"High Yield" Stuff that I think is important but Hoppe and Esper probably think otherwise Flashcards
Focal seizures with altered mental status sx
Usually frontal or temporal lobe involvement with automatism and impaired memory
Phenytoin MOA and use
Na+ channel blocker, for tonic-clonic seizures, high drug-drug interaction (oral contraceptives)
Side effects of phenytoin
gingival hyperplasia, hirsutism and others
Carbamazepine MOA and use
Na+ channel blocker, for focal seizure tx, induces own metabolism (increase dose over time to compensate
Lamotrigine MOA and use
Na+ channel blocker, 3rd choice for absence seizures, can cause Steven Johnsons syndrome, rash and other side effects
Lacosamide MOA and use
Na+ channel blocker, modulates NMDA receptor, adjunct for focal seizures
Ethosuximid MOA and use
decreases threshold for Ca2+ T-type currents (closer to depolarized state), used for 1st line absence seizures
Valproic acid MOA and use
Na+ and Ca+2 T-type channel blockers, increases GABA an d for both absence and focal seizures
Gabapentin MOA and use
increases GABA in synaptic cleft, not as potent/not 1st line
Pregabalin MOA and use
decreases excitatory NT’s, affects calcitonin, more potent than gabapentin, METABOLIZED by KIDNEYS (not liver)
Benzodiazepine use
chronic inhibition of seizures
Clonazepam MOA and use
is a BZ, indirectly inhibits Ca2+ T-type so used for tx of absence seizuires, lots of side effects=4th choice for tx
Phenobarbital use
focal, tonic-clonic, and resistant seizures. CAN MAKE ABSENCE SEIZURES WORSE
Vigabatrin MOA and use
increases GABA by GABA transaminase inhibition, for infantile seizures and focal epilepsy. Side effect=VISION LOSS
Tiagabine MOA
GABA inhibitor for reuptake (increases synaptic GABA)
Felbamate MOA and use
Inhibits NMDA receptors, tx for refractory epilepsy, CAN CAUSE APLASTIC ANEMIA AND LIVER FAILURE
Rufinamide MOA and use
inhibits mGluR5 in high doses/prolongs Na+ channels, tx for focal seizures, Lennox-Gastaut, and refractory seizures
Drug hierarchy for tx of status epilepticus
lorazepam/diazepam, fosphenytoin, phenobarbital, general anesthesia (propofol/midazolam)
Sign of absence seizure on EEG
3Hz spike and wave
Atonic vs myoclonic seizure
Atonic has brief impaired consciousness, myoclonic does not
Simple vs complex partial seizure
comples has LOC, simple does not, complex also has aura and amnesia
Sign of partial seizure with 2nd generalization
eye deviation
Benign febrile convulsions sx/age
4mo to 4 years, from rapid increase in temp
Tx for absence seizure (1st and 2nd line)
ethosuxamide and valproic acid
Tx for juvenile myoclonic epilepsy
depakote
West syndrome sx
infantile spasms, severe developmental delay
Lennox-Gastout syndrome sx
multiple seizure types (intractable), developmental delay
Diet for tx of seizures
ketogenic diet
Cause of cerebral palsy generally
nonprogressive injury to the brain
Specific causes of cerebral palsy (3)
intraparenchymal hemorrhages (thalamus/caudate), periventricular leukomalacia (infarcts), multicystic encephalopathy
Sx of Chiari Malformation type I
loss of pain/temp/m. strength of upper extremities
Assc with Chiari malformation
meningomyelocele anchoring spinal cord, increased intracranial pressure
Pachygyria
broad gyri with decreased number
Lissencephaly
smooth gyri surface, failure of cell migration
Assc with Down’s syndrome
Alzheimer’s by 4th decade
Trisomy of chromosomes 13-15 sx
midline defects/holoproencephaly
Developmental Reflexes/disappearance (8 of them)
stepping at 1-2m, galant at 1-2m, grasp at 3m, moro at 3-6m, tonic neck at 3-6m, root/suck at 4-7m, babinski at 1-2 yr, parachute starts at 8-9m and stays
Developmental milestones/appearance (7)
smile/recognize parents at 2m, roll back to front at 4m, roll front to back 5m, sit/recognize stranges at 6m, walk alone/use 2 words at 12 m
Only neuroprotective tx for neonates
hypothermia
Tx to prevent neonatal hemorrhages
antenatal corticosteroids
Assc of cerebral palsy (common cause)
periventricular leukomalacia
Aicardi syndrome causes/sx
absence of corpus callosum, more in females (X chromosome defect), seen infantile spasms
Possible cause of ADHD
prenatal tobacco exposure
Dx of ADHD
in more than 1 setting, longer than 6 months, before 7 yrs, some type of impaired function
Tx for ADHD
methylphenidate/dextroamphetamine (stimulants), atomoxetine (NE reuptake inhibitor)
Autism sx
enlarged head, regression/no attainment of language
Rett syndrome cause (genetically) and sx
MECP 2 gene mutation on Xq28. See smaller head, stereotypic hand movements and dementia. More in females
Sx of Neurofibromatosis-1 and cause
scoliosis, epilepsy, eye problems. From chromosome 17
Cause of NF-2
merlin/NF2 proteins on chromosome 22
Sx of NF
cafe au lait spots, axillary freckling, neurofribromas in 2nd/3rd decade
Sturge Weber sx
port wine stain on face, cerebral calcification, seizures. Can see trolley track lines in occipital lobe
Tuberous sclerosis triad
mental retardation, adenoma sebaceum, and epilepsy
Cause of tuberous sclerosis
hamartin and tuberin genes on chromosomes 9 and 16
Sx of maple syrup urine disease
seizures, hypoglycemia, hypertonia, delicious urine
Sx of homocystinuria
multiple thromboembolic events, ectopia lentis, seizures
Dx of Niemann Pick Disease
bone marrow x with decreased sphingomyelinase in leukocytes
Wilson disease sx
degeneration of basal nuclei, cirrohosis of liver, Kaysier Fleischer rings, onset 11-25 yrs