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. 2024 Mar 1;81(3):248-254.
doi: 10.1001/jamaneurol.2023.5549.

Risk of Stroke and Myocardial Infarction Among Initiators of Triptans

Affiliations

Risk of Stroke and Myocardial Infarction Among Initiators of Triptans

Christian Lund Petersen et al. JAMA Neurol. .

Abstract

Importance: Triptans are contraindicated in patients with ischemic heart disease or previous myocardial infarction, and caution is advised when prescribing these drugs to patients with vascular risk factors. However, controlled observational studies have either shown no association or an apparent lower risk, possibly owing to a channeling of triptans to individuals at low risk of cardiovascular outcomes, and it remains unclear whether avoiding triptan treatment for these patients is meaningful.

Objective: To establish whether an association between triptans and ischemic events could be demonstrated using a self-controlled design because this type of design is robust to the previously mentioned type of confounding.

Design, setting, and participants: All people in nationwide Danish registries who were initiating triptans and all the ischemic events that they experienced were identified. A case-crossover design was used to estimate odds ratios (OR) for associations between first-ever triptan use and ischemic outcomes, comparing triptan exposure in the 2-week period up to the event with four 2-week reference periods. Data were obtained for the period January 1995 to August 2022. Included from the population of Denmark were individuals redeeming a prescription for any triptan and experiencing at least 1 of 3 predefined ischemic outcomes. No one was excluded.

Exposure: Initiation of any triptan.

Main outcomes and measures: Acute myocardial infarction, ischemic stroke, or nonspecified stroke.

Results: Identified were a total of 429 612 individuals (median [IQR] age, 38 [28-48] years; 325 687 female [75.8%]) who redeemed a first prescription for a triptan in the study period. Of these patients, 11 (0.003%) had a myocardial infarction with the first triptan prescription in either a focal or referent window (odds ratio [OR], 3.3; 95% CI, 1.0-10.9), 18 (0.004%) had ischemic stroke (OR, 3.2; 95% CI, 1.3-8.1), and 35 (0.008%) had ischemic/nonspecified stroke (OR, 3.0; 95% CI, 1.5-5.9). Case patients had a median age of approximately 60 years and had a high-risk cardiovascular profile.

Conclusions and relevance: Results of this case-crossover study suggest that triptan initiation was associated with higher risk of ischemic stroke and myocardial infarction. For the individual patient with low background cardiovascular risk, the risk of an ischemic event after triptan initiation was very low.

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Conflict of interest statement

Conflict of Interest Disclosures: Dr Hougaard reported receiving speaker honoraria from AbbVie, Novartis, Teva, Lundbeck, Pfizer, and Eli Lilly outside the submitted work. Dr Gaist reported receiving speaker honoraria from Bristol Myers Squibb and Pfizer outside the submitted work. No other disclosures were reported.

Figures

Figure.
Figure.. Schematic Representation of the Case-Crossover Sampling Method With 4 Case Examples
Case 1 has an exposure in one of the reference windows and is not exposed during the focal window, while the opposite is true of case 2. Case 3 has no exposures in either the focal window or reference windows and does not contribute to the analysis. Like case 1, case 4 has an exposure in a reference window and contributes to the analysis in the same way as case 1 with regard to exposure status.

References

    1. Tfelt-Hansen P. Pharmacological strategies to treat attacks of episodic migraine in adults. Expert Opin Pharmacother. 2021;22(3):305-316. doi:10.1080/14656566.2020.1828347 - DOI - PubMed
    1. Rubio-Beltrán E, Labastida-Ramírez A, Villalón CM, MaassenVanDenBrink A. Is selective 5-HT1F receptor agonism an entity apart from that of the triptans in antimigraine therapy? Pharmacol Ther. 2018;186:88-97. doi:10.1016/j.pharmthera.2018.01.005 - DOI - PubMed
    1. Barra S, Lanero S, Madrid A, et al. . Sumatriptan therapy for headache and acute myocardial infarction. Expert Opin Pharmacother. 2010;11(16):2727-2737. doi:10.1517/14656566.2010.522567 - DOI - PubMed
    1. Welch KM, Mathew NT, Stone P, Rosamond W, Saiers J, Gutterman D. Tolerability of sumatriptan: clinical trials and postmarketing experience. Cephalalgia. 2000;20(8):687-695. doi:10.1046/j.1468-2982.2000.00116.x - DOI - PubMed
    1. Macintyre PD, Bhargava B, Hogg KJ, Gemmill JD, Hillis WS. The effect of IV sumatriptan, a selective 5-HT1-receptor agonist, on central haemodynamics and the coronary circulation. Br J Clin Pharmacol. 1992;34(6):541-546. - PMC - PubMed

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