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206 Cards in this Set

  • Front
  • Back
Stroke -
Types 2
Ischemic - 80%
emboli
thrombi
systemic hypoperfusion

hemorrhagic
Stroke -
Risk Factors
Age
male
race
HTN
diabetes
obesity
smoking
hypercholesterolemia
AF
carotid stenosis
coke
alcohol
IV drug user
Stoke -
Aphasia
Aphasia
Stoke -
neglect
MCA
Stoke -
gaze preference
MCA
Stoke -
homonymous hemianopsia
MCA
Stoke -
contralateral hemiparesis -
MCA
Stoke -
arm/face > leg
MCA
Stoke -
Amnesia
ACA
Stoke -
personality changes
ACA
foot drop
ACA
gait dysfunction
ACA
cognitive changes
ACA
contralateral hemiparesis -
ACA
leg > arm/face
ACA
Homonymous hemianopia
PCA
memory deficits
PCA
dyslexia/alexia
PCA
Coma
Basilar
CN palsies
Basilar
apnea
Basilar
visual Sxs
Basilar
drop attacks
Basilar
dysphagia
Basilar
Unilat pure motor or sensory
Lacunar
dysarthria -
Lacunar
clumsy hand syndrome
Lacunar
ataxic hemiparesis
Lacunar
Transient neuro deficits
last < 24 hours
TIA
TIA
most last
most last < 1 hour
Stoke -
Dx CT without contrast -
ischemic vs. hemorrhagic
Stoke
Dx
MRI
EKG
echocardiogram
Stoke
Dx
vascular studies -
carotid US
MRA
Stoke
Dx
transcranial doppler or MRA
screen for hypercoagulability
PE
Stoke -
Tx* Vigilance for signs of -
brain swelling
inc. ICP
herniation
Stoke -
Tx ischemic stroke
if admin within 3 hrs.
of onset of Sxs
* tPA -
Stoke -
Tx ischemic stroke presenting
within 48 hours
* ASA -
Stoke -
Tx * no hypo's
* no hypotension, hypoxemia,
hypoglycemia
Stoke -
Tx for periphery
* tx aspiration pneumonia,
UTI or DVT
Stoke -
Preventive and Long-Term
antiagregan
* ASA, clopidogrel or
dipyridamole/ASA
Stoke -
Preventive and Long-Term vascular
* carotid endarterectomy
Stoke -
Preventive and Long-Term anticoags
* anticoags
* management of
HTN, DM and
hypercholesterolemia
Carpal Tunnel Syndrome -
What is it
Median n. compression where
passes thru carpal tunnel
Carpal Tunnel Syndrome -

Risk factors
women 30-55
CTS
Risk factors
repetitive use injury
pregnancy
DM
CTS Risk factors
hypothyroidism
acromegaly
RA
obesity
CTS
pain location and funcionality
Wrist pain
numbness & tingling of 3 1/2
weak grip
dec. thumb opposition
CTS when aches
thenar atrophy
nocturnal pain & paresthesias
CTS Signs ??how worse
Sxs may awaken pt. at night
relieved by shaking wrist
CTS -
Workup Tinel's sign -
tap
tingle
CTS - Phalen's sign -
Phalen's sign -
ph-lex (flex)
paresthesias
CTS to confirm
EMG - to confirm
NCV - to confirm
eval for risk factors
Carpal Tunnel Syndrome -
Tx
Neutral wrist splint
modify activity
create ergonomic work envi
CTS Tx medications
NSAIDs
corticosteroids -
direct injection
CTS Tx surgery
if Sxs persist -
carpal tunnel release
Myasthenia Gravis -
What is it
Autoimmune
Ab that bind to postsynaptic
Ach receptors (nicotinic)
block receptors
lose receptors
MG age
young adult women
MG can be associated with -
thymoma
thyrotoxicosis
Muscle weakness inc. in
periods of activity
dec. after rest
MG
Sx come and go
onset can be sudden
fluctuating fatigable ptosis
MG
MG eye mouth2
diplopia (double vision)
dysphagia (swallowing)
dysarthria (speech)
Sxs worsen throughout day
MG
myasthenic crisis -
so severe,
resp. failure and aspiration
secondary to weakness
myasthenic crisis -often secondary to
often secondary to infection
(resp. muscles compromised)
Myasthenia Gravis -
Hx/PE ocular myasthenia -
common variant
if doesn't spread in 2-3 yrs,
probably won't
Myasthenia Gravis -
diagnostic testr
Edrophonium (tensilon test) -
Myasthenia Gravis -
Dx
abnormal single-fiber EMG
dec. response to
repetitive n. stimulation
Myasthenia Gravis - if thymoma
chest CT - eval for thymoma
