Migraine Disease

BASICS

DESCRIPTION
Paroxysmal headache lasting 4-72 hours. Episodes vary in frequency from more than once a week to less than one per year with symptoms abating completely between attacks. Prodromes consisting of non-specific symptoms occur frequently hours to days before headache. Most frequent sub-types are:
  • Without aura - (common migraine) defining over 80% of attacks
  • With aura - (classic migraine) characterized by focal disruption of neurological function begins and ends prior to headache onset
  • Variants of migraine include:
    • Transformed migraine - chronic headache pattern evolving from episodic migraine. Migraine-like attacks are superimposed on a daily or near-daily headache pattern, e.g., tension headache.
    • Basilar migraine - occipital headache, with aura symptoms of dysarthria, vertigo, tinnitus, ataxia, and bilateral paresis or bilateral paresthesias
    • Hemiplegic migraine - aura consisting of hemiplegia and/or hemiparesis
    • Ophthalmoplegic - palsy of the ipsilateral third cranial nerve during the headache phase
    • Retinal - symptoms of retinal vascular involvement during headache
    • Childhood periodic syndromes - (migraine equivalents) recurrent often cyclic episodes of symptoms
    • Status migrainous - persistent migraine which does not resolve spontaneously
    • Migrainous stroke - persistent or permanent neurologic deficits persisting beyond migraine attack usually with neuro-imaging changes
  • System(s) affected: Nervous, Musculoskeletal, Cardiovascular, Gastrointestinal
  • Genetics: > 80% of patients have positive family history. Identification of a chromosomal abnormality has been confirmed in familial hemiplegic migraine.
  • Incidence/Prevalence in USA:
    • Adults: 17.6% of females, 5.6% of males
    • Childhood unknown; may be significant
  • Predominant age: Childhood; increase in early adolescence, through 30s and 40s; decreases with age, attacks may persist into mature adulthood
  • Predominant sex:
    • Male ≥ Female in childhood
    • Female > Male (3:1) after menarche to mid-adult life
    • Female > Male (2:1) in postmenopausal female populations
SIGNS AND SYMPTOMS

Five phases of a migraine; symptoms vary from patient to patient or from attack to attack within the same individual

  • Prodrome (experienced by 50-80% of patients): A variety of "warnings" that precede migraine, frequently characterized by mood disruptions (e.g., euphoria, irritability, depression), fatigue, muscle tension, food craving, bloating, yawning, or subtle disruption of sensory processing. These symptoms are often not recognized by patients as associated with migraine.
  • Aura: Visual disruptions are most common, including scotoma, hemianopsia, fortification spectra, geometric visual patterns, and occasionally hallucinations. Somatosensory disruption in face or upper extremities is also common. Headache typically begins within 1 hour of aura resolution.
  • Headache: Unilateral (30-40% bilateral), throbbing (40% non-throbbing) pain of 4-72 hours; intensified by movement; associated with systemic manifestations, e.g., Nausea (87%), Vomiting (56%), Diarrhea (16%), Photophobia (82%), Phonophobia (78%), Muscle tenderness (65%), Lightheadedness (72%), Vertigo (33%).
  • Headache termination: Untreated, usually occurs with sleep; occasionally, vomiting or strong emotional experiences abort headache
  • Postdrome: Headache pain resolved but another manifestation lingers on, such as food intolerance, impaired concentration, fatigue, muscle soreness
CAUSES
  • Exact etiology unknown; appears to be a genetically linked, neuronal disease with vascular disruption as an epiphenomenon of underlying neurochemical disruption
  • Serotonin and norepinephrine metabolism abnormalities may play a role
  • Neurogenic inflammation and regional disruption of cerebral and/or extracranial blood flow may explain some clinical features
RISK FACTORS
  • Specific foods, alcohol, missing meals, menstrual cycle, excessive sleep, fatigue, emotional stress, let down (relief of stress)
  • Medications (estrogen replacement, BCP's, vasodilators)
  • Family history of migraine
  • Female gender
  • Young age
  • History of childhood cyclic vomiting, cyclic abdominal pain, motion sickness

