Toxicological seizures: characteristics, outcomes and recurrence.

IF 3.3
Kristy McCulloch, Ingrid Berling, Angela L Chiew, Katherine Wood, Keith Harris, Geoffrey Isbister, Brooke Sachs, Katherine Isoardi
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引用次数: 0

Abstract

Introduction: Seizures are a marker of severe toxicity following overdose. Research characterising toxicological seizures is limited. We aim to study toxicological seizures, causative agents, and recurrence.

Methods: This is a retrospective observational series of patients with seizure after drug overdose, presenting to three Australian clinical toxicology units between 1 January 2014 and 31 December 2022. Patients were identified from the database of each unit, and data were supplemented by the patient's medical record. Follow-up data were extracted in June 2024.

Results: Over the nine-year period, there were 38,493 presentations to the three toxicology units. A seizure occurred in 284 presentations (275 patients). The median age was 29 years (IQR: 21-39 years; range: 15-86 years), and there were 150 males (55%). A previous seizure disorder was documented in 29/275 (11%) patients. In 82 (30%) presentations, more than one proconvulsant drug was taken. In 202 single proconvulsant exposures, the most common agents were tramadol (18/202, 9%), 3,4-methylenedioxymetamfetamine (15/202, 7%), and quetiapine (15/202, 7%). The highest seizure rate, considering total presentations for each agent, was for synthetic cannabinoid receptor agonists (9/43, 21%), tramadol (18/524, 3.4%), cocaine (14/516, 2.2%), and propranolol (8/427, 1.9%). A single seizure occurred in 169 (60%) cases, while status epilepticus occurred in 62 (22%). The median seizure duration was 1 min (IQR:1-3 min). The median time to the first seizure was 2.5 h (IQR: 1.0-7.1 h). Seizures occurred within 12 h for immediate-release preparations and within 24 h for slow-release preparations. Follow-up occurred in 221/275 (80%) patients. Seizure recurrence occurred in 45/221 (20%) patients. In eight patients (4%), a new diagnosis of epilepsy was established.

Discussion: Both seizure recurrence and a subsequent diagnosis of epilepsy occurred more frequently than expected. A toxicological seizure may herald a propensity for future seizures and epilepsy.

Conclusions: In this series, toxicological seizures were most common after tramadol, 3,4-methylenedioxymetamfetamine, quetiapine and cocaine. Seizure recurrence was common, with 4% of patients later diagnosed with epilepsy, supporting toxicological seizures being investigated, managed and followed up as rigorously as unprovoked first seizures.

毒理学发作:特征、结局和复发。
癫痫发作是服药过量后出现严重毒性的标志。对毒理学发作特征的研究是有限的。我们的目标是研究毒理学癫痫发作,病原体和复发。方法:对2014年1月1日至2022年12月31日期间在澳大利亚三个临床毒理学单位就诊的药物过量后癫痫发作的患者进行回顾性观察。从每个单位的数据库中识别患者,并通过患者的病历补充数据。随访数据于2024年6月提取。结果:在9年的时间里,三个毒理学单位共收到38,493份报告。癫痫发作284例(275例)。中位年龄29岁(IQR: 21 ~ 39岁,范围:15 ~ 86岁),男性150例(55%)。275例患者中有29例(11%)既往有癫痫发作障碍。在82例(30%)病例中,服用了一种以上的抗惊厥药物。在202例单一惊厥药暴露中,最常见的药物是曲马多(18/ 202,9%)、3,4-亚甲基二氧基二甲非他明(15/ 202,7%)和喹硫平(15/ 202,7%)。考虑到每种药物的总表现,最高的癫痫发作率是合成大麻素受体激动剂(9/ 43,21%)、曲马多(18/524,3.4%)、可卡因(14/516,2.2%)和心得安(8/427,1.9%)。169例(60%)发生单次癫痫发作,62例(22%)发生癫痫持续状态。癫痫发作时间中位数为1分钟(IQR:1-3分钟)。至首次发作的中位时间为2.5 h (IQR: 1.0-7.1 h)。速释制剂在12 h内发作,缓释制剂在24 h内发作。221/275例(80%)患者进行了随访。221例患者中有45例(20%)癫痫复发。在8例(4%)患者中,新诊断为癫痫。讨论:癫痫复发和随后的癫痫诊断发生的频率比预期的要高。毒理学发作可能预示着未来发作和癫痫的倾向。结论:本研究中,曲马多、3,4-亚甲基二氧基甲基苯丙胺、喹硫平和可卡因后的毒理学发作最为常见。癫痫复发很常见,4%的患者后来被诊断为癫痫,支持对毒理性癫痫发作进行调查、管理和随访,就像首次无诱发性癫痫发作一样严格。
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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