Seizures Flashcards

1
Q

Phenytoin

A

Dilantin
Na+ channel
Treats partial seizers (and secondary)
SE: Gingival hyperplasia, coarsening of facial features, ataxia, hypersensitivity

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2
Q

Carbamazepine

A

Tegretol
Na+ channel
Treats Partial
SE: Hyponatremia, agranulocytosis, diplopia, hypersensitivity

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3
Q

Valproic acid

A

Depakote
Na+ channel GABA receptor
Treats partial, generalized, absence
SE: tremor, thrombocytopenia, weight gain, hair loss, hepatotoxicity, tremor, GI, accelerate osteoporosis, teratogen, PCOS

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4
Q

Phenobarbital

A

GABA receptor
For Partial, generalized seizures
SE: sedation

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5
Q

Ethosuximide

A

Zarontin
T-type CA channel
For absence seizures
GI symptoms

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6
Q

Gabapentin

A

Neurontin
for partial seizures
SE: Sedation, ataxia

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7
Q

Lamotrigine

A

Lamictal
For partial, generalized
SE: Rash, stevens-johnson syndrome

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8
Q

Topiramate

A

Topamax
Na+ channel,
For partial, generalized
SE: word-finding difficulty, renal stones, weight loss

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9
Q

Tiagabine

A

Gabitril
For partial
SE: Sedation

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10
Q

Levetiracetam

A

Keppra
For partial, generalized
SE: Insomnia, anxiety, irritability

special: low risk hypersensitivity, low drug drug interations with warfarin, Juvenile myoclonic epilepsy

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11
Q

Oxcarbazepine

A

Trileptal
Partial
Sedation, hyponatremia

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12
Q

Zonisamide

A

Zonegran
For partial, generazlied
SE: sedation, renal stones, weight loss

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13
Q

Periodic lateralizing discharges

A

Herpes encephalitis, focal brain lesions, nonketotic hyperglycemia, EtOH withdrawal, theophylline exposure.

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14
Q

Generalized periodic discharges

A

Anoxic brain injury, CJD, diffuse process

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15
Q

Stimulus Induced, Rhythmic, Periodic, or Ictal Discharges

A

critically ill

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16
Q

Burst supression

A

Anoxic encephalopathy or with medications (propofol, barbituates)

17
Q

How to treat Status Epilepticus

A

Benzos (esp IV Lorazepam) then phenytoin

18
Q

Jacksonian March

A

motor cortex

19
Q

Sensory phenomena

A

parietal seizures

20
Q

visual phenomena

A

occipital seizures

21
Q

gustatory, olfactory, psychic phenomena, deja vu, jamais vu, depersonalization

A

temporal seizures

22
Q

Lennox-Gastaut

A

asso with mental retardation,
Slow (1-2hx) spike and wave
TX: VPA, lamictal, felbamate

23
Q

Benign Rolandic epilepsy

A

nocturnal preponderance
EEG: Centrotemporal spikes
TX: CBZ, sometimes none

24
Q

Absence epilepsy

A

Hyperventilation as trigger
EEG: 3 hz spike and wave
TX: Ethosuximide, VPA

25
Q

Juvenile myoclonic epilepsy

A

Early morning preponderance
4-6 hx polyspike and wave
VPA, lamotrigine (in questions: levetiracetam)

26
Q

west syndrome

A
  1. Development delay
  2. Hypsarrhythmia on EEG (a high voltage, chaotic, disorganized pattern that is VERY, VERY abnormal)
  3. Infantile spasms
27
Q

Lennox Gastaut Syndrome

A
  1. Mental retardation (often profound)
  2. Multiple seizure types (including atypical absence seizures, atonic seizures,
    patients were helmets, knee pads, elbow pads, etc. to protect themselves from
    injury)
  3. 1 – 2 Hz spike-and-wave discharges interictally (i.e., between seizures) – in other
    words, even when they’re not actually seizing, their brain is constantly firing
    epileptic discharges
28
Q

Juvenile Myoclonic Epilepsy

A
  1. Absence seizures
  2. Myoclonic jerks, usually in the morning
  3. Generalized tonic clonic seizures, most commonly upon awakening
29
Q

Juvenile Absence Epilepsy:

A
  1. Staring spells without warning
  2. Hand, mouth automatisms
  3. 3 Hz spike-and-wave on EEG