antistriatal ab if thymoma
Myasthenia Gravis -
Tx
* Neostigmine (treat Sx)
* pyridostigmine (treat Sx)
* prednisone
* plasmapheresis or IVIG -
temp relief (wks) if severe
* thymoma resection
Amyotrophic Lat. Sclerosis -
What is it
Progressive neurodegen. dis
unknown etiology
ALS which nerves
degeneration of motor neurons
UMN and LMN degenerate
=> resp. failure and death
Amyotrophic Lat. Sclerosis -
Hx/PE
Slowly progressive weakness
may have fasciculations init
UMN and LMN
Amyotrophic Lat. Sclerosis -
Dx
Clinical presentation
EMG and n. conduction studies
ALS CT/MRI -
cervical spine
check for lesions
ALS r/o systemic causes -
CBC TSH SPEP UPEP
Ca2+ PTH PFTs
ALS urine for heavy metal -
(if h/o exposure)
Amyotrophic Lat. Sclerosis -
Tx
Supportive
pt. education
pulmonary specialist
ALS medication
riluzole
Thiamine (B1) Deficiency -
What are Signs/Sxs
Wernicke's
Wernicke's
inadeq intake or absorption
excessive alcohol interferes
with GI absorption
and liver storage
Wernicke's acute onset -
confusion
Wernicke's opthalmoplegia -
nystagmus
lat. rectus palsy
conjugate gaze palsy
abnormal pupils
Wernicke's ataxia -
vestibular dysfunction
cerebellar dysfunction
Wernicke's pts
Alcoholics
dialysis
hyperemesis
starvation
Wernicke's pts
cancer
AIDS
can be triggered by large-dose
glucose admin if deficient
Wernicke's tx
Reversible almost immediately
with thiamine admin
Korsakoff's Psychosis -
What is it
Late complication of
untreated pts. with Wernicke's
KP can be triggered by
severe or repeated DTs
can be triggered by SAH and
thalamic injuries
KP ????? memory affected
immediate memory affected
confabulation
Korsakoff's Psychosis -
Prognosis good
-
head injury and SAH
irreversible - others
B12 deficiency -
What are Signs/Sxs
Subacute combined degen
B12 deficiency -
Pts.
Pts with pernicious anemia
B12 deficiency -
Tx
B12 injections or
large oral doses
Folate Deficiency -
What are Signs/Sxs
Irritability
glossitis
diarrhea
depression
neural tube defects
Folate Deficiency -
glossitis
Folate Deficiency -
Pts
Alcoholics - alcohol
interferes with absorption
Pts. with pernicious anemia
Folate Deficiency -
prognosis
Reversible if corrected early
. Epilepsy -
seizure d/o
2+ seizures not related
to reversible stressors
. was seizure epileptic -
Hx
inc. prolactin = epileptic
seizure caused by -
. VITAMINS
vascular
infection
trauma
autoimmune
metabolic
idiopathic
neoplasm
sychiatric (faking it)
. anticonvulsant therapy
indicated?
. anticonvulsant therapy
indicated?
1st seizure not treated
when underlying cause unknown
Partial Seizures -
What are they
Arise from focus
limited to one side
consciousness usually not lost
can progress to generalized
simple partial & complex part
Partial Seizures -
Simple partial -
consciousness not impaired
Partial Seizures -motor -
Jacksonian march
They are unique in that they travel through the primary motor cortex in succession, affecting the corresponding muscles, often beginning with the fingers. This is felt as a tingling sensation.
It then affects the hand and moves on to more proximal areas. Symptoms often associated with a Jacksonian seizure are sudden head and eye movements, tingling, numbness, smacking of the lips, and sudden muscle contractions. Most of the time any one of these actions can be seen as normal movements, without being associated with the seizure occurring
Partial Seizures -
sensory
- parietal
Partial Seizures -
autonomic
- BP, HR, PVR
Partial Seizures -psychic -
fear, deja vu
Partial Seizures -psychic -
fear, deja vu
Partial Seizures postictally -
Todd's paralysis is focal weakness in a part of the body after a seizure.
