Department of Pharmacy, Iowa City Veterans Affairs Health Care System, Iowa City, IA, USA.
Department of Internal Medicine, University of Iowa Carver College of Medicine, Iowa City, IA, USA.
J Asthma. 2022 Dec;59(12):2360-2366. doi: 10.1080/02770903.2021.2018705. Epub 2022 Jan 3.
Neuropsychiatric events (NEs) reported with montelukast during post-marketing surveillance by the US Food & Drug Administration resulted in a 2008 safety alert and a black box warning in 2020. Our objective was to evaluate montelukast exposure and NEs risk using sequence symmetry analysis.
National Veterans Health Administration (VHA) administrative data were used to identify 11 840 patients prescribed incident montelukast during fiscal year 2014. Incident prescribing of neuropsychiatric medication was used as a proxy marker for incident NEs and included antidepressants, benzodiazepines, hypnotics, antipsychotics, mood stabilizers, and buspirone. Symmetry ratios were calculated as the ratio of patients with an incident neuropsychiatric event in the year following montelukast initiation to the year preceding initiation. Exposure counterfactual analyses were used to examine the relationship between potential therapeutic alternatives to montelukast and risk for NEs.
Incident NEs were observed in 2305 patients following montelukast initiation and 2734 patients preceding montelukast initiation (SR 0.84, 95% CI 0.80-0.89). Sensitivity analyses examining each of the 6 sub-types of psychiatric medications also failed to show increased risk of NEs following montelukast initiation. Therapeutic alternatives to montelukast, such as inhaled corticosteroids, were also not associated increased NE risk.
Initiation of montelukast was not associated with increased risk of a variety of NEs in this sequence symmetry analysis involving adult patients in the VHA. Our findings do not support the hypothesis that NEs are associated with montelukast initiation.
美国食品和药物管理局(FDA)在上市后监测期间报告的孟鲁司特引发的神经精神事件(NEs)导致 2008 年发布安全警示,并于 2020 年发布黑框警告。我们的目的是使用序列对称分析评估孟鲁司特暴露和 NEs 风险。
利用美国退伍军人健康管理局(VHA)的行政数据,确定了在 2014 财年有新处方孟鲁司特的 11840 名患者。神经精神药物的新处方被用作新发生 NEs 的替代标记物,包括抗抑郁药、苯二氮䓬类、催眠药、抗精神病药、心境稳定剂和丁螺环酮。对称比是通过在孟鲁司特起始后的一年中出现新的神经精神事件的患者与起始前一年的患者比例计算得出的。采用暴露反事实分析来研究孟鲁司特的潜在替代疗法与 NEs 风险之间的关系。
在孟鲁司特起始后有 2305 名患者出现新的 NEs,在孟鲁司特起始前有 2734 名患者出现新的 NEs(SR0.84,95%CI0.80-0.89)。对 6 种精神药物亚类的每一种进行敏感性分析也未能显示孟鲁司特起始后 NEs 风险增加。孟鲁司特的替代疗法,如吸入性皮质类固醇,也与增加的 NE 风险无关。
在这项涉及 VHA 成年患者的序列对称分析中,孟鲁司特的起始与多种 NEs 的风险增加无关。我们的研究结果不支持 NEs 与孟鲁司特起始有关的假设。