Department of Psychiatry & Psychotherapeutic Medicine, Medical University of Graz, Graz, Austria.
Department of Neurology, Klinik Donaustadt, Vienna, Austria.
Acta Psychiatr Scand. 2023 Jan;147(1):16-42. doi: 10.1111/acps.13505. Epub 2022 Oct 11.
Drug-associated delirium is a common but potentially preventable neuropsychiatric syndrome associated with detrimental outcomes. Empirical evidence for delirium-associated medication is uncertain due to a lack of high-quality studies. We aimed to further investigate the body of evidence for drugs suspected to trigger delirium.
A systematic update review and meta-analyses of prospective studies presenting drug associations with incident delirium in adult study populations was conducted. Two authors independently searched MEDLINE, PsycINFO, Embase, and Google Scholar dated from October 1, 2009 to June 23, 2020, after screening a previous review published in 2011. The most reliable results on drug-delirium associations were pooled in meta-analyses using the random-effects model. Quality of evidence was assessed using the GRADE-approach. This study is preregistered with OSF (DOI https://doi.org.10.17605/OSF.IO/4PUHY).
The 31 eligible studies, presenting results for 24 medication classes were identified. Meta-analyses and GRADE level of evidence ratings show no increased delirium risk for Haloperidol (OR: 0.96, 95% CI 0.72-1.28; high-quality evidence), Olanzapine (OR: 0.25, 95% CI 0.15-0.40), Ketamine (OR: 0.72, 95% CI 0.35-1.46) or corticosteroids (OR: 0.69, 95% CI 0.32-1.50; moderate quality evidence, respectively). Low-level evidence suggests a three-fold increased risk for anticholinergics (OR: 3.11, 95% CI 1.04-9.26). Opioids, benzodiazepines, H -antihistamines, and antidepressants did not reach reliable evidence levels in our analyses.
We investigated the retrievable body of evidence for delirium-associated medication. The results of this systematic review were then interpreted in conjunction with other evidence-based works and guidelines providing conclusions for clinical decision-making.
药物相关性谵妄是一种常见但可能可预防的与不良结局相关的神经精神综合征。由于缺乏高质量的研究,谵妄相关药物的实证证据尚不确定。我们旨在进一步研究可能引发谵妄的药物的证据。
对前瞻性研究进行了系统更新综述和荟萃分析,这些研究报告了成年研究人群中药物与新发谵妄的关联。两位作者独立检索了 MEDLINE、PsycINFO、Embase 和 Google Scholar,检索日期为 2009 年 10 月 1 日至 2020 年 6 月 23 日,此前还检索了 2011 年发表的一篇综述。使用随机效应模型对药物-谵妄关联的最可靠结果进行荟萃分析。使用 GRADE 方法评估证据质量。本研究在 OSF 上预先注册(DOI https://doi.org/10.17605/OSF.IO/4PUHY)。
确定了 31 项符合条件的研究,这些研究报告了 24 种药物类别的结果。荟萃分析和 GRADE 证据等级评价显示,氟哌啶醇(OR:0.96,95%CI 0.72-1.28;高质量证据)、奥氮平(OR:0.25,95%CI 0.15-0.40)、氯胺酮(OR:0.72,95%CI 0.35-1.46)或皮质类固醇(OR:0.69,95%CI 0.32-1.50)的谵妄风险无增加,分别为(中等质量证据)。低水平证据表明,抗胆碱能药物的风险增加三倍(OR:3.11,95%CI 1.04-9.26)。阿片类药物、苯二氮䓬类药物、H1 抗组胺药和抗抑郁药在我们的分析中未达到可靠的证据水平。
我们调查了与谵妄相关药物的可检索证据。然后,我们结合其他循证工作和指南的结果对系统评价的结果进行了解释,为临床决策提供了结论。