4a. Approach to Neuro Cases I Flashcards
What are the basic types of primary HA?
- tension-type HA
- migraine HA
- cluster HA
- other, including cold-stimulus HA
What should headache-specific history include?
Characteristics:
- gradual in onset, crescendo pattern
- pulsating
- moderate or severe intensity
- aggravated by routine physical activity
Appearance: pt rests in dark, quiet room
Duration: 4-72 hrs
Assoc. sx: n/v, photophobia/phonophobia, aura
Location: unilater in 60-70% adults, bifrontal/global in 30%; bilateral in children
migraines
Characteristics: pressure or tightness which waxes and wanes
Pt appearance: remain active or may need to rest
Duration: 30 min to 7 days
No assoc sx
Location: bilateral
tension-type HA
Characteristics:
- pain begins quickly, reaches crescendo w/in minutes
- pain is deep, continuous, excruciating, and explosive in quality
Pt appearance: active
Duration: 15 min to 3 hours
Assoc sx: ipsilateral lacrimation and redness of the eye; stuffy nose; rhinorrhea; pallor; sweating; Horner syndrome; restlessness or agitation; focal neurologic symptoms rare; senstivity to alcohol
Location: unilateral always (around eye or temple)
cluster HA
What to obtain for headache-specific physical exam?
- Obtain BP and pulse
- Listen for bruit
- Check eyes and head for signs of arteriovenous malformation
- Palpate head, neck, and shoulder regions
- Check temporal and neck arteries
- Examine the spine and neck muscles
- Mental status testing
- CN examination
- Fundoscopy and otoscopy
- Symmetry on motor, reflex, cerebellar, and sensory test
- Gait: toe walk, heel walk, tandem walk
- Station: get-up from seated position without support, Romberg test
What does SNOOP stand for?
- S: systemic symptoms, illness, or condxn
- N: neuro symptoms or abnormal signs
- O: onset is new
- O: other associated conditions
- P: previous HA hx w/ HA progression or change
What indicates need for emergency evaluation?
- sudden “thunderclap” HA
- acute or subacute neck pain or HA w/ Horner syndrome and/or neuro deficit
- HA w/ suspected meningitis or encephalitis
- HA w/ global or focal neurologic deficit or papilledema
- HA w/ orbital or periorbital sx
- HA and possible CO exposure
transient triggered episodes of vertigo caused by dislodged canaliths in the semicircular canals
BPPV
spontaneous episodes of vertigo caused by inflammation of the vestibular nerve or labyrinthine organs, usually from a viral infection
vestbular neuritis
spontaneous episodes of vertigo caused by abnormal bone growth in the middle ear and associated w/ conductive hearing loss
osteosclerosis
spontaneous episodes of vertigo associate w/ migraine headaches
vestibular migraine
continuous spontaneous episodes of vertigo caused by arterial occlusion or insufficiency, especially affecting the vertebrobasilar system
cerebrovascular disease
continuous spontaneous episodes of dizziness caused by vestibular schwanomma, infratentorial ependymoma, brainstem glioma, medulloblastoma, or neurogibromatosis
cerebellopontine angle and posterior fossa meningiomas
initially episodic, then often continuous episodes of dizziness w/o another cause and associated with psychiatric condition (e.g. anxiety, depression, bipolar disorder)
psychiatric