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Correspondence to:

VIEWS AND REVIEWS:
Marcelo E. Bigal and Richard B. Lipton
Excessive acute migraine medication use and migraine progression
Neurology 2008; 71: 1821-1828 [Abstract] [Full text] [PDF]
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[Read Correspondence] Excessive acute migraine medication use and migraine progression
Nitin K. Sethi, MD   (6 February 2009)

Excessive acute migraine medication use and migraine progression 6 February 2009
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Nitin K. Sethi, MD,
New York Presbyterian Hospital, Weill Cornell Medical Center
525 East 68th Street, New York, NY 10021

Send Correspondence to journal:
Re: Excessive acute migraine medication use and migraine progression

sethinitinmd{at}hotmail.com Nitin K. Sethi, MD

We read with interest the timely article by Bigal et al. commenting on migraine progression due to excessive use of acute migraine medication. [1]

Transformed migraine is common, invariably disabling, and frequently hard to treat. The authors mention that among acute migraine treatments, opiates and barbiturates are associated with progression of migraine to chronic migraine. The critical dose of exposure for opiates is only 8 days per month and 5 days per month for barbiturates which demonstrates that these medications are best avoided in the acute treatment of migraine.

Bigal et al. found anti-inflammatory medications (NSAIDS) protective in those with <10 days of headache. Our experience with migraine patients has been that they frequently underestimate and understate their frequency and duration of NSAID use. NSAIDS are widely available without prescription. They are the most frequently and widely used medications by patients and doctors for acute migraine treatment. In our experience, transformation of episodic migraine to chronic migraine frequently occurs in the setting of excessive NSAID use.

We would stress that migraine pathophysiology is complex and further investigation is needed. In addition, haphazard use of ibuprofen for headache may cause more harm than good.

Reference

1. Bigal ME, Lipton RB. Excessive acute migraine medication use and migraine progression. Neurology 2008; 71:1821-1828.

Disclosure: The author reports no disclosures.

Editor’s Note: The authors of the article were offered the opportunity to respond but declined.


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