Migraine Headache
Migraine Headache
Jennifer J. Mitchell
Tim Sprockel
Basics
Description
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Common cause of benign episodic headache:
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Sensory sensitivity
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Frequently altering activities of daily living
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Characterized by at least 2 of the following (1):
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Chronic
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Unilateral
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Throbbing or pulsating
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Worsened by movement or activity
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Moderate-to-severe pain intensity
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Including at least 1 of the following:
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Nausea
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Vomiting
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Photophobia
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Phonophobia
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Subtypes:
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Migraine without aura:
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Common migraine
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Most frequent variant
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No sensory, motor, or visual disturbances
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Migraine with aura:
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Classic migraine
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Characteristically with sensory, motor, and/or visual disturbances at onset
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Acephalgic migraine (less common subtype):
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Typical aura occurs, but no headache
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Basilar migraine (less common subtype):
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Headache with aura
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Disturbances in brainstem function; diplopia, dysarthria, paresthesias, tinnitus, vertigo
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No motor weakness
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Familial hemiplegic migraine (less common subtype):
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Headache with aura
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Hemiparesis or hemiplegia
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Patient with a 1st- or 2nd-degree relative with similar symptoms
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Medication overuse migraine (less common subtype):
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Excessive use or consumption of analgesic medications
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Menstrual migraine (less common subtype):
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Headaches present 2 days before through 1st 3 days of menses
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Retinal migraine (less common subtype):
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Headache with recurrent monocular visual disturbances
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Normal ophthalmologic exam in between migraine attacks
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Sporadic hemiplegic migraine (less common subtype):
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Headache with aura
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Hemiparesis or hemiplegia
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Epidemiology
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Females > Males (2)
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Before puberty, Males > Females
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Throughout puberty and adolescence, prevalence and incidence increase rapidly in females.
Risk Factors
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Family history of migraine headaches
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Female gender, in particular after onset of menses
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Certain foods (red wine, cheese, deli meats, MSG)
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Sleep cycle disturbances (lack of sleep)
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Emotional or psychological disturbances
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Oral contraceptive pills; estrogen therapy
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Missing or skipping meals
Genetics
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Migraine with aura has a hereditary component,
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Chromosome 19 associated with familial hemiplegic migraine
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MELAS syndrome (mitochondrial encephalopathy, lactic acidosis, and strokelike episodes):
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Extremely rare progressive neurological disorder leading to dementia:
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May present with migraine-like headaches
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Linked to a mutation in a mitochondrial gene
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General Prevention
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Identify and avoid triggers:
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Foods—cheeses, meats, MSG
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Red wine:
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Postulated causative agents tyramines and tannins (plant polyphenols)
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Inadequate sleep patterns
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Irregular eating times/skipping meals
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Consider discontinuation of:
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Oral contraceptive pills
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Hormone replacement therapy
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Establish and implement ways to manage emotional and/or psychological stressors.
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Evaluate association with menstrual cycle.
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Use medications for prophylactic treatment.
Etiology
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2 potential causes:
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Vascular theory:
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Vasodilation and vasoconstriction of cerebral blood vessels
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Neurovascular theory:
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Neuronal excitation in the gray matter with simultaneous vasodilation and vasoconstriction
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Excitation of sensory neurons in the occipital region, brainstem, hypothalamus, and thalamus
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Ongoing research examining the role of serotonin and calcitonin gene-related peptide as possible etiologies
Commonly Associated Conditions
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Anxiety (2)
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Asthma/allergy
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Atrial septal aneurysm
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Bipolar disorder
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Cerebrovascular accident: Ischemic, subclinical, or white matter abnormality
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Depression
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Epilepsy
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Fluctuations in BP
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Irritable bowel syndrome
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Mitral valve prolapse
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Panic disorder
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Patent foramen ovale
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Reynaud's phenomenon
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Sleep apnea/snoring
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Systemic lupus erythematosus
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Tourette's syndrome
Diagnosis
History
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Migraine without aura:
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Episodic headaches lasting 4–72 hr
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Includes at least 2 of the following:
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Unilateral
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Throbbing
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Worsened by movement
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Moderate or severe
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And includes at least 1 of the following:
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Nausea
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Vomiting
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Photophobia
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Phonophobia
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Migraine with aura:
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Headache consistent with migraine without aura AND
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Includes at least 1 temporary disturbance: Visual, sensory, speech
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Includes at least 2 of the following:
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Each disturbance lasts at least 5 min, not >60 min, and is fully reversible.
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1 disturbance develops slowly over time, and other disturbances appear in succession over time.
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Homonymous visual symptoms and/or unilateral sensory symptoms
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Aura is characterized, in order of incidence, by visual, sensory, language, motor disturbances
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Other associated symptoms include:
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Diarrhea
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Lightheadedness
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Muscular tenderness
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Vertigo
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Syncope
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Paresthesias
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P.389
Physical Exam
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General physical examination
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Detailed neurological examination
Diagnostic Tests & Interpretation
Lab
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Typically not needed, especially in those with established migraines with typical symptoms
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Labs to consider if concern for other diagnoses:
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Pseudotumor cerebri:
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Lumbar puncture (LP) with opening pressure
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No LP until after cerebral imaging to rule out intracranial mass, which could cause cerebral herniation
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Meningitis:
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CT or MRI 1st as above, then LP
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Temporal arteritis:
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Erythrocyte sedimentation rate
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C-reactive protein
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Hypoxia from carbon monoxide poisoning:
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Carbon monoxide level
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Imaging
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CT scan or MRI to rule out intracranial hemorrhage or tumor
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MRI is preferred over CT (3)[B].
