Migraine
Migraine (pronouced "Mee-grain" but also, and especially in American English, "My-grain") is a neurological disease,
of which the most common symptom is an intense and disabling episodic headache. Migraine headaches are usually
characterized by severe
pain on one or both sides of the head. Absent serious head injuries, stroke, and tumors, the
recurring severity of the pain indicates a vascular headache rather than a tension headache. Migraines are often
accompanied by photophobia (hypersensitivity to light), phonophobia (hypersensitivity to sound) and nausea.
The word migraine is French in origin and comes from the Greek hemicrania, as does the Old English term megrim. Literally,
hemicrania means "only half the head".
Migraines are a frustrating chronic illness which is widespread in the population (10% diagnosed, 5% undiagnosed), with
seriousness varying from a rare annoyance to a life-threatening daily experience. Treatments are typically expensive.
Periodic or unpredictable disability can cause impoverishment due to patients' inability to work enough or to hold a job
at all.
Migraines' secondary characteristics are inconsistent. Triggers precipitating a particular episode of migraine vary
widely. The efficacy of the simplest treatment, applying warmth or coolness to the affected area of the head, varies
between persons, sometimes worsening the migraine. A particular migraine rescue drug may sometimes work and sometimes not
work in the same patient. Some migraine types don't have
pain or may manifest symptoms in parts of the body other than the
head.
Available evidence suggests that migraine
pain is one symptom of several to many disorders of the serotonergic control
system, a dual hormone-neurotransmitter with numerous types of receptors. Two disorders — classic migraine with aura
(MA, STG) and common migraine without aura (MO, STG) — have been shown to have a genetic factor. Studies on twins show
that genes have a 60 to 65% influence on the development of migraine (PMID 10496258 and PMID 10204850 ). Additional
migraine types are suspected and could be proved to be genetic. Migraine understood as several or many disorders could
explain the inconsistencies, especially if a single patient has more than one genetic type.
However, still other migraine types might be functionally acquired due to hormone organ disease or injury. Three quarters
of adult migraine patients are female, although pre-pubertal migraine affects approximately equal numbers of boys and
girls. This reveals the strong correlation to hormonal cycling and hormonal-related causes or triggers. Hormonal migraine
is a likely consequence of periodically falling hormone levels causing reduction in protein biosynthesis of metabolic
components including intestinal tract serotonin.
Current Research
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Signs and Symptoms
The signs and symptoms of migraine vary among patients. Therefore, what a patient experiences before, during and
after an attack cannot be defined exactly. The four phases of a migraine attack listed below are common among
patients but are not necessarily experienced by all migraine sufferers. Additionally, the phases experienced and
the symptoms experienced during them can vary from one migraine attack to another in the same migraineur:
- The prodrome, which occurs hours or days before the headache.
- The aura, which immediately precedes the headache.
- The pain phase, aka headache phase.
- The postdrome.
Prodrome Phase
Prodromal symptoms occur in 40% to 60% of migraineurs. This phase may consist of altered mood, irritability,
depression
or euphoria, fatigue, yawning, excessive sleepiness, craving for certain food (e.g., chocolate), stiff muscles
(especially in the neck), constipation or diarrhea, increased urination, and other vegetative symptoms. These symptoms
usually precede the headache phase of the migraine attack by several hours or days, and experience teaches the patient
or observant family how to detect that a migraine attack is near.
Aura Phase
For the 20-30% of migraineurs who suffer migraine with aura, the migraine aura is comprised of focal neurological
phenomena that precede or accompany the attack. They appear gradually over 5 to 20 minutes and generally last less
than 60 minutes. The headache phase of the migraine attack usually begins within 60 minutes of the end of the aura
phase, but it is sometimes delayed up to several hours, and it can be missing entirely. Symptoms of migraine aura
can be visual, sensory, or motor in nature.
Visual aura is the most common of the neurological events. There is a disturbance of vision consisting usually of
unformed flashes of white or rarely of multicolored lights (photopsia) or formations of dazzling zigzag lines
(scintillating scotoma; often arranged like the battlements of a castle, hence the alternative terms "fortification
spectra" or "teichopsia"). Some patients complain of blurred or shimmering or cloudy vision, as though they were
looking through thick or smoked glass, or, in some cases, tunnel vision. The somatosensory aura of migraine consists
of digitolingual or cheiro-oral paresthesias, a feeling of pins-and-needles experienced in the hand and arm as well
as in the ipsilateral nose-mouth area. Paresthesia migrate up the arm and then extend to involve the face, lips and
tongue.
Other symptoms of the aura phase can include auditory or olfactory hallucinations, aphasia, vertigo, tingling or
numbness of the face and extremities, and hypersensitivity to touch.
The diagnosis of migraine without aura, according to the International Headache Society, can be made according to the
following criteria - 5 or more attacks, 4 hours to 3 days in duration 2 or more of - unilateral location, pulsating
quality, moderate to severe
pain, aggravation by or avoidance of routine physical activity and 1 or more accompanying
symptoms - nausea and/or vomiting, photophobia, phonophobia ("5, 4, 3, 2, 1 criteria"). For migraine with aura, only
two attacks are required to justify the diagnosis.
Pain Phase
The typical migraine headache is unilateral, throbbing, moderate to severe and can be aggravated by physical activity.
Not all of these features are necessary. The
pain may be bilateral at the onset or start on one side and become
generalized, usually alternates sides from one attack to the next. The onset is usually gradual. The pain peaks and
then subsides, and usually lasts between 4 and 72 hours in adults and 1 to 48 hours in children. The frequency of
attacks is extremely variable, from a few in a lifetime to several times a week, and the average migraineur experiences
from one to three headaches a month. The head pain varies greatly in intensity. The pain of migraine is invariably
accompanied by other features. Nausea occurs in almost 90 percent of patients, while vomiting occurs in about one third
of patients. Many patients experience sensory hyperexcitability manifested by photophobia, phonophobia, osmophobia and
seek a dark and quiet room. Blurred vision, nasal stuffiness, diarrhea, polyuria, pallor or sweating may be noted during
the headache phase. There may be localized edema of the scalp or face, scalp tenderness, prominence of a vein or artery
in the temple, or stiffness and tenderness of the neck. Impairment of concentration and mood are common. Lightheadedness,
rather than true vertigo and a feeling of faintness may occur. The extremities tend to be cold and moist.
Postdrome Phase
The patient may feel tired, "washed out", irritable, listless and may have impaired concentration, scalp tenderness
or mood changes. Some people feel unusually refreshed or euphoric after an attack, whereas others note
depression and
malaise. Often, some of the minor headache phase symptoms may continue, such as loss of appetite, photophobia, and
lightheadedness.
Pathophysiology
Migraine was once thought to be initiated by problems with blood vessels. This theory is now largely discredited.
