Division of Medical Toxicology, Department of Emergency Medicine, University of California at San Diego Medical Center, VA San Diego Healthcare System, an Diego, CA.
Division of Medical Toxicology, Department of Emergency Medicine, University of California at San Diego Medical Center, VA San Diego Healthcare System, an Diego, CA.
J Emerg Med. 2021 Nov;61(5):e99-e102. doi: 10.1016/j.jemermed.2021.07.011. Epub 2021 Aug 31.
Perampanel is a new antiepileptic used to treat partial-onset seizures and generalized tonic-clonic seizures in people older than 12 years old. Perampanel is a selective, non-competitive α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptor antagonist, with a prolonged half-life of approximately 105 hours. Few cases of significant toxicity have been reported, and effects in overdose are poorly understood.
This case describes a 20-month-old healthy female who ingested 8 mg of perampanel. She presented to a pediatric emergency department 1 hour after ingestion with ataxia, irritability, and somnolence. Vital signs were: heart rate 130 beats per minute, blood pressure 112/97 mmHg, temperature 99°F, respiratory rate 30 breaths per minute. She was admitted to the pediatric intensive care unit. During the hospitalization, she developed hypotension and bradycardia which improved with stimulation and fluid resuscitation. Intermittent bradycardia persisted for 32 hours after ingestion. Physical examination was notable for somnolence and truncal ataxia with irritability when aroused, all of which improved throughout the hospitalization. A quantitative level obtained on hospital day 3 (HD) was 750ng/ml. On HD 3 the patient was noted to be ataxic but otherwise had an age-appropriate neurologic examination. She was discharged on HD 4 with normal vital signs, return to baseline mental status, and baseline gait. The patient's cardiovascular, neurologic, and behavioral symptoms were attributed to perampanel toxicity. WHY SHOULD AN EMERGENCY PHYSICIAN BE AWARE OF THIS ?: Toxicity from a perampanel overdose is poorly understood both in adults and pediatric patients with significant cardiovascular, behavioral, and central nervous system abnormalities.
普瑞巴林是一种新的抗癫痫药,用于治疗 12 岁以上人群的部分发作性癫痫和全面强直阵挛性发作。普瑞巴林是一种选择性、非竞争性的α-氨基-3-羟基-5-甲基-4-异恶唑丙酸(AMPA)受体拮抗剂,半衰期约为 105 小时。报道的严重毒性病例很少,过量用药的影响知之甚少。
本病例描述了一名 20 月龄健康女性,摄入 8 毫克普瑞巴林。摄入后 1 小时,她出现共济失调、烦躁和嗜睡,到儿科急诊就诊。生命体征:心率 130 次/分钟,血压 112/97mmHg,体温 99°F,呼吸频率 30 次/分钟。她被收入儿科重症监护病房。住院期间,她出现低血压和心动过缓,经刺激和液体复苏后改善。摄入后 32 小时间歇性心动过缓持续存在。体格检查表现为嗜睡和躯干共济失调,唤醒时烦躁,整个住院期间均有所改善。摄入后第 3 天(HD)获得的定量水平为 750ng/ml。HD3 时,患者表现为共济失调,但其他方面神经检查正常。HD4 时,患者生命体征正常,精神状态恢复正常,步态正常出院。患者的心血管、神经和行为症状归因于普瑞巴林毒性。
成人和儿科患者普瑞巴林过量毒性的了解甚少,会出现严重的心血管、行为和中枢神经系统异常。