[EXCERPTS]
The criteria used to determine the categorization of the recommendations (Do, Do Not Do, and Do Not Know) are defined at the end of the "Major Recommendations" field. In addition, an explanation of the evidence source (i.e., types of evidence and corresponding "seed" guidelines) is also available.
The Guideline Development Group (GDG) considered the balance of benefits and harms for the interventions listed in the Alberta Guideline. Italicized statements relating to harm are included in the recommendations, where appropriate. These statements were sourced from the recommendations or elsewhere in the "seed" guidelines, or were created by the GDG.
Headache Diagnosis and Investigation
Recommendation | Evidence Source | |
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Approach to Headache Diagnosis | ||
Do |
Headache History For the patient presenting with headache for the first time or with a significant change in headache pattern, the headache history should include information on the following:
Refer to Appendix B: Headache History Guide in the original guideline document. |
EO (GDG) |
Do |
Physical Examination Patients presenting to a healthcare provider for the first time with headache, or with a headache that differs from their usual headache, should have a physical examination that includes the following: 1) a screening neurological examination; 2) a neck examination; 3) a blood pressure measurement; 4) a focused neurological examination, if indicated; and 5) an examination for temporomandibular disorders, if indicated. |
CS (G4) |
Do |
Screening Neurological Examination The screening neurological examination should consist of the following:
|
EO (G4) |
Do |
Neck Examination Physical examination of patients with headache should include an assessment of neck posture and range of motion, and palpation for muscle tender points. |
NRCS (G4) |
Do |
Focused Neurological Examination A focused neurological examination should be added if indicated by patient symptoms and/or abnormal signs on the screening examination (e.g., dysarthria would lead to more detailed assessment of lower cranial nerves; reflex asymmetry would lead to assessment of plantar responses). |
EO (GDG) |
Do |
Examination for Temporomandibular Disorders In the patient with headache and associated jaw complaints, the physical examination should include clinical assessment of jaw movements and palpation of the muscles of mastication for tender points. |
EO (GDG) |
Clinical Diagnosis | ||
Primary Headaches | ||
Do |
Patients with recurrent headache attacks and a normal neurological examination (other clinical symptoms may need to be considered as well, in some patients): |
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NRCS (G4) | |
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CS (G4) | |
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CS (G4) | |
Do |
Patients with headache on 15 or more days per month for more than 3 months and with a normal neurological examination: |
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EO (GDG) | |
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EO (GDG) | |
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EO (GDG) | |
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EO (GDG) | |
Do |
Although chronic migraine and chronic tension-type headache may result in continuous headache in some patients, two other less common headache syndromes should be considered in patients with continuous headache. Patients with continuous daily headache for more than 3 months with a normal neurological examination: |
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EO (GDG) | |
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EO (G4) | |
Secondary Headaches | ||
Do |
Cervicogenic headache should be considered in patients with neck pain and occipital head pain, with or without pain radiation to other head regions (or face), when pain is precipitated or aggravated by neck movements or sustained neck postures and there are abnormalities on examination of the neck (abnormal movement, muscle tone, or muscle tenderness). If the headache occurs after neck trauma and persists for more than 3 months, the term "chronic headache attributed to whiplash injury" should be used. Caution: Patients with migraine often complain of neck discomfort during a headache and may have muscular tender points. These appear to be secondary to the migraine pain, and do not necessarily indicate a neck disorder as cause of the headache. |
EO (GDG) |
Do |
Post-traumatic headache should be diagnosed when a new headache disorder begins within 7 days of a head injury. These may occur even after a mild head injury. If the headache persists for more than 3 months, it is termed a chronic post-traumatic headache. |
EO (GDG) |
Do |
Temporomandibular disorder should be considered in patients with headache and/or facial pain who have painful jaw clicking, jaw locking, tenderness of muscles of mastication, tenderness of the temporomandibular joints, or limitation of mandibular movement. |
EO (GDG) |
Diagnosis and Neuroimaging in the Emergent/Urgent Setting | ||
Do |