Current thinking is that a phenomenon known as cortical spreading
depression is responsible for the disorder. In
cortical spreading
depression, neurological activity is depressed over an area of the cortex of the brain. This results
in the release of inflammatory mediators leading to irritation of cranial nerve roots, most particularly the trigeminal
nerve, which conveys the sensory information for the face and much of the head.
This view is supported by neuroimaging techniques, which appear to show that migraine is primarily a disorder of the
brain (neurological), not of the blood vessels (vascular). A spreading depolarization (electrical change) may begin
24 hours before the attack, with onset of the headache occurring around the time when the largest area of the brain
is depolarized. The effects of migraine may persist for some days after the main headache has ended. Many sufferers
report a sore feeling in the area where the migraine was, and some report impaired thinking for a few days after the
headache has passed.
In 2005, research was published indicating that in some people with a patent foramen ovale (PFO), a hole between the
upper chambers of the heart, migraine might result and that the occurrence of migraines ends instantly if the hole is
patched. Several clinical trials are currently under way in an effort to determine if a causal link between PFO and
migraine can be found. Early speculation as to this relationship has centered on the idea that the lungs detoxify blood
as it passes through. The PFO allows uncleaned blood to go directly from the right side of the heart to the left without
passing through the lungs.
Migraine headaches can be a symptom of Hypothyroidism.
Types
Migraine Without Aura
This is the most commonly seen form of migraine; patients who primarily suffer from migraine without aura may also
have attacks of migraine with aura. According to the International Classification of Headache Disorders it is a
recurrent headache disorder manifesting in attacks lasting 4-72 hours. Typical characteristics of the headache are
unilateral location, pulsating quality, moderate or severe intensity, aggravation by routine physical activity and
association with nausea and/or photophobia and phonophobia.
In order to diagnose migraine without aura, there must have been at least 5 attacks not attributable to another cause
that fulfill the following criteria:
- Headache attacks lasting 4-72 hours when untreated
- At least two of the following characteristics:
- Unilateral location
- Pulsating quality
- Moderate or severe pain intensity
- Aggravation by or causing avoidance of routine physical activity
- During the headache there must be at least one of the following associated symptom clusters:
- Nausea and/or vomiting
- Photophobia and phonophobia
Where these criteria are not fully met, the problem may be classified as "probable migraine without aura"
but other diagnoses such as "episodic tension type headache" must also be excluded.
Migraine with Aura
This is the second most commonly seen form of migraine: patients who primarily suffer from migraine with aura may
also have attacks of migraine without aura. According to the International Classification of Headache Disorders
it is a recurrent disorder manifesting in attacks of reversible focal neurological symptoms that usually develop
gradually over 5-20 minutes and last for less than 60 minutes. Headache with the features of "migraine without
aura" usually follows the aura symptoms. Less commonly, the aura may occur without a subsequent headache or the
headache may be non-migrainous in type.
In order to diagnose migraine with aura, there must have been at least 2 attacks not attributable to another cause
that fulfill the following criteria:
- Aura consisting of at least one of the following, but no muscle weakness or paralysis:
- Fully reversible visual symptoms (e.g. flickering lights, spots, lines, loss of vision)
- Fully reversible sensory symptoms (e.g. pins and needles, numbness)
- Fully reversible dysphasia (speech disturbance)
- Aura has at least two of the following characteristics:
- Visual symptoms affecting just one side of the field of vision and/or sensory symptoms affecting just one
side of the body
- At least one aura symptom develops gradually over more than 5 minutes and/or different aura symptoms occur
one after the other over more than 5 minutes
- Each symptom lasts from 5-60 minutes
Where these criteria are not fully met, a diagnosis of "probable migraine with aura" may be considered, although
other neurological causes must also be excluded. If the picture complies with the criteria but includes one-sided
muscular weakness or paralysis, a diagnosis of "sporadic hemiplegic migraine" or "familial hemiplegic migraine"
should be considered.
Basilar Type Migraine
Basilar type migraine (BTM), formerly known as basilar artery migraine (BAM) or basilar migraine (BM), is an uncommon
type of complicated migraine with symptoms that result from brainstem dysfunction. Serious episodes of BTM can lead to
stroke, coma, or even death. The use of triptans and other vasoconstrictors as abortive treatments in BTM is
contraindicated. Abortive treatments for BTM often focus on vasodilation and restoration of normal blood flow to
the vertebrobasilar territory and subsequent return of normal brainstem function.
Familial Hemiplegic Migraine
Familial hemiplegic migraine 'FHM' is a type of migraine with a possible polygenetic component. These migraine attacks
may last 4-72 hours and are apparently caused by ion channel mutations, three types of which have been identified to
date. Patients who experience this syndrome have relatively typical migraine headaches preceded and/or accompanied by
reversible limb weakness on one side as well as visual, sensory or speech difficulties. A non-familial form exists as
well, "sporadic hemiplegic migraine" (SHM). It is often difficult to make the diagnosis between basilar-type migraine
and hemiplegic migraine. When making the differential diagnosis is difficult, the deciding symptom is often the motor
weakness or unilateral paralysis which can occur in FHM or SHM. While basilar-type migraine can present with tingling
or numbness, true motor weakness and/or paralysis occur only in hemiplegic migraine.
Abdominal Migraine
According to the International Classification of Headache Disorders abdominal migraine is a recurrent disorder of
unknown origin which occurs mainly in children. It is characterised by episodes of moderate to severe central abdominal
pain lasting 1-72 hours. There is usually associated nausea and vomiting but the child is entirely well between
attacks.
In order to diagnose abdominal migraine, there must be at least 5 attacks, not attributable to another cause, fulfilling
the following criteria:
- Attacks lasting 1-72 hours when untreated
- Pain must have ALL of the following characteristics:
- Location in the midline, around the umbilicus or poorly localised
- Dull or 'just sore' quality
- Moderate or severe intensity
- During an attack there must be at least two of the following:
- Loss of appetite
- Nausea
- Vomiting
- Pallor
Most children with abdominal migraine will develop migraine headache later in life and the two may co-exist
during adolescence.
Acephalgic Migraine
Acephalgic migraine is a neurological syndrome. It is a variant of migraine in which the patient may experience
aura symptoms such as scintillating scotoma, nausea, photophobia, hemiparesis and other migraine symptoms but does
not experience headache. Acephalgic migraine is also referred to as amigrainous migraine, ocular migraine, or optical
migraine.
Sufferers of acephalgic migraine are more likely than the general population to develop classical migraine with
headache.
The prevention and treatment of acephalgic migraine is broadly the same as for classical migraine. However, because of
the absence of "headache", diagnosis of acephalgic migraine is apt to be significantly delayed and the risk of
misdiagnosis significantly increased.
Visual snow might be a form of acephalgic migraine.
If symptoms are primarily visual, it may be necessary to consult an ophthalmologist to rule out potential eye disease before considering this diagnosis.
