epilepsy Flashcards

(55 cards)

1
Q

questions to ask

A
prodrome?
loss of urine/BM?
tongue biting?
describe seizure (witnesses?)
occupation?
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2
Q

seizure old def

A

paroxysmal event due to abnormal, excessive, hypersynchronous discharges from aggregate of CNS neurons

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3
Q

seizure new def

A

transient disturbance of cerebral function due to an abnormal paroxysmal neuronal discharge in the brain

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4
Q

epiplepsy

prevalence?

causes??

A

Recurrent seizure due to genetically or acquired brain disorder

0.5 to 1 % of pop

50% have a cause:
Head trauma, brain tumor, stroke, infection in brain, congenital

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5
Q

what is NOT considered epilepsy

A

etOH, metabolic derangements (PROVOKED)

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6
Q

seizure initiation phase

A

High frequency APs and hypersynchronization (all at same time)
Long lasting depol. of membrane due to influx of calcium which opens voltage dependent sodium channels–>repetitive action potentials
(abnormal e- activity)

location of activity determines type

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7
Q

if gets better w. prednisone

A

reduces vasogenic edema from brain mass

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8
Q

seizure propagation phase

A

can go all over from initial location

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9
Q

??? can lower seizure threshold by inhibiting (antagonizing) the effects of ??? at the receptors

A

PCN (dangerous!)

GABA

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10
Q

structural/metabolic causes

A

Pediatric – congenital
Metabolic – withdrawal alcohol, drugs, hypoglycemia
Trauma – post trauma, may not imply future seizure
Tumors – all patients > age 30 with seizure must have head imaging, focal seizures
Vascular – usually advanced age, >60
Infectious – AIDS, meningitis, encephalitis, syphilis, cysticercosis

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11
Q

hypoglycemic seizures are

A

reversible, give sucrose

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12
Q

assess for meningitis

A

nuchal rigidity
Kernig: flex knee and hip
Bruzinski: flex neck
stretching meninges

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13
Q

partial seizure: simple

A

motor, sensory, autonomic, or psychic signs
-preservation of consciousness
Jacksonian march: spread over larger regions of motor cortex
Todd’s paralysis: loc. paresis after seizure

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14
Q

partial seizure: complex

A

loss of consciousness
Frequently begins with aura

Automatisms:
Chewing, lip smacking, picking

EEG will be abnormal during seizure

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15
Q

partial with secondary generalization

A

Focal onset may not be clinically evident, but EEG would capture spikes/waves
Difficult to distinguish from generalized tonic clonic seizure

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16
Q

primarily generalized seizures: absence (petit mal)

A

“staring off into space”
Brief lapse of consciousness without loss of postural control

Frequently lasts seconds
Usually begins in childhood, ages 4-8
Can occur hundreds of times a day
Decline in school performance? Daydreaming?

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17
Q

primarily generalized seizures: tonic clonic (grand mal)

A

~10% of patients with epilepsy have this type

Most frequent type from metabolic derangements

Tonic contraction of muscles of expiration and larynx cause “ictal cry”

EEG will be abnormal during seizure

what worry about: airway, aspiration, most dangerous

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18
Q

other primarily generalized seizures:

A

tonic: stiffening
atonic: limp
myoclonic: shaking

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19
Q

unclassified:

A

neonatal

infantile

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20
Q

simple partial seizure symptoms

A

paresthesia, flashing lights, vertigo, flushing, altered smell/hearing

EEG will be abnormal during seizure, but hard to classify unless actually having seizure- use 24 hr EEG
how to provoke? sleep deprivation

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21
Q

generalized seizure arise from..

A

both hemispheres simultaneously

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22
Q

Juvenile Myoclonic Epilepsy

A

Bilateral myoclonic jerks single or repetitive

Most frequent in AM, worse with sleep deprivation

Respond well to anti convulsive therapy
-roll on side
hypoglycemic?