Emergency Red Flags: (need to be addressed immediately) |
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EO (GDG) | |
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CS (G4) | |
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CS (G4) | |
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NRCS (G4) | |
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CS (G4) | |
Do |
Urgent Red Flags (need investigation and referral within hours to days) |
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G (G4) | |
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NR (G4) | |
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EO (GDG) | |
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EO (GDG) | |
Neuroimaging and Diagnosis in the Outpatient Setting | ||
Do Not Do |
Imaging in Typical Migraine |
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As the diagnostic yield of neuroimaging in patients with typical recurrent migraine attacks is very low, neuroimaging is not indicated in patients with recurrent headaches with the clinical features of migraine, a normal neurological examination, and no red flags for potential causes of secondary headache. |
CS (G4) + qSR (IHE Database) | |
Sinus x-rays and cervical spine x-rays are not recommended for the routine evaluation of the patient with migraine. |
EO (G3) | |
Do |
Atypical Headaches and Changes in Headache Pattern Patients with headaches that do not fit the typical pattern of migraine or tension-type headache, and patients with a major change in headache pattern should be considered for specialist consultation and/or neuroimaging, depending on the clinical judgement of the practitioner. A non-contrast brain CT scan is usually sufficient to rule out a space-occupying lesion as a cause of headache. |
EO (G1) |
Do |
Unexplained Focal Signs in the Patient with Headache |
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Patients with unexplained focal neurological signs and recurrent headache require specialist referral and/or neuroimaging to exclude a space-occupying central nervous system (CNS) lesion. |
CS (G4) + qSR (IHE Database) | |
In the non-urgent setting, brain magnetic resonance imaging (MRI) is the neuroimaging procedure of choice, but a non-contrast brain CT is usually adequate to exclude a space-occupying lesion as a cause of headache. |
G (G4) | |
Do |
Unusual Headache Precipitants |
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Patients with headache clearly precipitated by exertion, cough, or valsalva should be considered for specialist referral and/or a brain MRI scan to exclude a Chiari 1 malformation or a posterior fossa lesion (but it must also be considered that patients with typical migraine may have exertion as one of their headache triggers). |
CS (G4) + qSR (IHE Database) | |
Patients in whom postural change has a major effect on headache intensity need specialist consultation and will require investigation. |
CS (G4) | |
For headache that worsens on standing, brain MRI scanning with gadolinium enhancement may be needed to look for indirect evidence of a CSF leak (dural enhancement, etc.). |
EO (GDG) | |
For headache that worsens on lying down, a brain CT or MRI scan can be used to exclude a space-occupying lesion. As the differential diagnosis includes cerebral venous sinus thrombosis, additional investigation may be required. |
EO (GDG) | |
Do |
Unusual Aura Symptoms For patients with unusual aura symptoms, consider referral to a neurologist for diagnosis and possible investigation. |
EO (GDG) |
Do |
Cluster Headache and Other Uncommon Primary Headache Syndromes In patients with new onset cluster headache or another trigeminal autonomic cephalalgia, hemicrania continua, or new daily persistent headache, specialist referral should be considered for treatment and investigation. |
CS (G4) + qSR (IHE Database) |
Do |
Late Onset Headache For patients with headache that begins after the age of 50 years and who have no other red flags, consider non-contrast brain CT scan for space-occupying lesion and/or complete blood count (CBC), ESR, and CRP to investigate for giant cell (temporal) arteritis. |
NR (G4) |
Do Not Do |
Neuroimaging for Patient Reassurance Clinicians considering neuroimaging primarily for patient reassurance in patients with headache should consider whether this is in the best interest of the patient, and a prudent use of resources, or whether other means of reassurance (i.e., careful explanation of the circumstances, patient education, or specialist referral) would be more advisable. Clinicians requesting neuroimaging should be aware that any imaging study, particularly MRI, can identify incidental findings which may or may not correlate with clinical findings, and which may cause unnecessary patient anxiety. |
RCT (G4) |
Do Not Do |
Electroencephalography (EEG) An EEG is not recommended for the routine evaluation of patients with headache. |
EO (G1, G3) |
Management of Migraine Headache
Recommendations | Evidence Source | |
---|---|---|
General Approach to Management | ||
Do |