Epidemiology
Migraine is an extremely common condition which will affect 12-28% of people at some point in their lives. However
this figure — the lifetime prevalence — does not provide a very clear picture of how many patients there are with
active migraine at any one time. Typically, therefore, the burden of migraine in a population is assessed by looking
at the one-year prevalence — a figure that defines the number of patients who have had one or more attacks in the
previous year. The third figure, which helps to clarify the picture, is the incidence — this relates to the number
of first attacks occurring at any given age and helps understanding of how the disease grows and shrinks over time.
Based on the results of a number of studies, one year prevalence of migraine ranges from 6%-15% in adult men and from
14%-35% in adult women. These figures vary substantially with age: approximately 4-5% of children aged under 12 suffer
from migraine, with little apparent difference between boys and girls. There is then a rapid growth in incidence
amongst girls occurring after puberty, which continues throughout early adult life. By early middle age, around 25%
of women experience a migraine at least once a year, compared with fewer than 10% of men. After menopause, attacks in
women tend to decline dramatically, so that in the over 70s there are approximately equal numbers of male and female
sufferers, with prevalence returning to around 5%.
At all ages, migraine without aura is more common than migraine with aura, with a ratio of between 1.5:1 and 2:1.
Incidence figures show that the excess of migraine seen in women of reproductive age is mainly due to migraine without
aura. Thus in pre-pubertal and post-menopausal populations, migraine with aura is somewhat more common than amongst
15-50 year olds.
Geographical differences in migraine prevalence are not marked. Studies in Asia and South America suggest that the
rates there are relatively low, but they do not fall outside the range of values seen in European and North American
studies.
Triggers
A migraine trigger is any factor that, on exposure or withdrawal, leads to the development of an acute migraine
headache. Triggers may be categorized as behavioral, environmental, infectious, dietary, chemical, or hormonal.
According to the National Library of Medicine's Medical Encyclopedia, Migraine attacks may be triggered by:
• Allergic reactions • Bright lights, loud noises, and certain odors or perfumes • Physical or emotional stress
• Changes in sleep patterns • Smoking or exposure to smoke • Skipping meals • Alcohol or caffeine • Menstrual cycle
fluctuations,
birth control pills • Tension headaches • Foods containing tyramine (red wine, aged cheese, smoked fish,
chicken livers, figs, and some beans), monosodium glutamate (MSG), or nitrates (like bacon, hot dogs, and salami)
• Other foods such as chocolate, nuts, peanut butter, avocado, banana, citrus, onions, dairy products, and fermented
or pickled foods
Many people report that one or more dietary, physical, hormonal, emotional, or environmental factors precipitate their
migraines. The most-often reported triggers include perfumes or fragrances (30% of sufferers) stress, over-illumination
or glare, alcohol, foods, too much or too little sleep, and weather. Some women experience migraines in conjunction with
monthly menstrual cycles.
Sometimes the migraine occurs with no apparent "cause". The trigger theory supposes that exposure to various
environmental factors precipitates, or triggers, individual migraine episodes. Migraine patients have long been
advised to try to identify personal headache triggers by looking for associations between their headaches and various
suspected trigger factors. Patients are urged to keep a "headache diary" in which to note what they eat and when they
get a headache, to look for correlations, and to try to avoid headache by avoiding factors they identify as triggers.
Typically this advice is accompanied by a list of trigger factors.
Food
In 2005, authors who reviewed the medical literature found that the available information about dietary trigger factors
relies mostly on the subjective assessments of patients. Some suspected dietary trigger factors appear to genuinely
promote or precipitate migraine episodes, but many other suspected dietary triggers have never been demonstrated to
trigger migraines. The review authors found that alcohol, caffeine withdrawal, and missing meals are the most important
dietary migraine precipitants. The authors say dehydration deserves more attention, and that some patients are sensitive
to red wine. The authors found little or no demonstrated evidence that notorious suspected triggers chocolate, cheese,
or that histamine, tyramine, nitrates, or nitrites normally present in foods trigger headaches. The artificial sweetener
aspartame (NutraSweet®) has not been shown to trigger headache, but in a large and definitive study monosodium glutamate
(MSG) in large doses (2.5 grams) was associated with adverse symptoms including headache more often than was placebo.
The review authors also note that general dietary restriction has not been demonstrated to be an effective migraine
therapy.
On the other hand, several headache clinics have had good results with individually tailored dietary restriction as a
therapy. Dr. Ian Livingstone, director of the Princeton Headache Clinic, recommends eliminating the following common
headache triggers from the diet: aged cheese, monosodium glutamate, processed fish and meats containing nitrates
(such as hot dogs), dark chocolate, aspartame, certain alcoholic beverages (including red wine), citrus fruits,
and caffeine. After a period of one to two months, these foods can be reintroduced one at a time to determine their
trigger potential for that individual. Adding large amounts of the suspected trigger in a short time may generate a
response that is easy to observe.
Dr. David Buchholz, a neurologist who treats headaches at Johns Hopkins Hospital, has a longer list of suspected
migraine triggers. He also recommends eliminating the triggers from the diet altogether, and then reintroducing them
slowly after many weeks to measure the effects. His list includes: coffee (including decaf), chocolate, monosodium
glutamate, processed meats and fish (aged, canned, preserved, processed with nitrates, and some meats that contain
tyramine), cheese and dairy products (the more aged, the worse), nuts, citrus and some other fruits, certain vegetables
(especially onions), fresh risen yeast baked goods, dietary sources of tyramine (including the foods listed above),
and whatever gives you a headache.
The National Headache Foundation has a more specific list of triggers, which differs slightly from David Buchholz's
list. For example, it says that decaffeinated coffee is allowed. The list details "Allowed", "Use with caution", and
"Avoid" triggers.
Weather
Several studies have found some migraines are triggered by changes in weather. One study(Prince, 2004) noted that
62% of the subjects in the study thought that weather was a factor, in fact 51% were actually sensitive to weather
changes. Among those whose migraines did occur during a change in weather, the subjects often picked a weather change
other than the actual weather data recorded. Most likely to trigger a migraine were, in order:
- Temperature mixed with humidity. High humidity plus high or low temperature was the biggest cause.
- Significant changes in weather
- Changes in barometric pressure
Another study(Cooke, 2000) researched whether chinook winds (warm westerly winds occurring in Alberta, Canada) are
a migraine trigger. Many patients had increased incidence of migraines immediately before and/or during the chinook
winds. The number of people reporting migrainous episodes during the chinook winds was higher on high-wind chinook
days. The probable cause is "through increased air positive ion concentrations."
Hair Wash Headache
Another trigger for Migraine has been proposed by Dr.K.Ravishankar, a neurologist and headache specialist from India.
He reported an unusual trigger for migraine seen among Indian women, Hair Wash Headache. It is described as a migraine
headache that originates with a head bath. Most Indian women have long hair and so wash their hair 2-3 times a week.
Very often they do not use a hair dryer and often plait their hair when wet. This results in a gradual build up of
pain which ultimately results in Migraine.
