TY - JOUR
T1 - Treatment of severe, disabling migraine attacks in an over-the-counter population of migraine sufferers
T2 - Results from three randomized, placebo- controlled studies of the combination of acetaminophen, aspirin, and caffeine
AU - Goldstein, J.
AU - Hoffman, H. D.
AU - Armellino, J. J.
AU - Battikha, J. P.
AU - Hamelsky, S. W.
AU - Couch, J.
AU - Blumenthal, H.
AU - Lipton, R. B.
PY - 1999/10/14
Y1 - 1999/10/14
N2 - 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. Design/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.
AB - 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. Design/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.
UR - http://www.scopus.com/inward/record.url?scp=0032832122&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0032832122&partnerID=8YFLogxK
U2 - 10.1046/j.1468-2982.1999.019007684.x
DO - 10.1046/j.1468-2982.1999.019007684.x
M3 - Article
C2 - 10524663
AN - SCOPUS:0032832122
SN - 0333-1024
VL - 19
SP - 684
EP - 691
JO - Cephalalgia
JF - Cephalalgia
IS - 7
ER -