Headache Diaries Consider encouraging patients to keep a headache diary to monitor headache frequency, intensity, triggering factors, and medication use. Refer to patient handout, Headache Diary Sheet . |
EO (G3) |
Do |
Additional Assessment of Disability The degree of migraine-related disability present should be assessed clinically. Practitioners may find formal disability scales helpful in selected patients. Headache Impact Test (HIT-6) , and the Migraine Disability Assessment Scale (MIDAS) . |
NRCS (G4) |
Do |
Psychiatric Comorbidities Assessment of patients with migraine should include a clinical evaluation for the presence of significant depression and/or anxiety. If present, these should be treated according to evidence-based mental health recommendations. |
NRCS (G3) |
Lifestyle and Migraine Trigger Management | ||
Do |
Lifestyle Factors Patients should be advised to adjust their lifestyle to avoid exacerbating their migraine (e.g., avoid missing meals; avoid dehydration; maintain adequate, regular sleep). A general exercise program should be considered part of comprehensive migraine management. |
EO (GDG) |
Do |
Specific Migraine Triggers Patients should be advised to consider whether some of the commonly reported migraine triggers, including food triggers, are important for them. A headache diary is helpful in this assessment. Refer to patient handouts: Headache Diary Sheet and Commonly Reported Food Triggers for Migraine Attacks . |
EO (GDG) |
Acute Pharmacological Therapy | ||
Do |
Assessment of the Need to Change a Patient's Acute Migraine Medication Patients should be specifically assessed at follow-up visits to determine if their acute migraine medications need to be changed. |
EO (GDG) |
Do |
Early Treatment of Migraine Attacks Advise patients to take their medication early in their migraine attack, where possible, to improve effectiveness. The strategy may not be appropriate for patients with frequent attacks who are at risk for medication overuse headache (see medication overuse recommendation). For patients with migraine with aura, it is usually advisable to take acute medication just as the headache phase is starting, rather than during the aura, although taking oral medication during the aura appears effective for many patients. |
EO (GDG) |
Do |
Rescue Medication For severe migraine attacks, consider providing an additional rescue medication if the patient's usual acute medication does not work consistently for every attack. |
EO (GDG) |
Acute Medications | ||
Do |
NSAIDs and Acetaminophen Acetylsalicylic acid 1000 mg, ibuprofen 400 mg, and naproxen sodium 500 to 550 mg are recommended for acute treatment in patients with migraine of all severities. Acetaminophen 1000 mg is recommended for acute treatment of migraine attacks of mild to moderate severity. Daily dosage should not exceed 4 grams per day to avoid liver dysfunction. If NSAIDs and/or acetaminophen are not effective by history or after a brief treatment trial, alternative medications (e.g., a triptan) should be tried. |
RCT (G4) + SR (IHE Database) |
NSAIDs can cause gastric irritation and bleeding and renal dysfunction. |
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Do |
Triptans |
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Oral triptans are recommended for acute treatment for all severities of migraine if previous attacks have not been controlled by simple analgesics. If a patient does not respond well to one triptan, a different triptan should be offered. |
SR (G3, G4) | |
Patients with recurrence of their migraine attack after initial relief from a triptan should be advised to take a second dose (within recommended dosage limits), as this is usually an effective strategy. |
RCT (G2) | |
Nasal zolmitriptan 5 mg and nasal sumatriptan 20 mg are recommended for acute treatment for all severities of migraine if previous attacks have not been controlled by simple analgesics. They may be helpful in patients with nausea and where oral triptans have been ineffective. |
SR (G2) | |
Subcutaneous sumatriptan 6 mg should be considered for patients with severe migraine, including those in whom other triptan formulations have been ineffective. It can be particularly helpful where vomiting precludes effective use of the oral route. |
SR (G2) | |
Triptans are vasoconstrictors and should be avoided in patients with cardiovascular disease. |
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Do |
Triptan and NSAID Combinations In patients with an inadequate response to triptans alone, a combination of sumatriptan 50 mg to 100 mg and naproxen sodium 500 to 550 mg may be more effective. This approach may be particularly helpful for patients with prolonged attacks and/or headache recurrence. Although demonstrated only for the sumatriptan-naproxen combination, it might be expected that combinations of naproxen sodium 500 to 550 mg (or other NSAIDs) with other triptans in the usual doses would also be helpful. |
RCT (G4) |
Do |
Antiemetics |
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Metoclopramide (10 mg up to 4 times per day orally) and domperidone (10 mg up to 3 times per day) are recommended to treat nausea and potential emesis in migraine. These drugs may improve the absorption of analgesics. Domperidone has fewer side effects than metoclopramide. |