resolves in 1-2 days
Partial Seizures Complex partial -
consciousness impaired
temporal lobe
auditory or visual hallucinat
deja vu
automatisms
Partial Seizures postictal -
confusion
amnesia
Partial Seizures Workup
EEG
Partial Seizures r/o systemic causes -
CBC
electrolytes
Ca2+
fasting glucose
LFTs
tox screen
RPR
renal panel
ESR
Partial Seizures r/o mass -
MRI or CT with contrast
Partial Seizures tx
Tx underlying cause
Partial Seizures -
Tx recurrent partial -
phenytoin
oxcarbazepine
tegretol
phenobarbital
valproic acid
Partial Seizures -
Tx kids -
phenobarbital
Partial Seizures -
Tx
intractable temporal lobe -
WADA testing
Partial Seizures -
Tx
ant. temporal lobectomy
Generalized Seizures -
What are they
Begin diffusely throughout
both sides
Generalized Seizures - consciousness
consciousness always lost
postictal confusion
most common types -
tonic-clonic (grand mal)
absence (petit mal)
Tonic-Clonic Seizures -
Start suddenly
with tonic extension of
back and extremities
rep. symm. clonic movements
Tonic-Clonic Seizures -
incontinence
tongue biting
may look cyanotic
consciousness slowly regained
Tonic-Clonic Seizures -may complain of -
muscle ache
headache
Tonic-Clonic Seizures -
Tx
Tx underlying cause
Tonic-Clonic Seizures -
Tx idiopathic -
Araklamaci gazeteci - 1st line
lama - adjunctive
topiramate - adjunctive
Tonic-Clonic Seizures -
Tx symptomatic -
same therapy as partial sz.
Absence (Petit Mal) Seizures-
What are they
Begin in childhood
subside before adulthood
often familial
Absence (Petit Mal) Seizures-
how often
Brief, often unnoticeable
episodes of
impaired consciousness
lasts 5-10 seconds
have 100's of times/day
eye flutters or lips smack
amnestic ???
amnestic during and
immediately after
can be precipitated by
hyperventilation
Absence (Petit Mal) Seizures-
Evaluation EEG -
3 Hz per sec. spike
& wave discharges
Absence (Petit Mal) Seizures-
Tx
eto- 1st line
araklamaci gazeteci
zonisamide
(West Syndrome) -
Infantile Spasms
Infantile Spasms
(West Syndrome) -
. infantile spasms
(generalized seizures)
symmetric
tonic
Infantile Spasms
(West Syndrome) -
5-10 at a time while drowsy
or upon awakening
. abnorm interictal EEG
. arrest of psychomotor dev.
Infantile Spasms Tx -
ACTH
prednisone
clonazepam
valproic acid
Status Epilepticus -
Brain in persist. state of Sz
1 cont. seizure or recurrent
w/o regaining cons. > 30 min.
med emergency - 20% mortality
Status Epilepticus -common causes -
anticonv. withdrawal/noncomp
anoxic brain injury
alcohol withdrawal
metab disturb (hypoNa+)
trauma
infection
Status Epilepticus -usual cause -
subtherapeutic or
noncompliance
Status Epilepticus -
Evaluation first
Airway, breathing, circulation
Status Epilepticus -
Evaluation labs -
electrolytes
anticonvulsants
Status Epilepticus -
Evaluation
get Hx
look for etiology if
no prior Hx
(tumor, encephalitis, SAH)
Evaluation of SE
(EEG, CT only when stable)
west syndrome
at age of onset
starts at 3-12 months
usu male
MR
Status Epilepticus -
Tx
Diazepam or lorazepam
Status Epilepticus -
Tx if continues -
phenytoin or fosphenytoin
Status Epilepticus -
Tx if continues -
phenobarbital
Status Epilepticus -
Txif continues -
midazalom or propoful
Headache -
Things to think about
(Evaluation)
Headache new or old
characteristics
any associated Sxs
any neurological Sxs
SAH suspected?
Migraine Headache - More commonly affects ????
and those with ???? Hx
????? & ???? abnorm
More commonly affects women
and those with family Hx
vascular & 5HT abnorm
Migraine Headache -triggers -
menses
OCP
chocolate
fasting
stress
bright lights
Migraine Headache -
Hx/PE
Throbbing > ???
usually lasts < ???
GIS symptoms
????phobia
sensitive to ???
Throbbing > 2 hrs
usually lasts < 24 hrs
n/v
photophobia
sensitive to noise
"classic" migraine -
visual aura precedes
unilat
"common" migraine -
80%
can be b/l, periorbital
Migraine Headache -
Dx
if have focal neuro deficits-
CT or MRI
Migraine Headache -
Sxs acute in onset -
r/o meningitis or SAH
Migraine Headache -
Tx
Avoid known triggers
aspirin/NSAIDs
sumatriptan
Migraine triggers
aspirin/NSAIDs
sumatriptan
Migraine prophylaxis -
beta-blockers
TCAs
Ca2+ channel blockers
valproic acid
Cluster Headache -
What is it
Men
~ 25 y/o - age of onset
Cluster Headache -
location
duration
Unilat, periorbital
30 min. - 3 hrs.
