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首页> 外文期刊>Clinical toxicology: the official journal of the American Academy of Clinical Toxicology and European Association of Poisons Centres and Clinical Toxicologists >Successful management of olanzapine-induced anticholinergic agitation and delirium with a continuous intravenous infusion of physostigmine in a pediatric patient.
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Successful management of olanzapine-induced anticholinergic agitation and delirium with a continuous intravenous infusion of physostigmine in a pediatric patient.

机译:成功管理奥烷扎滨诱导的抗胆碱能搅拌和谵妄,在儿科患者中连续静脉内输注粪症。

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摘要

Physostigmine effectively reverses anticholinergic delirium. However, continuous IV infusion of physostigmine is rarely used due to concern for cardiotoxicity and signs of cholinergic excess such as seizures, nausea, and vomiting. We report the successful use of continuous IV physostigmine in a 6-year-old boy with anticholinergic delirium. A 6-year-old, 30-kg boy with attention deficit hyperactivity disorder (ADHD) ingested 15-20 olanzapine (5 mg) tablets. He was agitated and was treated with lorazepam at a local hospital. His heart rate was 148 beats per min; respiratory rate, 32 breaths per minute; blood pressure, 111/70 mmHg; temperature, 96.8°F, and O2 saturation of 98% on room air. His pupils were 5-6 mm, and his skin was warm and initially flushed. Blood chemistry results were normal. A 12-lead ECG showed sinus tachycardia with normal QRS and QT intervals. The agitation worsened and did not respond to benzodiazepines. The patient was then given a dose of 0.6 mg physostigmine (0.02 mg/kg) intravenously with reversal of the agitation. But the effect only lasted 45 min requiring administration of a second bolus of 0.6 mg (0.02 mg/kg). A physostigmine intravenous infusion was administered at a rate of 0.5 mg/h (0.0167 mg/kg/h). Overnight, the patient became more agitated. The physostigmine was discontinued, and IV dexmedetomidine (0.2 μg/kg/h) was started at 21:00. The patient became over-sedated with pinpoint pupils resulting in discontinuation of the dexmedetomidine at 04:00. The patient again became agitated and developed visual hallucinations. Three 1-mg (0.03 mg/kg) boluses of physostigmine were administered over 45 min, and the physostigmine infusion was restarted at a rate of 1 mg/h (0.03 mg/kg/h) for 16.5 h. He received 19.5 mg of physostigmine with no return of anticholinergic symptoms and no signs of cholinergic excess except for a tremor that resolved when the infusion was stopped. He was discharged home without further sequelae. There are few publications describing a continuous infusion of physostigmine to reverse anticholinergic delirium. Our patient received a total dose of 25.5 mg with complete resolution of symptoms. We report the successful use of continuous infusion of physostigmine to reverse anticholinergic delirium in a pediatric patient who unintentionally ingested olanzapine.
机译:物质激素有效地逆转抗胆碱能谵妄。然而,由于心脏毒性的关注和胆碱能量过量的担心,即癫痫,恶心和呕吐,很少使用持续的IV输注粪症的输注。我们在一名6岁的男孩中举报了连续IV地震的成功使用抗胆碱能谵妄。一名6岁的30公斤男孩注意力缺陷多动障碍(ADHD)摄入了15-20个奥氮藻(5毫克)片剂。他被激动了,并在当地医院用洛拉西泮治疗。他的心率是每分钟的148次;呼吸速率,每分钟32次呼吸;血压,111/70 mmHg;温度,96.8°F和O2饱和度为室内空气98%。他的瞳孔为5-6毫米,他的皮肤温暖,最初冲洗。血液化学结果正常。一个12引导的心电图显示鼻窦心动过速,QRS和QT间隔。搅拌恶化并且没有对苯并二氮杂卓的反应。然后将患者静脉内给予患者的0.6mg的辐射物(0.02mg / kg)与搅拌的逆转。但效果仅持续45分钟,需要施用0.6mg(0.02mg / kg)的第二推注。以0.5mg / h(0.0167mg / kg / h)的速率施用静脉内输注。过夜,患者变得更加激动。停止了物质胺,在21:00开始IV德Xmedetomidine(0.2μg/ kg / h)。患者随着定位的瞳孔而变得过度镇静,导致在04:00停止Dexmedetomidine。患者再次变得激动并发生了视觉幻觉。在45分钟内施用三个1mg(0.03mg / kg)荧光剂,并以1mg / h(0.03mg / kg / h)的速率重新启动出火腿输注16.5小时。他收到19.5毫克的抗磷酸症状,除了在输注停止时解决的震颤,除了颤抖,没有胆碱能量过剩的迹象。没有进一步的后遗症,他被出发了回家。少数出版物描述了对逆转抗胆碱能谵妄的持续输注疫苗。我们的患者的总剂量为25.5毫克,完全分辨症状。我们报告了在无意中摄取奥氮滨的儿科患者中成功地使用持续输注抗嗜哪种抗体嗜睡。

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