Headache Disorders Flashcards

1
Q

What is our acronym for work up of secondary HA?

A
  • S - systemic symptoms, secondary risk factors
  • N - neurologic ssx, abnl signs
  • O - onset
  • O - older age onset (new and progressive, giant cell arteritis or CA)
  • P - pattern change
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2
Q

HA + wide based gait + dementia + incontinence

A

normal pressure hydrocephalus

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3
Q

sudden severe HA + nuchal rigidity

A

subarachnoid hemorrhage

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4
Q

sudden HA + localized findings + HTN

A

Intracerebral hemorrhage

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5
Q

HA + pt over 50 + tender temporal arteries

A

temporal arteritis

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6
Q

Pt 50 yo + presents with jaw claudication or occipital pain. Has a thickened non-pulsatile temporal artery.

Dx? How?

Tx?

If not treated, what could be sequelae?

What other disease is this often seen with?

A
  • Giant Cell Arteritis/Temporal Arteritis
    • granulomatous (giant cell) inflammation on biopsy
  • high dose corticosteroids - prednisone
  • irreversible blindness
  • Polymyalgia rheumatica
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7
Q

What is at the top of my ddx for a ‘thunderclap’ HA? When is the best time to find this on an LP and how do you know it is there?

A

subarachnoid hemorrhage

within 6 hours of onset - get an LP and the blood is not diluting over 4 tube draws of CSF

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8
Q

Pt is having recurrent thunderclap HA over 1-2 weeks. No aneurysmal SAH (but cortical SAH can be seen?), near normal CSF.

Dx?

What is happening?

A

Reversible Cerebral Vasoconstrictive Syndrome (RCVS)

multivessel, multifocal segmental vasoconstriction of cerebral blood vessels that reverses within 12 weeks of onset

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9
Q

Who normally gets RCVS? What are the HA triggered by and what are Risk Factors?

A
  • females in 40s and 50s
  • triggered by urinating, bathing, valsalva, sex
  • RF: postpartum, THC, antidepressants, stimulants including cold meds and migraines
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10
Q

How does RCVS compare to Primary CNS Angiitis?

A
  • RCVS
    • CSF normal
    • tx with CCBs
  • PACNS
    • CSF abnormal
    • tx with steroids/immunosuppressants
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11
Q

If my pt is sufferring from intracranial hypotension, what would my CSF opening pressure be on LP?

When are their symptoms better or worse?

How do I tx this?

A
  • opening pressure is <6 cm H2O
  • pain is better when laying down and worse when standing d/t CSF shifts
  • caffeine, rest, blood patch to stop CSF leak
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12
Q

What is the diagnostic criteria for Pseudotumor Cerebri?

A
  • any HA filling criterion C
  • idiopathic intracranial HTN (IIH) has been diagnosed with CSF pressure >250 mm H2O
  • evidence of causation by at least two of the following
    • HA developed in temporal relation to IIH or led to its discovery
    • HA is relieved by reducing intracranial HTN
    • HA is aggravated in temporal relation to increase in intracranial pressure
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13
Q

What neuroimaging would be consistent with Pseudotumor Cerebri/ IIH?

A
  • empty sella
  • orbital flattening
  • tortuous optic nerves
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14
Q

What happens during the prodrome phase of migraine? What causes this?

A
  • pt has fatigue, mood changes, food cravings, yawning, photophobia, muscle tenderness
  • HT dysfunction with increased parasympathetic tone activating meningeal nociceptors
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15
Q

When does the aura phase of a migraine occur and what happens?

A
  • 30-60 minutes prior to migraine
  • consists of focal neuro ssx that persist up to one hour
    • visual, sensory, language, ssx localizing brainstem
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16
Q

What is idiopathic recurrent moderate to severe midline abdominal pain with nausea and vomiting, lasting 2-72 hours with interval complete resolution called?

HA does not occur during these episodes

A

abdominal migraine

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17
Q

What do we call an episodic head tilt in an infant or young child a/w features such as pallor, irritability, malaise, vomiting, or ataxia?

A

benign paroxysmal torticollis

18
Q

Migraine is a disorder of what… People with migraine lack the ability to …

A

brain/brainstem hyperexcitability

habituate electrically to repetitive stimuli

19
Q

How is an aura prior of a migraine best described?

