Non-trauma Neurology Flashcards

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1
Q

Seizures

A

Really common – huge DDx
-The big question: Hx of same or first seizure?

Primary vs. Secondary seizure

  • Primary: occurs w/o provocation/cause - epilepsy
  • Secondary: response - toxic, metabolic, infectious, traumatic, vascular, neurologic, etoh withdrawal, eclampsia, fever, etc

Post-ictal state

  • Disorientation, sleepy, amnesia, HA, sonorous breathing, diaphoresis, lactic acidosis (high TCO2 on chem panel)
  • Commonly lasts 30min-1hr – gradually improves to normal
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2
Q

Generalized seizure - convulsive

A
  • Formerly “grand mal”
  • Involves both hemispheres
  • Loss of consciousness, amnesia
  • Tonic then clonic movements
    • Tonic: stiffen, arch back, cry out
    • Clonic: rhythmic jerking bilat arms/legs, facial grimace, clench teeth
  • Urinary incontinence, tongue biting
  • Resolve spontaneously, post-ictal state
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3
Q

Generalized seizure - non-convulsive

A
  • Absence Sz – formerly “petit mal”
    • More common in kids
    • “Daydream”, +/- LOC, +/- clonic sx’s
  • Lasts seconds – can go on as if nothing happened – no post-ictal state

Urinary incontinence and tongue biting are common if a generalized seizure occurred – helps determine if a seizure has occurred for someone who doesn’t remember and was alone

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4
Q

partial - 2 types

A
  • Limited area of brain

- Sx’s match area affected

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5
Q

focal aware seizure (simple partial)

A
  • Awareness, memory, consciousness is preserved

- Uncontrolled movement, visual, auditory sx, autonomic sx’s

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6
Q

focal impaired awareness seizure (complex partial)

A

-Any of: awareness, memory, consciousness is not preserved
-Temporal lobe Sz most common
-Aura common – déjà vu, jamais vu, sounds, smell, taste, numbness, automatisms, fear/panic
-Deja vu – unfamiliar is familiar
-Jamais vu – the familiar is unfamiliar (“who’s house is this?” this is your house!)
-Focal aware: THEY ARE AWAKE and watching their strange movements
Don’t need to know ECG pattern
-Why do we need to know which type of seizure? You need to be able to recognize the family’s description of what happened

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7
Q

Status epilepticus

A
  • Seizure activity lasting > 5min or repetitive seizures without clearing of mental state in between
  • Life-threatening – airway compromise
  • Seizures >5min OR seizures that don’t have a clearing of mental state inbetween!! are unlikely to spontaneously resolve
  • Often (almost always) result of secondary cause, so start looking…
    • Get D-stick right away – hypoglycemia is often the cause of status
    • Electrolytes (especially: glucose, sodium, magnesium)
    • Intracranial bleed, trauma
    • Tox, OD
  • Goal after ABC’s: abort seizure before neuronal injury occurs
    • Benzodiazepines 1st. Then 2nd or 3rd line drugs (Keppra, Valproic Acid, Fosphenytoin, Phenobarb, etc)
    • Intubation common because they are not ventilating during the seizure but remember – can’t see seizure if paralyzed – you have to be very careful!
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8
Q

Seizures: Hx and PE

A

History

  • Ever seized before?
    • Yes? Changing pattern?
  • Out of meds? Most common cause of seizures in ED
  • Witnesses: how long, how many?
  • Trauma – before, after
    • Head, tongue, extremities
  • EtOH? Drugs?
    • Stop? Why??
  • Recent illness? LMP?
  • Country of origin, travel

PE

  • Post-ictal or still seizing?
    • ABCDE’s first
    • IV, O2, monitor
  • VS improve with recovery
  • Tongue trauma, urinary incontinence
  • Head to toe exam
    • Trauma
    • Neuro deficit
    • Infection
    • Evidence other Dz
    • Stigmata of EtOH
    • Toxidrome
  • When the pattern in true epilepsy changes, that means your meds need to be changed
  • Seizure after trauma is concerning for brain bleed
  • LMP? Don’t want to miss eclampsia
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9
Q

