Epilepsy Flashcards

1
Q

social impact of having epilepsy

A
patients can't drive
poor school attendance
low education
cognitive difficulties
multiple financial difficulties
often don't have health insurance
dependant on caregivers to assist with medications, transport, and ensuring safety
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2
Q

causes of epilepsy

A

underlying cause is unknown
most common cause is head trauma or stroke
other are genetic deficits, CNS tumors, CNS infections, neurodegenerative diseases, HIV, neurocysticercosis infections

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3
Q

causes of isolated seizures

A
stroke
CNS trauma
CNS infections
metabolic disturbances (hyponatremia hypoglycemia)
hypoxia
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4
Q

drugs that may cause seizures

A
tramadol
bupropion
theophylline
some antidepressants
some antipsychotics
amphetamines
cocaine
imipenem
lithium
excessive doses of penicillins or cephalosporins
sympathomimetics
stimulants
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5
Q

NTs implicated in the pathophysiology of seizures

A

glutamate and GABA

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6
Q

Tonic-clonic seizures

A
primary generalized seizure
sudden loss of consciousness
tonic extension and rhythmic clonic contractions of major muscle groups
lasts 1-3 minutes
also called "grand mal" seizures
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7
Q

Absence seizures

A
Primary generalized seizure
sudden and brief loss of consciousness without muscle movements
last several seconds
described as daydreaming or blanking out
also called "petit mal"
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8
Q

Myoclonic seizures

A

Primary generalized seizure
single and brief jerk of all major muscle groups
patients may not lose consciousness
lasts less than 3-4 seconds
described as shoulder shurgs or spinal chills
may cluster and build into general tonic-clonic seizures

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9
Q

atonic seizures

A

primary generalized seizure
loss of consciousness and muscle tone
no muscle movements typically noted, patient goes limp
described as falling out

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10
Q

simple partial seizure

A

sensation of uncontrolled muscle movement of a portion of the body
no alteration of consciousness
dependent on location of seizure in brain

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11
Q

Complex partial seizure

A

localized in specific area of the brain

still an alteration in patient’s level of consciousness

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12
Q

secondarily generalized seizures

A

partial seizure
starts as a simple or complex partial seizure
spreads to involve entire brain
patient may report a warning or aura at the start of the seizure

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13
Q

Juvenile myoclonic epilepsy

A

Primary generalized epilepsy syndrome
usually starts in early to middle teenage years
strong familial component
myoclonic jerks and tonic-clonic seizure may also have absence seizures

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14
Q

Lennox-Gastaut seizures

A

cognitive dysfunction and mental retardation

usually consists of combination of tonic-clonic, absence, atonic, and myoclonic seizures

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15
Q

Mesial temporal lobe sclerosis

A

seizures consist of partial seizures arising from mesial temporal lobe of the brain
often associated with anatomical changed, described as hippocampal sclerosis
patients often have excellent surgical outcomes

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16
Q

Infantile spasms

A

occurs in infants less than 1 year old
characterized by specific EEG pattern and spasms or jitters
also knows as West’s syndrome
infants often develop other seizure types later in life

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17
Q

disorders that may be mistaken for seizures

A
convulsions
syncope
psychogenic nonepileptic events (pseudoseizures)
anxiety attacks
cardiac arrhythmias
hypoglycemia
TIA
tics
complicated migraine headaches
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18
Q

michaelis-menten metabolism

A

the maximum capacity of the hepatic enzymes is reached in the normal dose range
causes small changes in dose to create large jumps in serum concentrations
increased risk of sudden toxicity and side effects

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19
Q

which drug follows Michaelis-Menten metabolism?

A

phenytoin

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20
Q

How to adjust phenytoin doses

A

serum concentrations >7mcg/mL, increase total daily dose by 100mg
Concentrations between 7 and 12, increase by 50mg
Concentrations >12, increase by no more than 30mg

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21
Q

highly protein bound AEDs

A

phenytoin, tiagabine, VPA, carbamazepine, and clonazepam

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22
Q

populations with decreased protein binding

A
kidney failure
hypoalbuminemia
neonates
pregnant women
those taking multiple highly protein bound drugs
patients in critical care
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23
Q

which AED is an autoinducer?

