Seizures Flashcards

1
Q

What is the concept of kindling in regards to seizures?

A

seizures beget seizures

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2
Q

What is the irritative zone?

A

area of cortex that generates interictal spikes

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3
Q

What is the ictal onset zone?

A

area of cortex where seizures are generated

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4
Q

What is an epileptogenic lesion?

A

structural abnormality that is direct cause of epileptic seizures

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5
Q

What is a symptomatogenic lesion?

A

area of the brain that first manifests seizure symptoms

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6
Q

What is the functional deficit zone?

A

cortical area of nonepileptic dysfunction

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7
Q

What is the epileptogenic zone?

A

area of brain necessary and sufficient for initiating seizures; removal or disconnection required for amelioration of seizures

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8
Q

What is Todd’s paralysis? What causes it?

A

post ictal paralysis, could be due to decreased glucose or increased lactate

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9
Q

What EEG findings are seen on Absence seizures?

A

3 Hz Spike and Wave

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10
Q

What does pathology show on mesial temporal lobe sclerosis?

A

hippocampal atrophy with gliosis and neural loss in CA1, CA4, and dentate gyrus

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11
Q

What is West’s syndrome?

A

infantile spasms; repeated extension and flexion of the neck, trunk, and extremities

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12
Q

What is characterizes West’s syndrome (infantile spasms) on EEG?

A

hypsarrhythmia (chaotic background with random high voltage, slow spike and wave)

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13
Q

What is the treatment for infantile spasms (West syndrome)?

A

ACTH, vigabatrin, and ketogenic diet

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14
Q

What are Benign epilepsy of childhood with Rolandic spikes? What is the typical clinical course?

A

focal motor seizures typically of the face during sleep-wake transitions; conscious but aphasic post ictally

remits spontaneously by adolescences

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15
Q

What is Juvenile myclonic epilepsy?

A

myoclonus in the morning without loss of consciousness, affects upper > lower

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16
Q

What is the inheritance pattern of Juvenile myoclonic epilepsy?

A

Autosomal dominant

17
Q

What is the treatment of juvenile myoclonic epilepsy?

A

valproic acid for life

18
Q

What characterizes Lennox-Gastaut syndrome?

A

multiple seizure types with mental retardation

19
Q

What surgical options are available for patients with Lennox Gastaut syndrome?

A

VNS and corpus callosotomy

20
Q

What is the mechanism of action of phenytoin?

A

Na Channel blockade

21
Q

There are many side effects to phenytoin. What are some of the most serious ones?

A

Steven Johnson syndrome, cerebellar degeneration

22
Q

What is the mechanism of action of Carbamazepine/Oxacarbazepine?

A

Na channel blockade

23
Q

What are the side effects of Carbemazepine/Oxacarbazepine?

A

Pancytopenia and SIADH

24
Q

What is the MOA of Lacosamide?

A

Na channel blocker

25
What is the MOA of Ethosuximide?
Ca Channel blocker
26
What is the MOA of acetazolamide?
carbonic anhydrase inhibitor
27
What is the MOA of lamotrigine?
inhibit presynaptic glutamate release
28
What is the MOA of Topiramate?
affects Na channels, GABA, and Glutamate receptors
29
What is the MOA of Valproic acid?
inhibits Na and Ca channels increases GABA synthesis and activity
30
What are the side effects of Valproic acid?
Thrombocytopenia, hyperammonemia (hepatotoxicity in < 2 years)
31
What is the MOA of Felbamate?
NMDA receptor antagonist
32
What are the side effects of Felbamate?
aplastic anemia and hepatic failure
33
Absence seizures are thought to originate/involve what cerebral structure?
thalamus
34
What is the go to treatment for absence seizures?
Ethosuximide
35
WADA testing determines _______.
laterality of speech and memory
36
What is injected in a WADA test?
sodium amobarbital
37
Corpus callosotomy can be used for _______ and _______.
atonic seizures (drop attacks) seizures with secondary generalization