Antia Smita X, Sholevar Ellen H, Baron David A
Department of Psychiatry and Behavioral Sciences, Temple University School of Medicine, Philadelphia, Pennsylvania 19125, USA.
J Child Adolesc Psychopharmacol. 2005 Dec;15(6):970-85. doi: 10.1089/cap.2005.15.970.
We reviewed the available published data on intentional or unintentional secondgeneration antipsychotic overdoses in children and adolescents. The prescribing of secondgeneration antipsychotics has continued to increase over the past decade for children, adolescents, and adults. The authors reviewed the existing literature to determine the circumstances, presenting problems, treatment, and outcomes of youths who were exposed to nontherapeutic doses of these medications.
A systematic English-language Medline search of all reports (1989-2005) and a review of the bibliographies of all articles obtained was done to identify papers reporting an overdose or ingestion of a second-generation antipsychotic. Data were reviewed on clozapine, risperidone, olanzapine, ziprasidone, quetiapine, and aripiprazole. The annual reports of the American Association of Poison Control Centers National Data Collection System were reviewed from 1990 to 2003, the most recent report currently available. All fatalities in children and youths under 18 years of age were included.
The literature review identified 40 reports that included 63 patients, ranging in age from 1 day to 17 years of age. The clinical presentations included drowsiness, lethargy, agitation, irritability, combativeness, and tachycardia. There were 11 fatalities in the cases reviewed, 1 from clozapine overdose, 3 from risperidone overdose, 2 from olanzapine overdose, and 5 from quetiapine overdose. All other cases reported no significant sequelae and resolved without any reported clinical consequences. Duration of overdose symptoms ranged from 24 hours to 7 days. One case of clozapine intoxication showed resolution of symptoms in 6 hours and, in another case of olanzapine overdose, symptoms resolved in 13 days. The most frequently employed treatments included intubation, gastric lavage, activated charcoal, intravenous fluids, artificial respiration, and restraints or sedatives.
There is a need for future case reports to include serum medication level, weight of patient, coingestants, the health of the patient at baseline, relevant laboratory and toxicology studies and a standardized scale to rate the level of consciousness, such as the Glasgow Coma Scale. The existing pharmacovigilance data reports indicate these medications are relatively safe when taken in overdose, particularly when coingestants are not involved.
我们回顾了已发表的关于儿童和青少年有意或无意过量服用第二代抗精神病药物的可用数据。在过去十年中,第二代抗精神病药物在儿童、青少年和成人中的处方量持续增加。作者回顾了现有文献,以确定接触这些药物非治疗剂量的青少年的情况、出现的问题、治疗方法及结果。
对所有报告(1989 - 2005年)进行系统的英文医学文献检索,并查阅所有获取文章的参考文献,以确定报告第二代抗精神病药物过量或摄入的论文。对氯氮平、利培酮、奥氮平、齐拉西酮、喹硫平和阿立哌唑的数据进行了回顾。查阅了1990年至2003年美国毒物控制中心协会国家数据收集系统的年度报告,这是目前可获取的最新报告。纳入了所有18岁以下儿童和青少年的死亡病例。
文献回顾确定了40份报告,涉及63名患者,年龄从1天至17岁不等。临床表现包括嗜睡、昏睡、激动、易怒、好斗和心动过速。在所审查病例中有11例死亡,1例死于氯氮平过量,3例死于利培酮过量,2例死于奥氮平过量,5例死于喹硫平过量。所有其他病例均未报告有明显后遗症,且在未报告任何临床后果的情况下康复。过量症状持续时间从24小时至7天不等。1例氯氮平中毒病例症状在6小时内缓解,另1例奥氮平过量病例症状在13天内缓解。最常用的治疗方法包括插管、洗胃、活性炭、静脉输液、人工呼吸以及约束或使用镇静剂。
未来的病例报告需要包括血清药物水平、患者体重、合并摄入的物质、患者基线健康状况、相关实验室和毒理学研究,以及用于评估意识水平的标准化量表,如格拉斯哥昏迷量表。现有的药物警戒数据报告表明,这些药物过量服用时相对安全,尤其是在不涉及合并摄入其他物质的情况下。