Clinical Toxicology Center, Saitama Medical University Hospital, Saitama, Japan.
Department of Traumatology and Critical Care Medicine Faculty of Medicine, University of Miyazaki, Miyazaki, Japan.
Clin Toxicol (Phila). 2022 Mar;60(3):379-381. doi: 10.1080/15563650.2021.1953518. Epub 2021 Aug 18.
Lamotrigine toxicity can cause coma, seizures, and intraventricular conduction disturbances, and treatment options include good supportive care. We report two cases of lamotrigine poisoning in which multiple-dose activated charcoal may have shortened the elimination half-life of lamotrigine.
CASE 1: A 21-year-old woman ingested 15.6 g lamotrigine, 14 g levetiracetam, and 15 mg clonazepam. She became comatose and developed generalized tonic seizure. One hour post-ingestion, 50 g activated charcoal was administered. Starting 11 h post-ingestion, 25 g activated charcoal was administered every 4 h for 4 doses. The peak concentration of serum lamotrigine was 49.5 µg/mL, and the elimination half-life after commencement of multiple-dose activated charcoal was 6.5 h.
CASE 2: A 46-year-old woman ingested 0.3 g lamotrigine and 0.1 g topiramate twice, 2 h apart. She became drowsy, complained of blurred vision, vertigo, nausea, and vomited. An initial dose of 50 g activated charcoal was administered at 4.5 h post-second ingestion, and subsequent doses of 25 g (total of 3 doses) were administered every 4 h, commencing at 8.5 h post-second ingestion. The peak concentration of serum lamotrigine was 19.9 µg/mL, and the elimination half-life after commencement of multiple-dose activated charcoal was 9.3 h.
The mean elimination half-life of lamotrigine in healthy volunteers and epileptic patients receiving lamotrigine monotherapy is 22.8-37.4 h. In our two cases, multiple-dose activated charcoal may have shortened the elimination half-life of lamotrigine, possibly by inhibiting enterohepatic circulation. Multiple-dose activated charcoal should be considered an option for treating lamotrigine poisoning.
拉莫三嗪中毒可导致昏迷、癫痫发作和脑室传导障碍,治疗选择包括良好的支持性治疗。我们报告两例拉莫三嗪中毒病例,其中多次给予活性炭可能缩短了拉莫三嗪的消除半衰期。
病例 1:一名 21 岁女性摄入 15.6g 拉莫三嗪、14g 左乙拉西坦和 15mg 氯硝西泮。她昏迷并出现全身强直阵挛发作。摄入后 1 小时给予 50g 活性炭。摄入后 11 小时开始,每 4 小时给予 25g 活性炭共 4 剂。血清拉莫三嗪的峰值浓度为 49.5μg/mL,开始多次给予活性炭后消除半衰期为 6.5 小时。
病例 2:一名 46 岁女性分两次间隔 2 小时摄入 0.3g 拉莫三嗪和 0.1g 托吡酯。她变得昏昏欲睡,诉视物模糊、眩晕、恶心和呕吐。在第二次摄入后 4.5 小时给予初始剂量 50g 活性炭,随后每 4 小时给予 25g(共 3 剂),从第二次摄入后 8.5 小时开始。血清拉莫三嗪的峰值浓度为 19.9μg/mL,开始多次给予活性炭后消除半衰期为 9.3 小时。
健康志愿者和接受拉莫三嗪单药治疗的癫痫患者中,拉莫三嗪的平均消除半衰期为 22.8-37.4 小时。在我们的两个病例中,多次给予活性炭可能通过抑制肠肝循环缩短了拉莫三嗪的消除半衰期。多次给予活性炭应被视为治疗拉莫三嗪中毒的一种选择。