FDA approved indications:
Non-FDA approved indications:
The American Headache Society and the American Academy of Neurology: 2012 evidence-based guideline update indicated that Petasites (butterbur) demonstrates effectiveness for migraine prevention and is a valid option for patients with migraine to reduce both the severity and frequency of migraine attacks (Level A). The recommendation was questioned and then retracted in 2016.
Butterbur (leaves of Petasites japonicus) has been found to be effective in the prophylaxis of adult migraines in multiple studies. Based on these trials, the American Headache Society gave the herb a level A recommendation and declared it to be effective in the prevention of migraine headaches. Similarly, the Canadian Headache Society guidelines give butterbur a strong recommendation for use in migraine prophylaxis. Although the American Academy of Neurology recommended butterbur, it has retracted its current guidelines on it. In the United Kingdom and Germany, butterbur is not authorized for official use due to concerns about safety. In one randomized, parallel-group study from 2004, the group given butterbur had a response rate of 45% whereas the group who used placebo had a response rate of 15%. In another randomized controlled trial from 2004, butterbur reduced the frequency of migraines by 48% in the experimental group whereas the placebo reduced the frequency by 26% in the control group.
Similar to adult migraines, there is evidence for Petasites in the prevention of pediatric migraines. In one randomized controlled trial from 2005, butterbur reduced the frequency of attacks by at least 50% in 77% of the pediatric experimental group. In another randomized controlled trial from 2008, butterbur reduced the frequency of attacks by 59% in the experimental group whereas the placebo reduced the frequency of attacks by 31% in the control group.
Butterbur has been used in countries in Asia as a herbal treatment of asthma and allergic diseases.There is a limited body of evidence from randomized controlled trials that butterbur may be useful as a therapy for asthma and allergic rhinitis, but not as effective as in the prevention of migraine.
Studies have found that butterbur may potentially be effective in the treatment of Alzheimer's disease due to its neuroprotective effect. However, only studies involving in vitro and in vivo models have been performed.
Mechanism of action for the treatment of migraines:
Mechanism of action for the treatment of Asthma and Allergic Rhinitis:
Mechanism of action for the treatment of Alzheimer's:
Butterbur is given almost exclusively via oral administration. The recommended daily dose is between 50mg to 150mg.
Previous randomized controlled trials have found no serious adverse effects and good overall tolerance of the drug. Minor effects include gastrointestinal symptoms (belching is most common), dyspepsia, headache, itchy eyes, drowsiness, fatigue, and asthma. Long-term use of butterbur may rarely lead to cholestatic hepatitis (estimated incidence of 1:175,000). Patients who are allergic to ragweed and daisies may also have similar allergic reactions to butterbur.
One major area of concern with regards to safety is with pyrrolizidine alkaloids which are commonly found in the butterbur plant. These substances can cause hepatotoxicity, lung toxicity, carcinogenesis, and thrombosis. Fortunately, the commercial preparation process of butterbur typically removes these substances. Thus, it is recommended for consumers of butterbur to only buy brands that are free of alkaloids and other plant carcinogens.
Severe hepatotoxicity may be associated with butterbur use, but the evidence is unclear. From the World Health Organization's Vigibase, one study reported 40 cases of hepatotoxicity including two liver transplants associated with the use of Petasites formulations. However, these cases may be the result of the use of butterbur contaminated with alkaloids. Another article reported detecting levels of toxic alkaloids in seven out of 21 commercially available compounds. Therefore, at least some brands are inadequately removing alkaloids from their butterbur formulations. In summary, it is unclear if hepatotoxicity is due to alkaloids in the formulation or the butterbur itself. To evaluate the hepatotoxic effects of butterbur more clearly a future study can collect data on brands that claims to be alkaloid-free, by thoroughly reviewing the literature and the Periodic Update Safety Report. The data can then be analyzed with the Roussel Uclaf Causality Assessment Method test to determine if butterbur carries an association with hepatotoxicity.
Butterbur use is contraindicated in patients using anticholinergic medications. Also, there have not been studies establishing safety criteria in children under six years of age, pregnant or lactating women. Therefore, butterbur use is not recommended in these groups.
The list of side effects of butterbur is in the adverse effects section. Long-term use of butterbur may rarely lead to reversible cholestatic hepatitis (estimated incidence of 1:175,000). Butterbur may also interact with anticholinergic medications. There is no known antidote for butterbur overdose. The recommendation in such cases is to cease using the drug.
There have been no formal studies examining interprofessional care and its relationship to butterbur. Nevertheless, close coordination amongst physicians, nurses, pharmacists, and other healthcare providers is recommended to monitor for side effects and interactions with other medications especially anticholinergics. As a herbal remedy, butterbur may often not appear on a patient's official prescribed medication list. Therefore, it is essential for every healthcare provider to inquire about alternative or natural remedies when interviewing patients and record it in the patient's chart.
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