Treatment
Conventional treatment focuses on three areas: trigger avoidance, symptomatic control, and preventive drugs. Patients
who experience migraines often find that the recommended treatments are not 100% effective at preventing migraines.
Trigger Avoidance
Patients can attempt to identify and avoid factors that promote or precipitate migraine episodes. Moderation in alcohol
and caffeine intake, consistency in sleep habits, and regular meals may be helpful. Beyond an often pronounced placebo
effect, general dietary restriction has not been demonstrated to be an effective approach to treating migraine.
Nonetheless, some people fervently claim that they have successfully identified foods that are likely to result in
migraines, and by avoiding them, can decrease the likelihood of an episode.
Symptomatic Control to Abort Attacks
Migraine sufferers usually develop their own coping mechanisms for the
pain of a migraine attack. A cold or hot shower
directed at the head, a hot or cold wet washcloth, a warm bath, or resting in a dark and silent room may be as helpful
as medication for many patients, but both should be used when needed.
Some headache sufferers are surprised to learn that a simple cup of coffee is used daily around the world to control
minor vascular headaches that are not quite migraines. Minor vascular headaches are frequently associated with the
hormonal fluctuations of menstrual periods, irregular eating, and unusually hard work. For migraineurs, a well-timed
cup of coffee can prevent outright migraine under the same conditions.
A simple treatment, which has been effective for some, is a counteracting "ice cream headache", briefly provoked by
placing spoonfuls of ice cream on the soft palate at the back of the mouth. (Hold them there with your tongue until
they melt or become intolerable.) This directs cooling to the hypothalamus, which is suspected to be involved with
the migraine feedback cycle, and for some it can stop even a severe headache very quickly.
For patients who have been diagnosed with recurring migraines, doctors recommend taking migraine abortive medicines to
treat the attack as soon as possible. Migraine without aura presenting without prodrome or nausea can present with
sudden onset. Many patients avoid taking their medications when an attack is beginning, hoping that "it will go away".
However, in many cases once an attack is underway, it can become intensely painful, last for a long time (sometimes
even for several days), and become somewhat resistant to medical treatment. In contrast, treating the attack at the
onset can often abort it before it becomes serious, and can reduce the near-term frequency of subsequent attacks.
The first line of treatment is over-the-counter (OTC) abortive medication. Patients themselves often start off with
paracetamol (known as acetaminophen in the USA), aspirin, ibuprofen, or other simple analgesics that are useful for
tension headaches. Some patients find relief from taking Benadryl, an OTC sedative antihistamine, or anti-nausea
agents. OTC drugs may provide some relief, although they are typically not effective for most sufferers. It is one
of doctors' practical diagnoses of migraine head
pain when patients say typical OTC drugs "won't touch it".
If the patient hasn't tried it, doctors may suggest the simple analgesics combined with caffeine. During a migraine
attack, emptying of the stomach is slowed, resulting in nausea and a delay in absorbing medication. Caffeine has been
shown to partially reverse this effect, and probably accounts for its benefit. Excedrin is an example of an aspirin
with caffeine product. Caffeine is recognized by the U.S. FDA as an OTC treatment for migraine.
If over-the-counter medications do not work, or if triptans are unaffordable, the next step for many doctors is to
prescribe fioricet or fiorinal, which is a combination of butalbital (a barbiturate), acetaminophen (in fioricet) or
acetylsalicylic acid (more commonly known as aspirin and present in fiorinal), and caffeine. While the risk of
addiction
is low, butalbital can be habit-forming if used daily, and it can also lead to rebound headaches. Barbiturate-containing
medications are not available in many European countries.
Narcotic pain killers (for example, codeine, morphine or other opiates) provide variable relief, but their side effects,
the possibility of causing rebound headaches or analgesic overuse headache, and the risk of
addiction contraindicates
their general use.
Amidrine (a cocktail of a
pain reliever, a sedative, and a vasoconstrictor) is sometimes prescribed for migraine
headaches.
Anti-emetics by suppository or injection may be needed in cases where vomiting dominates the symptoms. The earlier these
drugs are taken in the attack, the better their effect.
Until the introduction of sumatriptan (Imitrex®/Imigran®) in 1991, ergot derivatives (see ergoline) were the primary
oral drugs available to abort a migraine once it is established.
Ergot drugs can be used either as a preventive or abortive therapy, though their relative expense and cumulative side
effects suggest reserving them as an abortive rescue medicine. However, ergotamine tartrate tablets (usually with
caffeine), though highly effective, and long lasting (unlike triptans), have fallen out of favour due to the problem
of ergotism — temporarily disabling calf pai
pain n caused by overuse. Oral ergotamine tablet absorption is reliable unless
the patient is nauseated. Anti-nausea administration is available by ergotamine suppository (or Ergostat sublingual
tablets made until circa 1992). Ergotamine-caffeine 1/100 mg fixed ratio tablets (like Cafergot, Ercaf, etc.) are much
less expensive per headache than triptans, and are commonly available in Asia. They are difficult to obtain in the USA.
Ergotamine-caffeine can't be regularly used to abort evening or night onset migraines due to debilitating caffeine
interference with sleep. Pure ergotamine tartrate is highly effective for evening-night migraines, but is rarely or
never available in the USA. Dihydroergotamine (DHE), which must be injected or inhaled, can be as effective as ergotamine
tartrate, but is much more expensive than $2 USD Cafergot tablets.
Sumatriptan and related selective serotonin receptor agonists are now the therapy of choice for chronic migraine attacks.
Triptans are a mid-line treatment suitable for many migraineurs with typical migraines. They may not work for atypical
or unusually severe migraines, transformed migraines, or status (continuous) migraines.
Triptans are highly effective, reducing the symptoms or aborting the attack within 30 to 90 minutes in 70-80% of patients.
Many patients have a recurrent migraine later in the day, and only one such recurrence in a day can be treated with a
second dose of a triptan.
Triptans have few side effects if used in correct dosage and frequency. Although there is a theoretical risk of coronary
spasm in patients with established heart disease, no clinically significant problems have ever been reported in practice.
Some members of this family of drugs are:
- Sumatriptan (Imitrex®, Imigran®)
- Zolmitriptan (Zomig®)
- Naratriptan (Amerge®, Naramig®)
- Rizatriptan (Maxalt®)
- Eletriptan (Relpax®)
- Frovatriptan (Frova®, Migard®)
- Almotriptan (Almogran®)
Evidence is accumulating that these drugs are effective because they act on serotonin receptors in nerve endings as well
as the blood vessels. This leads to a decrease in the release of several peptides, including CGRP and Substance P.
These drugs have been available only by prescription (US, Canada and UK), but sumatriptan became available
over-the-counter in the U.K in June, 2006. The brand name of the OTC product in the UK is Imigran Recovery. Injectable
sumatriptan should be available in generic formula in early 2007 as the patent on Imitrex STATDose expires in December,
2006. The patent on Imitrex tablets expires in the USA in 2009, and the generic sumatriptan tablets should be available
shortly thereafter. Many migraine sufferers do not use them only because they have not sought treatment from a
physician, but others don't because they know that they can't afford them at current prescription prices.
