Seizures + Epilepsy Flashcards

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1
Q

What is a seizure?

A
  • Clinical event in which there is a sudden disturbance of neurological function caused by abnormal/excessive neuronal excitation.
  • Can be epileptic or non-epileptic.
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2
Q

Causes of epilepsy in children?

A

1) Idiotpathic
2) Secondary: cerebral dysgenesis/malformation, vascular occlusion, or damage (infection, hypoxic-ischaemic encephalopathy).
3) Cerebra tumour
4) Neurodegenerative disease

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3
Q

Causes of non-epileptic seizures?

A

1) Febrile seizures
2) Meningitis/encephalitis
3) Metabolic - hypoglycaemia, hypomagnesiaemia, hypocalcaemia, hypo/hypernatraemia.
4) Posions/toxins
5) Head trauma

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4
Q

What are febrile seizures?

A
  • Single tonic-clonic, symmetrical generalised seizure lasting <15 minutes occurring alongside fever - typically in a normal developing child (6m-6yrs).
  • Does NOT cause brain damage.
  • Complex febrile seizures (focal, prolonged, or repeated in same illness) have an increased risk of developing into epilepsy.
  • 10% risk if child has a first-degree relative with febrile seizures.
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5
Q

Presentation and diagnosis of febrile seizures?

A

Sx: Generalised tonic-clonic seizure lasting <15 minutes

Dx: Seizure normally occurs in a viral infection when the temperature rises rapidly. If there is neck-stiffness - think meningitis.
AVOID LP in post-octal periods as CNS assessment impossible.

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6
Q

Complex seizure causes?

A

IF:

1) Focal CNS signs/abnormality
2) >15 minutes
3) >1 attack in 24 hours
4) Previous Hx of epilepsy

THINK:
Meningo-encephalitis, trauma, epilepsy, CNS lesion, hypoglycaemia, hypocalcaemia, hypomagnesiaemia.

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7
Q

Treatment of febrile seizure?

A

1) Put in recovery position
2) If seizure >5 minutes give benzodiazepine e.g. rectal diazepam or buccal midazolam.
3) Find underlying infection
4) Educate and reassure parents

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8
Q

What are paroxysmal disorders? Aetiology?

A
  • Cause funny turns and mimic epilepsy.

Ax:
- Breath-holding attack - toddlers: precipitated by anger, holds breath, goes blue then limp, rapid recovery.

  • Reflex anoxic seizures - toddlers: triggered by pain/discomfort from minor head trauma/fear/fright. After triggering event - child becomes very pale and falls to the floor. Hypoxia may induce a generalised tonic-clonic seizure. Episodes due to cardiac systole from vagal inhibition. Rapid recovery.
  • Syncope - due to hot and stuffy environment, clonic movements may occur.
  • Migraine
  • Benign paroxysmal vertigo - recurrent episodes of vertigo, lasting from one to several minutes, associated with nystagmus, unsteadiness and falling.
  • Primary headache disorder occasionally due to viral labrynthitis.
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9
Q

Childhood epilepsy definition and Ax?

A
  • Chronic neurological disorder characterised by recurrent, unprovoked seizures, consisting of transient signs of excess and abnormal neuronal activity in the brain.
  • RF: FH
  • Idiopathic, infection (meningitis), hyponatraemia, hypoglycaemia, hypocalcaemia, hypomagnesaemia, CNS tumours, flickering lights.
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10
Q

Childhood epilepsy PPx?

A
  • Generalised: discharge arises from both hemispheres - absence, myoclonic, tonic, tonic-clonic, atonic.
  • Focal - seizures arise from one part/hemisphere:
    1) Frontal seizures - Involve motor/premotor cortex - may lead to clonic movements - Jacksonian March
    2) Temporal seizures (MOST COMMON) - strange warning feelings or aura with smell and taste abnormalities and distortions of sound and shape. Lip-smacking, plucking nothing and walking in a non-purposeful manner.
    3) Occipital seizures - vision distortion
    4) Parietal lobe seizures - contralateral dysaesthesias (altered sensation) or distorted body image.
  • Conscious may or may not be altered, or the seizure may be followed by generalised tonic-clonic seizure.
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11
Q

Ddx of childhood epilepsy?

A

1) Arrhythmias (prolonged QT)
2) Migraine, narcolepsy, night terrors
3) Paroxysmal disorders (reflex anoxic seizure)

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12
Q

Dx of childhood epilepsy?

A
  • Primarily clinical diagnosis
  • Focused on specific triggers and if child has any impairments
  • Check skin markers for a neurocutaneous syndrome/neurological abnormality
  • EEG
  • MRI/CT head
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13
Q

Tx of childhood epilepsy?

A
  • Generalised seizures:
    1) Tonic-clonic - Sodium Valproate (weight gain and drowsiness) or Carbamazepine (agranulocytosis, rash)
    2) Absence - Sodium Valproate
    3) Myoclonic - Sodium Valproate
  • Focal seizures:
    1) Carbamazepine, Sodium Valproate
    2) Lamotrigine

Other: Ketogenic diet, vagal stimulation, temporal lobectomy
Advice: Avoid baths/swimming alone, don’t sit too close to TV (f photophobic), do not drive until 1 year after seizure.

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14
Q

Name 4 childhood epilepsy syndromes?

A

1) West syndrome
2) Lennox-Gastaut syndrome
3) Absence epilepsy
4) Juvenile myoclonic epilepsy

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15
Q

West syndrome brief:

A
  • 4-6 months
  • Violent flexor spasms of head, trunk and limbs - followed by extension of the arms
  • Social interaction deteriorates
  • Most develop learning disability or epilepsy
  • Treatment - Vigabatrin or corticosteroids
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16
Q

Lennox-Gastaut syndrome brief?

A
  • 1-3 yrs
  • Mostly drop attacks (astatic seizures), atonic, or atypical absence seizures
  • Neurodevelopment arrest or regression/behavioural disorder
  • Poor prognosis
17
Q

Absence epilepsy?

A
  • 4-12 years (mostly female)
  • Stares and stops moving momentarily (my twitch eyelids)
  • Lasts few seconds
  • Child has no recall - maybe realises they have missed something
  • Developmentally normal but can interfere in schooling
  • Episodes can be induced by hyperventilation - child can be asked to blow on a piece of paper or windmill for 2-3 mins - useful test
  • Good prognosis
18
Q

Juvenile myoclonic epilepsy?

A
  • Adolescence/adulthood
  • Throwing cereal or drinks in the morning - myoclonus occurs at this time
  • Responds well to Tx but lifelong