Epilepsy Flashcards

1
Q

Differential diagnosis of epilpesy

A
  • syncope
  • transient ischaemic attacks
  • REM sleep disorder
  • migraine
  • hypoglycaemia
  • pyschogenic epsiodes
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2
Q

Causes of epilepsy

A
  • idiopathic- no obvious pathology/ most common
  • brain tumour
  • alcohol
  • autoimmune condition- can cause localised encephalitis
  • brain injury/ trauma- provides an epileptic focus which persists long after the injury has healed
  • infections- inflammation provides an epileptic focus
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3
Q

Common factors lowering seizure threshold

A
  • sleep deprivation
  • alcohol withdrawal
  • television flicker
  • epileptogenic drugs
  • head trauma
  • systemic infection
  • recreational drugs
  • menstruation
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4
Q

Occasional factors lowering seizure threshold

A
  • dehydration
  • barbiturate withdrawal
  • benzodiazepine withdrawal
  • hyperventilation
  • flashing lights
  • diet and missed meals
  • stress
  • intense exercise
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5
Q

Ideal AED

A
  • low risk of interaction
  • low protein binding
  • long elimination half life
  • linear kinetics
  • complete absorption
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6
Q

Established AED’s

A
  • phenytoin
  • phenobarbitone
  • primidone
  • carbamazepine
  • ethosuximide
  • clonazepam
  • clobazam
  • sodium valproate
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7
Q

Newer AED’s

A
  • gabapentin
  • pregablin
  • lacosamide
  • topiramate
  • lamotrigine
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8
Q

Risks of sodium valproate

A
  • high risk of serious developmental disorders

- congenital malformations

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9
Q

patient education of sodium valproate

A
  • risks associated
  • need to use effective contraception
  • need for regular review for treatment
  • the need to rapidly consult if she is planning a pregnancy or becomes pregnant
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10
Q

what AED’s can worsen absence seizures?

A

carbamazepine and phenytoin

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11
Q

what seizure type does ethosuximide have efficacy against

A
  • absence seizures but not others
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12
Q

phenytoin kinetics

A
  • zero order kinetics
  • small therapeutic window
  • highly protein bound
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13
Q

carbamazepine

A
  • induces its own metabolism at initiation
  • repeated dosing reduces half life to 1/3
  • metabolism is readily induced by drugs that induce hepatic microsomal enzymes
  • use of slow release formulations can reduce peak concentrations and improve tolerance
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