Seizure red flags

A
  • First seizure: Why??
  • Head trauma: Bleed, ICP
  • VS not resolving: Why??
  • Alcohol withdrawal
  • Fever, infection: Need LP? Shock?
  • Rash: Meningitis?
  • Vomiting: Airway, aspiration risk
  • Electrolytes: Which ones?
  • Stimulants: Bleed? CVA?
  • Prolonged post-ictal state: Why?
  • Focal neuro deficit: CVA, bleed?
  • Travel/Endemic area?
    • Neurocystercercosis
  • Malignancy: Mets to brain?
  • Renal/liver Dz: Uremic or encephalopathic??
  • HIV: Toxo-, histo-, infection
  • Coumadin/Plavix: Bleed?
  • Pregnancy: Eclampsia
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10
Q

seizure work-up if pt has history of seizures

A
  • D-stick on all, upreg
  • Observe, reassess
  • Safety: bedrails, etc
  • Measure drug levels
    • Dilantin, Carbamazepine, Valproic acid, Phenobarb
    • ?Keppra, not Lamictal, etc
  • Alcohol, urine tox screen
  • Chem for electrolytes
    • If cause not obvious
    • Sz causes lactic acidosis
  • Creatinine Kinase (CK) if prolonged down-time
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11
Q

seizure work-up if this is the first seizure

A
  • D-stick on all, upreg
  • If sz stops, pt now normal, no obvious cause:
    • Chem panel
    • Magnesium, phosphorus if EtOH
    • EtOH, U tox
    • Coumadin? PT/INR
    • HIV test
  • Head CT non-con
  • Add lumbar puncture only if fever, suspect SAH, encephalitis, etc
  • EEG: on admission or as outpt
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12
Q

seizure tx

A
  • Active tonic/clonic seizure in ED
    • Protect pt, abort the seizure with meds
    • When stop: suction oral blood/secretions, O2, time the event
    • Recheck d-stick, re-examine, cardiac monitor
  • Abortive Tx 1st line: Benzodiazepines – know 3
    • Lorazepam (2mg IM/IV)
    • Midazolam (2-5mg IM/IV), Diazepam (5mg IV)
  • Hx seizure? Give regular med in ED – refill meds, f/u
  • New Sz, now well and no Red Flags? Neurology consult to initiate EEG, tx and follow up.
  • Alcohol related sz’s are not prevented with meds
  • Alcohol related seizures are NOT prevented with meds. Phenobarbital is the longest lasting and has the best chance of preventing alcohol related seizures but its not reliable!
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13
Q

febrile seizure in kids

A
  • Rapid rise in temperature, not the number itself
  • Risks: hx same, family hx
  • Get a d-stick on all
  • Search for source of fever or occult infection
    • CBC, Chem, UA, CXR
    • Blood and +/- stool culture depending on whether or not they have diarrhea
  • No CT. No LP if dx clear and kid looks great
    • Yes LP if recent abx use
    • LP, +/-CT if kid looks sick
    • Clear Dx = no anti-sz meds
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14
Q

eclampsia seizures

A
  • Usually >20wks

- Get a Upreg!

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15
Q

alcohol withdrawal siezure

A
  • Common but dangerous
  • Tx w/d agressively
  • Admit
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16
Q

pseudoseizure

A
  • Psych, emotional distress
  • Atypical movements
  • Brief post-ictal period
  • Good Soc Hx
  • Refer to psych, EEG output
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17
Q

syncope

A
  • Transient LOC, loss of postural tone with spontaneous recovery
    • Brief clonic activity common – mimics seizure
  • Loss of cerebral perfusion leads to loss of O2 and glucose needed by the brain and RAS to function
  • DDx is large; most benign, some life threatening
  • Hx is key – drives work up (like everything else…)
    • Ever had this before? What was the Dx?
    • Really lose consciousness? Fall? Hurt yourself?
    • What were you doing? Last thing you remember?
    • Sick lately? Upset? EtOH, drugs?
    • PMHx, Meds, Fam Hx, Soc Hx
  • Near-syncope, “pre-syncope” – treated like true syncope
  • RAS: Reticular Activating System – neuro network in the brainstem that controls level of consciousness
  • There may be brief clonic activity in syncope – this does NOT mean they are seizing!! Don’t be fooled!
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18
Q

syncope red flags

A
  • Syncope in person >50yrs
  • Syncope w/ exertion or when supine – think cardiac
  • Hx – before/after event
    • Chest pain
    • Palpitations
    • Headache
    • SOB
    • Abd pain
    • Back pain – thoracic aorta dissection
    • Bleeding (coumadin)
  • Recent hospitalization, surgery, procedure
  • Fam Hx of sudden death
  • Syncope PE findings:
    • Abnormal VS (Hypotension, Tachy-, bradycardia, Fever)
    • Diaphoresis
    • Confusion, focal deficit
    • Cardiac murmur
    • Rales, wheeze, edema
    • Melena
    • Head trauma
    • Pregnancy
    • Pacemaker
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19
Q

syncope ddx

A

The Biggies

  • Cardiac
    • Arrhythmia
    • Aortic stenosis (severe)
    • Hypertrophic, other cardiomyopathies
  • Intracerebral
    • Hemorrhage, SAH
    • Ischemic stroke: rarely
  • Aorta
    • Dissection, aneurysm
  • GI Bleed, anemia
  • Ectopic pregnancy
  • Pulmonary embolus

