Treatment of Severe, Disabling Migraine Attacks in an Over-The-Counter Population of Migraine Sufferers: Results From Three Randomized, Placebo-Controlled Studies of the Combination of Acetaminophen, Aspirin, and Caffeine

Author:

Goldstein J1,Hoffman HD2,Armellino JJ2,Battikha JP2,Hamelsky SW2,Couch J3,Blumenthal H4,Lipton RB5

Affiliation:

1. San Francisco Headache Clinic

2. San Francisco, CA, USA; Bristol-Myers Squibb Company

3. Hillside, NJ, USA; Oklahoma University Neurological Center

4. Oklahoma City, OK, USA; Neurological Associates of Tulsa

5. Tulsa, OK, USA; and Albert Einstein College of Medicine, Montefiore Headache Unit, Bronx, NY and Innovative Medical Research, Stamford, CT, USA

Abstract

Objective: To examine the benefits of acetaminophen, aspirin, and caffeine (AAC) in the treatment of severe, disabling migraine attacks, in a population of migraine sufferers for whom over-the-counter (OTC) medications are appropriate. Background: Subjects ( n = 1220) who met the International Headache Society criteria for migraine with or without aura were included in three independent clinical studies. Designl Methods: Post-hoc analysis of 172 subjects who met the criteria for severe, disabling migraine reported a history of migraine attacks characterized by at least severe pain and severe disability, and treated attacks with severe pain and at least severe disability. Subjects who usually vomited with 20% or more of their migraine attacks, and those with incapacitating disability (subjects who required bed rest for more than 50% of their attacks) were not eligible for enrollment. Results: From 1 h and continuing through 6 h postdose, the proportion of responders was significantly greater ( p≤0.01) for AAC than placebo. The pain intensity difference from baseline was significantly greater ( p≤0.05) for AAC than placebo from 0.5 h through 6 h. The proportion of subjects reporting improvement in functional disability, photophobia, and phonophobia was significantly greater for AAC than placebo from 2 h through 6 h postdose. Conclusions: The nonprescription combination of AAC was well tolerated and effective.

Publisher

SAGE Publications

Subject

Clinical Neurology,General Medicine

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