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February 24, 2004; 62 (4) Articles

Triptans in migraine

The risks of stroke, cardiovascular disease, and death in practice

Gillian C. Hall, Martin M. Brown, Jingping Mo, Kenneth D. MacRae
First published February 23, 2004, DOI: https://doi.org/10.1212/01.WNL.0000110312.36809.7F
Gillian C. Hall
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Martin M. Brown
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Jingping Mo
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Kenneth D. MacRae
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Citation
Triptans in migraine
The risks of stroke, cardiovascular disease, and death in practice
Gillian C. Hall, Martin M. Brown, Jingping Mo, Kenneth D. MacRae
Neurology Feb 2004, 62 (4) 563-568; DOI: 10.1212/01.WNL.0000110312.36809.7F

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Abstract

Background: Triptans are widely used to treat migraine but have been associated with stroke, myocardial infarction (MI), and ischemic heart disease (IHD) in case reports.

Objective: To estimate the incidence of stroke, cardiovascular events, and death in a migraine cohort, stratified by triptan prescription, and investigate whether the risk of these events was increased in those treated with triptans.

Methods: Migraine patients and matched nonmigraine control subjects were identified from the General Practice Research Database. Computerized records were searched for triptan prescriptions, stroke, TIA, MI, IHD, death, arrhythmia, and confounding variables. Incidence rates were calculated and migraine groups compared with controls using a Cox model, adjusting for confounders.

Results: Of 63,575 migraine patients, 13,664 were prescribed a triptan. There was no association between triptan prescription and stroke (hazard ratio [HR] 1.13; 95% CI 0.78, 1.65), MI (HR 0.93; 95% CI 0.60, 1.43), or other outcomes studied. The larger group of migraine patients not prescribed a triptan had an increased risk of stroke (HR 1.51; 95% CI 1.26, 1.82) and IHD (HR 1.35; 95% CI 1.18, 1.54) and a decreased risk of all-cause mortality (HR 0.72; 95% CI 0.65, 0.80).

Conclusions: In general practice, triptan treatment in migraine does not increase the risk of stroke, MI, cardiovascular death, IHD, or mortality. Triptans are prescribed to those less at risk of these events.

  • Received June 20, 2003.
  • Accepted October 28, 2003.
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