Neuro Flashcards
Types of strokes (3)
Embolic (ischemic)
thrombotic (ischemic)
Hemorrhagic (SAH and IPH)
Seizure: causes
Vascular (stroke) Infection (meningitis/encephalitis) Trauma (TBIs and brain bleeds) Autoimmune (lupus cerebritis) Metabolic (ca, Na, glucose) Ingestion/withdrawal(benzos/EtoH) Neoplasm Psychiatric
VITAMINS
Status epilepticus: TX progression
Benzos (a lot of lorazepam) –> IV fosphenytoin and intubation –> midazolam and propofol –> phenobarbital
Broad spectrum anti-epileptics good for general epilepsy
valproate, lamotrigine, levetiracetam
Myoclonic: features and tx
no LOC and no loss of tone
valproate
Atonic: features and tx
No LOC, but loss of tone
valproate
Parkinsons disease: clinical features (4)
bradykinesia
cogwheel rigidity
resting tremor
gait/postural instability
Parkinsons disease: TX
NOTE: amantadine is wrong
COMT-inhibitors (-capones)
MOA-B inhibitors (selegeline)
Dopamine agonists (ropimerole, promipexole)
carbidopa/levodopa
If <70 and functional: start with dopamine agonist
If >70 or not functional: start with levodopa/carbidopa, then COMT and MOA-B inhibitors as dopaminergic neurons continue to degenerate in substantia niigra
Types of primary headaches (4)
Tension
Analgesic rebound
cluster
migraine
Tension HA: clinical features and TX
features: BL vice-like, with radiation down to neck
TX: NSAIDs, acetominenophen
Cluster HA: clinical features and TX
vascular pathology
asymptomatic for months, but then HA 8-10x/day with unilateral eye pain with a Horner syndrome-type presentation
TX: abortive–O2, then sumitriptan
ppx–ccbs (verapamil)
F/U with 1x brain imaging
Migraine HA: clinical features and TX
pathology is vascular
unilateral, pulsatile pain that is debilitating and lasts 4-72 houyrs w/o abortion
TX:
Abortive
mild–NSAIDs
mod-severe–triptans and ergots
PPX
propranolol
valproate
topiramate
Idiopathic intracranial HTN
female taking OCPs and/or acne meds with ICP (papilledema, FND, N/V, HA especially in morning)
negative CT
LP with high opening pressure (>25cmH20) and symptomatic relief
TX: acetazolamid, serial LPs, VP shunt
Reflexes to assess for brain stem function
corneal reflex (with Q-tip)
cold-water calorics (cold water causes opposite beating nystagmus in normal brainstem, and warm water same)
Dolls eye reflex (eyes should move when you turn head
Alzheimers: initial impairment
memory
Picks disease: initial impairment
personality (memory is retained)
Picks: CT finding
fronto-temporal atrophy
Lewy-Body dementia: features
parkinsonian type features albeit predominantly with dementia and also with visual hallucinations
Fluctuating cognition
Alzheimers: treatment
donepezil
Normal pressure hydrocephalus
Path: increased ICP
Wet, wacky, wobbly (ataxia early in disease)
DX: CT showing hydrocephalus and dilated ventricles
LP provides improvement
TX: VP shunt
CJD: DX
MRI
Clinically: behavioral change and myoclonus +/- seizures
Peripheral vertigo causes (3)
BPPV
labrynthitis/vestibular neuritis
Menieres
Menieres: clinical features and tx
Triad of hearing loss, vertigo, and tinnitus lasting <1hr but >30 minutes
Tx: salt restriction, thiazide duiretics, and meclizine
Labrynthitis/vestibular neuritis: clinical features and tx
4wks after a viral URI
vertigo with hearing loss, N/V lasting up to a week
TX: steroids and meclizine
BPPV: path, clinical features, and Dx/TX
path from otolith in vestibular system
recurrent, reproducible vertigo lasting <1 minute with positional changes
Dx: dix-hallpike maneuver
Tx: Epley maneuver
Multiple sclerosis: MRI findings
Periventricular white matter
NOTE: get this for initial diagnosis of MS before committing to high dose steroids
Multiple sclerosis: chronic tx
IFN
glatiraner
fingolonod
Bethanocol for urinary retention
amitriptyline for urinary iconinence
baclofen for spasms
gabapentin for neuropathic pain
Ascending paralysis and hyporeflexia in s/o recent diarrheal illness
GBS
NOTE: can also proceed URI and be accompanied by paresthesias and dysarthria