RCT (G2) | |
Intravenous metoclopramide (10 mg) can be used in the acute treatment of patients with migraine. Side effects include akathisia and dystonia. |
SR (G4) | |
Do |
Dihydroergotamine (DHE) DHE by nasal spray or subcutaneous/intramuscular injection may be considered for patients who do not respond well to triptans. |
RCT (G1, G3) |
Do Not Do |
Ergotamine Ergotamine is not recommended for routine use in patients with acute migraine, although it may be helpful for selected patients where triptans are not an option. |
SR (G4) |
Because it is a vasoconstrictor, it should not be used in patients with cerebrovascular or cardiovascular disease. |
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Do Not Do |
Opioids |
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Opioid analgesics and combination analgesics containing opioids (e.g., codeine) are not recommended for routine use for the treatment of migraine owing to their potential for causing medication overuse headache. |
CS (G4) | |
Opioids may be necessary when other medications are contraindicated or ineffective, or as a rescue medication when the patient's usual medication has failed. |
EO (GDG) | |
For more information on the use of opioids for chronic non-cancer pain, consult the National Guideline Clearinghouse summary of the National Opioid Use Guideline Group's Canadian guideline for safe and effective use of opioids for chronic non-cancer pain (guideline endorsed by the College of Physicians and Surgeons of Alberta). |
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Do Not Do |
Butalbital The use of butalbital-containing combination analgesics in migraine management should be avoided and limited to exceptional circumstances where other acute medications are contraindicated and/or ineffective. When used, they should be carefully monitored to avoid medication overuse (use on less than 10 days per month) and dependence. |
RCT (G1) |
Pharmacological Prophylactic Therapy | ||
Do |
Indications for Migraine Preventive Medication Consider migraine pharmacological prophylactic therapy in the following situations:
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EO (GDG) |
Goals for Migraine Prophylactic Therapy | ||
Do |
Choosing a Specific Migraine Preventive Medication A preventive medication should be chosen based on the following:
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EO (GDG) |
Do |
Prescribing a Migraine Preventive Medication
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EO (G3, G4) |
Medications for Migraine Prophylaxis | ||
Do |
Beta-Blockers The following beta-blockers are recommended for migraine prophylaxis: |
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SR (G2,G4) | |
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RCT (G1) | |
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RCT (G1, G2) | |
Beta-blockers may be helpful in patients with comorbid anxiety. |
G (G4) | |
Side effects of beta-blockers include fatigue and hypotension. They should be avoided or used with caution in patients with asthma, diabetes, bradycardia, and peripheral vascular disease. |
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Do |
Antidepressants |
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Amitriptyline is recommended for migraine prophylaxis:
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RCT (G1, G2, G4) | |
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EO (GDG) | |
Common side effects are dry mouth and sedation. |
G (G4) | |
Venlafaxine 75 mg to 150 mg daily is an alternative to amitriptyline for migraine prophylaxis, although evidence for its efficacy is limited. |
RCT (G2, G4) | |
Nortriptyline can be considered for migraine prophylaxis. The dosage is similar to that of amitriptyline. |
EO (G1) | |
Do Not Do |
Selective serotonin reuptake inhibitors are not recommended in the prophylaxis of migraine. |
SR (G4) |
Do |
Antiepileptics |
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Topiramate 50 mg to 200 mg daily (usual target dose 100 mg daily) is recommended for migraine prophylaxis. |
SR (G4) | |
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SR (G4) | |
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EO (GDG) | |
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EO (GDG) | |
Divalproex sodium 750 mg to 1500 mg daily is recommended for migraine prophylaxis. |
SR (G4) | |
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G (G4) | |
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G (G4) | |
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RCT (G1) | |
Gabapentin (900 to 2400 mg daily) is recommended for migraine prophylaxis. |
RCT (G4) | |
Do |
Vitamins, Minerals and Herbals The following vitamins, minerals, and herbal compounds are recommended for migraine prophylaxis. They may have lower efficacy than drug prophylactics (expert opinion), but all have minimal side effects: |
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RCT (G2) | |
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RCT (G1, G2) | |
