Clinical effects of acute lamotrigine overdose (ATOM-10).

IF 3 3区 医学 Q2 TOXICOLOGY
Angela L Chiew, Geoffrey K Isbister, Kiet Nguyen, Kristy McCulloch, Úna Nic Ionmhain, Katherine Z Isoardi
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引用次数: 0

Abstract

Introduction: Lamotrigine overdose is not typically associated with severe toxicity. However, both severe toxicity and serotonin toxicity is occasionally reported following large ingestions. We aimed to investigate the clinical effects of lamotrigine overdose.

Methods: This was a prospective observational study from July 2020-March 2024. Patients >14 years-old with acute lamotrigine overdose (≥2 g ingestion) were recruited from the Australian Toxicology Monitoring study or identified from three toxicology units. Data extracted included clinical features, lamotrigine concentrations, management, and outcomes.

Results: Fifty-four patients were included, median age 29 years (IQR: 21-42 years), 37 (69%) were female. The median ingested dose was 4.8 g (IQR: 3.2-6.3 g) and 41 patients (76%) co-ingested other substances. The median maximum lamotrigine concentration was 18.5 mg/L (IQR: 12.4-25.0 mg/L) at a median time of 4.3 h (IQR: 3.2-10.8 h) post-ingestion. Clinical effects and their management included sedation in 44 (81%) with 29 patients (54%) endotracheally intubated, tachycardia in 39 (72%), hypotension in 21 (39%) with 15 (28%) receiving inotropes, and seizures in 11 (20%). Serotonin toxicity occurred in 23 (43%) patients with four having severe toxicity characterised by temperature >38.5 °C and/or rigidity treated with muscle paralysis. Higher peak lamotrigine concentrations were correlated with severe outcomes such as endotracheal intubation for coma (P <0.0001), patients with hypotension receiving inotropes (P = 0.0269) and patients developing seizures (P = 0.0002). Patients who co-ingested another serotonin agent (some in therapeutic doses) had a higher incidence of developing serotonin toxicity (22/33 [67%]) versus those who had not (1/21 [5%]); P <0.0001).

Discussion: Severe toxicity was associated with higher peak lamotrigine concentrations. Serotonin toxicity was common in those who were exposed to another serotonergic agent.

Conclusion: Coma, seizures and hypotension following lamotrigine overdose appeared to be concentration dependent. Serotonin toxicity occurred in those who co-ingested another serotonergic agent and was unrelated to lamotrigine concentration.

急性拉莫三嗪过量(ATOM-10)的临床疗效。
拉莫三嗪过量通常不伴有严重的毒性。然而,严重的毒性和血清素毒性偶尔会在大量摄入后报道。我们的目的是探讨拉莫三嗪过量的临床效果。方法:这是一项前瞻性观察研究,时间为2020年7月至2024年3月。14岁急性拉莫三嗪过量(≥2g摄入)患者从澳大利亚毒理学监测研究中招募或从三个毒理学单位中确定。提取的数据包括临床特征、拉莫三嗪浓度、管理和结果。结果:纳入患者54例,中位年龄29岁(IQR: 21 ~ 42岁),女性37例(69%)。中位摄入剂量为4.8 g (IQR: 3.2-6.3 g), 41例(76%)患者共摄入其他物质。中位最大拉莫三嗪浓度为18.5 mg/L (IQR: 12.4 ~ 25.0 mg/L),中位时间为4.3 h (IQR: 3.2 ~ 10.8 h)。临床效果及处理包括镇静44例(81%),经气管插管29例(54%),心动过速39例(72%),低血压21例(39%),使用肌力药物15例(28%),癫痫发作11例(20%)。23例(43%)患者出现血清素毒性,其中4例出现严重毒性,表现为体温低于38.5°C和/或僵硬,并伴有肌肉麻痹。较高的拉莫三嗪峰值浓度与严重后果相关,如昏迷患者气管插管(P = 0.0269)和癫痫发作(P = 0.0002)。同时摄入另一种5 -羟色胺药物的患者(有些是治疗剂量)发生5 -羟色胺毒性的发生率(22/33[67%])高于未服用的患者(1/21 [5%]);P讨论:严重的毒性与较高的拉莫三嗪峰浓度相关。血清素毒性在暴露于另一种血清素能剂的人群中很常见。结论:拉莫三嗪过量后出现昏迷、癫痫发作和低血压的浓度依赖性。血清素毒性发生在同时摄入另一种血清素能剂的患者中,与拉莫三嗪浓度无关。
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
Clinical Toxicology
Clinical Toxicology 医学-毒理学
CiteScore
5.70
自引率
12.10%
发文量
148
审稿时长
4-8 weeks
期刊介绍: clinical Toxicology publishes peer-reviewed scientific research and clinical advances in clinical toxicology. The journal reflects the professional concerns and best scientific judgment of its sponsors, the American Academy of Clinical Toxicology, the European Association of Poisons Centres and Clinical Toxicologists, the American Association of Poison Control Centers and the Asia Pacific Association of Medical Toxicology and, as such, is the leading international journal in the specialty.
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