» Articles » PMID: 19586594

Overuse of Acute Migraine Medications and Migraine Chronification

Overview
Date 2009 Jul 10
PMID 19586594
Citations 48
Authors
Affiliations
Soon will be listed here.
Abstract

Among individuals with episodic migraine, the influence of excessive acute medication use on the development of chronic migraine depends upon within-person characteristics (eg, headache frequency), class of drug, and frequency of medication use. Available data suggest that opioids induce migraine chronification (progression), and the effect is dose dependent (critical dose around 8 days of exposure per month) and more pronounced in men. Barbiturates also induce migraine progression, and the effect is dose dependent (critical dose around 5 days of exposure per month) and more pronounced in women. Triptans induce migraine progression only in those with high migraine frequency at baseline (10-14 days per month), but not overall. NSAIDs protect against migraine progression unless individuals have 10 or more headache days per month (when they become inducers, rather than protective). Finally, caffeine-containing over-the-counter products increase risk of progression. While we await randomized trials, these findings should inform the choice of acute migraine treatments with the goal of reducing the risk of migraine progression to chronic migraine.

Citing Articles

Erenumab escalation in migraine - double dose without additional benefit - a retrospective experience.

Heintz S, Storch P, Burow P, Maier P, Obermann M, Stoessel G Acta Neurol Belg. 2024; 124(5):1663-1670.

PMID: 39066884 PMC: 11615020. DOI: 10.1007/s13760-024-02603-z.


A Narrative Review of Intestinal Microbiota's Impact on Migraine with Psychopathologies.

Francavilla M, Facchetti S, Demartini C, Zanaboni A, Amoroso C, Bottiroli S Int J Mol Sci. 2024; 25(12).

PMID: 38928361 PMC: 11203823. DOI: 10.3390/ijms25126655.


Comparative effectiveness of erenumab versus rimegepant for migraine prevention using matching-adjusted indirect comparison.

Mahon R, Tiwari S, Koch M, Ferraris M, Betts K, Wang Y J Comp Eff Res. 2024; 13(3):e230122.

PMID: 38174577 PMC: 10945420. DOI: 10.57264/cer-2023-0122.


Multimodal Migraine Management and the Pursuit of Migraine Freedom: A Narrative Review.

Blumenfeld A, Lipton R, Silberstein S, Tepper S, Charleston 4th L, Landy S Neurol Ther. 2023; 12(5):1533-1551.

PMID: 37542624 PMC: 10444724. DOI: 10.1007/s40120-023-00529-x.


L-arginine and aged garlic extract for the prevention of migraine: a study protocol for a randomised, double-blind, placebo-controlled, phase-II trial (LARGE trial).

Chaliha D, Vaccarezza M, Corti E, Takechi R, Dhaliwal S, Drummond P BMC Neurol. 2023; 23(1):122.

PMID: 36973718 PMC: 10041759. DOI: 10.1186/s12883-023-03149-y.


References
1.
Scher A, Stewart W, Liberman J, Lipton R . Prevalence of frequent headache in a population sample. Headache. 2004; 38(7):497-506. DOI: 10.1046/j.1526-4610.1998.3807497.x. View

2.
King T, Ossipov M, Vanderah T, Porreca F, Lai J . Is paradoxical pain induced by sustained opioid exposure an underlying mechanism of opioid antinociceptive tolerance?. Neurosignals. 2005; 14(4):194-205. DOI: 10.1159/000087658. View

3.
Bigal M, Lipton R . Excessive acute migraine medication use and migraine progression. Neurology. 2008; 71(22):1821-8. DOI: 10.1212/01.wnl.0000335946.53860.1d. View

4.
Sullivan L, Chawarski M, OConnor P, Schottenfeld R, Fiellin D . The practice of office-based buprenorphine treatment of opioid dependence: is it associated with new patients entering into treatment?. Drug Alcohol Depend. 2005; 79(1):113-6. DOI: 10.1016/j.drugalcdep.2004.12.008. View

5.
Bigal M, Lipton R . Modifiable risk factors for migraine progression. Headache. 2006; 46(9):1334-43. DOI: 10.1111/j.1526-4610.2006.00577.x. View