4.7 Article

Evidence-based guideline update: NSAIDs and other complementary treatments for episodic migraine prevention in adults Report of the Quality Standards Subcommittee of the American Academy of Neurology and the American Headache Society

Journal

NEUROLOGY
Volume 78, Issue 17, Pages 1346-1353

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1212/WNL.0b013e3182535d0c

Keywords

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Funding

  1. American Academy of Neurology
  2. American Headache Society
  3. Albert Einstein College of Medicine
  4. AGA
  5. Allergan
  6. Boston Scientific
  7. Capnia
  8. Coherex
  9. Endo Pharmaceuticals
  10. GlaxoSmithKline
  11. Lilly
  12. MAP
  13. Medtronic
  14. Merck
  15. NINDS
  16. NuPathe
  17. St. Jude Medical
  18. Valeant Pharmaceuticals
  19. Advanced Neurostimulation Systems
  20. St Jude Medical, Inc.
  21. NINDS/NIH
  22. Mayo Clinic
  23. Forest Laboratories
  24. Eli Lilly
  25. Neurogesx
  26. Pfizer
  27. NIH

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Objective: To provide updated evidence-based recommendations for the preventive treatment of migraine headache. The clinical question addressed was: Are nonsteroidal anti-inflammatory drugs (NSAIDs) or other complementary treatments effective for migraine prevention? Methods: The authors analyzed published studies from June 1999 to May 2009 using a structured review process to classify the evidence relative to the efficacy of various medications for migraine prevention. Results: The author panel reviewed 284 abstracts, which ultimately yielded 49 Class I or Class II articles on migraine prevention; of these 49, 15 were classified as involving nontraditional therapies, NSAIDs, and other complementary therapies that are reviewed herein. Recommendations: Petasites (butterbur) is effective for migraine prevention and should be offered to patients with migraine to reduce the frequency and severity of migraine attacks (Level A). Fenoprofen, ibuprofen, ketoprofen, naproxen, naproxen sodium, MIG-99 (feverfew), magnesium, riboflavin, and subcutaneous histamine are probably effective for migraine prevention (Level B). Treatments considered possibly effective are cyproheptadine, Co-Q10, estrogen, mefenamic acid, and flurbiprofen (Level C). Data are conflicting or inadequate to support or refute use of aspirin, indomethacin, omega-3, or hyperbaric oxygen for migraine prevention. Montelukast is established as probably ineffective for migraine prevention (Level B). Neurology (R) 2012; 78: 1346-1353

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