A

spreading cortical depression (SCD)

result of accumulation of extracellular K+ due to repeated depolarization and repolarization of hyperexcitable neurons

20
Q

If aura occurs for the first time after the age of 40, is fast in onset, brief, purely negative in nature, a/w weakness or not followed by a migraine HA…

A

think TIA and refer to neurology

21
Q

What is contraindicated in women with aura migraines?

A

synthetic estrogens

22
Q

Migraine with visual aura is a/w

A

incidental a fib, stroke/TIA

23
Q

What is the thought behind Trigeminovascular Activation?

A
  • CGRP and other vasoactive neuropeptides activate the trigeminal ganglion
  • afferents from here converge at the Trigeminal cervical complex (TCC) (extracranial structures also converge here)
  • TCC activates the Superior Salivatory Nuc. and other structures projecting to the cortices
24
Q

What features will a migraine without aura have?

A
  • unilateral
  • pulsating
  • at least one of
    • N/V
    • photophobia or phonophobia
25
What are features of tension type HA?
* bilateral * pressing or tightening (nonpulsating) * not aggravated by routine physical activity * BOTH * NO Nausea or Vomiting * NO more than 1 of photophobia or phonophobia
26
What rx should I avoid in pts with a typical aura but without HA?
avoid triptans or vasoconstrictors
27
Preventative rx tx should be for those pts who ...
experience more than 1-2 HA/week or one severe prolonged episode monthly
28
My pt has a migraine HA for longer than 72 hours. Dx? Tx?
Status Migrainous * IV fluids * valproic acid IV * Magnesium sulfate IV * Diphenhydramine IV * Metoclopromide IV * Solumedrol IV * DHE IV (Raskin Protocol)
29
What is the Rasking Protocol?
* Metoclopramide or prochlorperazine 10 mg IV over 60 seconds * wait 5 min * DHE 0.5 mg IV over 60 s * wait 3-5 min * may repeat 0.5 mg IV if no relief follow with dexamethasone 4-12 mg IV
30
Who is DHE contraindicated in?
pts at risk for MI
31
What are examples of migraines with atypical auras? What is contraindicated in these pts?
* hemiplegic Migraine - CL motor paralysis * migraine with brainstem aura * TIAs must be excluded
32
repeated attacks of monocular visual disturbance, including scintillations, scotoma or blindness, a/w migraine HA dx? What else must be ruled out?
retinal migraine amaurosis fugax
33
What are four types of trigeminal autonomic cephalgias?
* cluster * paroxysmal hemicrania * hemicrania continua * SUNA/SUNCT
34
What is usually a trigger of a cluster HA and what is the primary symptom?
etoh orbital/temporal stabbing, boring pain; rapid, severe onset
35
What is the acute tx for cluster HA? What rx could prevent cluster HA?
sumatriptan SC with O2 verapamil
36
How is Paroxysmal Hemicrania different from a cluster HA
* more in females * shorter attack, but higher daily frequency * tends to be chronic (lasting about a year) * always unilateral * completely responsive to indomethacin
37
What is unique to Hemicrania Continua?
* unremitting pain lasting 30 minutes to 3 days * unilateral HA * pain not as bad as cluster or paroxysmal * complete response to indomethacin
38
What is unique to SUNA/SUNCT? How do I tx it?
* Short-lasting Unilateral Neuralgiform * attacks only 1-600 seconds, occur up to 100x /day * tx - Iamotrigine
39
What should I be thinking clinically with trigeminal autonomic cephalgias?
* r/o other with MRI and pituitary testing * cluster responds to short acting verapamil * avoid PO in acute cluster * if clusterlike without trigger in a female, think paroxysmal hemicrania
40
What are three causes for medication overuse HA?
* butalbital \>5 d/mo * opioids \>8 d/mo * triptans/NSAIDs/analgesics \>10 d/mo
41
How can you differentiate Trigeminal neuralgia from cluster HA?
Trigeminal neuralgia will likely include V2/3 while cluster is mostly V1
42
Eagle's syndrome is a calcified stylohyoid ligament that could cause ...
glossopharyngeal neuralgia