The Common

  • Volume depletion
    • Dehydration, n/v/d
  • Medication effect
  • Drug/EtOH effect
  • Vasomotor (vasovagal)
  • Emotional event/reaction
  • Mimic – unwitnessed seizure
  • Hypoglycemia**
20
Q

ED work up of syncope

A
  • Syncope in young, healthy, completely recovered person:
    • All get: EKG; consider D-stick, Hct
    • All females (12-55yrs) get Upreg
    • CT, CBC, Chem, troponin, etc; not routine part of w/u
  • Other diagnostics driven by age, Hx, PE
    • IV hydration, O2, monitor, labs, troponin
    • CXR, +/-CT. Echocardiogram, Holter Monitor
    • > 50yo – higher risk, more extensive work up
  • Dispo:
  • Young, healthy, completely recovered, stable?
    • Likely benign cause. Home if stable w/ return precautions
    • Close follow-up, PO hydration, avoid risks
  • > 50yo – bigger work up, home if w/u all neg, no risks
  • The reason she says “consider” D stick – if your sugar was low enough to faint, how did you come back to consciousness?
  • All females 12-55 get a upreg
21
Q

Dizziness vs vertigo

A
  • Vertigo
    • Sensation of motion, room spinning
    • Major question for us = Central or Peripheral?
    • Peripheral is usually benign
    • Central causes usually serious – red flag!
  • Dizzy: Near-syncope/”feeling faint”, lose balance, disequilibrium, anxiety, etc
  • “Dizzy” is difficult to describe and used to describe many things across cultures
  • A detailed Hx is essential
    • Describe what you feel
    • OPQRST the sx to death
    • Trauma, recent illness?
    • Hearing changes, tinnitus?
    • Headache, weakness?
    • Associated sx’s – fever, bleeding, etc…
22
Q

peripheral vertigo sxs:

A

-Peripheral: sudden onset, intense, paroxysmal, w/ movement; nystagmus is horizontal/torsional, fatigable; tinnitus, n/v, +/- normal TM, no focal neuro deficit

23
Q

Peripheral vertigo types

A
  • BPPV – benign paroxysmal peripheral vertigo
    • Most common cause
    • Otolyth in the semicircular canal
    • Vertigo lasts seconds, positional
  • Labrynthitis: inflammation, viral
    • Vertigo for days, ear/hearing sx’s
    • Movement exacerbates, post viral
  • Vestibular Neuritis: inflammation
    • Vertigo for days, no ear sx’s
    • Movement worse, post viral
  • Meniere’s – 40-70 age group
    • Episodic, chronic, incurable
    • SN hearing loss, tinnitus
  • Cerebellar pontine angle tumor

-Drugs cause peripheral sx’s – ear sx’s predominate

24
Q

Central vertigo types

A
  • Cerebellar CVA, hemorrhage
  • Vertebrobasilar vascular insufficiency/CVA
  • Basilar artery migraine
  • Multiple sclerosis
  • Temporal lobe seizure
25
Q

Vertigo PE and red flags

A
  • Vertigo is miserable; but most benign causes do not hurt
    • Severe headache, chest pain, neck pain are Red Flags
  • Eyes
    • Nystagmus present in all: type, direction, duration matter
    • Pupils, reaction (tox, CVA, tumor)
    • Ptosis? (CVA, CN Palsy, Botulism, Myasthenia Gravis)
  • Ears – test hearing, then look inside
    • Vesicles, cholesteatoma, perforated TM?

-Carotid bruits

  • Thorough Neuro exam
    • Focal neuro deficit, sit/stand/gait (get help if ataxic)

-Fever

26
Q

HINTS exam

A
  • Bedside peripheral vs. central vertigo test
    • Useful but not adequately validated
  • Head impulse
    • Abnormal (saccade) suggests peripheral
    • Normal in central causes
  • Nystagmus
    • Peripheral: one direction: horizontal/torsional – never vertical, fast phase away from affected ear, intensity decreases w/ fixation, fatigues on repeat (Exception: BPPV may not fatigue)
    • Central: any direction (vertical, rotary), fast toward lesion, little effect with fixation/gaze direction change, does not fatigue
  • Test of Skew
    • Cover one eye, uncover, repeat. Eye position deviation when uncover, corrects.
    • Positive suggests central cause
27
Q

Head impulse test

A

-Hold pt’s head, tell them to stare continuously at your nose. Abruptly turn their head 20 degrees to either side. Observe if the pt’s eyes must move or adjust to continue to fixate on your nose – this is the saccade. Repeat to the other side. In a person with active vertigo, if saccade is present, then the issue is located on the same side and they likely have a peripheral cause for their vertigo.

