Department of Emergency Medicine & Clinical Toxicology, Prince of Wales Hospital, Randwick, NSW, Australia.
Clinical Pharmacology & Toxicology Unit, Calvary Mater Newcastle Hospital, Waratah, NSW, Australia.
Br J Clin Pharmacol. 2023 Feb;89(2):903-907. doi: 10.1111/bcp.15588. Epub 2022 Nov 20.
Olanzapine pamoate is an intramuscular depot injection for the treatment of schizophrenia. Approximately 1.4% of patients develop a serious adverse event called post-injection delirium/sedation syndrome (PDSS), characterised by drowsiness, anticholinergic and extrapyramidal symptoms. The objective is to investigate olanzapine PDSS presentations including clinical features and treatment approach. This is a retrospective review of olanzapine PDSS patients from three toxicology units and the NSW Poisons Information Centre between 2017 and 2022. Adult patients were included if they had intramuscular olanzapine then developed PDSS criteria. Clinical symptoms, treatment, timing and length of symptoms were extracted into a preformatted Excel database. There were 18 patients included in the series, with a median age of 49 years (interquartile range [IQR]: 38-58) and male predominance (89%). Median onset time post injection was 30 min (IQR: 11-38). PDSS symptoms predominate with drowsiness, confusion and dysarthria. Median length of symptoms was 24 h (IQR: 20-54). Most common treatment included supportive care without any pharmacological intervention (n = 10), benzodiazepine (n = 4) and benztropine (n = 3). In one case, bromocriptine and physostigmine followed by oral rivastigmine were given to manage antidopaminergic and anticholinergic symptoms respectively. This proposed treatment combination could potentially alleviate some of the symptoms but needs further studies to validate the findings. In conclusion, this case series supports the characterisation of PDSS symptomology predominantly being anticholinergic with similar onset (<1 h) and duration (<72 h). Bromocriptine is proposed to manage PDSS if patients develop severe dopamine blockade and physostigmine followed by rivastigmine for anticholinergic delirium.
奥氮平癸酸酯是一种用于治疗精神分裂症的肌肉注射长效制剂。大约有 1.4%的患者会出现一种称为注射后谵妄/镇静综合征(PDSS)的严重不良事件,其特征为嗜睡、抗胆碱能和锥体外系症状。本研究旨在探讨奥氮平 PDSS 的表现,包括临床表现和治疗方法。这是对 2017 年至 2022 年间三个毒理学单位和新南威尔士毒物信息中心的奥氮平 PDSS 患者进行的回顾性研究。如果患者接受肌肉注射奥氮平后出现 PDSS 标准,则纳入成人患者。将临床症状、治疗方法、症状出现时间和持续时间提取到预格式化的 Excel 数据库中。该系列共纳入 18 例患者,中位年龄 49 岁(四分位距 [IQR]:38-58),男性居多(89%)。中位注射后发病时间为 30 分钟(IQR:11-38)。PDSS 症状以嗜睡、意识模糊和构音障碍为主。中位症状持续时间为 24 小时(IQR:20-54)。最常见的治疗方法包括支持性治疗,而无任何药物干预(n=10)、苯二氮䓬类(n=4)和苯海索(n=3)。在 1 例患者中,给予溴隐亭和毒扁豆碱,随后口服利伐斯的明,分别用于治疗抗多巴胺能和抗胆碱能症状。这种拟议的治疗组合可能会缓解一些症状,但需要进一步的研究来验证这些发现。总之,本病例系列支持 PDSS 症状学的特征主要为抗胆碱能,其发病时间(<1 小时)和持续时间(<72 小时)相似。如果患者出现严重的多巴胺阻断,建议使用溴隐亭治疗 PDSS,随后使用毒扁豆碱和利伐斯的明治疗抗胆碱能谵妄。