Lec 42 Epilepsy Flashcards

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1
Q

What is a seizure?

A

release of excessive and uncontrolled electrical activity in the brain

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2
Q

What is epilepsy?

A

seizure disorder –> neurologic condition cahracterized by 2 or more unprovoked seizures

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3
Q

When does epilepsy usually present?

A

childhood or elderly

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4
Q

What is intractable epilepsy?

A

epilepsy that is at least partially resistant to drug treatment
found in ~30% of those with epilepsy

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5
Q

What is differential diagnosis for epilepsy [other things that look like epilepsy but aren’t]?

A
  • syncope attack due to loss of cerebral blood flow
  • cardiac arrhythmias
  • migraines
  • hypoglycemia
  • narcolepsy
  • panic attacks
  • pseudoseizures [psychosomatic disorder]
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6
Q

What are the 2 main categories of epileptic siezures?

A
  • partial/focal/localization related

- primary generalized

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7
Q

What are possible causes of primary generalized epilepsy?

A
  • genetic causes, starts in childhood, adolescence
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8
Q

What are possible causes of focal epilepsy?

A
  • trauma, tumor, stroke, encephalitis [infection]
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9
Q

What is onset/symptoms of primary generalized seizures?

A
  • onset in both hemispheres, no aura, lasts 2-3 minutes, see EEG changes in al leads
  • symptoms: generalized, post-ictal confusion, incontinence, amnesia
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10
Q

What is the difference simple vs complex seizures?

A
  • both are types of partial seizures

simple = have full consciousness, onset in 1 site or lobe

complex = impaired consciousness, onset in 1 site then spreads, most common site is MTL [medial temporal lobe]

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11
Q

What is secondary generalized tonic-clonic seizure? common causes?

A
  • a partial complex seizure that starts at a focus and then spreads to the rest of brain
  • becomes secondarily generalized
  • associated with trauma, stroke, drugs, old brain trauma, drug withdrawal
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12
Q

What is absence seizure [petit mal]? characteristic EEG?

A
  • type of generalized seizure
  • common in kids
  • sudden behavior arrest without falling
  • EEG = 3Hz/s spikes
  • no post-ictal confusion
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13
Q

What are myoclonic jerks?

A

type of generalized seizure

  • brief, rapid movement
  • may or may not lose consciousness, no aura, may precede tonic-clonics
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14
Q

What is juvenile myoclonic epilepsy? etiology?

A
  • myoclonic jerk generalized epilepsy
  • need life-long treatment
  • due to familial/genetic
  • associated with channelopathy
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15
Q

What are tonic-clonic seizures [grand mal]?

A
  • loss of consciousness
  • alternating stiffening/jerking
  • not preceded by aura
  • amnestic for the event
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16
Q

What are atonic seizures?

A
  • drop seizure

- fall to the floor, mistaken for fainting

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17
Q

What is reflexive epilespy?

A
  • epilepsy brought on by particular triggers for seizure to occur
    ex. triggered by flashing light or by reading
18
Q

What is delta wave?

A

< 4Hz
seen in slow wave stage 3+4 sleep
also seen in encephalopathy, delirium, diffuse lesions

19
Q

What is theta wave?

A

4-8 Hx

drowsiness and stage 1+2 sleep

20
Q

What is alpha wave?

A

8-13 Hz

when awake, relaxed, eyes closed

21
Q

what is beta wave?

A

> 13 Hz
seen in anterior head regions
increasingly common in pts on benzos/barbs
normally sen when pt eyes open, alert, active thinking

22
Q

What type of EEG waveforms suppressed or promoted by caffeine/stimulants?

A
  • suppress theta and alpha

- promote beta

23
Q

What are epilepsy auras?

A
  • perceptual disturbance considered a simple seizure but often followed by secondary generalized seizure = considered “warning” sign

manifests as: intense fear, deja vu, olfactory or gustatory hallucinations, rising abdominal sensation, moving sensory symptoms or visual/motor symptoms

24
Q

What is status epilepticus?

A

continuous seizure for > 30 min OR recurrent seizures without regaining consciousness between seizures for > 30 min
= medical emergency

25
Q

What regions are most prone to being epiletogenic?

A

medial temporal = hippocampus, enterorhinal cortex, amygdala

26
Q

what are signs of temporal lobe seizure?

A
  • epigastric rise at beginning
  • intense fear
  • deja vu
  • olfactory hallucinations
  • automatisms [lip smacking, chewing, button picking]
27
Q

What are signs of frontal lobe seizure?

A
  • can be bilateral without loss of awareness
  • often nocturnal
  • contralateral muscle jerks [due to motor cortex involvement] = jacksonian march
28
Q

What are signs of occipital lobe seizure?

A
  • complex figures or colors in part of visual field
29
Q

What is mesial temporal sclerosis?

A
  • hippocampal sclerosis causing temporal lobe epilepsy [TLE]
  • important cause of refractory epilepsy [ie epilepsy poorly controlled by meds]
  • characterized by neuronal loss in CA1, CA3, and CA4 regions of hippocampus + atrophy and gliosis
30
Q

What is clinical presenation of mesial temporal sclerosis?

A
  • aura of rising epigastric fullness
  • intense fear
  • impaired consciousness
  • automatisms –> lip smacking, chewing, button picking

EEG –> anterior temporal spikes
MRI –> hyperintensity + atrophy of hippocampus

31
Q

What are signs of frontal lobe epilepsy?

A
  • often nocturnal
  • brief vocalizations, shaking, forced head turn to opposite side from epiletpic foci
  • jacksonian march = myoclonus begins in one pat of body and migrates along the pattern of the motor homunculus
32
Q

What is todd’s paralysis?

A
  • post-ictal condition of focal weakness in one part of body
  • helps you discriminate between primary and secondary generalized seizure b/c region of weakness = region of focus
  • can be confused with stroke
33
Q

How do you distinguish frontal lobe epilepsy vs frontal stroke?

A

epilepsy: pt looks away from epileptic foci, promotes contralateral eye movement
stroke: pt looks toward lesion due to unopposed ipsilateral eye movement from preserved hemisphere

34
Q

What is rolandic seizure?

A
  • benign epilepsy with centrotemporal spikes
  • resolves by adolescence
  • usually occurs shortly after falling asleep

signs: unilateral parasthesia and clonus of tongue, lip, pharynx, dysarthria, drooling

35
Q

What is lennox-gaustat syndrome?

A
  • triad: mental retardation, slow spike and wave, multiple seizure types
  • diagnosed before age 8
  • tonic seizures out of sleep
36
Q

What is west syndrome?

A
  • infantile spasms age 3-12 mo
  • sudden jerk followed by stiffening
  • treat with ACTH if AEDs fail
  • may be due to tuberous sclerosis
37
Q

What are febrile seizures?

A
  • benign simple seizure, less than 15 min with shaking
  • occurs in 3mos - 5yos with fever
  • treatment not required
38
Q

Tumors in which locations of brain are more or less likely to cause seizures?

A

more common: near rolandic fissure, temporal lobes, insular cortex

cerebellum/brainstem tumors do not causes seizures

39
Q

When is it safe to withdraw treatment from pt with epilepsy?

A
  • if seizure free for 3 years –> perform slowly + carefully
40
Q

Are epileptic drugs safe for pegnant?

A
  • risk of teratogenicity especially with valproate

- withdrawing drug therapy in pregnancy more risky than continuation