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米氮平过量不太可能导致严重毒性。

Mirtazapine overdose is unlikely to cause major toxicity.

机构信息

Department of Clinical Toxicology and Pharmacology, Calvary Mater Newcastle , Newcastle, NSW , Australia.

出版信息

Clin Toxicol (Phila). 2014 Jan;52(1):20-4. doi: 10.3109/15563650.2013.859264. Epub 2013 Nov 14.

Abstract

OBJECTIVE

There is limited information on mirtazapine overdose, but cases of severe effects (seizures, serotonin toxicity and coma) have been reported. We aimed to investigate the clinical effects and complications of mirtazapine overdose.

METHODS

This was an observational case series of mirtazapine overdoses (> 120 mg) identified from admissions to a toxicology unit between January 1987 and August 2013. Demographic information, details of ingestion, clinical effects, ECG parameters (HR, QT and QRS), and length of stay were extracted from a clinical database.

RESULTS

From 267 mirtazapine overdoses, there were 89 single-agent mirtazapine ingestions and 178 cases where mirtazapine was taken with at least one other drug. The median age of the 89 single-agent mirtazapine ingestions was 36 years [interquartile range (IQR): 26-49 years; Range: 15-81 years]; 45 were female (51%). The median ingested dose was 420 mg (IQR: 270-750 mg; Range: 150-1350 mg) and 41 patients (46%) had a Glasgow coma score (GCS) < 15, but the minimum GCS was 10. There were no seizures, serotonin toxicity or delirium. Tachycardia occurred in 29 patients (33%) and hypertension in 32 patients (36%). The median QRS was 80 ms (Range: 80-120 ms) and there were no cases with QT prolongation. There were no arrhythmias and no deaths. The median length of stay was 14 h (IQR: 8.8-18.2 h; Range:2.2-75 h). No single-agent mirtazapine patient was admitted to intensive care. The 178 patients taking co-ingestants had more severe toxicity depending on the co-ingested drug.

CONCLUSION

Mirtazapine appears to be relatively benign in overdose, associated with tachycardia, mild hypertension and mild CNS depression not requiring intervention.

摘要

目的

有关米氮平过量的信息有限,但已有严重影响(癫痫发作、血清素毒性和昏迷)的报告。我们旨在研究米氮平过量的临床效果和并发症。

方法

这是一项观察性病例系列研究,纳入了 1987 年 1 月至 2013 年 8 月间在毒理学单位住院的米氮平过量(>120mg)患者。从临床数据库中提取人口统计学信息、摄入细节、临床效果、心电图参数(心率、QT 和 QRS)以及住院时间。

结果

在 267 例米氮平过量中,有 89 例为单一药物米氮平摄入,178 例为米氮平与至少一种其他药物同时摄入。89 例单一药物米氮平摄入者的中位年龄为 36 岁[四分位间距(IQR):26-49 岁;范围:15-81 岁];45 例为女性(51%)。摄入的中位剂量为 420mg(IQR:270-750mg;范围:150-1350mg),41 例(46%)格拉斯哥昏迷评分(GCS)<15,但最低 GCS 为 10。无癫痫发作、血清素毒性或意识模糊。29 例(33%)出现心动过速,32 例(36%)出现高血压。中位 QRS 为 80ms(范围:80-120ms),无 QT 延长病例。无心律失常,无死亡。中位住院时间为 14 小时(IQR:8.8-18.2 小时;范围:2.2-75 小时)。没有单一药物米氮平患者入住重症监护病房。同时摄入其他药物的 178 例患者的毒性更严重,取决于同时摄入的药物。

结论

米氮平过量似乎相对良性,与心动过速、轻度高血压和轻度中枢神经系统抑制有关,无需干预。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ea6/3894718/2048fb8df13a/CTX-52-20-g001.jpg

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