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Red flags to prompt imaging:
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1st or worst headache
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Subacute headaches with increased frequency and/or severity
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Progressively worsening headache
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Headache always on the same side
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Not responding to treatment
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New-onset headache in immunocompromised individuals or with history of malignancy
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New-onset headache after age 50
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Seizures with headaches
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Headache with:
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Signs of meningitis:
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Fever
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Stiff neck
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Altered mental status
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Sick contacts
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Focal neurological deficits
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Papilledema
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Cognitive impairment
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Personality changes
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Differential Diagnosis
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Acid/base disturbance
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Acute ischemic cerebrovascular accident (CVA)
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Cerebral aneurysm/vascular malformation
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Cluster headache
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Dental abscess
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Exertional headache
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Head trauma
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Hemorrhagic CVA
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Hypoglycemia
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Hypoxia
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Intracranial infection
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Intracranial malignancy
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Medication side effects (eg, nitroglycerin, sildenafil)
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Nonintracranial infections
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Poor visual acuity
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Pseudotumor cerebri
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Psychiatric disorder
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Secondary gain
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Sinus infection or congestion
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Substance withdrawal or exposure
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Temporal arteritis
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Temporomandibular joint disorders
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Transient ischemic attack
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Tension headache
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Uncontrolled HTN
Treatment
Preventive treatment (4)[A]:
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Determining initiation:
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Significantly impacting patient's daily life
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Failure or contraindication to abortive medications
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Overuse of abortive medications
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Patient preference
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Start at low dose and increase slowly until desired effect
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Allow adequate time for medication to work:
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6–8 wks for some
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Examples of preventive medications with recommended doses:
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Anticonvulsants:
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Topiramate 15–25 mg PO at bedtime
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Antidepressants:
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Amitriptyline 10 mg PO at bedtime
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Venalfaxine 37.5 mg PO in morning
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Beta-blockers:
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Atenolol 50 mg PO daily
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Propranolol 40 mg PO b.i.d.
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Calcium channel blockers:
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Verapamil 80 mg PO b.i.d. or t.i.d.
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Flunarizine 5 mg PO at bedtime
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Selective serotonin reuptake inhibitors not effective (5)
Medication
Medication contraindications/cautions:
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Serotonin agonists contraindicated in patients with:
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Coronary artery disease
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Peripheral vascular disease
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Uncontrolled HTN
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Patients with a complicated migraine course
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Do not use serotonin agonists in patients who:
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Have taken ergotamine derivatives within 24 hr
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Have taken other serotonin agonists within 24 hr
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Utilize monamine oxidase inhibitors.
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Do not use NSAIDs or ASA in patients with known gastric ulcers.
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Do not use NSAIDs in patients with liver or renal compromise.
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Do not use narcotics if suspected secondary gain.
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Avoid medications in patients with suspected or documented allergy to that substance.
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Consider that frequent use of a medication may lead to overuse headache or rebound headache.
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Pregnancy:
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Serotonin agonists are not FDA-approved for use during pregnancy, Category C
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Ergot derivatives are contraindicated, Category X
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Narcotic medications are Category B and C
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Serotonin agonists pass through breast milk.
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Pediatrics:
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Serotonin agonists are not recommended for use in patients under 18 yrs of age.
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First Line
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OTC medications:
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NSAIDs
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Aspirin (ASA)
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Acetaminophen (APAP)
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Combination medications that include caffeine, ASA, and APAP
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Prescription medications:
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Ketorolac 30–60 mg IM/IV
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Midrin 2 caps PO at onset of headache
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Serotonin agonists (triptans) chosen based on:
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Onset of action
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Mode of delivery
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Cost to patient
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Examples:
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Sumatriptan 25 mg PO or 5 mg nasal spray or 4 mg SC
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Zolmitriptan 2.5 mg PO or 5 mg nasal spray
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Ergotamine use has declined since the introduction of serotonin agonists
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Potential problems with medication use:
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Medication overuse
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Withdrawal/rebound headaches (6)[A]
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P.390
Second Line
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Use of narcotic in refractory migraine headaches:
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Morphine 2–4 mg IV
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Meperidine 50–100 mg IM/IV
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Caution advised with use of narcotics (6)[A]
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Adjunct therapy (antiemetics) (6)[A]:
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Promethazine 25–50 mg PR/IM/IV
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Metoclopramide 10 mg IV/IM
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Prochlorperazine 5–10 mg PO
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Ondansetron 4 mg IV/IM
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Some antiemetics themselves treat migraine pain.
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Otherwise, used as adjunctive treatment to allow patient to tolerate oral abortive medications
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Additional Treatment
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Remove from known environmental stimuli or stressors.