28
Q

test of skew

A

-Pt asked to stare at your nose. Cover one eye for 3-5 seconds , then quickly uncover this eye and cover the other eye. Observe if the eye you are uncovering “drifts” or has to correct to stare back at your nose when it is uncovered. If the eye deviates when uncovered, this is a positive test of skew and a symptom of a central lesion.

29
Q

Dix-Hallpike test

A
  • Specific test for BPPV
    • Debris in semicircular canal; posterior most common
  • Goal is to determine affected side while watching nystagmus
  • Nystagmus is upward and toward ear with head off bed on affected side - may have rotary quality
    • Diagnostic for BPPV
  • Initial delay (latency) – fatigues
  • Purely vertical, rotational, no latency or does not fatigue suggests central cause of the vertigo
30
Q

Epley Maneuver

A
  • Purpose: to reposition the debris – reduce sx’s of BPPV
  • Done right after Dix-Hallpike if it is positive, on positive side
  • Wait until nystagmus stops during Dix-Hallpike, go slow
  • Will reproduce vertigo sx’s
  • May repeat both tests
  • May completely relieve sx’s of BPPV
31
Q

Vertigo treatment

A
  • Peripheral – no labs (upreg)
  • Antihistamines – Meclizine
  • Antiemetics, IV hydration
  • Benzodiazepines
    • Diazepam, Lorazepam PO/IV
  • Safety, return precautions, f/u
  • Epley in ED; Semont maneuver in ED and/or at home**
  • ENT referral if recurrent, hearing loss, ear findings
  • Central vertigo w/u as appropriate – MRI test of choice
32
Q

Peripheral motor weakness

A
  • Not central nervous system
    • CVA/TIA is sudden onset, unilateral
  • Motor weakness
    • Slower onset, progressive, bilateral
    • Neuromuscular junction vs. muscles
    • Respiratory compromise concerns
  • Hx – OPQRST – recognition is key
    • How did it start, how is it worse now?
  • PE – thorough neuro exam
    • Strength testing
    • DTR’s: +2 is normal
    • Cranial nerves
    • Sensation testing
    • Cerebellar testing
33
Q

Guillain barre

A
  • Most common cause of acute, bilateral, flaccid paralysis
  • Autoimmune, demyelinating, progressive, symmetrical
  • Ascending pattern – legs first
  • Loss of DTR’s: is key
  • 2/3 have preceding viral illness (also Zika, etc)
    • 1/6 GB cases after Flu shot
  • Hand paresthesia, muscle pain, may involve CN’s
  • Dx is clinical; worry about respiratory issues, dysautonomia
  • Neurology consult. Admit.
  • Tx: immunoglobulins, plasmapheresis
  • Miller-Fischer variant: descending; ataxia, areflexia, ophthalmoplegia - rare
34
Q

Myasthenia Gravis

A
  • Most common disorder of neuromuscular transmission
  • Autoimmune, gradual, progressive
  • Bimodal peak: 30’s (female predominant), 80’s (male)
  • Eye, facial, swallowing, speech muscle sx’s predominate
    • Bilateral or unilateral ptosis, diplopia, vision changes (Peek sign: close eyes -> can’t maintain, can see sclera)
    • Flat expression, “lost their smile”
    • Gets “tired” talking, chewing fatigue, difficulty swallowing
    • Generalized weakness, fatigue, can’t climb stairs
  • Key: sx’s get worse with use, better with rest
  • Descending, DTR’s intact
  • ED Dx: Tensilon (Enlon) test, ice pack test. Neuro consult, Admit.
  • The improvement of MG with cooling probably occurs by lesser acetylcholinesterase activity in temperatures below 28ºC, providing increasing amount of ACh molecules in the synaptic cleft
  • Tx MG: anti-acetylcholinesterase drugs, steroids, immunosuppressants, thymectomy, etc
35
Q

Botulism

A
  • C. Botulinum: home canned foods, honey/corn syrup in infants, skin popping/IVDU (wound botulism)
  • Sudden, severe, symmetric, bilateral weakness – eyes, face, neck first; extremities last
  • Diplopia, ptosis, blurred vision (pupils dilated), facial weakness, dysphagia, weak voice, neck weak (can’t hold head up)
  • Descending, DTR’s intact
  • Mental status, sensory intact
  • Infants: floppy, lethargic
  • These pt’s are sick: recognition is key, respiratory concerns
  • Tx: Antitoxin, supportive care. Neuro consult. Admit
36
Q