DIAGNOSIS

LABORATORY

Only useful to rule out secondary causes of headache

Drugs that may alter lab results: N/A
Disorders that may alter lab results: N/A

PATHOLOGICAL FINDINGS
  • Changes in blood serotonin levels and serotonin metabolites in the urine are reported
  • Changes in regional blood flow
  • Changes in sophisticated imaging studies
SPECIAL TESTS
Only to rule out underlying pathology
IMAGING
Occasionally required; indicated for new onset of headache for patient over age 50, and in patients with a change in established headache pattern
DIAGNOSTIC PROCEDURES
Based on careful history and physical findings

TREATMENT

APPROPRIATE HEALTH CARE

Outpatient. For status migrainous or cases complicated by concurrent medical problems or significant medication-withdrawal issues, hospitalization may be required.

GENERAL MEASURES
  • Compression to ipsilateral temporal artery or tender areas of scalp or neck
  • Cold compresses to area of pain
  • Rest with pillows comfortably supporting head or neck in an area devoid of sensory stimulation, including light, sound, and odors
  • Withdrawal from stressful surroundings
  • Sleep is desirable
  • Biofeedback and early psychologic intervention in appropriate cases or when pain behaviors are first identified
  • Most patients manage attacks with self-care
SURGICAL MEASURES

N/A

ACTIVITY

In bed in a dark quiet environment

DIET

Maintain fluid intake. Avoid dietary precipitants of migraine.

PATIENT EDUCATION
  • Emphasize migraine cannot be cured, but symptoms can be managed
  • Encourage use of diary and patient education
  • Emphasize proper use of all medications
  • Encourage lifestyle modifications

FOLLOW UP

PREVENTION/AVOIDANCE
  • Avoid precipitants of attacks
  • Prescribe biofeedback and psychologic intervention early if pain behavior evident
  • Prophylactic therapy: If attacks significantly interfere with lifestyle or are not adequately controlled by appropriate acute interventions, daily prophylactic therapy may be appropriate. Regularly scheduled follow-up is mandatory.
    • Propranolol (Inderal) 80–320 mg daily
    • Atenolol (Tenormin) 50–100 mg daily
    • Nadolol (Corgard) 40–80 mg daily
    • Timolol (Blocadren) 10–20 mg daily
    • Metoprolol (Lopressor) 100–450 mg daily
    • Amitriptyline (Elavil) 10–150 mg daily
    • Nortriptyline (Pamelor) 10–150 mg daily
    • Verapamil (Calan, Isoptin) 80–120 mg daily
    • Isradipine (DynaCirc) 2.5–10 mg bid
    • Valproic acid (Depakene) or divalproex (Depakote) 250–1500 mg daily
    • Methysergide (Sansert) 5–8 mg daily (cannot be used concomitantly with 5-HT-1 agonists)
    • Cyproheptadine (Periactin) 4–16 mg daily
  • Consultation/referral
    • Obscure diagnosis, concomitant medical conditions, significant psychopathology
    • Unresponsive to usual treatment
    • Analgesic-dependent headache patterns
POSSIBLE COMPLICATIONS
  • Rare status migrainosus
  • Rare cerebral ischemic events
  • Iatrogenic effects of treatment
EXPECTED COURSE AND PROGNOSIS
  • With age – reduction in severity, frequency, and disability of attacks
  • Most attacks subside within 72 hours

MISCELLANEOUS

ASSOCIATED CONDITIONS

Depression, panic disorders, sleep disturbance, cerebral vascular disease, myocardial disease, peripheral vascular disease and seizure

AGE-RELATED FACTORS

Pediatric: Recurrent abdominal pain and cyclic vomiting may predominate; attacks may be of shorter duration. Headache description by younger children may appear atypical.
Geriatric: Rare onset of acephalic migraine (aura without subsequent headache) after the age of 40. Possible relationship to transient global amnesia. Late onset of migraine requires diagnostic evaluation.
Others: Migraine affects all races, social classes, intelligence levels

PREGNANCY

Attacks frequently diminish, esp. in 2nd/3rd trimester. No treatment drug has FDA approval in pregnancy; ergotamines are contraindicated.

OTHER NOTES

N/A

ABBREVIATIONS

N/A

Clinical Investigations

ROLE OF HOMOEOPATHY

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