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
Drugs recommended for absence seizures
lamotrigine
26
Drugs recommended for simple and complex partial seizures
carbamazepine, gabapentin, lamotrigine, oxcarbazepine, phenobarbital, phenytoin, topiramate, valproate
27
AED common adverse effects
sedation ataxia diplopia
28
AED chronic adverse effects
peripheral neuropathy cerebellar atrophy extension of acute adverse effects osteoporosis
29
method for switching between AEDs
start the new drug low and titrate up slowly. | once therapeutic, slowly taper the old one down until gone
30
Criteria to meet before discontinuing antiepileptic drugs
``` no seizures for 2-5 years normal neurologic examination normal IQ single type of partial or generalized seizure normal EEG with treatment ```
31
how to withdraw AEDs
slowly, tapering dose over 1-3 months
32
determining dosing of AEDs
``` general guidelines response of patient serum concentrations (but treat patient not number) ```
33
CYP1A2 Inducers
carbamazepine phenytoin phenobarbital rifampin
34
CYP1A2 inhibitors
cimetidine ciprofloxacin erythromycin clarithromycin
35
CYP2C9 inducers
carbamazepine phenytoin phenobarbital rifampin
36
CYP2C9 inhibitors
amiodarone cimetidine fluconazole VPA
37
CYP2C19 inducers
none
38
CYP2C19 inhibitors
flebamate ticlopidine topiramate zonisamide
39
CYP2D6 inducers
carbamazepine
40
CYP2D6 inhibitors
none
41
CYP3A4 inducers
carbamazepine phenytoin phenobarbital rifampin
42
CYP3A4 inhibitors
amiodarone erythromycin propoxyphene ketoconazole
43
UGT inducers
lamotrigine phenobarbital phenytoin OCs
44
UGT inhibitors
VPA
45
more teratogenic AEDs
valproate and carbamazepine
46
How can teratogenic risk be reduced
1-4mg folic acid daily
47
monitoring efficacy in AED patients
seizure counts!! keep a calendar/journal/diary | compare notes monthly
48
Monitoring toxicity in AED patients
monitor at each visit | question patients about AEs and weigh the impact of AEs against benefit of treatment
49
Status epilepticus
seizure lasting >30 minutes (conventially >5 minutes), with or without loss of consciousness having recurrent seizures without regaining consciousness
50
Recommended treatment for Status Epilepticus
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
Carbamazepine AEs
``` aplastic anemia hyponatremia leucopenia osteoporosis rash ```
52
gabapentin AEs
peripheral edema | weight gain
53
Lamotrigine AEs
Rash
54
Levetiracetam AEs
Depression
55
Oxcarbazepine AEs
hyponatremia | 25-30% cross sensitivity in patients hyth hypersensitivity to carbamazepine
56
phenobarbital AEs
``` ADD cognitive impairment hyperactivity osteoporosis passive-aggressive behavior ```
57
phenytoin AEs
``` anemia gingival hyperplasia hirsutism lymphadenopathy osteoporosis rash ```
58
pregabalin AEs
edema | weight gain
59
Topiramate AEs
``` acute glaucoma metabolic acidosis oligohidrosis paresthesia renal calculi weight loss ```
60
Valproic acid AEs
Hepatotoxicity osteoporosis pancreatitis weight gain