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RCT (G1) | |
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RCT (G2) | |
Do Not Do |
Feverfew is not recommended for migraine prophylaxis. |
SR (G4) |
Do |
Other Medications |
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Candesartan 8 mg daily for one week, then 16 mg daily is recommended for migraine prophylaxis. It has few side effects, but experience with this drug in migraine prophylaxis is limited. |
RCT (G2) | |
Pizotifen 1.5 mg to 4 mg daily is recommended for migraine prophylaxis. Side effects are common and include somnolence and weight gain. |
RCT (G1) | |
Flunarizine 10 mg at bedtime is recommended for migraine prophylaxis. It should not be used in patients with a history of depression. Side effects are common and include weight gain and depression. |
RCT (G1, G2) | |
OnabotulinumtoxinA (botulinum toxin A) 155 to 195 Units injected as per protocol every 3 months by clinicians experienced in its use for headache is recommended for prophylaxis of chronic migraine only (migraine with headache on more than 14 days a month). |
EO (GDG) | |
Do Not Do |
NSAIDs are not recommended for migraine prophylaxis. |
EO (GDG) |
Do Not Know |
There is insufficient evidence to recommend for or against the use of verapamil for migraine prophylaxis. |
EO (GDG) |
Non-Pharmacological Therapy | ||
Do |
Relaxation Training, Biofeedback, and Cognitive Behavioural Therapy (CBT) Psychological therapies, including relaxation training, biofeedback, and CBT (alone or in combination), are treatment options for motivated patients with migraine. These therapies are considered to be effective components of stress management training. Specific recommendations regarding which of these therapies to use for specific patients cannot be made. |
SR (G3, IHE Database) |
Do |
Acupuncture Acupuncture can be considered in the prophylactic treatment of patients with migraine. Treatment should consist of at least one to two sessions per week for several (2 or more) months, with each treatment lasting approximately 30 minutes. |
SR (G4, IHE Database) |
Do Not Do |
Homeopathy Homeopathy is not recommended for migraine prophylaxis. |
RCT (G2) |
Do Not Know |
Hyperbaric Oxygen There is insufficient evidence to recommend for or against hyperbaric oxygen for acute treatment of migraine attacks and migraine prophylaxis. Lack of availability and cost would make this therapy impractical for routine use. |
RCT (G1) + SR (IHE Database) |
Do Not Know |
Normobaric Oxygen There is insufficient evidence to recommend for or against the use of 100% normobaric oxygen for acute migraine treatment. |
EO (GDG) |
Do Not Know |
There is insufficient evidence to make a recommendation for or against the use of the following interventions for migraine management: |
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EO (G4) | |
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RCT (G1) | |
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RCT (G4) | |
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SR (G4, IHE Database) | |
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SR (G4) | |
Menstrual Migraine | ||
Do |
Acute Medications The acute treatment of menstrual migraine attacks is similar to the acute treatment of non-menstrual migraine attacks. If patients do not respond to simple analgesics (acetaminophen, NSAIDs), a triptan should be used. |
RCT (G4) + SR (IHE Database) |
Do |
Prophylactic Treatment For patients with refractory menstrual migraine headache, frovatriptan 2.5 mg twice a day can be considered, with frovatriptan administration starting 2 days before the anticipated onset of the menstrually associated migraine attack and continuing for a total of 6 days. |
RCT (G4) + SR (IHE Database) |
Migraine Treatment in Pregnancy | ||
Acute Medications | ||
Do Not Do |
Drugs for migraine should be avoided during pregnancy where possible. |
EO (G4) |
Ergot alkaloids should not be used during pregnancy. |
EO (G2) | |
Do |
When necessary, acetaminophen 1000 mg and metoclopramide 10 mg can be used for the treatment of migraine in pregnancy. As with any medication used during pregnancy, acetaminophen should be taken at the lowest effective dose for the shortest time necessary. The total daily dose should not exceed 4 grams. |
EO (G2, G4) |
Where analgesia beyond acetaminophen is needed, acetaminophen - codeine combination analgesics can be used in pregnancy. |
EO (GDG) | |
Ibuprofen 400 mg can be used for acute migraine attacks during the second trimester of pregnancy. All NSAIDs, including ibuprofen, should be avoided in the third trimester of pregnancy. |
EO (G4) | |
Do Not Know |
The risks associated with the use of sumatriptan during pregnancy appear to be minimal, but there is insufficient evidence to make a recommendation for or against the use of sumatriptan in pregnancy. Sumatriptan should not be used routinely in pregnancy, but may be considered for use when other medications have failed and the benefits outweigh the risks. There is much less information or experience available regarding the safety of the other triptans during pregnancy. |