GBS: managment
NEVER steroids
give IVIG or do plasmapharesis, or try one then the other
Myasthenia gravis: TX
Chronic: cholinesterase-inhibitor, give steroids, remove thymoma if diagnosed on CT
Acute crisis: IVIG or plasmaphoresis
Eaton lambert disease: clinical features
Initial fatiguability, improvement with use
Issues with proximal muscles
EMG shows increased amplitude of impulses with more attempts
CT can show small cell lung cancer (paraneoplastic syndrome)
Neuromuscular junction diseases
MG
Lambert eaton syndrome
organophosphate poisoning
botulism
Muscle fibers
muscular dystrophies
polymyositis and dermatomyositis
hypothyroidism
corticosteroids
HIV myopathy
Peripheral nerve diseases (5)
hereditary primary motor sensory neuropathy
GBS
diabetic neuropathy
amyloid neuropathy (MM)
Lead poisoining
Anterior horn cell neuropathies (4)
Poliomyelitis
spinal muscular atrophy
ALS
paraneoplastic syndromes
Upper motor neuron disorders
leukodystrophy
vasculitis
brain mass
vit B12
Non eccymotic swelling in scalp on newborn that was not present at birth and involves one cranial bone
cephalohematoma
caput succedaneum is eccymotic and crosses suture lines
Serotonin syndrome vs neuroleptic malignant syndrome
Serotonin syndrome: triad of AMS, autonomic instability, and neuromuscular excitability (tremor, hyperreflexia, and myoclonus)
Neuroleptic malignant syndrome: tetrad of AMS, autonomic instability, rigidity, and fever
Lithium toxicity
coarse tremors, ataxia, AMS, N/V, hypotension
Cholinesterase inhibitors used in alzheimers disease
donepezil, galantamine, and rivastigmine
Normal CSF values
Cells: O-3
glucose: 50-100
protein: 20-45
Pressure: 100-200
CSF values in viral/aseptic meningitis
Cells: >100 lymphocytes
glucose: 50-100
protein: 20-45
Pressure: 100-200
CSF values in bacterial meningitis
Cells: >1000 PMNs
glucose: <50
protein: 100
Pressure: >200
pseudotumor cerebri =
idiopathic intracranial HTN
peripheral nerve lesion: EMG findings
fasciculations/fibrilations at rest
Intrinsic muscle disease: EMG findings
no muscle activity at rest
Decreased amplitude of muscle contraction upon stimulation
Broca vs wernickes area: location
Broca: dominant frontal lobe
Wernicke: dominant temporal lobe
Midbrain cranial nerves
3 and 4
Pons cranial nerves
5,6,7, &8
Medulla cranial nerves
9-12
Seizure with no post-ictal state
absence seizure
Normal age range for febrile seizure
6months old - 5 years old
25 year old with pmh of mr who has inability to relax grip =
myotonic dystrophy (autosomal dominant) Tx involves genetic counseling
Shy-Drager syndrome =
Parkinsoism predominantly with orthostasis
Medication used chronically in multiple sclerosis that can cause progressive multifocal leukoencephalopathy
Natalizumab
Paralysis of entire side of the face, involving forehard
bells palsy
Paralysis on one side of face, but can still wrinkle forehead =
stroke until proven otherwise
Bells palsy: TX
prednisone +/- acyclovir
Herpes simplex encephalitis: CSF findings and most accurate imaging
CSF Cells: >100 WBCs (90% lymphocytes) glucose: 50-100 protein: elevated (>100) Pressure: 100-200 RBCs present (from destruction of temporal lobe)
Imaging
MRI most accurate (CT nl in 50% of cases)
Wernickes encephalopathy: clinical features
triad of sxs
encephalopathy (confusion)
oculomotor dysfunction (nystagmus)
gait disturbance (broad based)
Spinal epidural abscess: TX
vancomycin and ceftriaxone (staph aureus most likely causative organism)
Contralateral hemiparesis and sensory loss due to ___
putaminal hemorrhage and involvement of adjacent internal capsule
Transient, focal neurologic deficit occurring after a seizure
Todd paralysis
Digoxin toxicity
N/V, diarrhea, vision changes, and arrythmias (percieved as palpitations)
Small-vessel lipohylanosis is caused by ____ and inturn causes___
atherosclerosis
thrombotic small-vessel occlusions–> lacunar strokes and pure contralateral motor or pure sensory deficits