Department of Clinical Pharmacology, Odense University Hospital, Odense, Denmark.
Department of Radiology, University Hospital of Southern Denmark, Odense, Denmark.
JAMA Neurol. 2024 Mar 1;81(3):248-254. doi: 10.1001/jamaneurol.2023.5549.
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.
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.
Initiation of any triptan.
Acute myocardial infarction, ischemic stroke, or nonspecified stroke.
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.
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.
曲坦类药物禁用于缺血性心脏病或既往心肌梗死患者,并且在为有血管危险因素的患者开处方时应谨慎。然而,对照观察性研究表明,两者之间没有关联,或者关联风险明显较低,这可能是由于曲坦类药物被分配给了心血管结局风险较低的个体,目前尚不清楚避免这些患者使用曲坦类药物是否有意义。
使用自我对照设计来确定曲坦类药物与缺血性事件之间是否存在关联,因为这种设计对于先前提到的混杂因素具有很强的稳健性。
设计、环境和参与者:在全国性的丹麦注册中心中,所有开始使用曲坦类药物的患者以及他们经历的所有缺血性事件都被确定。使用病例交叉设计来估计首次使用曲坦类药物与缺血性结局之间的比值比(OR),将事件前 2 周的曲坦暴露与 4 个 2 周的参考期进行比较。数据来源于 1995 年 1 月至 2022 年 8 月的丹麦人群。该人群包括服用任何一种曲坦类药物且至少发生了 3 种预先定义的缺血性结局之一的个体。没有人被排除在外。
任何曲坦类药物的起始使用。
急性心肌梗死、缺血性卒中和未特指的卒中。
研究期间共确定了 429612 名(中位[IQR]年龄,38[28-48]岁;325687 名女性[75.8%])首次开处方使用曲坦类药物的个体。其中,11 名患者(0.003%)在第一次开曲坦类药物处方时,在局部或参考窗口发生了心肌梗死(比值比[OR],3.3;95%CI,1.0-10.9),18 名患者(0.004%)发生了缺血性卒(OR,3.2;95%CI,1.3-8.1),35 名患者(0.008%)发生了缺血性/未特指的卒(OR,3.0;95%CI,1.5-5.9)。病例患者的中位年龄约为 60 岁,且具有较高的心血管风险特征。
这项病例交叉研究的结果表明,曲坦类药物的起始使用与缺血性卒中和心肌梗死的风险增加相关。对于低背景心血管风险的个体患者,曲坦类药物起始使用后发生缺血性事件的风险非常低。