Yang Xuelian, Yang Yulian, Miao Gelan, Yang Chaobing, Liu Li, Lei Xianying
Department of Intensive Care Unite, The Affiliated Hospital of Southwest Medical University, Luzhou, China.
Department of Anesthesiology, The Affiliated Hospital of Southwest Medical University, Luzhou, Sichuan, China.
BMJ Open. 2024 Dec 10;14(12):e091172. doi: 10.1136/bmjopen-2024-091172.
Remimazolam is a novel ultra-short-acting benzodiazepine that allosterically modulates γ-aminobutyric acid type A receptors to induce sedative effects. Remimazolam was approved by China for procedural sedation in 2020. Intensive care unit (ICU) patients frequently exhibit impaired liver and renal function as well as haemodynamic instability; thus, the pharmacokinetic properties of remimazolam may offer advantages for ICU sedation. A comprehensive evaluation of the relevant studies warrants further discussion. This systematic review aims to compare the efficacy and safety of the novel intravenous anaesthetic remimazolam with that of commonly used anaesthetics in the ICU.
The following databases will be searched: Embase, Cochrane Library, PubMed, MEDLINE, Web of Science, CNKI and WanFang to retrieve relevant randomised controlled trials (RCTs). This protocol was developed by the Preferred Reporting Items for Systematic Reviews and Meta-Analyses Protocols 2020. RCTs about the use of remimazolam for sedation during ICU mechanical ventilation will be included. Two investigators will independently screen articles and extract data according to predefined inclusion and exclusion criteria. Following a qualitative evaluation of each study, data analysis will be conducted using Review Manager 5.4 software. The planned start and end dates for the study were placed on 1 June 2024 and 31 October 2024, respectively.
This protocol for the systematic evaluation and meta-analysis does not involve individual patient data; thus, ethical approval is not required. This will be the first meta-analysis to assess the sedative efficacy and safety of remimazolam in the ICU and to provide evidence to inform clinical decision-making. The findings will be disseminated through conference presentations and publications in peer-reviewed journals relevant to the field.
CRD42024554425.
瑞马唑仑是一种新型超短效苯二氮䓬类药物,可通过变构调节γ-氨基丁酸A型受体来产生镇静作用。瑞马唑仑于2020年在中国获批用于手术镇静。重症监护病房(ICU)患者常出现肝肾功能受损以及血流动力学不稳定的情况;因此,瑞马唑仑的药代动力学特性可能为ICU镇静带来优势。对相关研究进行全面评估值得进一步探讨。本系统评价旨在比较新型静脉麻醉药瑞马唑仑与ICU常用麻醉药的疗效和安全性。
将检索以下数据库:Embase、Cochrane图书馆、PubMed、MEDLINE、Web of Science、中国知网和万方,以检索相关随机对照试验(RCT)。本方案依据2020年系统评价与Meta分析方案的首选报告项目制定。将纳入关于瑞马唑仑在ICU机械通气期间用于镇静的RCT。两名研究人员将根据预定义的纳入和排除标准独立筛选文章并提取数据。在对每项研究进行定性评估后,将使用Review Manager 5.4软件进行数据分析。该研究计划的开始和结束日期分别为2024年6月1日和2024年10月31日。
本系统评价和Meta分析方案不涉及个体患者数据;因此,无需伦理批准。这将是第一项评估瑞马唑仑在ICU中的镇静疗效和安全性并为临床决策提供依据的Meta分析。研究结果将通过会议报告和在该领域相关的同行评审期刊上发表进行传播。
PROSPERO注册号:CRD42024554425。