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23
Q

Lennox-Gastaut Syndrome (triad)

A

1) multiple seizure types (ie: generalized tonic clonic, atonic, atypical)
2) an EEG showing slow spike and wave discharges
3) impaired cognitive function

24
Q

a normal brain is…

A

capable of having a seizure, there are differences in the threshold or susceptibility
i.e. 2 kids w/ fevers, 1 gets seizure, other doesn’t

25
a variety of conditions have high chance of chronic seizure disorder
i. e. penetrating brain trauma, 50% chance of epilepsy | - ppx anticonvulsants
26
seizures are ??
episodic | May go months to years between episodes
27
things to exclude
``` syncope TIA (stroke-like, resolves w.in 24 hrs) migraine acute psychosis (pseudo seizure) other causes of episodic cerebral dysfunction ```
28
how to dx pseudoseizure??
dx of exclusion 24 hr EEG HAVE episode, NORMAL EEG trick: "hand drop" doesn't fall on face
29
ddx syncope from seizure
``` (convulsant syncope can pass out and shake gray vision, lightheaded) see slide 21 seizures longer biting of tongue ```
30
hit ground fast with no prodrome
cardiac arrhythmia
31
if hx of epilepsy
``` consider tx, SEs, serum levels e-lytes (hypoNa) CBC (leukocytosis) L/RFTs tox screen (ecstasy: hypothermic, thirsty-->hypoNa) ```
32
no hx epilepsy
same labs + serum glucose, Ca, Mg, UA
33
do what first?
head CT w. w.out contrast contrast better for masses no contrast better for bleeds
34
+ metab. screen
metab/inf disorder
35
no hx epilepsy, neg metab. screen
``` MRI scan or EEG ? if neg: idiopathic seizure if pos: mass, stroke, etc-tx underlying disorder for both: controversial: antiepileptic meds ```
36
ddx seizure
TIA Panic Attack Syncope Psychogenic Nonepileptic Seizure (PNES): Check prolactin, which can be high 15-30 minutes after a tonic-clonic seizure in most patients CK may also be high post convulsion
37
check ?? level after seizure | why ??
``` CK rhabdomyalgia (tightened musc.) ```
38
chance my child will have it again?
It is possible, but unlikely
39
childhood febrile seizure
Simple febrile – brief, symmetric Complex febrile - >15 minutes, focal features 1/3-1/2 of children will have another seizure, but
40
evaluation
``` ABCs Hx/exam (neuro focus) lab studies EEG brain imaging psychogenic seizure prolactin level (rises in seizure) ```
41
lab studies
CMP, Magnesium, UDS LP if meningeal signs on exam HIV patient? Must do LP.
42
EEG
Recording electrodes on scalp, potential differences recorded Normal awake, 8-13Hz alpha rhythm, variable faster >13Hz beta waves Sleep deprivation helps induce seizure, consider 24 hour continuous EEG; may be normal 60% of the time
43
brain imaging
Almost all patients, except children may not need this *MRI better than CT to detect any anatomical abnormalities
44
status epilepticus how does it wreak havoc?
Repeated seizures without recovery between them; a fixed and enduring epileptic condition lasting > or = 30 minutes Medical Emergency: can "fry" brain, airway issues May lead to irreversible neuronal injury
45
seizure tx
Treat underlying cause if metabolic Avoid alcohol if alcoholic Single seizure, started AED is controversial
46
status epilepticus tx
Typically intubation, lorazepam (ativan), and AED (anti-epileptic drugs) all together If no IV, can give rectal diazepam (valium) *resp. depression is issue with lots of benzos*-intubate-->ventilator
47
first line tx: tonic-clonic
*valproic acid* | lamotrigine
48
FLD: partial
carbamazepine phenytoin (dilantin) lamotrigine *valproic acid*
49
FLD: absence
*valproic acid* ethosuximide "sucks to have an absence seizure"
50
FLD: atypical absence, myoclonic, atonic
*valproic acid*
51
phenytoin (dilantin) OD SEs
diplopia, skin rashes (SJS), ataxia, nystagmus, gingival hyperplasia
52
carbamazepine (tegretol, carbatrol) OD SEs
leukopenia, aplastic anemia
53
valproic acid OD SEs
thrombocytopenia, hepatic toxicity
54
can you ever stop the medicine?
it depends | after 2 yrs seizure free
55
Lamictal SEs OD
SJS, skin rash