Regarding comparative effectiveness of these drugs used to abort migraine attacks, a 2004 placebo-controlled trial
reveals that high dose acetylsalicylic acid (1000 mg), sumatriptan 50 mg and ibuprofen 400 mg are equally effective
at providing relief from
pain, although sumatriptan was superior in terms of the more demanding outcome of rendering
patients entirely free of pain. Acetylsalicylic acid is OTC aspirin, ibuprofen is OTC Advil, and since migraineurs
know they don't provide much relief, the results of this study are unexpected. They may be partly related to the dosage
of acetylsalicylic acid used, which was considerably higher than the one or two 300 mg tablets normally recommended for
OTC use. High doses of aspirin and ibuprofen may cause ringing of the ears, which is a sign of drug toxicity to the
inner ear.
Triptan therapy has been shown to result in a reduction in lost productivity. Sumatriptan has been shown to result in
an average of 0.5 fewer missed workdays during the first three months of therapy and 0.7 fewer missed workdays within
the first six months, as well as a reduction in the number of days spent working while symptomatic. The average reduction
in lost productivity has been estimated at $1,249, at a cost of $25 per day of disability avoided. The annual net
savings in reduced health care costs and lost productivity, over the increased cost of triptan therapy, has been
estimated at between $114 and $540 per patient; thus the use of these pharmaceuticals represents a cost savings as well
as an improvement in the patients' quality of life.
Triptans' cost, typically $20 USD per dose and frequently two doses per headache, is a serious problem for low-income
patients. In most non-US countries these costs are considerably lower — typically $5-10 per dose. To their credit,
drug companies often provide them free to low-income patients in the USA. Cost will become less of a problem if patents
end on schedule and generics become available. Drug patent expiration and generics becoming available have not always
happened as expected.
Intravenous chlorpromazine has proven very effective in treating status migrainosus—intractable and unremitting
migraine.
Status migraine is an extremely rare life-threatening condition. In otherwise uncomplicated, non-nauseated cases,
it can be treated with 20 mg of prednisone tablets every eight hours until the migraine ends, followed by mandatory
tapering off doses (the classic steroid taper). Prednisone is a cortisol-like semi-synthetic adrenal hormone, a
non-anabolic steroid, which strongly stimulates biosynthesis of proteins from DNA. The replicated proteins include
enzymes that cure the migraine through numerous metabolic boosts, including molecular construction of more natural
serotonin to be stored in blood platelets.
Prednisone use is a gamble that saves many lives, frequently has frightening side effects, occasionally causes serious
harm, and requires a lot of bicycle-like how-to learning by the patient. Balanced against its risks of immune system
suppression, adrenal axis suppression, non-addictive dependence, and long-term
osteoporosis, prednisone is very
inexpensive for low income migraineurs who may be willing to trade quality of life for length of life. Vitamin
antioxidants taken with calcium and magnesium may reduce the damage caused by the extra free radicals released, and
the bone lost, during long term prednisone use.
Preventive Drugs
Following treatment of an acute migraine, it is important to consider preventive measures. Factors that prompt
consideration of such measures include: 1) more than two migraines per month with disabilities lasting three or more
days per month; 2) failure of acute treatments; 3) contraindications to acute treatments; 4) adverse reactions from
acute treatments; 5) use of acute treatments more than twice a week; or 6) presence of uncommon symptoms such as
hemiplegia, prolonged, aura, or migraine infarction.
The main goal of preventive therapy is to reduce the frequency, severity, and durations of migraines, and to increase
the effectiveness of abortive therapy. Another reason is to avoid medication overuse headache (MOH), otherwise known
as rebound headache, which is an extremely common problem among migraneurs. This occurs in part due to overuse of pain
medications. MOH results in the development of chronic daily headache due to "transformed" migraine.
Preventive medication has to be taken on a daily basis, usually for a few weeks, before the effectiveness can be
determined. Supervision by a neurologist is advisable. A large number of medications with varying modes of action can
be used. Selection of a suitable medication for any particular patient is a matter of trial and error, since the
effectiveness of individual medications varies widely from one patient to the next. Often preventive medications do
not have to be taken indefinitely. Sometimes as little as six months of preventive therapy is enough to "break the
headache cycle" and then they can be discontinued.
The most effective prescription medications include several drug classes:
- Beta blockers such as propranolol and atenolol. A meta-analysis by the Cochrane Collaboration of nine
randomized controlled trials or crossover studies, which together included 668 patients, found that
propranolol had an "overall relative risk of response to treatment (here called the 'responder
ratio')" was 1.94.
- Anticonvulsants such as valproic acid and topiramate. A meta-analysis by the Cochrane Collaboration of
ten randomized controlled trials or crossover studies, which together included 1341 patients, found
anticonvulsants had an "2.4 times more likely to experience a 50% or greater reduction in frequency
with anticonvulsants than with placebo" and a number needed to treat of 3.8. However, concerns
have been raised about the marketing of gabapentin.
- Antidepressants include tricyclic antidepressants (TCAs) such as amitriptyline and the newer selective
serotonin reuptake inhibitors (SSRIs) such as fluoxetine. A meta-analysis by the Cochrane Collaboration
found selective serotonin reuptake inhibitors are no more effective than placebo. Another meta-analysis
found benefit from SSRIs among patients with migraine or tension headache; however, the effect of SSRIs
on only migraines was not separately reported. A randomized controlled trial found that amitriptyline
was better than placebo and similar to propranolol.
Other drugs:
- Sansert was withdrawn from the US market by Novartis, but is available in Canadian pharmacies. Although
highly effective, it has rare but serious side effects, including retroperitoneal fibrosis.
- Namenda, memantine HCI tablets, which is used in the treatment of Alzheimer's Disease, is beginning to
be used off label for the treatment of migraines. It has not yet been approved by the FDA for the
treatment of migraines.
Alternative Approaches
Because the conventional approaches to migraine prevention are not 100% effective and can have unpleasant side
effects, many seek alternative treatments.
Physical Therapy
Many physicians believe that exercise for 15-20 minutes per day is helpful for reducing the frequency of migraines.
Massage therapy and physical therapy are often very effective forms of treatment to reduce the frequency and intensity
of migraines. However, it is important to be treated by a well-trained therapist who understands the pathophysiology
of migraines. Deep massage can 'trigger' a migraine attack in a person who is not used to such treatments. It is
advisable to start sessions as short in duration and then work up to longer treatments.
Prism Eyeglasses
At least two British studies have shown a relationship between the use of eyeglasses containing prisms and a reduction
in migraine headaches.
