A cluster headache is one-sided head pain that may involve tearing of the eyes and a stuffy nose. Attacks occur regularly for 1 week to 1 year, separated by long pain-free periods that last at least 1 month, possibly longer.
Histamine headache; Headache - histamine; Migrainous neuralgia; Headache - cluster; Horton's headache
Cluster headaches are a fairly common form of chronic, repeated headaches. They are four times more common in men than women. The headaches can occur at any age but are most common in adolescence and middle age. They tend to run in families, passed down through genes.
Scientists do not know exactly what causes cluster headaches, but they appear to be related to the body's sudden release of histamine or serotonin. A problem in a small area at the base of the brain called the hypothalamus may be involved.
The following may trigger cluster attacks:
A cluster headache begins as a severe, sudden headache. The headache most commonly strikes 2 to 3 hours after you fall asleep. However, the headache may occur while you are awake. The headache tends to occur at the same time of day.
The pain occurs on one side of the head. It may be described as:
The pain may occur in, behind, and around one eye. It may:
The strongest pain may last 30 minutes to 2 hours.
The eye and nose on the same side as the head pain may also be affected. Symptoms can include:
Cluster headaches may occur daily for months, alternating with periods without headaches (episodic), or they can recur for a year or more without stopping (chronic).
Your health care provider can diagnose this type of headache by performing a physical exam and asking questions about your symptoms and medical history.
If a physical exam is done during an attack, the exam will usually reveal Horner syndrome (one-sided eyelid drooping or a small pupil). These symptoms will not be present at other times. No other nervous system (neurological) changes will be seen.
Tests, such as an MRI of the head, may be needed to rule out other causes of the headaches.
Treatment for cluster headaches involves:
TREATING CLUSTER HEADACHES WHEN THEY OCCUR
Your doctor may recommend the following treatments for when the headaches occurs:
You may need more than one of these treatments to control headache symptoms. Your doctor may have you try several medications before deciding which works best for you.
Painkillers and narcotics do not usually relieve the pain from cluster headaches. Generally, they take too long to work.
PREVENTING CLUSTER HEADACHES
Avoid smoking, alcohol use, certain foods, and other factors that seem to trigger your cluster headaches. A headache diary can help you identify your headache triggers. When you get a headache, write down the day and time the pain began. The diary should include notes about:
The headaches may go away on their own, or you may need treatment to prevent them. The following medications may also be used to treat or prevent headache symptoms:
In rare cases, a device that delivers tiny electrical signals to a certain nerve near the brain may be placed. This device is called a neurostimulator. However, it is not yet an established therapy for cluster headaches.
Cluster headaches are not life threatening and usually cause no permanent changes to the brain. However, they are chronic and often painful enough to interfere with work or lifestyle. Rarely, the pain may be so severe that some people may consider harming themselves.
Call for an appointment with your health care provider if:
Danger symptoms require immediate medical care. Some of these symptoms include:
If prone to cluster headache, stop smoking. Alcohol use and any foods that are associated with cluster headache may need to be avoided. Medications may prevent cluster headaches in some cases.
Francis GJ, Becker WJ, Pringsheim TM. Acute and preventive pharmacologic treatment of cluster headache. Neurology. 2010;75(5):463-473.
Law S, Derry S, Moore RA. Triptans for acute cluster headache. Cochrane Database Syst Rev. 2010;(4)::CD008042.
Silberstein SD, Young WB. Headache and facial pain. In: Goetz CG. Textbook of Clinical Neurology. 3rd ed. St. Louis, Mo: WB Saunders; 2007:chap 53.