Ostuzzi Giovanni, Gastaldon Chiara, Papola Davide, Fagiolini Andrea, Dursun Serdar, Taylor David, Correll Christoph U, Barbui Corrado
Department of Neuroscience, Biomedicine and Movement Sciences, Section of Psychiatry, WHO Collaborating Centre for Research and Training in Mental Health and Service Evaluation, University of Verona, Piazzale L.A. Scuro, 10, Verona, 37134, Italy.
Department of Neuroscience, Biomedicine and Movement Sciences, WHO Collaborating Centre for Research and Training in Mental Health and Service Evaluation, Section of Psychiatry, University of Verona, Verona, Italy.
Ther Adv Psychopharmacol. 2020 Jul 20;10:2045125320942703. doi: 10.1177/2045125320942703. eCollection 2020.
People with coronavirus disease (COVID-19) might have several risk factors for delirium, which could in turn notably worsen the prognosis. Although pharmacological approaches for delirium are debated, haloperidol and other first-generation antipsychotics are frequently employed, particularly for hyperactive presentations. However, the use of these conventional treatments could be limited in people with COVID-19, due to the underlying medical condition and the risk of drug-drug interactions with anti-COVID treatments. On these premises, we carried out a rapid review in order to identify possible alternative medications for this particular population. By searching PubMed and the Cochrane Library, we selected the most updated systematic reviews of randomised trials on the pharmacological treatment of delirium in both intensive and non-intensive care settings, and on the treatment of agitation related to acute psychosis or dementia. We identified medications performing significantly better than placebo or haloperidol as the reference treatment in each population considered, and assessed the strength of association according to validated criteria. In addition, we collected data on other relevant clinical elements (i.e. common adverse events, drug-drug interactions with COVID-19 medications, daily doses) and regulatory elements (i.e. therapeutic indications, contra-indications, available formulations). A total of 10 systematic reviews were included. Overall, relatively few medications showed benefits over placebo in the four selected populations. As compared with placebo, significant benefits emerged for quetiapine and dexmedetomidine in intensive care unit (ICU) settings, and for none of the medications in non-ICU settings. Considering also data from indirect populations (agitation related to acute psychosis or dementia), aripiprazole, quetiapine and risperidone showed a potential benefit in two or three different populations. Despite limitations related to the rapid review methodology and the use of data from indirect populations, the evidence retrieved can pragmatically support treatment choices of frontline practitioners involved in the COVID-19 outbreak, and indicate future research directions for the treatment of delirium in particularly vulnerable populations.
冠状病毒病(COVID-19)患者可能有多种导致谵妄的风险因素,而谵妄反过来又可能显著恶化预后。尽管针对谵妄的药物治疗方法存在争议,但氟哌啶醇和其他第一代抗精神病药物仍被频繁使用,尤其是用于治疗多动型谵妄。然而,由于潜在的基础疾病以及与抗COVID治疗药物相互作用的风险,这些传统治疗方法在COVID-19患者中的应用可能受到限制。基于这些前提,我们进行了一项快速综述,以确定针对这一特定人群可能的替代药物。通过检索PubMed和考克兰图书馆,我们选择了关于在重症和非重症监护环境中谵妄药物治疗以及与急性精神病或痴呆相关的激越治疗的最新随机试验系统评价。我们确定了在每个考虑的人群中疗效显著优于安慰剂或作为对照治疗的氟哌啶醇的药物,并根据验证标准评估了关联强度。此外,我们收集了其他相关临床要素(即常见不良事件、与COVID-19药物的药物相互作用、每日剂量)和监管要素(即治疗适应症、禁忌症、可用剂型)的数据。总共纳入了10项系统评价。总体而言,在四个选定人群中,相对较少的药物显示出优于安慰剂的效果。与安慰剂相比,在重症监护病房(ICU)环境中,喹硫平和右美托咪定显示出显著益处,而在非ICU环境中,没有一种药物显示出显著益处。考虑到来自间接人群(与急性精神病或痴呆相关的激越)的数据,阿立哌唑、喹硫平和利培酮在两到三个不同人群中显示出潜在益处。尽管快速综述方法存在局限性且使用了来自间接人群的数据,但检索到的证据可以切实支持参与COVID-19疫情防控的一线从业者的治疗选择,并为特别脆弱人群谵妄的治疗指明未来研究方向。