A

carbamazepine

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24
Q

Drugs recommended for tonic-clonic seizures

A
carbamazepine
lamotrigine
oxcarbazepine
phenobarbital
phenytoin
topiramate
VPA
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25
Q

Drugs recommended for absence seizures

A

lamotrigine

26
Q

Drugs recommended for simple and complex partial seizures

A

carbamazepine, gabapentin, lamotrigine, oxcarbazepine, phenobarbital, phenytoin, topiramate, valproate

27
Q

AED common adverse effects

A

sedation
ataxia
diplopia

28
Q

AED chronic adverse effects

A

peripheral neuropathy
cerebellar atrophy
extension of acute adverse effects
osteoporosis

29
Q

method for switching between AEDs

A

start the new drug low and titrate up slowly.

once therapeutic, slowly taper the old one down until gone

30
Q

Criteria to meet before discontinuing antiepileptic drugs

A
no seizures for 2-5 years
normal neurologic examination
normal IQ
single type of partial or generalized seizure
normal EEG with treatment
31
Q

how to withdraw AEDs

A

slowly, tapering dose over 1-3 months

32
Q

determining dosing of AEDs

A
general guidelines
response of patient
serum concentrations (but treat patient not number)
33
Q

CYP1A2 Inducers

A

carbamazepine
phenytoin
phenobarbital
rifampin

34
Q

CYP1A2 inhibitors

A

cimetidine
ciprofloxacin
erythromycin
clarithromycin

35
Q

CYP2C9 inducers

A

carbamazepine
phenytoin
phenobarbital
rifampin

36
Q

CYP2C9 inhibitors

A

amiodarone
cimetidine
fluconazole
VPA

37
Q

CYP2C19 inducers

A

none

38
Q

CYP2C19 inhibitors

A

flebamate
ticlopidine
topiramate
zonisamide

39
Q

CYP2D6 inducers

A

carbamazepine

40
Q

CYP2D6 inhibitors

A

none

41
Q

CYP3A4 inducers

A

carbamazepine
phenytoin
phenobarbital
rifampin

42
Q

CYP3A4 inhibitors

A

amiodarone
erythromycin
propoxyphene
ketoconazole

43
Q

UGT inducers

A

lamotrigine
phenobarbital
phenytoin
OCs

44
Q

UGT inhibitors

A

VPA

45
Q

more teratogenic AEDs

A

valproate and carbamazepine

46
Q

How can teratogenic risk be reduced

A

1-4mg folic acid daily

47
Q

monitoring efficacy in AED patients

A

seizure counts!! keep a calendar/journal/diary

compare notes monthly

48
Q

Monitoring toxicity in AED patients

A

monitor at each visit

question patients about AEs and weigh the impact of AEs against benefit of treatment

49
Q

Status epilepticus

A

seizure lasting >30 minutes (conventially >5 minutes), with or without loss of consciousness
having recurrent seizures without regaining consciousness

50
Q

Recommended treatment for Status Epilepticus

A

remove patient from harmful suroundings
ensure safe airway to prevent respiratory collapse or aspiration
BDZs are first med administered followed by initiation of AED
identify and treat underlying cause

51
Q

Carbamazepine AEs

A
aplastic anemia
hyponatremia
leucopenia
osteoporosis
rash
52
Q

gabapentin AEs

A

peripheral edema

weight gain

53
Q

Lamotrigine AEs

A

Rash

54
Q

Levetiracetam AEs

A

Depression

55
Q

Oxcarbazepine AEs

A

hyponatremia

25-30% cross sensitivity in patients hyth hypersensitivity to carbamazepine

56
Q

phenobarbital AEs

A
ADD
cognitive impairment
hyperactivity
osteoporosis
passive-aggressive behavior
57
Q

phenytoin AEs

A
anemia
gingival hyperplasia
hirsutism
lymphadenopathy
osteoporosis
rash
58
Q

pregabalin AEs

A

edema

weight gain

59
Q

Topiramate AEs

A
acute glaucoma
metabolic acidosis
oligohidrosis
paresthesia
renal calculi
weight loss
60
Q

Valproic acid AEs

A

Hepatotoxicity
osteoporosis
pancreatitis
weight gain