Dextromethorphan Overdose with Refractory Status Epilepticus and Reversible Cranial Nerve Reflex Loss: A Case Report.

IF 1 Q3 MEDICINE, GENERAL & INTERNAL
Akifumi Okamoto, Naoki Yonezawa, Kazuhiro Yoshizawa, Reiki Kumashiro, Shinya Suzuki
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引用次数: 0

Abstract

BACKGROUND Dextromethorphan is a widely used over-the-counter antitussive medication. Generally safe within the recommended dosages, its misuse can lead to severe adverse effects, particularly in large amounts. However, comprehensive descriptions of severe overdose cases - including pharmacokinetic data of dextromethorphan and its active metabolite (dextrorphan) - are scarce. CASE REPORT A 21-year-old woman with schizophrenia ingested 20 280 mg of dextromethorphan along with other prescribed medications during a suicide attempt. She was discovered semiconscious and experienced a generalized seizure en route to the hospital. Despite intensive treatments - including endotracheal intubation and administration of propofol and midazolam - she continued to experience refractory status epilepticus. Subsequent neurological examination revealed cranial nerve reflex loss. The serum concentration of dextromethorphan was 5.8 mg/L on admission and decreased to 2.2 mg/L by day 1 and 1.1 mg/L by day 2, contrasting with that of dextrorphan, which remained within the therapeutic limits. By day 4, her condition stabilized; she became alert, responsive to commands, and was successfully extubated. She was discharged on day 9 without any sequelae. CONCLUSIONS This report describes the case of a patient who survived a massive dextromethorphan overdose, who presented with refractory status epilepticus followed by reversible suppression of cranial nerve reflexes. The pharmacokinetic profiles suggested that dextromethorphan, rather than dextrorphan, was responsible for the symptoms. High-dose dextromethorphan ingestion can lead to varied and potentially fatal outcomes, especially when compounded by metabolism-altering factors such as CYP2D6 inhibition, genetic variability, or co-ingested medications. This case underscores the importance of prompt, intensive supportive care in managing severe dextromethorphan toxicity.

右美沙芬过量致顽固性癫痫持续状态和可逆性脑神经反射丧失1例报告。
右美沙芬是一种广泛使用的非处方止咳药物。在推荐剂量范围内通常是安全的,但误用会导致严重的不良反应,特别是大量误用时。然而,对严重用药过量病例的全面描述——包括右美沙芬及其活性代谢物(右美沙芬)的药代动力学数据——很少。病例报告:一名患有精神分裂症的21岁女性在企图自杀时服用了20280毫克右美沙芬和其他处方药。她被发现处于半意识状态,在去医院的途中经历了全身癫痫发作。尽管进行了强化治疗——包括气管插管、异丙酚和咪达唑仑——她仍然经历着难治性癫痫持续状态。随后的神经学检查显示脑神经反射丧失。入院时右美沙芬的血药浓度为5.8 mg/L,第1天降至2.2 mg/L,第2天降至1.1 mg/L,右美沙芬仍在治疗范围内。第四天,她的病情稳定下来;她变得警觉起来,对命令有反应,并成功拔管。她于第9天出院,没有任何后遗症。结论:本报告描述了一例大量服用右美沙芬后幸存的患者,其表现为难治性癫痫持续状态,随后出现可逆性脑神经反射抑制。药代动力学分析表明,右美沙芬,而不是右美沙芬,是导致这些症状的原因。大剂量右美沙芬摄入可导致各种潜在的致命结果,特别是当代谢改变因素如CYP2D6抑制、遗传变异或共摄入药物时。本病例强调了在处理严重右美沙芬毒性时及时、强化支持性护理的重要性。
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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来源期刊
American Journal of Case Reports
American Journal of Case Reports Medicine-Medicine (all)
CiteScore
1.80
自引率
0.00%
发文量
599
期刊介绍: American Journal of Case Reports is an international, peer-reviewed scientific journal that publishes single and series case reports in all medical fields. American Journal of Case Reports is issued on a continuous basis as a primary electronic journal. Print copies of a single article or a set of articles can be ordered on demand.
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