Headaches Flashcards

1
Q

Migraine Diagnostic criteria

A
  • > 5 attacks
  • 4-72 hrs duration
  • > 2: pulsatility, moderate/severe intensity, aggravated by physical activity, unilateral
  • > 1 : n/v, photophobia & photophonia, not attributed to another disorder
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2
Q

FDA approved therapies for migraines

A
  • Propranolol
  • Timolol
  • Divalproex sodium
  • Topiramate
  • Trial 2-3 months, maxn6 months
  • Selection of agent based on SE profile and comorbid conditions
  • Often can use lower doses than other indications
  • Start low and go slow
  • Continue 6-12 months after frequency of headache reduces
  • May be able to taper to lower dose or discontinue altogether
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3
Q

First line for mild-mod migraines

A
  • Simple analgesics (APAP & APAP/caffeine/ASA)
  • NSAIDS (Aspirin, diclofenac, ibuprofen, ketorolac, naproxen, tolfenamic acid, and combination therapy)
  • Metoclopramide = speed absorption of analgesic and alleviate N/V
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4
Q

Pharmacological tx: migraines

A
  • Acetaminophen 1000 mg every 4 hours as needed; max dose 3-4 gm/24 hours
  • Excedrin Migraine (ASA/APAP/caffeine) 2 tabs every 6 hours as needed
  • ASA 500-1000 mg every 4 hours as needed (max 4 gm/day)
  • Ibuprofen 200-800 mg every 4 hours as needed (max 2.4 gm/day)
  • Naproxen sodium 550-825 mg at onset, may repeat 220 mg 3-4 hours later
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5
Q

opiates for migraines

A

-Use is controversial
-CNS sensitization is likely
Increased risk for overuse headache
-Maybe reasonable with moderate to severe infrequent headaches

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6
Q

Ergot alkaloids for migraines

A
  • Useful for moderate to severe attacks
  • Nonselective 5-HT receptor agonists
  • Constrict intracranial blood vessels and inhibit development of neurogenic inflammation in trigeminovascular system
  • Agonist at dopamine receptors
  • Contraindications: renal or hepatic failure, coronary dz, cerebral dz, PVD, uncontrolled HTN, sepsis, pregnant or nursing
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7
Q

Ergotamine

A
  • Oral, sublingual, rectal
  • Caffeine may be given to enhance absorption and analgesic effects of oral and rectal routes
  • Use is limited due to poor efficacy and side effects (nausea), associated with rebound headache
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8
Q

Dihydroergotamine

A
  • Intranasal, IV, IM, SQ routes
  • Relatively safe, not associated with rebound headache
  • Side effects: Common: N/V, abdominal pain, weakness, paresthesias, muscle pain, diarrhea, chest tightness
  • Rare: Severe peripheral ischemia (ergotism), vasoconstrictor effects, gangrene, MI, hepatic necrosis, bowel & brain ischemia
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9
Q

Triptans: First line for mild-severe HAs

A
  • Selective agonists of 5-HT1B and 5-HT1D receptors
  • Normalization of dilated intracranial arteries through enhanced vasoconstriction
  • Inhibit vasoactive peptide release from perivascular trigeminal neurons
  • Inhibit transmission through second order neurons ascending to the thalamus
  • Sumatriptan provides relief in 70% of patient at 2 hours; SQ has most rapid onset
  • Do not use triptan within 24 hours of ergotamine derivative
  • Zolmitriptan
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10
Q

Triptan s/e

A

-generally mild – moderate, short duration
-Paresthesia’s, Fatigue, Dizziness, Flushing
Warm sensations, Somnolence
-Contraindicated: history ischemic heart dz, uncontrolled HTN, cerebrovascular dz, pregnancy, hemiplegic or basilar migraines
-Postmenopausal women and men over 40 years of age – cardiovascular assessment prior to use; first dose with supervision

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11
Q

Triptan drug interactions

A
  • Avoid sumatriptan, rizatriptan, and zolmitriptan within 2 weeks of MAOIs
  • Eletriptan should not be given with CYP3A4 inhibitors: macrolide abx, antifungals, and some antiviral therapies
  • SSRI or SNRI + triptan may increase risk for serotonin syndrome
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12
Q

Prophylactic therapies: BB

A
  • Reduce frequency 50%, in greater than 50% of patients
  • May raise migraine threshold by modulating adrenergic or serotonergic neurotransmitters in cortical or subcortical pathways
  • May be useful if concomitant HTN
  • Caution if concomitant CHF, PVD, Atrioventricular conduction disturbances, asthma, depression, diabetes
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13
Q

Prophylactic therapies: Antidepressants

A
  • Amitriptyline and venlafaxine demonstrated effectiveness
  • Other agents are controversial; anecdotal evidence
  • Watch for serotonin syndrome if using venlafaxine with triptans
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14
Q

Prophylactic therapies: Anticonvulsants

A
  • Enhancement of GABA-mediated inhibition, modulation of excitatory NT glutamate
  • Inhibition of Na and Ca channel activity
  • Useful with comorbid seizures, anxiety, bipolar
  • Sodium valproate or divalproex sodium
  • Topiramate is most studied – benefit as soon as 2 weeks possible
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15
Q

Aimovig (erenumab-aooe)

A

-Monoclonal antibody, inhibits Calcitonin Gene-Related Peptide
-Prevention of episodic and chronic migraines (with and without aura)
-70-140 mg SQ monthly, upper arm
-Side Effects: constipation, hypertension
Can be significant
-Cost and insurance coverage can be a barrier

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16
Q

Cluster HA

A
  • Most severe of primary headache disorder
  • Excruciating, unilateral head pain
  • Lasting series of weeks – months
  • Remission months – years
  • Relatively uncommon: lifetime prevalence 0.12%
  • Treatment: oxygen, triptans, ergotamine derivatives
  • Prophylaxis: verapamil, lithium, corticosteroids, others