Turville, A. E. (1934) Refraction and migraine. Br. J. Physiol. Opt. 8, 62–89, contains a good review of the literature
and theories existing in 1934, and includes the vascular theory of migraine, which is popular today. In that study,
Turville suggests that many patients were provided with complete relief from migraine symptoms with proper eyeglass
prescriptions, which included prescribed prism.
Wilmut, E. B. (1956) Migraine. Br. J. Physiol. Opt. 13, 93–97, replicated Turville's work. Both studies are subject
to criticism because of sample bias, sample size, and the lack of a control group.
Turville's and Wilmut's conclusions have largely been ignored since 1956 and it is widely believed that vision problems
are not migraine triggers.
Most optometrists avoid prescribing prism because, when incorrectly prescribed, it can cause headaches.
Herbal and Nutritional Supplements
50 mg or 75 mg/day of butterbur (Petasites hybridus) rhizome extract was shown in a controlled trial to provide 50% or
more reduction in the number of migraines to 68% of participants in the 75 mg dose group, 56% in the 50 mg dose group
and 49% in the placebo group after four months. Native butterbur contains some carcinogenic compounds, but a purified
version, Petadolex®, does not.
Cannabis was a standard treatment for migraines from the mid-19th century until it was outlawed in the early 20th
century in the USA. It has been reported to help people through an attack by relieving the nausea and dulling the head
pain, as well as possibly preventing the headache completely when used as soon as possible after the onset of
pre-migraine symptoms, such as aura. There is some indication that semi-regular use may reduce the frequency of attacks.
Further studies are being conducted. A pharmaceutical company is currently conducting trials of a whole cannabis extract
spray for migraine.
Supplementation of coenzyme Q10 has been found to have a beneficial effect on the condition of some sufferers of
migraines. In a well-controlled trial, Young and Silberstein found that 61.3% of patients treated with 100 mg/day
had a greater than 50% reduction in number of days with migraine, making it more effective than most prescription
prophylactics. Fewer than 1% reported any side effects.
The plant feverfew (Tanacetum parthenium) is a traditional herbal remedy believed to reduce the frequency of migraine
attacks. Clinical trials have been carried out, and appear to confirm that the effect is genuine (though it does not
completely prevent attacks).
Kudzu root (Pueraria lobata) has been demonstrated to help with menstrual migraine headaches and cluster headaches.
While the studies on menstrual migraine assumed that kudzu acted by imitating estrogen, it has since been shown that
kudzu has significant effects on the serotonin receptors. Kudzu Monograph at Med-Owl.
Magnesium citrate has reduced the frequency of migraine in an experiment in which the magnesium citrate group received
600mg per day oral of trimagnesium dicitrate. In weeks 9-12, the frequency of attacks was reduced by 41.6% in the
magnesium citrate group and by 15.8% in the placebo group.
Non-Drug Medical Treatments
Botox has been used by some sufferers in an attempt to reduce the frequency and/or severity of migraine attacks
(Botox for Migraines).
Spinal cord stimulators are an implanted medical device sometimes used for those who suffer severe migraines several
days each month.
Transcranial Magnetic Stimulation (TMS): At the 49th Annual meeting of the American Headache Society in June 2006,
scientists from Ohio State University Medical Center presented medical research on 47 candidates that demonstrated
that TMS — a medically non-invasive technology for treating
depression, obsessive compulsive disorder and tinnitus,
among other ailments — helped to prevent and even reduce the severity of migraines among its patients. This treatment
essentially disrupts the aura phase of migraines before patients develop full-blown migraines. In about 74% of
the migraine headaches, TMS was found to eliminate or reduce nausea and sensitivity to noise and light. Their research
suggests that there is a strong neurological component to migraines. A larger study will be conducted soon to better
assess TMS's complete effectiveness.
Other Alternatives
Some migraine sufferers find relief through acupuncture, which is usually used to help prevent headaches from
developing. Sometimes acupuncture is used to relieve the
pain of an active migraine headache. In one controlled
trial of acupuncture with a sham control in migraine, the acupuncture was not more effective than the sham acupuncture
but was more effective than delayed acupuncture.
Additionally acupressure is used by some for relief. For instance pressure between the thumbs and index finger to help
subside headaches if the headache or migraine isn't too severe.
Incense and smells are shown to help. The smell and incense of apples and lavender have been proven to help with
migraines and headaches more so than most other scents.
Biofeedback has been used successfully by some to control migraine symptoms through training and practice.
There is evidence that magnesium supplements or epsom salts (magnesium sulfate) might reduce the frequency of migraine
headaches.
Sleep is often a good solution if a migraine is not so severe as to prevent it, as when a person awakes the symptoms
will have most likely subsided.
Diet, visualization, and self-hypnosis are also alternative treatments and prevention approaches.
Bruxism, clenching or grinding of teeth, especially at night, is a trigger for many migraineurs. A device called a
nociceptive trigeminal inhibitor (NTI) takes advantage of a reflex limiting the force of clenching. It can be fitted
by dentists and clips over the front teeth at night, preventing contact between the back teeth. It has a success rate
similar to butterbur and co-enzyme Q10. Massage therapy of the jaw area can also reduce such pain.
Sexual activity has been reported by a proportion of male and female migraine sufferers to relieve migraine pain
significantly in some cases.
In many cases where a migraine follows a particular cycle, attempting to interrupt the cycle may prolong the symptoms.
Letting a headache "run its course" by not using painkillers can sometimes decrease the length of an episode. This is
especially true of cases where vomiting is common, as often the headache will subside immediately after vomiting.
Curbing the
pain may delay vomiting, and prolong the headache.
History
The history of humanity's suffering from headache dates back to 9000 years ago when basic drastic therapy of that time
was trepanation. Headache with neuralgia was recorded in the medical documents of the ancient Egyptians as early as 1200
BC. In 400 BC Hippocrates described the visual aura that can precede the migraine headache and the relief which can be
induced by vomiting. Aretaeus of Cappadocia is credited as the discoverer of migraine because of his classic description
of the symptoms of a unilateral headache associated with vomiting with headache-free intervals in between attacks in the
2nd century. Galenus of Pergamon used the term "hemicrania", from which the word "migraine" was derived. He thought there
was a connection between the stomach and the brain because of the nausea and vomiting that often accompany an attack. For
relief of migraine, Spanish-born physician Abulcasis, also known as Abu El Quasim, suggested application of a hot iron to
the head or insertion of garlic into an incision made in the temple. In the Medieval Ages migraine was recognized as a
discrete medical disorder with treatment ranging from hot irons to blood letting and even witchcraft. Followers of Galenus
explained migraine as caused by aggressive yellow bile. Ebn Sina (Avicenna) described migraine in his textbook "El Qanoon
fel teb" as "... small movements, drinking and eating, and sounds provoke the pain... the patient cannot tolerate the
sound of speaking and light. He would like to rest in darkness alone." Abu Bakr Mohamed Ibn Zakariya Râzi noted the
association of headache with different events in the lives of women, "...And such a headache may be observed after
delivery and abortion or during menopause and
dysmenorrhea."
