• Shuffle
    Toggle On
    Toggle Off
  • Alphabetize
    Toggle On
    Toggle Off
  • Front First
    Toggle On
    Toggle Off
  • Both Sides
    Toggle On
    Toggle Off
  • Read
    Toggle On
    Toggle Off
Reading...
Front

Card Range To Study

through

image

Play button

image

Play button

image

Progress

1/72

Click to flip

Use LEFT and RIGHT arrow keys to navigate between flashcards;

Use UP and DOWN arrow keys to flip the card;

H to show hint;

A reads text to speech;

72 Cards in this Set

  • Front
  • Back
type of seizure due to a lesion
focal
type of seizure that is primarily genetic
generalized
types of partial seizures
simple and complex
simple partial
no loss of consciousness
complex partial
loss of consciousness
generalized seizures
absence, myoclonic, tonic, clonic, tonic-clonic, atonic, secondary generalized
Carbamazepine Indications
seizure disorders, trigeminal neuralgia, bipolar disorder, alcohol withdrawal prophylaxis
Carbamazepine dose related AEs
CNS: sedation, fatigue, dizziness, confusion GI: n/v
CBZ non-dose related AE
SIADH, aplastic anemia, thrombocytopenia, anemia, leukopenia
Pts with HLA-B1502 and take CBZ
will develop a RASH
OXCBZ vs CBZ
hyponatremia is more common with CBZ; blood dyscrasias are less common with OXCBZ; no autoinduction and rash = 30% cross rxn with cbz
phenytoin suspension
must shake very very well
dose related AEs-phenytoin
nystagmus, ataxia, drowsiness, cognitive impairment
non-dose related AEs-phenytoin
gingival hyperplasia, hirsutism, acne, rash, hepatotoxicity, coarsening of facial features
Fosphenytoin indications
parenteral formularion for loading or maintenance dosing of phenytoin; status epilepticus
Dosage forms of fosphenytoin
IM, IV-in PE
Fosphenytoin AEs
hypotension, itching,
Rufinamide PKs
dose-dependent absorption. Food Increases absorption, low protein binding-metabolism is increased by inducers. Renal elimination
Rufinamide Indication
Lennox-Gastaut Syndrome
Rufinamide CI
in pts with familial short QT syndrome
Rufinamide AEs
somnolence, coordination problems, ataxia
Drugs that enhance fast Na channel inactivation
Rufinamide, Phenytoin, OXCBZ, CBZ
Locosamide MOA
Enhances slow Na channel invactivation. Binds to the collapsin-response mediator protein 2 (CRMP-2): may help prevent rearragement of neuronal connections and may protect neurons from excitatoxicity and apoptosis.
Locosamide common AEs
common-sedation, dizziness, nausea, ataxia, nystagmus
Locosamide rare AEs
PR interval prolongation
Locosamide AE @ 800 mg dose
Euphoria
FDA-approved schedule 5 for adjuncative therapy of…
partial-onset seizures
Lamotrigine MOA
dec glutamate and aspartate release, delays repetitive firing of neurons, enhances fast Na channel inactivation, inibits Ca channels
Lamotrigine AE
RASH-TITRATION
GABA
receptor mediates chloride influx, chloride influx causes hyperpolarization and inhibits firing
Phenobabital MOA
increases GABA mediated Cl influx
Phenobarbital AEs
sedation, hyperactivity, cognitive impairment
Tiagabine MOA
blocks GABA reuptake in the presynaptic neuron
Tiagabine AEs
generalized weakness (1%), new onset seizures in non-epiplepsy pts (usually takin other meds known to lower the seizure threshold)
Topiramate MOA
enhances fast sodium channel inactivation, enhances GABA activity, anatagonizes AMPA/kainate activity, weak carbonic anhydrase inhibitor
Common Topiramate AEs
dizziness, drowsiness, parasthesis, psychomotor slowing (titrate), wt loss
Rare Topiramate AEs
renal stone (2-4 x greater incidence-more common in men, FH, other carbonic anhydrase inhibitors, ketogenic diet…prevent with hydration); oligohydrosis/hyperthermia, acute angle glaucoma, metabolic acidosis
