There are many different types of headache. A migraine is a type of headache where the person often has an intense throbbing headache and additional symptoms such as nausea, vomiting or increased sensitivity to bright light, noise or smell.
There are two recognised forms of migraine. A migraine is often described as a classic migraine with ‘aura’ if the person gets some form of visual distortions prior to the headache. These visual distortions are often in the form of zigzag or flashing patterns across their vision. Non-classic or common migraine does not have this aura.
Migraines are thought to be caused by changes in the chemicals of the brain, in particular serotonin. Serotonin levels are believed to decrease during a migraine, which can cause the blood vessels in the brain to spasm and then dilate, causing the headache. Other triggers can be hormonal changes, certain food items, environmental situations, emotions, stress and physical triggers (for example muscular tension or poor sleep).
Acute migraines are usually treated using painkillers and anti-sickness medications. For people whose migraine does not respond to over-the-counter medications, stronger painkillers may be prescribed by a doctor. If a person suffers from regular debilitating migraines they may need to be prescribed preventative (prophylactic) medications, which they take to stop them getting migraines. There are various drugs currently prescribed for migraine prophylaxis, including beta-blockers and certain antidepressants or anticonvulsants.
The National Institute for Health and Clinical Excellence (NICE) looked at a systematic review that had identified all randomised controlled trials comparing the toxin type A with placebo for people with chronic headache. Two large trials were identified, and in both of these trials, the injections reduced the frequency of headache days, which was the main trial outcome that the researchers were interested in. The injections also helped to improve quality of life on validated scales, but was no more effective than placebo in reducing the use of painkillers to treat acute pain.
In the reviewed trials the most frequently reported adverse reaction were neck pain, headache, migraine, eyelid drooping, muscular stiffness and muscular weakness. Neck pain was the only adverse effect that occurred at a rate of 5% or more in the toxin type A groups compared with the placebo groups. Other recognised adverse effects are itching, injection site pain and other muscular effects such as aching, tightness or spasms.
The manufacturer’s summary of product characteristics states that “in general, adverse reactions occur within the first few days following injection and, while generally transient, may have a duration of several months or, in rare cases, longer”.
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