Cluster Headache -attacks in clusters -
same part of head
same time of day
same time of year
Cluster Headache - precipitators
can be precip by alcohol or
vasodilators
ipsilat tearing of eye
Cluster Headache -
Dx
HX
Cluster Headache -
Tx Acute therapy with
high-flow O2
(100% nonrebreather O2)
sumatriptan
corticosteroids
prophylaxis -
Ca2+ channel blockers
valproic acid
methylsergide
prophylaxis important -
by the time abortive meds take
effect, has already resolved
methylsergine (sansert) - careful??
need drug holiday every several months to avoid risk of retroperitoneal fibrosis
MC type diagnosed in adults
chronic
Tension Headache -
Tension Headache - describe
Tight, bandlike pain
occipital and neck
Tension Headache - exacerbated by -
noise
bright lights
stress
fatigue
Tension Headache - Dx
Dx of exclusion
Tension Headache -
Tx
Avoid exacerbating factors
NSAIDs - 1st line
Tension Headache -
prophylaxis -
Ca2+ channel blockers
alpha blockers
TCAs
Benign Paroxysmal
Peripheral vertigo
otoliths dislodge from
usual position
migrate over time into
semicircular canals
abnorm fluid displacement
=> vertigo
Benign Paroxysmal
Positional Vertigo -
Hx/PE
Sudden onset of severe
vertigo and nystagmus
vertigo with head movement in
direction of affected ear
happens turning head in bed
5 sec. - 1 min.
n/v
Sxs dec. with repetitive tests
usu h/o recent trauma
Benign Paroxysmal
Positional Vertigo -
Dx
Nylen-Barany Maneuver
(Dix-Hallpike)
Benign Paroxysmal
Positional Vertigo -
Tx
Usually subsides spontan.
in wks to months
Epley Repositioning Maneuver
Meniere's Disease
(Endolymphatic Hydrops) -
What is it
Peripheral vertigo
from buildup of endolymphatic
fluid in inner ear
Meniere's Disease
= V and P change
risk factors -
head trauma
syphilis
Meniere's Disease
(Endolymphatic Hydrops) -
Hx/PE
Sudden attacks of vertigo
lasts up to 24 hours
attacks can last hrs to days
n/v
ear fullness
tinnitus
hearing loss
signif permanent hearing loss
can occur over period of yrs
Meniere's Disease
(Endolymphatic Hydrops) -
Dx
Audiometry -
low-freq. pure tone
hearing loss
Meniere's Disease
(Endolymphatic Hydrops) -
Tx
Low-salt diet
acetazolamide
Meniere's Disease
(Endolymphatic Hydrops) -
Tx acute -
antihistamines
antiemetics
benzos
Meniere's Disease
(Endolymphatic Hydrops) -
Tx if refractory -
surgical decompression
Parkinsonism cause antiemetics
(metoclopramide),
Parkinsonism cause indole alkaloid antipsychotic and antihypertensive drug
reserpine.
Poisoning from 4.................................................... are also causes of Parkinsonism.
MPTP, carbon monoxide, cyanide, and
manganese
Patients who have
survived an episode of encephalitis can develop
postencephalitic Parkinsonism.
Parkinsonism + vertical gaze palsy
= supranuclear palsy
Parkinsonism + prominent ataxia
= olivopontocerebellar atrophy
Parkinsonism + prominent orthostatic hypotension
= Shy-Drager syndrome
Severe ................................. can cause a paucity of
spontaneous movement that can mimic Parkinsonism.
depression
111111111 can be mistaken
for the tremor of Parkinson disease, but the lack of other neurologic symptoms and a positive
22222222 of tremor and its amelioration with 3333333333 distinguish the two entities.
1 Essential tremor
2family history
33alcohol
11111 can present with ataxia and gait disturbances, which can
also be mistaken for Parkinson disease. The presence of 2222 and 333333
with 44444 on a CT scan of the head can help identify this disorder
1A normal pressure hydrocephalus
2dementia
3urinary incontinence
4dilated ventricles
medications available for the medical treatment of Parkinson disease indirecdy
increase the amount of dopamine available
(COMT inhibitors, selegiline, amantadine),
Direct-acting dopamine agonists such as ----------------can be used alone as initial
therapy or in combination with small doses of levodopa/carbidopa.
pramipexole or ropinirole
Two other dopamine
agonists are
bromocriptine and pergolide.
Bromocriptine and pergolide
are 111111 and can cause 222222
1ergot derivatives
2cardiac toxicity.
Anticholinergics such as benztropine and trihexyphenidyl are used in patientsyounger than 60 years old mosdy to relieve
tremor and rigidity. Avoid with 22222
BPH and glaucoma.