Zonisamide MOA
enhances slow sodium channel inactivation, blocks T-type Ca currents, weak carbonic anhydrase inhibitor
Zonisamide and Allergies
CI in pts with hypersensitivity to sulfonamides-even non-arylamines
Zonisamide AEs
depression, psychomotor slowing, parasthesias, kidney stones, blood dyscrasias, oligohydrosis/hyperthermia, metabolic acidosis
Valproic Acid (VA)-MOA
blocks t-type Ca currents, enhances fast Na channel inactivation, increases GABA production
VA indications
seizure prophylaxis: partial seizures and absence seizures; also for bipolar and migraine prevention
Common AEs-VA
sedation, n/v, wt gain, tremor, alopecia
AEs-rare-VA
hepatotoxicity (monitor baseline and periodic LFTs), interference with platelet aggregation; pancreatitis (abd. Pain, n/v, anorexia); hyperammonemic encephalopathy
Hyperammonemic Encephalopathy
Rare AE assoc with VA. Occurs in pts with urea cycle disorders. May be increased with topiramate combo. Sxs: altered consciousness, vomiting, lethargy. Assess serum ammonia conc screen for urea cycle enzyme deficiency, EEG. Tx: d/c VA, carnitine
Ethosuximide MOA
blocks t-type Ca currents
Ethosux Indication
absence seizures
Gabapentin MOA
unknown-increases brain levels of GABA
Gabapentin PKs
eliminated renally-adjustments for renal dysfunction and hemodialysis
Gabapentin AEs
wt gain, pedal edema
Gabapentin Pediatric AEs
emotional instability, hostility, conc probs, hyperkinesia
Pregabalin MOA
unknown
Pregabalin Indications
postherpetic neuralgia, diabetic neuropathy, partial onset seizures-adjunctive therapy
Pregabalin AEs
drowsiness, blurred vision, wt gain, pedal edema (may be more common with concomitant thiazolidinedione antidiabetic agents), angioedema, creatinine kinase elevations
Pregabalin schedule
4-insomnia, n, ha, diarrhea, reported after abrupt d/c
Levetiracetem and AED interactions
NONE
Levetiracetem AEs
asthenia, somnolence, behavioral sxs (aggression, agitation, anger, apathy, etc), dizziness, depression, coordination difficulties
Partial Seizure DOCs
CBZ, Gabapentin, Lamotrigine, OXCBZ, Phenobarb, Phenytoin, Topiramate, Valproate, Lacosamide
Tonic-Clonic Seizure DOCs
same as Partial DOCs EXCEPT lacosamide
Absence seizure DOCs
ethosux, lamotrigine, valproate
Atonic seizure DOCs
lamotrigine, OXCBZ, phenytoin, topiramate, valproate
Myoclonic seizure docs
lamotrigine, OXCBZ, phenytoin, topiramate, valproate (same as atonic)
Cat D AEDs
CBZ, Phenobarb, phenytoin, VA … All others are Cat C
CBZ cat D
hand and face abnormalities
Phenobarb Cat D
10.7% risk major malformations, hand and face abnormalities, hemorrhagic dz of newborn, lower verbal IQ
Phenytoin cat D
fental hydantoin syndromw, hemorrhagic dz of newborn
VA cat D
10.7-17.% risk of major malformation, spina bifida, lower verbal IQ
AED teratogenicity risk
greater risk with polytherapy, VA, 5 or more convulsive seizures during prenancy lower verbal IQ. Seizures increase risk of fetal loss and injury.
Pregnancy Recommendations and epilepsy
seizure control is primary goal. Avoid VA in women of childbearing age. Serum conc should be used to adjust dose Q 1-3 mo, but every 2-4 wks or lamotrigine and OXCBZ. Folic acid at least 1gm/d to all women of childbearing potential
Medication discontinuation criteria
Seizure free for at least 2 yrs and normal neurological exam and EEG. Requires slow tapering
Factors assoc with successful d/c AED
seizure free for 2-4 yrs, seizure control within 1 yr, onset after 2 but before 35 yrs, normal exam and EEG
Factors assoc with failure d/c AED
high frequency of seizures, SE, combo of seizure types, abnl mental functioning