Seizures/Epilepsy Flashcards

1
Q

What is a seizure? What is epilepsy?

A
  • Seizure: episodic neurological phenomena resulting from excessive, hypersynchronous activity from neurons in cerebral cortex
  • Epilepsy:
    • = a group of diverse neurological disorders in which people have an enduring predisposition to epileptic seizures
    • classical definition used in paediatrics is recurrent (two or more), unprovoked (afebrile) epileptic seizures
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2
Q

How many children have seizures, and what is the most common cause?

A

5% children have one or more in lifetime - febrile seizures most common cause.

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3
Q

Aetiology of seizures in children.

A

○ Febrile seizures (3%)
○ Acute symptomatic seizures
- In the setting of an acute medical issue, which will cease when the acuteness passes.
- eg. meningitis, trauma, hypo? (1%)
○ Single or recurrent, unprovoked seizures ie. Epilepsy (1%)

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4
Q

Differentiate the two broad types of seizures

A

Generalised:

  • Bilateral
  • LOC always
  • No aura
  • Mechanism of types distinctly different
  • Symptoms of types generally similar

Focal:
- Unilateral
- LOC not always - more probable if association areas are impacted
• Focal with impaired consciousness (formerly complex partial)
• Focal -> bilaterally convulsive (formerly secondary generalised)
- Aura
- Mechanism of types roughly the same
- Types symptomatically different

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5
Q

Roughly describe the different types of generalised seizure.

A
  • Tonic clonic (few mins)
  • Absence
    • light switch, on and off (but can happen in focal too e.g. TL)
    • around 5-30s
  • Myoclonic (sudden, brief jerks)
  • Tonic
    • 1-10s of gen muscle stiffening
    • Often when asleep
    • Associated: apnoea, colour change, drooling
  • Atonic - can cause head nods, or even sudden falling (drop attacks)
  • Spasm
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6
Q

What is the acute mx for uncomplicated afebrile seizures?

A
  • Most convulsions are brief and self limiting, generally ceasing within 5 - 10 minutes
  • Supportive care 5-10 mins:
    ○ DRS ABC
  • IV access:
    ○ BSL
    ○ Calcium/UEC
    ○ VBG
  • Benzodiazepine (midazolam/diazepam)
    ○ Repeat after 5 mins of continuing seizures
    ○ Switch to phenytoin/phenobarbitone if convulsion continues for further 5-10 mins
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7
Q

When does epilepsy have its highest incidence? Why?

A
  • highest incidence in infancy (cf spectrum of childhood), due to immaturity of CNS
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8
Q

What is the outcome of epilepsy in childhood?

A
  • favourable outcome, often with remission in >50%
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9
Q

Generally, what pathology do many genetic epilepsies involve?

A

Genes coded in ion channels

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10
Q

What are the broad groups of aetiologies of childhood epilepsy?

A
  1. idiopathic (presumed genetic predisposition to seizures)

2. symptomatic (underlying lesion or genetic/metabolic disorder)

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11
Q

List the main groups of childhood epilepsies.

A
  1. Genetic generalised (idiopathic, generalised)
  2. Benign focal (idiopathic, focal)
  3. Symptomatic generalised (epileptic encephalopathies)
  4. Symptomatic (lesional) focal
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12
Q

What are some DDx for childhood epilepsy?

A

Normal phenomenon
- sleep jerks, tantrums, inattention/day dreaming

Syncope and related episodes
- vasovagal attacks, breath-holding spells, long QT syndrome

Parasomnias and related sleep disturbances
- confusional arousals, night terrors, sleep walking, cataplexy

Migraine variant and neurovascular episodes
- complicated migraine, benign paroxysmal vertigo, TIAs

Movement disorders
- tics, clonus, chorea, shuddering attacks, tremor, stereotypies

Behavioural and psychiatric disturbances
- mannerisms, psychogenic seizures, rage attacks

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13
Q

Breath-holding spells:

  • What happens and pathophysiology
  • Outcome
A
  • Not to do with electrical hypersynchrony, but cerebral ischaemia
  • Initial noxious stimulus e.g. accident, change in breathing patterns, HR slows -> unconscious
  • Benign, no Tx needed. Grow out of it ~ 6yo
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14
Q

What Ix could you conduct to investigate epilepsy?

A
  • Biochemistry e.g. glucose, electrolytes, Ca/Mg → all afebrile convulsive seizures
  • EEG → all afebrile epileptic seizures
  • MRI → all potentially “symptomatic” epilepsies
  • Metabolic and genetic investigations → MRI negative “symptomatic” epilepsies
  • video-EEG monitoring ,specialised neuroimaging → uncontrolled epilepsies
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15
Q

What kind of general management points must you advise a family on with a dx of epilepsy?

A

Counselling child and family
- e.g. information, Epilepsy Foundation, emergency management, epilepsy Mx plan

Avoid precipitating factors
- e.g. sleep deprivation, flashing lights

Lifestyle precautions/restrictions
- e.g. bathing and hot water (try showers), swimming, heights, alcohol, driving, vocational

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