EO (G2, G4) |
Prophylactic Treatment | ||
Do Not Do |
Preventive drugs for migraine should be avoided during pregnancy where possible. |
EO (GDG) |
Do |
Preventive drugs for migraine should be gradually discontinued prior to the commencement of a planned pregnancy or should be stopped as soon as possible during an unplanned pregnancy. |
EO (GDG) |
When it is necessary to continue migraine prophylaxis during pregnancy, obtaining specialist advice should be considered. |
EO (GDG) |
Management of Tension-Type Headache (TTH)
Recommendation | Evidence Source | |
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Acute Pharmacological Therapy | ||
Do |
The following drugs are recommended for the acute treatment of TTH (use on 15 days a month or more should be avoided):
Combination analgesics containing caffeine are drugs of second choice. Combining caffeine with ibuprofen and acetaminophen increases efficacy, but possibly also the risk for developing medication overuse headache. |
RCT (G6) |
Do Not Do |
The following drugs are not recommended for routine use in acute treatment of TTH: |
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NR (G6) | |
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CS (G6) | |
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RCT (G6) | |
Pharmacological Prophylactic Therapy | ||
Do |
Drug of first choice:
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SR (G4) |
Drugs of second choice: |
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SR (G6) | |
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RCT (G6) | |
Do Not Do |
OnabotulinumtoxinA (botulinum toxin A) is not recommended for prophylaxis of chronic TTH. |
RCT (G4) |
Non-Pharmacological Therapy | ||
Do |
Cognitive Behavioural Therapy (CBT), Biofeedback, and Relaxation Training CBT, biofeedback, and relaxation training may be considered for patients with frequent TTH. |
EO (GDG) |
Do |
Exercise A therapeutic exercise program, based on an assessment by an appropriately trained health professional, may be considered for patients with TTH. |
EO (GDG) |
Do |
Physical Therapy and Acupuncture Physical therapy and acupuncture may be considered for patients with frequent TTH. |
SR (G6) |
Do Not Know |
There is insufficient evidence to make a recommendation for or against the use of the following interventions for the treatment of patients with TTH: |
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EO (GDG) | |
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SR (G4) | |
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SR (G4) | |
TTH Treatment in Pregnancy | ||
Acute Medication | ||
Do Not Do |
Drugs for TTH should be avoided during pregnancy where possible. |
EO (G4) |
Do |
Acetaminophen in a dose of 500 mg to 1000 mg is the treatment of choice in pregnant patients with TTH when headache pain is sufficient to require analgesia. As with any medication used during pregnancy, acetaminophen should be taken at the lowest effective dose for the shortest time necessary. The total daily dose should not exceed 4 grams. |
EO (G4) |
If acetaminophen provides insufficient analgesia, ibuprofen 400 mg can be used in the second trimester of pregnancy. All NSAIDs, including ibuprofen, should be avoided in the third trimester of pregnancy. |
EO (G4) | |
Prophylactic Treatment | ||
Do Not Do |
Preventive drugs for TTH should be avoided during pregnancy where possible. |
EO (GDG) |
Do |
Preventive drugs for TTH should be gradually discontinued prior to the commencement of a planned pregnancy or should be stopped as soon as possible during an unplanned pregnancy. |
EO (GDG) |
Prophylactic treatment for TTH would only rarely be considered necessary in pregnancy. When necessary, obtaining specialist advice should be considered. |
EO (GDG) |
Management of Medication Overuse Headache
Recommendation | Evidence Source | |
---|---|---|
Prevention and General Approach to Management | ||
Do |
Consider a diagnosis of medication overuse headache in patients with headache on 15 days a month or more, and assess the patient for possible medication overuse. |
EO (GDG) |
Do |
When medication overuse headache is suspected, the patient should also be evaluated for the presence of the following: |
NRCS (G4) |
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NRCS (G4) | |
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EO (GDG) | |
Do |
Headache diaries that record acute medication intake should be used by patients with frequent migraine or other headache types to monitor acute medication use. Careful monitoring of acute medication use by both the patient and the physician is important in the prevention of medication overuse headache. Refer to theHeadache Diary Sheet . |
EO (G3) |
Do |
Treatment Treatment plans for the patient with medication overuse headache should include:
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EO (GDG) |
Do |
