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In a case-control study, Wammes-van der Heijden et al. investigated whether the intensity of triptan and ergotamine use is associated with the risk of ischemic complications. Triptan overuse did not increase this risk. Overuse of ergotamine proved to be a risk factor, especially in patients with concomitant use of cardiovascular drugs (8.5-fold increase).
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Triptan and ergotamine overuse in patients with headache at risk for vasoconstrictive complications
Commentary by Mark Obermann, MD, and Zaza Katsarava, MD, PhD, MSc
Medication overuse headache (MOH) has developed into the third most common type of headache after tension-type headache (TTH) and migraine. The prevalence of MOH is approximately 1% of the worlds population and may be increasing: recent studies show that it occurs at all ages, often starting in childhood. Virtually any anti-headache drug is capable of inducing MOH1: triptans, ergots, opioids, and other analgesics, as well as commonly used combinations
The study by Wammes-van der Heijden et al. reviews the possible risk of vasoconstrictive complications in patients with MOH using triptans and ergots. They found that triptan overuse was not associated with an increased risk for vasoconstrictive complications, even in patients with concomitant cardiovascular risk factors, while patients who overused ergotamine had a two times higher risk for ischemic complications. The risk of ergotamine was increased almost fourfold in patients with additional cardiovascular risk factors.
This study has methodologic limitations: ICD-9 codes may not accurately reflect the patients diagnosis; exact time period of triptan and ergotamine intake could not be defined; possible confounders were not well controlled, e.g., type of associated risk factors, possible interactions of co-medication. However, the study contributes important information on the safety of triptan use in clinical neurology practice and underlines the apparent dangers associated with ergotamine in headache treatment especially in older patients at risk for cardiovascular complications. The prevalence for MOH in the general population is on the rise in all age groups.2 In the past triptans may have been prescribed less frequently because of concerns about their cardiovascular side effects.3 If the concerns about cardiovascular side effects are unwarranted, wider use of triptans might prevent the development of MOH.
This study was not able to distinguish among cerebral, coronary, and peripheral vasoconstrictive events and could not quantify the safety in low vs high cardiovascular risk patients. Therefore, triptan prescription still has to be carefully evaluated for the individual patient. General recommendations cannot be given until further, prospective research is conducted. This study suggests that a prospective trial of triptans is justified in patients who would previously have been excluded from treatment.
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References
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