Epilepsy Flashcards

1
Q

seizure

A

*the clinical symptom of an abnormal, hypersynchronous discharge of a population of cortical neurons
*may produce clinical symptoms or may only be apparent as electrical activity on the EEG
*a singular event!

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2
Q

epilepsy

A

*RECURRENT seizures (2+) which are not provoked by systemic or acute neurologic insults

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3
Q

focal (partial) seizures

A

*affect one area of the brain (BEGINS in one area on EEG)
*commonly originate from temporal lobe
*may be preceded by a seizure aura
*can be focal aware or focal impaired awareness

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4
Q

focal aware seizures

A

*no alteration of consciousness
*can be motor, sensory, autonomic, psychic

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5
Q

focal impaired awareness seizures

A

*impaired consciousness (may range from mild confusion to loss of consciousness)
*clinical manifestations vary with site of origin and propagation of electrical activity through brain
*duration typically < 2 minutes
*often present as “staring spells”

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6
Q

focal to bilateral tonic-clonic seizures

A

*BEGINS focally, with or without obvious focal neurological symptoms
*variable symmetry, intensity, and duration of tonic (stiffening) and clonic (jerking) phases
*typical duration 1-3 minutes
*postictal confusion, somnolence, with or without transient focal deficit

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7
Q

non-motor generalized seizures (typical absence seizures)

A

*brief staring spells with impairment of awareness
*3-20 seconds
*sudden onset & sudden resolution
*often provoked by hyperventilation
*onset typically between 4 and 14 years of age
*often resolve by 18 years of age
*normal development and intelligence
*EEG: generalized 3 Hz spike-wake discharges

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8
Q

what is the EEG finding for non-motor generalized seizures (typical absence seizures)

A

generalized 3 Hz spike-wave discharges

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9
Q

what type of seizure is characterized by generalized 3 Hz spike-wave discharges

A

non-motor generalized (typical absence seizures)

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10
Q

motor generalized seizures

A

*associated with loss of consciousness and post-ictal confusion/lethargy
*duration 30-120 seconds
* tonic phase: stiffening and fall; may be associated with ictal cry
*clonic phase: rhythmic extremity jerking
*EEG: generalized polyspikes

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11
Q

etiologies of seizures and epilepsy - infancy and childhood onset

A

-prenatal or birth injury
-inborn error of metabolism
-congenital malformation

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12
Q

etiologies of seizures and epilepsy - childhood and adolescence onset

A

-idiopathic/genetic syndrome
-CNS infections
-trauma

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13
Q

etiologies of seizures and epilepsy - adolescence and young adult onset

A

-head trauma
-maturation effects of structural foci
-drug intoxication and withdrawal

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14
Q

etiologies of seizures and epilepsy - older adult onset (50+)

A

-STROKE
-brain tumor
-acute metabolic disturbances
-neurodegenerative

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15
Q

Lennox Gastaut Syndrome

A

*multiple seizure types
*slow (< 3 Hz) spike and wave on EEG
*developmental delay

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16
Q

examples of structural causes of epilepsy

A

-medial temporal sclerosis
-migration abnormality

17
Q

evaluation after a first seizure

A

-history and physical
-blood tests
- +/- lumbar puncture
-blood or urine screen for drugs
-EEG (best if pt is sleep deprived)
-MR brain scan

18
Q

seizure precipitants

A

-metabolic and electrolyte imbalance
-sleep deprivation
-ASM non-compliance
-hormonal variations
-stress
-fever/infection
-head injury
-stimulants and other drugs

19
Q

medications that can trigger a seizure

A

*wellbutrin
*diphenhydramine (benadryl)
*tramadol
*some stimulants or antibiotics

20
Q

key metabolic abnormalities associated with triggering a seizure

A

1) hyponatremia (low sodium in blood)
2) hypoglycemia

21
Q

electroencephalogram (EEG)

A

*graphical depiction of cortical electrical activity, usually recorded from the scalp
*advantage of high temporal resolution, but poor spatial resolution of cortical disorders
*most important neurophysiological study for the diagnosis, prognosis, and treatment of epilepsy

22
Q

background abnormalities on EEG

A

significant asymmetries and/or degree of slowing inappropriate for clinical state or age, may not relate to seizures

23
Q

interictal abnormalities associated with seizures and epilepsy

A

**spike-wave complexes are pathognomonic for epilepsy
-spikes (< 70 msec)
-sharp waves (< 200 msec)

24
Q

psychogenic non-epileptic spells

A

*NOT seizures (“functional neurologic disorder”)
*females > males; h/o abuse; may coexist with epilepsy
*psychiatric mechanism - dissociation, conversion - malingering is rare
*common association with physical, emotional, or sexual abuse
*NO EEG CORRELATION

25
cellular mechanisms for seizure generation
*too much excitation -ionic: inward Na+ and Ca++ currents -neurotransmitter: glutamate and aspartate *too little inhibition -ionic: inward Cl-, outward K+ currents -neurotransmitter: GABA
26
vagus nerve stimulator
*intermittent programmed electrical stimulation of left vagus nerve *may improve seizures, etc
27
ethosuximide only works for what type of seizures
absence seizures
28
epidiolex (CBD) for seizures
*only approved for: 1) Dravet syndrome (SCM1A) 2) tuberous sclerosis complex 3) Lennox Gastaut syndrome
29
Stevens-Johnson Syndrome (SJS)
-blisters and erosions of the skin, particularly palms and soles and mucous membranes -fever and malaise -rare condition -rapid titration of lamotrigine especially in combination with valproate increases risk
30
surgical treatment for epilepsy - potentially curative
-resection of epileptogenic region avoiding significant new neurologic deficit -laser thermal ablation
31
surgical treatment for epilepsy - palliative
-partial or staged resection of epileptogenic region -disconnection procedures to prevent seizure spread (callostomy)
32
surgical treatment for epilepsy - devices
-responsive neurostimulation -deep brain stimulation
33
status epilepticus
*a medical emergency *traditionally, > 30 minutes of convulsive seizure activity or 2+ sequential seizures without full recovery between seizures for > 30 minutes *current: defines earliest time when treatment should be started (t1) and the time when long term consequences are increasingly likely (t2) t1 = 5 min and t2 = 30 min
34
sudden unexpected death in epilepsy (SUDEP)
sudden, unexpected, witnessed or unwitnessed, nontraumatic and non-drowning death in a patient with epilepsy where the autopsy does not reveal any other cause of death