In Bibliotheca Anatomica, Medic, Chirurgica, published in London in 1712, five major types of headaches are described,
including the "Megrim", recognizable as classic migraine. Graham and Wolff (1938) published their paper advocating
ergotamine tart for relieving migraine. Later in the 20th century, Harold Wolff (1950) developed the experimental
approach to the study of headache and elaborated the vascular theory of migraine, which has come under attack as the
pendulum again swings to the neurogenic theory.
Economic Impact
In addition to being a major cause of
pain and suffering, chronic migraine attacks are a significant source of both
medical costs and lost productivity. Medical costs per migraine sufferer (mostly physician and emergency room visits)
averaged $107 USD over six months in one 1988 study, with total costs including lost productivity averaging $313.
Annual employer cost of lost productivity due to migraines was estimated at $3,309 per sufferer. Total medical costs
associated with migraines in the United States amounted to one billion dollars in 1994, in addition to lost productivity
estimated at thirteen to seventeen billion dollars per year. Employers may benefit from educating themselves on the
effects of migraines in order to facilitate a better understanding in the workplace. The workplace model of 9-5, 5 days
a week may not be viable for a migraine sufferer. With education and understanding an employer could compromise with
an employee to create a workable solution for both.
Migraine and Cardiovascular Risks
Recent studies have suggested that migraine sufferers may be at increased risk of stroke in later life. A meta-analysis
of several such studies published in the British Medical Journal in 2005 appeared to confirm this association, with
young adult sufferers and women taking the oral contraceptive pill at particular risk. The mechanism of any association
is unclear, but chronic abnormalities of cerebral blood vessel tone may be involved.
Women who experience auras have been found to have twice the risk of strokes and heart attacks over non-aura migraine
sufferers and women who do not have migraines.
(adapted from Wikipedia, the free encyclopedia http://en.wikipedia.org/wiki/Migraine)
Authors: Hill DL, Daroff RB, Ducros A, Newman NJ, Biousse V.
Departments of Ophthalmology (DLH, NJN, VB), Neurology (NJN, VB), and Neurological Surgery (NJN), Emory University School of
Medicine, Atlanta Georgia; Department of Neurology and Office of the Vice Dean (RBD), Case Western Reserve University School
of Medicine, Cleveland, Ohio; and Acute Headache Center and Department of Neurology (AD), Hopital Lariboisiere, Paris,
France.
BACKGROUND:: Monocular visual loss has often been labeled "retinal migraine." Yet there is reason to believe that many such
cases do not meet the criteria set out by the International Headache Society (IHS), which defines "retinal migraine" as
attacks of fully reversible monocular visual disturbance associated with migraine headache and a normal neuro-ophthalmic
examination between attacks. METHODS:: We performed a literature search of articles mentioning "retinal migraine," "anterior
visual pathway migraine," "monocular migraine," "ocular migraine," "retinal vasospasm," "transient monocular visual loss,"
and "retinal spreading
" using Medline and older textbooks. We applied the IHS criteria for retinal migraine to
all cases so labeled. To be included as definite retinal migraine, patients were required to have had at least two episodes
of transient monocular visual loss associated with, or followed by, a headache with migrainous features. RESULTS:: Only 16
patients with transient monocular visual loss had clinical manifestations consistent with retinal migraine. Only 5 of these
patients met the IHS criteria for definite retinal migraine. No patient with permanent visual loss met the IHS criteria for
retinal migraine. CONCLUSIONS:: Definite retinal migraine, as defined by the IHS criteria, is an exceedingly rare cause of
transient monocular visual loss. There are no convincing reports of permanent monocular visual loss associated with
migraine. Most cases of transient monocular visual loss diagnosed as retinal migraine would more properly be diagnosed as
"presumed retinal vasospasm."
Journal: J Neuroophthalmol. 2007 Mar;27(1):3-8.
Authors: Lampl C, Voelker M, Diener HC.
Dept. of Neurology, Pain and Headache Center, Krankenhaus der Barmherzigen Schwestern, Seilerstatte 4, A-4010, Linz,
Austria.
Migraine is often associated with health consequences including impaired quality of life, and the cost of treating migraine
headaches places a significant financial burden on patients who suffer from migraines. Nonsteroidal anti-inflammatory drugs
(NSAIDs) and triptans are commonly used for the treatment of acute migraine attacks. Aspirin is widely accepted as a
treatment option for migraine
relief and could provide an alternative not only for treatment of moderate migraine
attacks, but also for severe migraine attacks. The efficacy and safety of 1,000 mg effervescent aspirin (eASA) was evaluated
in comparison to 50 mg sumatriptan and placebo in an individual patient data meta-analysis of three randomized,
placebo-controlled, single- dose migraine trials. Pain-relief at 2 h, pain-free at 2 h and sustained pain-free up to 24 h
were calculated. For eASA, the response rates were 51.5 % (95 % CI: 46.6-56.5 %), 27.1 % (95 % CI: 22.6-31.4 %), and 23.5 %
(95 % CI: 19.3-27.7 %). For sumatriptan, the response rates were 46.6 % (95% CI: 40.0-53.2 %), 29% (95 % CI: 23.0-34.9 %),
and 22.2 % (95 % CI: 16.7-27.6 %). The corresponding rates for placebo were 33.9 % (95% CI: 29.1-38.6 %), 15.1 % (95 % CI:
11.5-18.7 %), and 14.6 % (95 % CI: 11.0-18.1 %). The treatment effect of eASA and sumatriptan were significantly different
from placebo (p < 0.001), but differences between eASA and sumatriptan were not significant. The remission of
accompanying symptoms and the subgroup analyses of patients with moderate or severe migraine pain at baseline revealed no
significant differences between eASA and sumatriptan. Safety was evaluated based on the frequency of reported adverse events,
and treatment with eASA was associated with lower incidence of adverse events than was with sumatriptan. This individual
patient data meta-analysis provided evidence that eASA 1,000mg is as effective as sumatriptan 50mg for the treatment of
acute migraine attacks and has a better side effect profile. This is also true for patients with moderate as well as severe
headache at baseline. Patients therefore should be advised to use eASA first for migraine attacks and use a triptan in case
of no response.
Journal: J Neurol. 2007 Apr 10;
Authors: Stella CL, Jodicke CD, How HY, Harkness UF, Sibai BM.
Division of Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, University of Cincinnati College of Medicine,
Cincinnati, OH 45267-0526, USA.
