Barrueto F, Williams K, Howland M A, Hoffman R S, Nelson L S
Department of Emergency Medicine, New York University School of Medicine and the New York City Poison Control Center, New York, New York, USA.
J Toxicol Clin Toxicol. 2002;40(7):881-4. doi: 10.1081/clt-120016959.
Levetiracetam (Keppra) is a new anticonvulsant used to treat partial complex seizures that is also being investigated for its mood-stabilizing properties. Although its precise mechanism of action is unknown, levetiracetam does not appear to directly interact with the GABA system. We report the first intentional overdose with levetiracetam including clinical effects and serial serum concentrations.
A 38-year-old woman reportedly ingested 60 (500 mg) tablets of levetiracetam that she used as a mood-stabilizing medication for bipolar disorder. She had no other prescription medications available and no other medical history. She vomited 4 hours after ingestion and presented to the ED 2 hours later. In the ED, the patient was obtunded and was intubated secondary to respiratory depression. Her only other significant clinical finding was diminished deep tendon reflexes. Serum ethanol, lithium, carbamazepine, phenytoin, and valproic acid levels were all negative as was a subsequent urine screen for drugs of abuse. Her levetiracetam serum concentration was 400 microg/mL at 6 hours, 72 microg/mL at 18 hours, and 60 microg/mL at 20.5 hours (therapeutic serum concentration is 10-37 microg/mL). The elimination half-life was calculated to be 5.14 hours. She was extubated the next hospital day and recovered without sequelae.
In overdose, levetiracetam is sedating and causes respiratory depression, however, recovery is rapid with supportive care. This is the first reported case of levetiracetam overdose; serial serum concentrations suggest first-order elimination even at concentrations 10-40 fold higher than therapeutic.
左乙拉西坦(开浦兰)是一种用于治疗部分性癫痫发作的新型抗惊厥药物,其情绪稳定特性也正在研究中。尽管其确切作用机制尚不清楚,但左乙拉西坦似乎不直接与γ-氨基丁酸(GABA)系统相互作用。我们报告首例左乙拉西坦故意过量服用病例,包括临床效应和系列血清浓度。
据报道,一名38岁女性摄入了60片(每片500毫克)她用作双相情感障碍情绪稳定剂的左乙拉西坦。她没有其他可用的处方药,也没有其他病史。摄入后4小时她呕吐,2小时后就诊于急诊科。在急诊科,患者意识不清,因呼吸抑制而插管。她唯一的其他重要临床发现是深部腱反射减弱。血清乙醇、锂、卡马西平、苯妥英和丙戊酸水平均为阴性,随后的尿液药物滥用筛查结果也是如此。她的左乙拉西坦血清浓度在6小时时为400微克/毫升,18小时时为72微克/毫升,20.5小时时为60微克/毫升(治疗血清浓度为10 - 37微克/毫升)。计算得出消除半衰期为5.14小时。次日她在医院拔管,康复且无后遗症。
过量服用时,左乙拉西坦具有镇静作用并导致呼吸抑制,然而,通过支持治疗恢复迅速。这是首例报告的左乙拉西坦过量服用病例;系列血清浓度表明即使在高于治疗浓度10 - 40倍时仍为一级消除。