Migraine: 
Definition
Migraine is a primary headache disorder characterized by recurrent episodes of head pain, typically unilateral and localized, often associated with nausea, vomiting, photophobia (sensitivity to light), and phonophobia (sensitivity to sound). Approximately 25% of migraine patients experience an aura, which consists of transient, reversible neurological symptoms preceding or accompanying the headache. Migraine is primarily a clinical diagnosis, and neuroimaging is generally not required unless atypical features or “red flags” are present.
Epidemiology
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Prevalence:
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Women: ~17%
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Men: ~6%
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Peak incidence: 30–39 years
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Relative frequency: Second most common type of headache; most common cause among patients presenting to emergency departments with headache.
Etiology
The exact cause of migraine remains incompletely understood, but it is thought to involve a combination of genetic susceptibility and environmental triggers.
Genetic Predisposition
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Individuals with migraine may have hyperexcitable brains due to altered neuronal habituation.
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Familial cases, especially hemiplegic migraine, demonstrate autosomal dominant inheritance patterns.
Common Triggers
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Dietary: chocolate, alcohol, tyramine-containing foods, dairy, citrus, nicotine
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Lifestyle: fasting, dehydration, poor sleep, stress
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Hormonal: menstruation, hormonal therapy (oral contraceptives)
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Environmental: weather changes, sensory stimuli (light, noise)
Pathophysiology
Migraine involves complex neurovascular and neuroinflammatory mechanisms:
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Activation of meningeal nociceptors
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Leads to pain perception.
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Trigeminovascular pathway activation
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Trigeminal neurons release vasoactive peptides (substance P, CGRP) → vasodilatation and neurogenic inflammation.
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Cortical spreading depression (CSD)
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Waves of cortical excitation and inhibition → activation of meningeal nociceptors, triggering aura.
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Autonomic system dysregulation
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Hypothalamic responses to stress or hormonal changes influence cranial vascular tone and parasympathetic output.
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Vasodilation
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Considered secondary, not the primary cause of pain.
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Clinical Features
Migraine attacks typically follow four stages, though not all stages occur in every patient.
1. Prodrome (24–48 hours before headache)
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Mood changes (irritability, euphoria, depression)
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Fatigue or excessive yawning
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Food cravings or anorexia
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Difficulty concentrating, reading, or writing
2. Aura (25% of cases)
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Typical aura: fully reversible, lasts ≤ 60 minutes
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Visual: scintillating scotoma, flashing lights, fortification spectra, central scotoma, color distortion
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Sensory: paresthesia, numbness
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Speech: dysphasia/aphasia
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Gradual onset, spreads over minutes
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Atypical aura: may include paresis, persistent or prolonged symptoms, cranial nerve III palsy (rare, usually with vascular lesions)
3. Headache
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Localization: usually unilateral, but may be bilateral; commonly frontal, frontotemporal, or retro-orbital
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Duration: 4–24 hours, rarely >72 hours
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Character: pulsating, throbbing, or pounding
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Exacerbating factors: physical activity, movement
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Associated symptoms: nausea, vomiting, photophobia, phonophobia
Mnemonic: “POUND” – Pulsatile, One-day duration, Unilateral, Nausea, Disabling intensity
4. Postdrome
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Fatigue, euphoria, muscle weakness, anorexia or cravings
Migraine Subtypes and Variants
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Migraine with aura – includes visual, sensory, speech, or motor symptoms
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Migraine without aura – no preceding neurological symptoms
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Hemiplegic migraine – motor weakness in aura, may be familial or sporadic
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Brainstem aura (basilar-type) – reversible brainstem symptoms (vertigo, dysarthria, diplopia), no motor deficits
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Vestibular migraine – episodic vertigo associated with migraine
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Retinal migraine – monocular visual symptoms, fully reversible
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Silent migraine – aura occurs without headache
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Chronic migraine – ≥15 headache days/month for ≥3 months; ≥8 days with migraine features
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Menstrual migraine – linked to menstrual cycle; can be pure (only during menstruation) or menstrually related
Diagnosis
Clinical
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Diagnosis is based on history and physical examination.
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Rule out “red flags” suggesting secondary headaches (e.g., infection, hemorrhage, intracranial mass).
