Department of Anesthesiology, The Second Clinical Medical College, North Sichuan Medical College, Nanchong Central Hospital, Nanchong, China.
School of Humanities and Management, Key Laboratory for Quality of Life and Psychological Assessment and Intervention, Guangdong Medical University, Dongguan, China.
JMIR Res Protoc. 2024 Jun 12;13:e55948. doi: 10.2196/55948.
Postinduction hypotension (PIHO) is a hemodynamic abnormality commonly observed during the induction of general anesthesia. Etomidate is considered a safer drug for the induction of anesthesia because it has only minor adverse effects on the cardiovascular and pulmonary systems. Recent evidence indicates that the novel benzodiazepine remimazolam has minimal inhibitory effects on the circulation and respiration. However, the efficacy and safety of remimazolam versus etomidate in the induction of anesthesia are unclear.
To further understand the potential of remimazolam in anesthesia induction, it is necessary to design a meta-analysis to compare its effects versus the classic safe anesthetic etomidate. The aim of this study is to determine which drug has more stable hemodynamics and a lower incidence of PIHO. Our study will also yield data on sedation efficiency, time to loss of consciousness, time to awakening, incidence of injection pain, and postoperative nausea and vomiting with the two drugs.
We plan to search the Web of Science, Cochrane Library, Embase, PubMed, China National Knowledge Infrastructure, and Wanfang databases from the date of their creation until March 31, 2025. The language is limited to English and Chinese. The search terms are "randomized controlled trials," "etomidate," and "remimazolam." The incidence of PIHO is the primary outcome measure. Secondary outcomes include depth of anesthesia after induction, sedation success rate, time to loss of consciousness, hemodynamic profiles, recovery time, incidence of injection pain, and postoperative nausea and vomiting. Reviews, meta-analyses, case studies, abstracts from conferences, and commentaries will not be included. The heterogeneity of the results will be evaluated by sensitivity and subgroup analyses. RevMan software and Stata software will be used for data analysis. We will evaluate the quality of included studies using version 2 of the Cochrane risk-of-bias tool. The confidence of the evidence will be assessed through the Grading of Recommendations, Assessments, Developments, and Evaluations system.
The protocol was registered in the international PROSPERO (Prospective Register of Systematic Reviews) registry in November 2023. As of June 2024, we have performed a preliminary article search and retrieval for further review. The review and analyses are expected to be completed in March 2025. We expect to submit manuscripts for peer review by the end of June 2025.
By synthesizing the available evidence and comparing remimazolam and etomidate, we hope to provide valuable insights into the selection of anesthesia-inducing drugs to reduce the incidence of PIHO and improve patient prognosis.
PROSPERO CRD42023463120; https://tinyurl.com/333jb8bm.
INTERNATIONAL REGISTERED REPORT IDENTIFIER (IRRID): PRR1-10.2196/55948.
诱导后低血压(PIHO)是全麻诱导期间常见的血流动力学异常。依托咪酯被认为是一种更安全的麻醉诱导药物,因为它对心血管和呼吸系统只有轻微的不良影响。最近的证据表明,新型苯二氮䓬类药物 remimazolam 对循环和呼吸的抑制作用最小。然而, remimazolam 与依托咪酯在麻醉诱导中的疗效和安全性尚不清楚。
为了进一步了解 remimazolam 在麻醉诱导中的潜力,有必要设计一项荟萃分析来比较其与经典安全麻醉药依托咪酯的效果。本研究的目的是确定哪种药物具有更稳定的血流动力学和更低的 PIHO 发生率。我们的研究还将提供两种药物镇静效率、意识丧失时间、苏醒时间、注射疼痛发生率和术后恶心呕吐的数据。
我们计划从创建之日起至 2025 年 3 月 31 日,在 Web of Science、Cochrane 图书馆、Embase、PubMed、中国国家知识基础设施和万方数据库中搜索,语言限于英语和中文。搜索词为“随机对照试验”、“依托咪酯”和“ remimazolam ”。PIHO 的发生率是主要的观察结果。次要结果包括诱导后麻醉深度、镇静成功率、意识丧失时间、血流动力学特征、恢复时间、注射疼痛发生率和术后恶心呕吐。综述、荟萃分析、病例研究、会议摘要和评论将不包括在内。通过敏感性和亚组分析评估结果的异质性。RevMan 软件和 Stata 软件将用于数据分析。我们将使用第 2 版 Cochrane 偏倚风险工具评估纳入研究的质量。通过 Grading of Recommendations, Assessments, Developments, and Evaluations 系统评估证据的可信度。
该方案于 2023 年 11 月在国际 PROSPERO(系统评价前瞻性登记)注册。截至 2024 年 6 月,我们已对进一步审查进行了初步文章搜索和检索。预计将于 2025 年 3 月完成审查和分析。我们预计将在 2025 年 6 月底提交同行评审的手稿。
通过综合现有证据并比较 remimazolam 和依托咪酯,我们希望提供有关选择麻醉诱导药物的有价值的见解,以降低 PIHO 的发生率并改善患者预后。
PROSPERO CRD42023463120;https://tinyurl.com/333jb8bm。
国际注册报告标识符(IRRID):PRR1-10.2196/55948。