42B Peds Seizure Disorder Flashcards

(39 cards)

1
Q

What can induce an absence seizure?

A

hyperventilation

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2
Q

Age of onset for absence seizures?

A

childhood

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3
Q

Has an aura?

A

complex partial seizure

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4
Q

Abrupt onset?

A

absence seizure

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5
Q

Duration of absence seizure vs complex partial seizure?

A

sec vs minutes

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6
Q

Abrupt termination?

A

absence seizure

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7
Q

Frequency of absence seizure?

A

can be multiple times per day

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8
Q

Post-ictal phase?

A

complex partial seizure

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9
Q

Focal lesions on imaging?

A

complex partial seizure

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10
Q

MC type of childhood seizure?

Peak incidence?

A

febrile

18mo

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11
Q

Complex vs simple febrile seizure?

A

simple = isolated, generalized, brief

complex = multiple, focal, prolonged

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12
Q

How commonly do febrile seizures recur?

A

90% of kids have recurrence w/in 1 yr of onset

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13
Q

Risk factors for febrile seizure recurrence?

A
  • young age of onset (<18mo)
  • febrile seizure of 1st degree relative
  • low grade fever in ER
  • brief duration between fever and seizure
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14
Q

Risk factors for epilepsy in children w/ febrile seizures?

A
  • complex febrile seizures
  • family hx epilepsy
  • neuro impairment prior to febrile seizure
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15
Q

Common infections associated with febrile seizures?

A

HHV-6B

HHV-7

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16
Q

Infantile spasms:

Age of onset?

17
Q

Infantile spasms:

Characterized?

A

brief, bil, symm contraction of neck, trunk and extremities

18
Q

Infantile spasms:

MC type of spasm seen?

A

flexor spasms, arms an legs drawn up

19
Q

Infantile spasms:

Non-motor symptoms?

A

crying or giggling

flushing or becoming pale/cyanotic

20
Q

Infantile spasms:

EEG?

A

hypsarrhythmia with high voltage, chaotic activity between seizures

21
Q

West Syndrome =

A

triad of infantile spasms, hypsarrhythmia, developmental arrest/regression

22
Q

Lennox-Gastaut:

Age of onset?

23
Q

Lennox-Gastaut:

Triad?

A
  1. at least 2 seizures (tonic, atypical absence atonic)
  2. slowing of mental dev
  3. EEG = “slow spike and wave”
24
Q

Lennox-Gastaut:

Prognosis?

A

life-long seizures that are hard to control

25
Childhood absence epilepsy: | Age of onset?
4-8 y/o
26
Childhood absence epilepsy: | Neurological status?
nml
27
Childhood absence epilepsy: | EEG?
generalized 3Hx spike-and-wave discharges w/ nml EEG background
28
Childhood absence epilepsy: | Characterized?
multiple absence seizures per day
29
Juvenile myoclonic epilepsy: | Age of onset?
adolescence ``` 7-13 = abs 12-18 = myocl 13-20 = tonic-cl ```
30
Juvenile myoclonic epilepsy: | Characterized?
tonic-clonic, myoclonic or absence seizures (different seizures = different age of onset) *myoclonic = brief, bil asymm jerks in arms (or legs), conscious
31
Juvenile myoclonic epilepsy: | MC time for myoclonic?
early morning (drop things)
32
Juvenile myoclonic epilepsy: | Ppt factors?
- sleep deprivation - ETOH - stress - awakening from nocturnal or daytime sleep - photic stim
33
Juvenile myoclonic epilepsy: | Etiology?
genetic (AD, chr 6)
34
Benign Rolandic Epilepsy: | Location of discharges?
lower Rolandic area
35
Benign Rolandic Epilepsy: | Age of onset?
4-12 (*8-9)
36
Benign Rolandic Epilepsy: | Most specific type of seizure?
facial motor
37
Benign Rolandic Epilepsy: | MC presentation?
nocturnal generalized tonic-clonic
38
Benign Rolandic Epilepsy: | Prognosis?
usually stops by 14-16
39
Benign Rolandic Epilepsy: | EEG?
central-temporal spikes