Headache Prophylaxis Pharmacological prophylaxis should be considered in patients with suspected medication overuse headache, with the prophylactic medication started prior to or during medication withdrawal. Many migraine prophylactics are used (beta-blockers, tricyclics, and others) but topiramate (with the drug titrated slowly to a target dose of 100 mg daily, see migraine prophylaxis section), and OnabotulinumtoxinA (100 to 200 Units injected at intervals of 3 months by clinicians experienced in its use for headache) have the best evidence for efficacy in the setting of chronic migraine with medication overuse. |
EO (GDG) |
Do |
Stopping Medication Overuse Withdrawal of the overused medication should be attempted in all patients with suspected medication overuse headache. For most motivated patients, treatment can be carried out in an outpatient setting. A headache diary should be used to ensure that medication withdrawal targets are being met. Refer to the Headache Diary Sheet . |
EO (GDG) |
Abrupt withdrawal should be advised for patients with suspected medication overuse headache caused by simple analgesics (acetaminophen, NSAIDs) or triptans, although gradual withdrawal is also an option. |
RCT (G4) | |
Gradual withdrawal should be advised for patients with suspected medication overuse headache caused by opioids and opioid-containing analgesics. |
NR (G4) |
Management of Cluster Headache
Recommendation | Evidence Source | |
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Do |
Referral Cluster headache is an uncommon condition and specialist advice should be considered early if the patient is not responding well to therapy or unusual medication doses are required. |
EO (GDG) |
Acute Pharmacological Therapy | ||
Do |
Effective options for the acute treatment of cluster headache attacks are: |
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RCT (G4, G5) | |
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RCT (G4, G5) | |
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NRCS (G5) | |
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RCT (G5) | |
For more information on triptan use (e.g., maximum daily dose, side effects, etc.) see migraine medications see Appendix A: Table A.1. Medications Used for Acute (Symptomatic) Treatment of Migraine in the original guideline document. | ||
Pharmacological Prophylactic Therapy | ||
Do |
For prophylaxis of cluster headache: |
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RCT (G4,G5) | |
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EO (G4) | |
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NRCS (G5) | |
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RCT (G5) | |
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NRCS (G5) |
Other Headache Disorders
Recommendation | Evidence Source | |
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Hemicrania Continua | ||
Do |
Referral Patients with hemicrania continua require specialist referral. |
NR (G4) |
Do |
Pharmacological Therapy Indomethacin (25 mg to 75 mg three times a day) will provide headache relief. Long term use of indomethacin is often problematic because of side effects (gastric irritation and bleeding, and renal dysfunction). |
NR (G4) |
Cervicogenic Headache | ||
Do |
Referral If the headache history and examination of the neck indicates that neck problems may be playing a significant role in the patient's headache, referral to a musculoskeletal therapist or specialist should be considered. |
EO (GDG) |
Non-Pharmacological Therapy | ||
Do |
Exercise Although there is insufficient evidence to recommend any specific exercise for the treatment of cervicogenic headache, a therapeutic exercise program based upon an assessment by an appropriately trained health professional may be considered. |
EO (GDG) |
Do |
Cervical Spinal Manipulation Cervical spinal manipulation, defined as the application of high velocity, low amplitude manual thrusts to the spinal joints slightly beyond the passive range of joint motion, may be considered in the management of patients with cervicogenic headache. |
SR (G4, IHE Database) |
Do |
Cervical Spine Mobilization Cervical spine mobilization, defined as the application of manual force to the spinal joints within the passive range of joint motion that does not involve a thrust, may be considered in the management of patients with cervicogenic headache. |
SR (G4, IHE Database) |
Headache Secondary to Temporomandibular Disorders | ||
Do |
Referral For patients with headache and symptoms and signs of a temporomandibular disorder (TMD), referral to a therapist or specialist in TMD may be appropriate. |
EO (GDG) |
Non-Pharmacological Therapy | ||
Do |
Exercise A therapeutic exercise program based upon an assessment by an appropriately trained health professional may be considered for patients with TMD. |
EO (GDG) |
Definitions:
Summary of Criteria to Determine the Categorization of Recommendations
Do |
|
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Do Not Do |
|
Do Not Know |
|
Evidence Source
Recommendations are based on a review of six "seed" guidelines (referenced as G1 to G6; published between 2000 and 2010) and additional systematic reviews (Institute of Health Economics [IHE] Database), or were created by the GDG based on their collective professional opinion and an analysis of relevant evidence.
