AEDs Flashcards

(18 cards)

1
Q

classical AEDs

A

phenytoin, carbamazepine, ethosuximide, valproic acid

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2
Q

newer AEDs

A

oxacarbazepine, gabapentin, lamotrigine, topiramate, levetiracetam, zonisamide

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3
Q

classical AED with the least sedation

A

valproic acid

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4
Q

cons of classical AEDs

A
  • decreased bone mineral density
  • increase metabolism of BC
  • teratogenic
  • hypersensitivity- skin rxns; hematotoxicity
  • multiple doses/day
  • long half lives
  • recommended TDM
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5
Q

a number of classical AEDS contains

A

the ureide structure

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6
Q

phenytoin (Dilantin) MOA

A

slows rate of recovery of Na channels

- effective in partial & tonic-clonic seizures

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7
Q

phenytoin elimination

A
  • rate of elimination varies as a function of its concentration
  • half-life increases with dose increase
  • [drug] in plasma increases disproportionately when dose is increased
  • age dependent metabolism
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8
Q

phenytoin ADRs

A

cns depression, gingival hyperplasia, osteomalacia, megaloblastic anemia, hirsutism, hyperglycemia, teratogenic

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9
Q

carbamazepine (Tegretol)

A
  • slows recovery of Na channel
  • primary drug for partial and tonic-clonic seizures
  • induces its own metabolism
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10
Q

carbamazepine ADRs

A
  • acute intoxication
  • long term therapy- drowsiness, vertigo, ataxia, diplopia, blurred vision
  • seizure may increase with overdose
  • N/V
  • hematological
  • retention of water in the elderly, teratogenic, skin rxns (SJS & TEN)
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11
Q

ethosuximide (Zarontin)

A
  • blocks T type channels in thalamus
  • first line for absence seizures
  • GI & CNS problems
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12
Q

valproic acid (Depakene)

A
  • multiple actions- Na & Ca channel blocker, enhances GABA transmission
  • DOC for unclassified forms of seizures
  • GI, weight gain, hair loss
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13
Q

oxacarbazepine (Trileptal)

A
  • blocks Na channels
  • can be effective in pts who didnt respond to cbz
  • prodrug
  • decreases plasma levels of eithinyl estradiol & levonorgestrel
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14
Q

Gabapentin (neurontin)

A
  • GABA molecule bound to a cyclohexane ring, but does NOT mimic GABA
  • MOA not well understood, promotes release of GABA at synapse
  • useful in neuropathic pain, migraine, spasticity
  • no known interactions with other AEDs
  • no metabolism
  • used as a second line adjunct
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15
Q

lamotrigine (Lamictal)

A
  • delays Na channel recovery
  • not an enzyme inducer
  • anti-folate acticity
  • mono & adjunct therapy
  • mood stabilizer
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16
Q

topiramate (Topamax)

A
  • multiple MOA- blcosk AMPA, NA channels & activated hyperpolarizing K channel
  • mono & adjuncttherapy
  • adr: cognitive impairment w/ too fast titration
  • teratogenic
17
Q

levetiracetam (Keppra)

A
  • unknown MOA
  • myoclonic, partial & tonic-clonic >4yo
  • eliminated renally mostly unchanged
  • modest side effects
  • limied evidence for anti-epileptogenic properties
18
Q

Zonisamide (Zonegran)

A
  • blocks Na & T-type Ca channels
  • adjunct for partial seizures
  • 85% renal elimination unchanged
  • long half-life
  • no interactions