Therapeutic single-dose mirtazapine-induced symptomatic bradycardia: a case report

Pınar D Gündoğmuş, İbrahim Gündoğmuş, Emrah Burak Olcu, A. Karagoz, A. Algul
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引用次数: 2

Abstract

Therapeutic single-dose mirtazapine-induced symptomatic bradycardia: a case report Cardiotoxicity is an important adverse effect of some psychotropic drugs. However, cardiac side effects with mirtazapine, which is used for an effective treatment of depression and anxiety, are rare. In this article, a forty-eight-year-old woman referred to psychiatric clinics with depressive symptoms. According to Diagnostic and Statistical Manual of Mental Disorders Fifth Edition (DSM-5) criteria, major depressive disorder was diagnosed and mirtazapine 30mg/day was started. 30 minutes after the first dose of mirtazapine was brought to the emergency room with syncope, nausea, vomiting. She was examined in emergency service. Routine blood tests and ECG was studied. During the examination, the patient was followed up with a heart rate of 33 beats per minute, blood pressure arterial 80/50mmHg and a temperature of 36.1°C. 0.5mg atropine IV and theophylline inhaler were administered and cardiology consultation was requested. After atropine and theophylline administration, the heart rate was 48 beats/min in the second ECG. To the best of our knowledge, it is the first bradycardia developed after mirtazapine use in the literature. Bradycardia has been resolved after the half-life of mirtazapine has passed (37 hours for women). The initial heart rate of our patient was within normal limits prior to mirtazapine administration. There was no reason to explain bradycardia, we think that symptomatic bradycardine is caused by mirtazapine. In conclusion, this case report suggests that mirtazapine may cause bradycardia in patients. Risk factors for bradycardia caused by mirtazapine are unknown. Although in many patients this bradycardine does not cause a clinical outcome, clinicians should be aware of this and should perform ECG monitoring in patients with underlying cardiac disease, especially when prescribing mirtazapine.
治疗性单剂量米氮平诱导症状性心动过缓1例报告
治疗性单剂量米氮平致症状性心动过缓1例心脏毒性是一些精神药物的重要不良反应。然而,用于有效治疗抑郁和焦虑的米氮平的心脏副作用是罕见的。在这篇文章中,一位48岁的女性因抑郁症状来到精神科诊所。根据《精神障碍诊断与统计手册》第五版(DSM-5)标准,诊断为重度抑郁症,开始使用米氮平30mg/天。第一剂米氮平30分钟后被送到急诊室,伴有晕厥,恶心,呕吐。她在急救中心接受了检查。研究了血常规和心电图。检查期间,随访患者心率33次/分,血压动脉80/50mmHg,体温36.1℃。给予静脉阿托品0.5mg及茶碱吸入器,并要求进行心内科会诊。给予阿托品和茶碱后,第二次心电图心率为48次/分。据我们所知,这是文献中使用米氮平后出现的第一例心动过缓。在米氮平的半衰期(女性37小时)过去后,心动过缓得到缓解。在使用米氮平之前,患者的初始心率在正常范围内。没有理由解释心动过缓,我们认为症状性心动过缓是由米氮平引起的。总之,本病例报告提示米氮平可能导致患者心动过缓。米氮平引起心动过缓的危险因素尚不清楚。虽然在许多患者中,这种慢速卡丁药不会引起临床结果,但临床医生应该意识到这一点,并对有潜在心脏病的患者进行心电图监测,特别是在开米氮平处方时。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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