Evidence Source Legend
- SR: Systematic Review
- qSR: Quasi-Systematic Review
- RCT: Randomized Control Trial
- NRCS: Non-Randomized Comparative Study
- CS: Case Series Study
- G: Guideline
- NR: Narrative Review
- EO: Expert Opinion as cited by the seed guideline(s)
- EO (GDG): collective EO of the Ambassador GDG
- IHE: Institute of Health Economics
"Seed" Guidelines"
The guidelines are not presented in any specific order. G1, G2, etc., are randomly assigned and for the purpose of organization only.
G1 |
Frishberg BM, Rosenberg JH, Matchar DB, McCrory DC, Pietrzak MP, et al. Evidence based guidelines in the primary care setting: neuroimaging in patients with non-acute headache. St Paul, MN: US Headache Consortium; 2000. Available from:http://tools.aan.com/professionals/practice/pdfs/gl0088.pdf (accessed July 3, 2012). Matchar DB, Young WB, Rosenberg JH, Pietrzak MP, Silberstein SD, et al. Evidence-based guidelines for migraine headache in the primary care setting: pharmacological management of acute attacks. St Paul, MN: US Headache Consortium; 2000. Available from: http://tools.aan.com/professionals/practice/pdfs/gl0087.pdf (accessed July 3, 2012). Ramadan NM, Silberstein SD, Freitag FG, Gilbert TT, Frishberg BM. Evidence-based guidelines for migraine headache in the primary care setting: pharmacological management for prevention of migraine. St Paul, MN: US Headache Consortium; 2000. Available from: ttp://tools.aan.com/professionals/practice/pdfs/gl0090.pdf (accessed July 3, 2012). Campbell JK, Penzien DB, Wall EM. Evidence-based guidelines for migraine headache: behavioral and physical treatments. St Paul, MN: US Headache Consortium; 2000. Available from: http://tools.aan.com/professionals/practice/pdfs/gl0089.pdf (accessed July 3, 2012). |
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G2 |
Evers S, Afra J, Frese A, Goadsby PJ, Linde M, May A, et al. EFNS guideline on the drug treatment of migraine - revised report of an EFNS task force. European Journal of Neurology 2009;16(9):968-81. |
G3 |
Géraud G, Lantéri-Minet M, Lucas C, Valade D. French Society for the Study of Migraine Headache (SFEMC). French guidelines for the diagnosis and management of migraine in adults and children. Clinical Therapeutics 2004;26(8):1305-18. |
G4 |
Scottish Intercollegiate Guidelines Network (SIGN). Diagnosis and management of headache in adults. A national clinical guideline. SIGN Publication No. 107. Edinburgh: SIGN; 2008. Available from:http://www.sign.ac.uk/guidelines/fulltext/107/index.html (accessed July 3, 2012). |
G5 |
May A, Leone M, Afra J, Linde M, Sandor PS, Evers S, et al. EFNS guidelines on the treatment of cluster headache and other trigeminal-autonomic cephalalgias. European Journal of Neurology 2006;13(10):1066-77. |
G6 |
Bendtsen L, Evers S, Linde M, Mitsikostas DD, Sandrini G, Schoenen J. EFNS guideline on the treatment of tension-type headache - Report of an EFNS task force. European Journal of Neurology 2010;17(11):1318-25. |
An algorithm for management of headache in adults titled "Quick Reference Guide" is provided in Appendix B of the original guideline document.
Definitions: Summary of Criteria to Determine the Categorization of Recommendations/Evidence Source Legend [available online]
[Free full-text Guideline for Primary Care Management of Headache in Adults PDF | National Guideline Clearinghouse version]
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