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病例报告:在包括氯氮平在内的心理药物治疗基础上额外单次服用唑吡坦后出现的多动性谵妄。

Case report: Hyperactive delirium after a single dose of zolpidem administered additionally to psychopharmacotherapy including clozapine.

作者信息

Preiss Maximilian, Rabl Ulrich, Popper Valentin, Watzal Victoria, Treiber Michael, Ivkic Dominik, Praschak-Rieder Nicole, Naderi-Heiden Angela, Fugger Gernot, Frey Richard, Rujescu Dan, Bartova Lucie

机构信息

Department of Psychiatry and Psychotherapy, Clinical Division of General Psychiatry, Medical University of Vienna, Vienna, Austria.

Comprehensive Center for Clinical Neurosciences and Mental Health, Medical University of Vienna, Vienna, Austria.

出版信息

Front Psychiatry. 2023 Jul 27;14:1204009. doi: 10.3389/fpsyt.2023.1204009. eCollection 2023.

DOI:10.3389/fpsyt.2023.1204009
PMID:37575586
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10413097/
Abstract

The non-benzodiazepine hypnotic zolpidem is frequently administered as a short term psychopharmacotherapy for insomnia. Although it is well-established in a broad clinical routine and often well-tolerated, severe delirium and complex sleep behavior were reported in rare cases. Hereby, it remains unclear whether zolpidem's potential for delirium might be enhanced when combined with further psychopharmacotherapeutics. The present case report portrays a young male Caucasian inpatient with schizoaffective disorder, who was admitted due to severe hyperactive delirium after a single dose of zolpidem 10 mg that was administered in addition to already established psychopharmacotherapy including clozapine 200 mg/day, aripiprazole 15 mg/day and cariprazine 4.5 mg/day. In detail, disorientation, agitation, confabulations, bizarre behavior, and anterograde amnesia occurred shortly after ingestion of zolpidem and gained in intensity within a couple of hours. Once zolpidem was discontinued, the abovementioned symptoms subsided completely and did not reoccur. Since a clear temporal association could be drawn between the intake of zolpidem and the onset of hyperactive delirium, the present clinical experience should serve as a cautionary note for combining potent sedative-hypnotics and substances with anticholinergic properties, even in young adults in a good general condition. Moreover, our case argues for the necessity of further research into the pathomechanism of the interaction potential of non-benzodiazepines as zolpidem, especially with substances exerting anticholinergic properties, which are known for their potential to precipitate delirium. Therefore, the metabolic pathways of the concurrently administered substances should be further taken into account.

摘要

非苯二氮䓬类催眠药唑吡坦常用于短期失眠的心理药物治疗。尽管它在广泛的临床常规应用中已得到充分确立,且通常耐受性良好,但仍有罕见病例报告出现严重谵妄和复杂睡眠行为。在此,尚不清楚唑吡坦与其他心理药物联合使用时,其导致谵妄的可能性是否会增加。本病例报告描述了一名患有精神分裂症的年轻白人男性住院患者,在已确立的包括氯氮平200毫克/天、阿立哌唑15毫克/天和卡立普唑4.5毫克/天的心理药物治疗基础上,加用一剂10毫克唑吡坦后,因严重的多动性谵妄入院。具体而言,服用唑吡坦后不久出现定向障碍、躁动、虚构、怪异行为和顺行性遗忘,并在数小时内加重。一旦停用唑吡坦,上述症状完全消退且未再出现。由于唑吡坦摄入与多动性谵妄发作之间存在明确的时间关联,即使是身体状况良好的年轻人,目前的临床经验也应作为联合使用强效镇静催眠药和具有抗胆碱能特性物质的警示。此外,我们的病例表明有必要进一步研究唑吡坦等非苯二氮䓬类药物相互作用潜力的发病机制,尤其是与已知有诱发谵妄潜力的具有抗胆碱能特性的物质。因此,应进一步考虑同时使用药物的代谢途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9341/10413097/b455e35a235e/fpsyt-14-1204009-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9341/10413097/b455e35a235e/fpsyt-14-1204009-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9341/10413097/b455e35a235e/fpsyt-14-1204009-g0001.jpg

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