Low back pain and weakness: weakness

A
  • Must consider this Dx in anyone w/ low back pain!
  • Symptoms: Unilateral or asymmetric radicular back pain with:
    • True leg weakness, bilat or unilateral
    • Bladder incontinence or retention, hesitancy
    • Stool incontinence, loss of anal tone
    • Numbness in the “saddle” and perineal distribution; genitals
    • Loss of or reduced lower extremity DTR’s
  • Cause: mechanical compression on “horse’s tail”
    • Disc, fracture, infection, tumor
  • Charting should reflect all of above in low back pain pt’s
  • MRI, call neurosurgery

-SADDLE DISTRIBUTION should be in your chart!

37
Q

Transverse myelitis

A
  • Inflammatory condition of the spinal cord
  • Bilateral motor and sensory loss w/ radicular back pain, B/B dysfunction/incontinence, sensory changes, +/- fever
  • Rapidly progressive. Pain on spinal palpation
  • Risks: Herpes, MS, vasculitis, Lyme dz, TB, IVDU, IMZ, etc
  • MRI, call neurosurgery
38
Q

Spinal epidural abscess

A
  • Risks: IVDU, surgery, bacteremia, spine osteo
  • Fever + back pain, radicular sx’s
  • Bilat motor weakness, sensory changes, B/B sx’s
  • Pain on spinal palpation
  • 2-3 days sx’s then cord compression
  • MRI, call neurosurgery
39
Q

Multiple sclerosis

A
  • Young, female > male, autoimmune?
  • Episodic weakness, paresthesias, disequilibrium – atypical pattern
  • Gait changes
  • Monocular vision change – optic neuritis
  • Labs, lumbar puncture
  • MRI for Dx – MS plaques
40
Q

Polymyositis

A
  • Abrupt, progressive, bilat, proximal muscle weakness – legs usually before arms
  • Can’t rise from chair, brush hair, lift, etc
  • May have dysphagia
  • Elevated CK. CBC, Chem, ESR, RA, ANA often all neg
  • Rash to face, chest, upper back (“shawl pattern”)? Consider dermatomyositis – think cancer somewhere
41
Q

hypokalemic periodic paralysis

A
  • Low K+, Fam Hx, meds (diuretics)
  • Weakness local or generalized
  • Descending, DTR’s diminished
  • Triggers: carbs, cold, exercise
42
Q

tick paralysis

A
  • Suggestive Hx
  • Ascending, DTR’s diminished
  • Remove tick – resolves 24-48hrs
43
Q

Radial nerve palsy

A
  • Prolonged compression of the radial nerve
    • Arm over rail, ‘bridegroom palsy”, nerve compressed against humerus, forearm
  • Painless, temporary
    • Wrist drop
    • Sensory changes (Radial nerve distribution)
    • DTR’s depend on compression location
  • Splint with wrist in extension
    • Resolves weeks to months
  • Consider occult Fx
  • Referral to PMD, neurologist
44
Q

Bell’s palsy

A
  • CN VII mononeuropathy
  • Sudden onset, isolated, unilateral facial nerve weakness
  • Forehead is involved in Bell’s
    • CN VII LMN innervation of forehead, lids is from UMN’s in both hemispheres – Bell’s blocks both
  • Forehead is spared in CVA
    • CVA/tumor: UMN lesion in only one hemisphere. Other hemisphere still innervates forehead
  • Steroid taper is Tx (no antivirals)
  • Look for vessicles, HIV test
45
Q

Diplopia - isolated CN palsy

A
  • Commonly palsy of CN III, IV, VI
  • Idiopathic, traumatic; central: tumor, etc vs. peripheral: vascular (DM, vascullitis), cavernous sinus thrombosis
  • Exam is key
    • Monocular or binocular? Evoke the diplopia
    • Do the eyes line up on EOM’s/cover test?
    • Ptosis? Pupils?
  • CN III – occulomotor – DM, temporal arteritis
    • Ptosis, “down and out” gaze, non-reactive, dilated pupil
  • CN IV – trochlear – rare, idopathic, kids
    • “head-tilt” to opposite shoulder to avoid diplopia, eye “down and away”
  • CN VI – abducens – DM, increased ICP
    • Lose lateral gaze, horizontal diplopia, cover affected eye – diplopia resolves
  • Consider: Cavernous Sinus Thrombosis, Lupus, Lyme’s, Botulism, Wernicke’s, Syphilis, Thyroid, Vit B deficiency
  • Labs, CT head/face