth injuries
  • Localised gliosis
  • Can stay localised or can spread
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4
Q

What are generalised tonic-clonic seizures?

A
  • Whole brain is affected
  • Way they metabolise neurotransmitters, ion-channelopathy, difference in binding sites
  • Result of genetic problems
  • Genetic Generalised Epilepsy (GGE)
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5
Q

What are the features of focal seizures?

A
  • Can be aware or have impaired awareness
  • History of trauma or birth injury
  • Focal aura/sequalae (gustatory/sensory/motor)
  • Post-attack confusion/drowsiness
  • Nocturnal events
  • Motor onset:
    • Automatisms
    • Atonic
    • Clonic
    • Epileptic spasms
    • Hyperkinetic
    • Myoclonic
    • Tonic
  • Non-motor onset:
    • Autonimic
    • Behaviour arrest
    • Cognitive
    • Emotional
    • Sensory
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6
Q

What are the features of GGE?

A
  • Photosensitivity
  • Age of onset 8-26yrs
  • Alcohol
  • Sleep deprivation
  • Lack of aura
  • Seizures within 2 hrs of awakening
  • FHx of IGE
  • Abnormal EEG
  • Motor
    • Tonic-clonic
    • Clonic
    • Tonic
    • Myoclonic
    • Myoclonic-tonic clonic
    • Myoclonic-atonic
    • Atonic
    • Epileptic spasms
  • Non-motor (absence)
    • Typical
    • Atypical
    • Myoclonic
    • Eyelid myoclonia
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7
Q

What can EEG be used for in epilepsy?

A
  • EEG can be used to classify epilepsy and is useful to tell you the risk of recurrence
  • Cannot be used for undiagnosed blackouts
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8
Q

How is focal epilepsy treated?

A
  • Lamotrigine
  • Carbamazepine
  • Levetiracetam
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9
Q

How is generalised epilepsy treated?

A
  • Valproate
  • Levetiracetam
  • Lamotrigine
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10
Q

How is status epilepticus managed?

A
  • General measures
    • ABCDE
    • Establish aetiology
    • Alert anaesthetist/ITU it established
    • Transfer to ICU if refractory
  • AED therapy
    • Prehospital
      • Diazepam 10-20mg PR or Midazolam 10mg bucally
    • Early status
      • Lorazepam IV 0.1mg/kg repeated after 10-20 minutes
      • Give AED if already on treatment
    • Established status
      • Phenytoin infusion
    • Refractory status
      • Propofol
      • Midazolam
      • Thiopental sodium
      • Continue 12-24 hrs after last clinical seizure or elctrographic seizure
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11
Q

Dravet syndrome

A
  • An epilepsy with a genetic cause
  • Onset in 1st yer of life with febrile seizures (typically 3-9 months)
  • Prolonged unilateral or generalised clonic seizures
  • Other seizure types by 1-4 years
    • Myoclonus
    • Focal seizures
    • Atypical absences
  • Hyperthermia often precipitant (bathing, fever)
  • Onset in absence of an infection or structural brain lesion
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12
Q

Classification of non-epileptic seizures and events

A
  • Syncopes
  • Psychological/behavioural events
  • Sleep related events
  • Paroxysmal movement disorders
  • Migraine and disorders possibly related to migraine
  • Miscellaneous neurological and non-neurological events
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13
Q

Reflex anoxic seizure/reflex asystolic syncope

A
  • Syncope triggered by an unpleasant event, often a bump on the head, scratch, seeing blood
  • Neurogenic syncope with profound bradycardia and asystole
  • Child goes white as a sheet, may have an anoxic seizure, children may sleep for a while after event
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14
Q

Prolonged expiratory apnoea/breath holding

A
  • Anoxic seizure after not breathing back in following an unpleasant stimulus/crying
  • Child goes progressively blue
  • May become cyanosed and then have an anoxic seizure
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15
Q

Behavioural events

A
  • Often defined as involuntary, patterend, coordinated, repetitive, often rhythmic, non-reflexive movements that are goal directed and ocur in the same fashion with each repitition
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16
Q

Narcolepsy with cataplexy

A
  • Excessive daytime sleepiness
  • Cataplexy
  • Hypnagogic hallucinations
  • Sleep paralysis
  • Disturbed night time sleep
17
Q

Management of generalised tonic-clonic seizures (tonic - muscle tensing, clonic - muscle jerking)

A
  • 1st - sodium valproate
  • 2nd - lamotrigrine or carbamazepine
18
Q

Management of focal seizures (hearing, speech, memory, emotions)

A
  • 1st - carbamazepine or lamotrigine
  • 2nd - sodium valproate or levetiracetam
19
Q

Management of myoclonic seizures (brief muscle contractions, awake throughout)

A
  • 1st - sodium valproate
  • 2nd - lamotrigine, levetiracetam or topiramate
20
Q

Management of absence seizures (becomes blank)

A
  • 1st - sodium valproate or ethosuximide
21
Q

Management of atonic seizures (drop attacks, brief loss in muscle tone)

A
  • 1st - sodium valproate
  • 2nd - lamotrigine
22
Q

Management of infantile spasms (clusters of full body spasms)

A
  • Prednisolone
  • Vigabatrin
23
Q

Side effects of sodium valproate

A
  • Teratogenic
  • Liver damage and hepatitis
  • Hair loss
  • Tremor
24
Q

Side effects of carbamazepine

A
  • Agranulocytosis
  • Aplastic anaemia
  • Induces the P450 system
25
Q

Side effects of phenytoin

A
  • Folate and vitamin D deficiency
  • Megaloblastic anaemia (folate deficiency)
  • Osteomalacia (vitamin D deficiency)
26
Q

Side effects of ethosuximide

A
  • Night terrors
  • Rashes
27
Q

Side effects of lamotrigine

A
  • SJS or DRESS syndrome
  • Leukopenia
28
Q

What is the definition of status epilepticus?

A
  • Status epilepticus (SE) is a single seizure lasting more than five minutes or two or more seizures within a five-minute period without the person returning to normal between them.