不良临床事件报告

T. Mcevoy
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引用次数: 0

摘要

一名43岁女性患者在开始使用甲硝唑(总剂量= 28 g)治疗幽门螺杆菌约20天后出现突发性双侧听力丧失、共济失调和眩晕。体格检查显示嗜睡、脑病、口齿不清和冷漠。尽管肌肉张力正常,但身体右侧的肌肉力量下降。感染病因筛查呈阴性。脑磁共振成像显示齿状核、胼胝体脾和脑白质双侧对称t2加权高信号病变。停用甲硝唑,开始用左旋肉碱和辅酶Q10治疗,3天内观察到听力和行走有明显改善。根据给药与症状的出现和缓解之间的时间关系,作者得出结论,该患者经历了甲硝唑诱导的脑病和神经毒性。其作用机制可能包括线粒体功能障碍、与神经RNA结合抑制蛋白质合成、修饰小脑和前庭g-氨基丁酸受体。Agah E等人(A Tafakhori,神经免疫学研究协会,普遍科学教育和研究网络,伊朗德黑兰;电子邮件:a_tafakhori@sina.tums.ac.ir)甲硝唑引起的神经毒性表现为突发性双侧听力丧失、脑病和小脑功能障碍。中华临床医学杂志73:249-250 (2)2017
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Reporting on Adverse Clinical Events
A 43-year-old female patient developed sudden bilateral hearing loss, ataxia, and vertigo approximately 20 days after starting metronidazole (total dose = 28 g) as part of a regimen for the treatment of Helicobacter pylori. A physical examination revealed lethargy, encephalopathy, slurred speech, and apathy. Despite normal muscle tone, the muscle force was decreased on the right side of the body. Screenings for infectious etiologies were negative. A brain magnetic resonance imaging demonstrated bilateral symmetric T2-weighted hypersignal lesions in dentate nucleus, the splenium of corpus callosum, and cerebral white matter. Metronidazole was discontinued and treatment with L-carnitine and coenzyme Q10 was initiated with significant improvements observed in hearing and walking within 3 days. The authors concluded that this patient experienced metronidazoleinduced encephalopathy and neurotoxicity based on the temporal relationship between the administration of the drug and the appearance and resolution of symptoms. Suggested mechanism of action included mitochondrial dysfunction, inhibition of protein synthesis by binding to neural RNA, and modifying cerebellar and vestibular g-aminobutyric acid receptors. Metronidazole [“Flagyl”] Agah E et al (A Tafakhori, NeuroImmunology Research Association, Universal Scientific Education and Research Network, Tehran, Iran; e-mail: a_tafakhori@sina.tums.ac.ir) Metronidazole-induced neurotoxicity presenting with sudden bilateral hearing loss, encephalopathy, and cerebellar dysfunction. Eur J Clin Pharmacol 73:249–250 (Feb) 2017
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