OBJECTIVE: Headache is a common finding in the postpartum period, and there are limited data describing the cause and
treatment of women with postpartum headache. Our objective was to describe our experience with women who were hospitalized
for postpartum headache and to develop a management algorithm for these women. STUDY DESIGN: Data for 95 women with headache
>24 hours after delivery from 2000-2005 were reviewed retrospectively. Maternal assessment included an evaluation for
benign and serious causes of headache that included preeclampsia, dural puncture, and neurologic lesions. Neurologic imaging
were performed on the basis of initial neurologic findings and clinical course. Outcomes that were studied included cause,
a need for cerebral imaging, neurologic findings, maternal complications, and long-term follow-up evaluations. RESULTS: The
mean onset of headache was 3.4 days (range, 2-32 days) after delivery. Tension-type/migraine headache was the most common
cause (47%). Preeclampsia/eclampsia and spinal headache comprised 24% and 16% of cases, respectively. Anesthesia evaluation
was required in 15 patients because of suspected spinal headache; blood patch was required in 12 of these patients.
Cerebral imaging was performed in 22 patients because of focal neurologic deficits and/or failure to respond to initial
therapy; 15 of these women (68%) had abnormal findings. Ten patients had serious cerebral pathologic findings, such as
hemorrhage, thrombosis, or vasculopathy. There were no deaths; 2 women had minor residual neurologic damage on follow-up
evaluation. CONCLUSION: The evaluation of persistent headaches that develop >24 hours after delivery must be performed
in a stepwise fashion and requires a multidisciplinary approach. Preeclampsia should be considered initially in women with
and proteinuria. Normotensive women should be evaluated initially for tension-type/migraine headache or spinal
headache. Patients with headache that is refractory to usual therapy and patients with neurologic deficit require cerebral
imaging to detect the presence of life-threatening causes.
Journal: Am J Obstet Gynecol. 2007 Apr;196(4):318.e1-7.
Authors: Kelman L.
Headache Center of Atlanta, Atlanta, GA, USA.
The aim of this study was to evaluate and define the triggers of the acute migraine attack. Patients rated triggers on a
0-3 scale for the average headache. Demographics, prodrome, aura, headache characteristics, postdrome, medication
responsiveness, acute and chronic disability, sleep characteristics and social and personal characteristics were also
recorded. One thousand two hundred and seven International Classification of Headache Disorders-2 (1.1-1.2, and 1.5.1)
patients were evaluated, of whom 75.9% reported triggers (40.4% infrequently, 26.7% frequently and 8.8% very frequently).
The trigger frequencies were stress (79.7%), hormones in women (65.1%), not eating (57.3%), weather (53.2%), sleep
disturbance (49.8%), perfume or odour (43.7%), neck pain (38.4%), light(s) (38.1%), alcohol (37.8%), smoke (35.7%),
sleeping late (32.0%), heat (30.3%), food (26.9%), exercise (22.1%) and sexual activity (5.2%). Triggers were more likely
to be associated with a more florid acute migraine attack. Differences were seen between women and men, aura and no aura,
episodic and chronic migraine, and between migraine and probable migraine.
Journal: Cephalalgia. 2007 Mar 30;
Authors: Ishkanian G, Blumenthal H, Webster CJ, Richardson MS, Ames M.
Elkind Headache Center, Mount Vernon, New York, USA.
BACKGROUND:: Many patients and physicians interpret episodic headache in the presence or absence of nasal symptoms as
"sinus' headache, while ignoring the possible diagnosis of migraine. OBJECTIVE:: The purpose of this study was to assess
the efficacy and tolerability of sumatriptan succinate 50-mg tablets in patients with migraine presenting with "sinus"
headache. METHODS:: A randomized, double-blind, placebo-controlled, multicenter study was conducted in adult (aged 18-65
years) migraine patients presenting with self-described or physician-diagnosed "sinus" headache. From November 2001 to
March 2002, patients meeting International Headache Society criteria for migraine (with >/=2 of the following:
unilateral location, pulsating quality, moderate or severe intensity, aggravation by moderate physical activity; and
>/=1 of: phonophobia and phonophobia, nausea and/or vomiting) and with no evidence of bacterial rhinosinusitis were
enrolled and randomized in a 1:1 ratio via computer-generated randomization schedule to receive either 1 sumatriptan 50-mg
tablet or matching placebo tablet. The primary efficacy end point was headache response (moderate or severe headache pain
reduced to mild or no headache
) at 2 hours after administration. The presence or absence of migraine-associated
symptoms and sinus and nasal symptoms was also measured. Tolerability was assessed through patient-reported adverse events
(AEs). RESULTS:: Two hundred sixteen patients with self-described or physician-diagnosed "sinus" headache received a
migraine diagnosis and treated 1 migraine attack with sumatriptan 50 mg. The efficacy (intentto-treat) analysis included
215 patients treated with sumatriptan 50 mg (n = 108; mean [SD] age, 39.6 [12.3] years; mean [SD] weight, 77.7 [17.7] kg;
sex, 71% female; race, 69% white) or placebo (n = 107; mean [SD] age, 41.0 [11.3] years; mean [SD] weight 80.7 [20.9] kg;
sex, 69% female; race, 64% white). Significantly more patients treated with sumatriptan 50 mg achieved a positive headache
response at 2 and 4 hours after administration compared with those treated with placebo (69% vs 43% at 2 hours and 76% vs
49% at 4 hours, respectively; both, P < 0.001). Significantly more sumatriptan-treated patients were free from sinus
compared with placebo recipients at 2 hours (63% vs 49% placebo, P = 0.049) and 4 hours (77% vs 55%, P = 0.001). All
treatments were generally well tolerated. The most common drug-related AEs reported in the sumatriptan and placebo groups,
respectively, were dizziness (5% vs < 1%), nausea (3% vs 2%), other pressure/tightness (defined as sense of heaviness;
heaviness of upper body, upper extremities; jaw tension; neck tension) (4% vs 0%), and temperature sensations (defined as
warm feeling of back of neck, or flushing) (2% vs 0%). No patients experienced any serious AEs. CONCLUSIONS:: Sumatriptan
50-mg tablets were effective and generally well tolerated in the treatment of these patients presenting with migraine
headaches that were self-described or physician-diagnosed as sinus headaches.
Journal: Clin Ther. 2007 Jan;29(1):99-109.
Authors: Alstadhaug K, Salvesen R, Bekkelund S.
Department of Neurology, Nordlandssykehuset, Bodo, Norway.
It is a general belief that migraine attacks are prone to occur on days off. Only a few studies, however, have addressed
this issue. The objective of this study was to investigate the periodicity of migraine with respect to weekly (circaseptan)
variations. Eighty-nine females of fertile age who had participated in a previous questionnaire-based study volunteered to
record in detail every migraine attack for 12 consecutive months. Eighty-four patients completed recordings for a mean of
311 days (s.d. = 95.9, range 30-365). A total of 2314 attacks were recorded. Migraine occurrence was almost equally
distributed during the week, except on Sundays, when there were significantly fewer attacks (t = -4.42, d.f. = 83, P <
0.001). A Mantel-Haenszel estimate of the relative risk of having an attack on a holiday vs. another day, not Sundays
included, was 0.64 (95% CI 0.49-0.85). Our study suggests that days off protect against migraine.
Journal: Cephalalgia. 2007 Apr;27(4):343-6.
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