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评估瑞芬太尼与快速起效的神经肌肉阻滞剂相比,用于有胃内容物误吸风险的患者进行快速序贯诱导和插管的效果:一项非劣效性简单盲随机对照试验(REMICRUSH 研究)的研究方案。

Assessment of remifentanil for rapid sequence induction and intubation in patients at risk of pulmonary aspiration of gastric contents compared to rapid-onset paralytic agents: study protocol for a non-inferiority simple blind randomized controlled trial (the REMICRUSH study).

机构信息

Université de Nantes, CHU Nantes, Pôle Anesthésie-Réanimation, Service d'Anesthésie Réanimation Chirurgicale, Hôtel Dieu, Nantes, F-44093, France.

CHU de Lille, Pole Anesthésie Réanimation, Hôpital Claude Huriez, Lille, France.

出版信息

Trials. 2021 Mar 30;22(1):237. doi: 10.1186/s13063-021-05192-x.

Abstract

BACKGROUND

Rapid-onset paralytic agents are recommended to achieve muscle relaxation and facilitate tracheal intubation during rapid sequence induction in patients at risk of pulmonary aspiration of gastric contents. However, opioids are frequently used in this setting. The study's objective is to demonstrate the non-inferiority of remifentanil compared to rapid-onset paralytic agents, in association with an hypnotic drug, for tracheal intubation in patients undergoing  procedure under general anesthesia and at risk of pulmonary aspiration of gastric contents.

METHODS

The REMICRUSH (Remifentanil for Rapid Sequence Induction of Anaesthesia) study is a multicenter, single-blinded, non-inferiority randomized controlled trial comparing remifentanil (3 to 4 μg/kg) with rapid-onset paralytic agents (succinylcholine or rocuronium 1 mg/kg) for rapid sequence induction in 1150 adult surgical patients requiring tracheal intubation during general anesthesia. Enrolment started in October 2019 in 15 French anesthesia units. The expected date of the final follow-up is October 2021. The primary outcome is the proportion of successful tracheal intubation without major complications. A non-inferiority margin of 7% was chosen. Analyses of the intent-to-treat and per-protocol populations are planned.

DISCUSSION

The REMICRUSH trial protocol has been approved by the ethics committee of The Comité de Protection des Personnes Sud-Ouest et Outre-Mer II and will be carried out according to the principles of the Declaration of Helsinki and the Good Clinical Practice guidelines. The results of this study will be disseminated through presentations at scientific conferences and publications in peer-reviewed journals. The REMICRUSH trial is the first randomized controlled trial powered to investigate whether remifentanil with hypnotics is non-inferior to rapid-onset paralytic agents with hypnotic in rapid sequence induction of anesthesia for full stomach patients considering successful tracheal intubation without major complication.

TRIAL REGISTRATION

ClinicalTrials.gov NCT03960801. Registered on May 23, 2019.

摘要

背景

在有胃内容物吸入风险的患者中,快速序贯诱导时推荐使用快速起效的麻痹剂来实现肌肉松弛并便于气管插管。然而,在这种情况下经常使用阿片类药物。本研究的目的是证明与催眠药物联合使用时,瑞芬太尼与快速起效的麻痹剂相比在全麻下进行手术且有胃内容物吸入风险的患者中进行快速序贯诱导时用于气管插管不劣于后者。

方法

REMICRUSH(瑞芬太尼用于全麻下快速序贯诱导)研究是一项多中心、单盲、非劣效性随机对照试验,比较了瑞芬太尼(3 至 4μg/kg)与快速起效的麻痹剂(琥珀胆碱或罗库溴铵 1mg/kg)用于全麻下 1150 例需要气管插管的成年手术患者的快速序贯诱导。2019 年 10 月在 15 个法国麻醉单位开始入组。预计最终随访日期为 2021 年 10 月。主要结局是无严重并发症的气管插管成功率。选择了 7%的非劣效性边界。计划进行意向治疗和方案人群的分析。

讨论

REMICRUSH 试验方案已获得 Sud-Ouest et Outre-Mer II 保护委员会的伦理委员会批准,并将根据赫尔辛基宣言和良好临床实践指南的原则进行。该研究的结果将通过在科学会议上的演讲和同行评议期刊上的发表进行传播。REMICRUSH 试验是第一项旨在研究在考虑成功进行无严重并发症的气管插管的情况下,瑞芬太尼联合催眠药与快速起效的麻痹剂联合催眠药在全麻下快速序贯诱导时用于饱胃患者是否不劣于前者的随机对照试验。

试验注册

ClinicalTrials.gov NCT03960801。于 2019 年 5 月 23 日注册。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b5c/8010986/f084168dc14d/13063_2021_5192_Fig1_HTML.jpg

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