Diagnostic Criteria (ICHD-3)
| Feature | Migraine without aura | Migraine with aura |
|---|---|---|
| Attacks | ≥5 lifetime | ≥2 lifetime |
| Duration | 4–72 hrs | N/A |
| Characteristics | ≥2: unilateral, pulsating, moderate/severe, worsened by activity | ≥1 aura symptom (visual, sensory, speech, motor, brainstem, retinal) |
| Concomitant | ≥1: nausea/vomiting, photophobia, phonophobia | ≥3 aura features: gradual spread ≥5 min, multiple aura in succession, each 5–60 min, unilateral, positive symptoms; headache within 60 min |
Investigations
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Laboratory tests: usually not indicated; pregnancy test in women of childbearing age
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Imaging: MRI preferred if red flags present or atypical features (e.g., first aura after age 40, prolonged aura, change in baseline pattern)
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Peripheral findings: usually normal; nonspecific white-matter changes may be seen
Differential Diagnosis
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Paroxysmal hemicrania
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Medication overuse headache
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TIA or stroke in atypical aura
Management
Acute Treatment
General Measures
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Reduce sensory stimuli (light/noise)
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Rest in a dark, quiet room
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Ensure adequate hydration
Mild–Moderate Headache
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NSAIDs (ibuprofen, aspirin)
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Acetaminophen
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Combination therapy with caffeine (e.g., acetaminophen-aspirin-caffeine)
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Parenteral NSAIDs if nausea/vomiting (ketorolac, diclofenac)
Moderate–Severe Headache
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First-line: Triptans (sumatriptan, zolmitriptan) orally, subcutaneously, or intranasally
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Second-line: Ergot alkaloids (dihydroergotamine)
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Adjuncts: Antiemetics (metoclopramide, prochlorperazine), IV dexamethasone to prevent recurrence
Caution: Avoid opioids as first-line therapy; monitor for serotonin syndrome if combining triptans with other serotonergic drugs.
Migraine Prophylaxis
Indications
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≥3 attacks/month or attacks with severe disability
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Poor response to acute therapy
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Specific subtypes (hemiplegic, brainstem aura)
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Contraindication to acute therapy
Non-Pharmacologic
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Lifestyle modifications: regular sleep, moderate exercise, trigger avoidance, healthy diet
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Behavioral therapy: relaxation, biofeedback, CBT
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Acupuncture or noninvasive neuromodulation (adjunctive evidence)
Pharmacologic
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Beta-blockers: propranolol, metoprolol
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Anticonvulsants: topiramate, valproate
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Antidepressants: amitriptyline, venlafaxine
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CGRP-targeted therapies: monoclonal antibodies (erenumab, fremanezumab), oral antagonists (ubrogepant, rimegepant)
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Others: candesartan, botulinum toxin for chronic migraine
Menstrual Migraine
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Short-term prophylaxis with triptans (frovatriptan preferred) for 5–7 days around menstruation
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Continuous combined hormonal contraception can be considered in women without aura
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Migraine with aura is an absolute contraindication for estrogen-containing contraceptives
Special Populations
Pregnancy
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Acute: acetaminophen first-line; sumatriptan has evidence for safety
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Avoid: NSAIDs in 3rd trimester, opioids, ergot derivatives
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Prophylaxis: calcium channel blockers, cyproheptadine; avoid beta-blockers unless specialist-approved
Children
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Shorter attack duration (2–72 hours), often bilateral headaches
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Aura uncommon; photophobia/phonophobia inferred from behavior
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Treatment: ibuprofen preferred; triptans for older children (≥6 yrs)
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Avoid aspirin (Reye syndrome risk)
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Preventive therapy: lifestyle, amitriptyline + CBT, topiramate, propranolol
Complications
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Status Migrainosus: debilitating migraine lasting ≥72 hours; may require hospitalization
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Stepwise treatment: IV fluids, antiemetics, NSAIDs, dihydroergotamine, dexamethasone, valproate, magnesium sulfate (under specialist guidance)
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Medication overuse headache
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Rare: persistent neurological deficits, vascular events in migraine with aura
Summary of Acute Management Checklist
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Evaluate for red flags → consider imaging if indicated.
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Reduce sensory stimuli and maintain hydration.
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Initiate pharmacologic therapy early:
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Mild–moderate: NSAIDs, acetaminophen
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Moderate–severe: triptans or ergot alkaloids + antiemetics
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Prevent recurrence: IV dexamethasone
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Status migrainosus: escalate therapy, consider hospitalization.
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Counsel on lifestyle modification and preventive strategies.
Disposition and Follow-Up
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Most patients can be managed outpatient.
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Hospitalize for:
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Status migrainosus refractory to initial therapy
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Inability to maintain hydration/nutrition
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Chronic migraine with medication overuse requiring supervised withdrawal
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Neurology or headache clinic referral for:
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Frequent, severe, or disabling migraines
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Preventive therapy optimization
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