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
Juvenile myoclonic epilepsy
Early morning preponderance 4-6 hx polyspike and wave VPA, lamotrigine (in questions: levetiracetam)
26
west syndrome
1. Development delay 2. Hypsarrhythmia on EEG (a high voltage, chaotic, disorganized pattern that is VERY, VERY abnormal) 3. Infantile spasms
27
Lennox Gastaut Syndrome
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
Juvenile Myoclonic Epilepsy
1. Absence seizures 2. Myoclonic jerks, usually in the morning 3. Generalized tonic clonic seizures, most commonly upon awakening
29
Juvenile Absence Epilepsy:
1. Staring spells without warning 2. Hand, mouth automatisms 3. 3 Hz spike-and-wave on EEG