Epilepsy Flashcards

1
Q

Seizure

A

occasional, sudden, excessive and rapid discharge of gray matter –> positive sx

Post-seizure –> negative sx (post-ictal period)

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2
Q

Posictal period mechanisms

A

neuronal exhaustion, inhibitory inputs to seizure area

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3
Q

Signs of epileptic seizures

A

paroxysmal change in behavior or movement, or altered consciousness

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4
Q

Partial seizure

A

begins in one area of cortex

remains localized or spreads (may spread to whole cortex –> grand mal seizure)

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5
Q

Generalized epilepsy

A

due to whole cortex hyper-irritability (genetic). Overreaction to deep gray matter inputs –> seizure

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6
Q

Difference between partial complex seizures and absence seizures

A

partial complex seizures –> postictal state

no postictal state in absence seizures

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7
Q

DDx of episodic epilepsy sx

A

Syncope/near syncope (circulatory, altered blood state like hypoxia), movement disorders (myoclonus, paroxysmal dyskinesia), fasciculation, stroke/TIA, Migraine, sleep disorder, psychogenic/behavioral

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8
Q

Focal seizures, consciousness preserved

A

motor signs (Jacksonian, aversive), somatosensory sx, autonomic s/sx, psychic sx

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9
Q

Focal seizures, loss/impaired conciousness

A

Partial onset –> impaired consciousness; OR impairment of consciousness on onset

Can evolve into convulsive seizure

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10
Q

Generalized seizures

A

tonic-clonic, tonic, atonic, myclonic, absence

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11
Q

Epilepsy

A

chronic disease of recurrent, unprovoked sizures. 2+ unprovoked seizures, more than 24h apart OR 1 seizure with studies suggesting further risk for seizures

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12
Q

Drug resistant epilepsy

A

36% of cases

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13
Q

symptomatic seizures

A

30% with structural abnormality (tumor, arteriovenous malformation). Half remit

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14
Q

Idiopathic seizures

A

genetic. Usually children

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15
Q

Benign epilepsy

A

easily treated, normal intelligence, normal tests.

Genetic, remission by teen years

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16
Q

Catastrophic epilepsy

A

Med resistant. Affects development –> mental retardation, shortened lifespan of child

Abnormal EEG, MRI. Symptomatic seizures

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17
Q

Febrile seizures

A

age 6mo-3y. seizure c fever without evidence of intracranial infection or defined cause

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18
Q

Simple seizure

A

generalized, less than 10-15min, do not recur in less than 24h

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19
Q

Complex seizure

A

focal, > 10-15 min, recur in less than 24h. 30% of febrile seizures

20
Q

Timing of febrile seizures

A

within first 24h of illness

21
Q

Risk factors for recurrence of febrile seizure

A

less than 1 yo, family hx, low grade fever, brief fever

22
Q

Seizure’s effect on cognition

A

nearly all children have normal cognition. prolonged or complex seizures –> increased risk of cognitive problems (most do well)

Tendency for sleep problems

23
Q

Risk factors for developing epilepsy

A

Complex febrile seizure, neurologically abnormal prior to seizure, family hx of afebrile seizures

24
Q

Treatment of seizure now

A

DOES NOT prevent later epilepsy

25
Lennox Gastaut syndrome
Generalized seizures, cognitive dysfunction (may evolve later), usually children 1-7y
26
Causes of Lennox Gastaut syndrome
malformations, hypoxic-ischemic injury, encephalitis, meningitis, TUBEROUS SCLEROSIS 30% of pts with infantile spasms --> LGS
27
When do you treat seizures?
after someone has 2 seizures or if there is an acute reason for seizure (tumor, stroke, etc) --> anticonvulsants
28
How long should a patient be seizure free before we consider weaning off meds?
2 years
29
Myoclonic seizure tx
lamotrigine
30
Generalized seizure tx
phenytoin, carbamazepine, oxcarbazepine, gabapentin
31
valproic acid contraindications
teen girls (polycystic ovarian disease), pregnant women, children
32
Topiramate and zonisamide contraindications
acidosis
33
Old, partial seizure meds
phenytoin, carbamazepine
34
Old, broad spectrum seizure meds
phenobarbital, valproic acid, ethosuxamide, benzodiazepines
35
New partial antiseizure meds
Tiagabine, Oxcarbazepine, gabapentin, pregabalin, lacosamide, exogabine, eslicarbazepine
36
New broad seizure meds
lamotrigine, zonisamide, topiramate, levoteracetam, felbamate, clobazam, rufinamide, perampanel
37
"Special" seizure meds
Vigabatrin, ACTH
38
Ketogenic diet
starvation --> ketone bodies --> antiepileptic effect Diet (creams and MCT oils) continues ketosis (enough calories and protein to grow) Children > adults Used with generalized > partial seizures
39
Ketogenic diet adverse effects
hunger, hypoglycemia, drosiness, lethargy, irritability, acidosis (excessive ketosis) Serious: kidney stones, prolonged QT, increased bruising with bleeding, pancreatitis, immunosuppression
40
Vagal nerve stimulation
pacemaker implanted in left chest wall --> stops seizures For chronic intractable seizures, stopping clustered/prolonged seizures
41
vagal nerve stimulation side effects
temporary hoarseness, ticking in throat, dyspnea
42
Epilepsy surgery
for partial epilepsies
43
Epilepsy surgery in adults
temporal lobe
44
Epilepsy surgery in children
extratemporal, hemispherectomy
45
Focal epilepsy surgery
lesionectomy, lobectomy, corticectomy, multiple subpial transection
46
Generalized epilepsy surgery
corpus callosotomy for drop
47
Indications for epilepsy surgery
Drug-resistant with poor prognosis and natural hx (Rassmussen's, Sturge Weber, hemimegalencephaly, focal cortical dysplasia, hippocampal sclerosis), rapid regression of development status, lesion/focus in area not critical for function, predominant seizure type and frequency