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Encourage sleep.
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Avoid known triggers.
Complementary and Alternative Medicine
Preventive therapies (4)[A]:
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Evidence of efficacy in reducing frequency:
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Riboflavin 400 mg (vitamin B2) daily
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Butterbur extract 75 mg b.i.d.
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Acupuncture effective as prophylaxis alone or in conjunction with analgesics, antidepressants, beta-blockers or anticonvulsants (7)
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No evidence of efficacy:
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Botulinum toxin type A (Botox)
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Herbal supplements such as feverfew
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In-Patient Considerations
Initial Stabilization
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ABCs
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IV fluids
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Medications:
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Analgesics
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Antiemetics
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Removal from environmental stimuli
Admission Criteria
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Unstable vital signs
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Neurologic exam with focal deficits that do not resolve
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Unclear diagnosis or to exclude life-threatening illness
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Intractable migraine despite appropriate therapy
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Intractable nausea and vomiting
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Electrolyte imbalance
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Potential self-harm or harm to others due to symptoms or medications
Discharge Criteria
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Resolution or improvement of symptoms
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Certain of diagnosis
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Life-threatening pathology ruled out
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Able to tolerate oral liquids/food and medications
Ongoing Care
Return to play criteria:
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No neurological or cognitive deficits
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Resolution of symptoms:
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Movement or activity can worsen migraine symptoms
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Play with ongoing symptoms could create difficulty in evaluation if the athlete sustains a concussion.
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Migraine headache after concussion:
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May not return to play until all symptoms resolved (increased risk for 2nd impact syndrome if still symptomatic)
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High school and college athletes with migraine after concussion may have increased neurocognitive impairment.
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Consider potential medication side effects and how these may affect performance.
Follow-Up Recommendations
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Patient education on:
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Etiology
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Natural course of illness
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Cautions concerning progression of illness
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Use of medications/avoiding overuse
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Headache journal to identify potential triggers
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Discuss lifestyle modifications:
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Avoidance of triggers
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Abortive treatment
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Follow-up visits based on patient's:
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Understanding of condition
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Ability to self-assess and self-treat
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Frequency of headaches
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P.391
Prognosis
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Most migraines last from 4–72 hr:
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If persisting, must consider other pathology
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Most patients dramatically reduce the number of migraine episodes by avoiding triggers.
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Remission increases with age.
Complications
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Status migrainous:
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Migraine lasting >72 hr
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Severely alters patient's activities
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Migrainous stroke:
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Presence of 1 or more aura symptoms
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Associated lesion demonstrated on brain imaging
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Chronic migraine:
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Headache without aura
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Present for at least 15 days per month
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Over a time span >3 mos (8)
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Medication overuse migraines
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Medication side effects
References
1. Headache Classification Subcommittee of the International Headache Society. The international classification of headache disorders: 2nd edition. Cephalgia. 2004;24(Suppl 1):1–160.
2. Bigal ME, Lipton RB. The epidemiology, burden, and comorbidities of migraine. Neurol Clin. 2009;27:321–334.
3. Evans RW. Diagnostic testing for migraine and other primary headaches. Neurol Clin. 2009;27:393–415.
4. Silberstein SD. Preventive migraine treatment. Neurol Clin. 2009;27:429–443.
5. Moja L, Cusi C, Sterzi R, et al. Selective serotonin re-uptake inhibitors (SSRIs) for preventing migraine and tension-type headaches. Cochrane Database of Systematic Reviews 2005;3:CD002919. DOI: 10.1002/14651858.CD002919.pub2.
6. Tepper SJ, Spears RC. Acute treatment of migraine. Neurol Clin. 2009;27:417–427.
7. Linde K, Allais G, Brinkhaus B, et al. Acupuncture for migraine prophylaxis. Cochrane Database of Systematic Reviews. 2008;2:CD001218. DOI: 10.1002/14651858.CD001218.pub2.
8. Vargas BB, Dodick DW. The face of chronic migraine: epidemiology, demographics, and treatment strategies. Neurol Clin. 2009;27:467–479.
Additional Reading
Goadsby PJ. Pathophysiology of migraine. Neurol Clin. 2009;27:335–360.
Lay CL, Broner SW. Migraine in women. Neurol Clin. 2009;27:503–511.
Codes
ICD9
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346.00 Migraine with aura, without mention of intractable migraine without mention of status migrainosus
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346.10 Migraine without aura, without mention of intractable migraine without mention of status migrainosus
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346.20 Variants of migraine, not elsewhere classified, without mention of intractable migraine without mention of status migrainosus
Clinical Pearls
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Differentiate benign-natured migraine headache and more serious intracranial pathology.
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Key to prevention is avoiding known triggers
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Allow enough time for prophylactic therapies to work; up to 6–8 wks
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If imaging is needed, MRI is preferable to CT.
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Serotonin agonists are not approved in:
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Coronary artery disease
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Peripheral vascular disease
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Uncontrolled HTN
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Pregnancy
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Patients under 18 yrs of age
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Excessive medication use can promote rebound headaches.