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瑞马唑仑-氟马西尼与丙泊酚用于脊柱大手术麻醉后延迟苏醒的比较:一项多中心、单盲、随机对照试验方案

Comparison of remimazolam-flumazenil versus propofol on delayed emergence from anaesthesia in major spine surgery: protocol for a multicentre, single-blinded, randomised controlled trial.

作者信息

Sun Jingjing, Luo Wei, Wen Liang, Xiao Yanying, Dai Ruping

机构信息

Department of Anesthesiology, The Second Xiangya Hospital, Central South University, Changsha, Hunan Province, China.

Anesthesiology Research Institute, Central South University, Changsha, Hunan, China.

出版信息

BMJ Open. 2025 Aug 8;15(8):e097541. doi: 10.1136/bmjopen-2024-097541.

Abstract

INTRODUCTION

Prolonged infusion of anaesthetics is associated with delayed emergence (DE) from general anaesthesia due to residual drug effects. Remimazolam besylate, a novel ultrashort-acting benzodiazepine, exhibits minimal accumulation, and its sedative effects can be reversed with flumazenil. This study aimed to evaluate the incidence of DE from anaesthesia using remimazolam-flumazenil or propofol in patients undergoing major spine surgery.

METHODS AND ANALYSIS

This multicentre, randomised controlled trial will be conducted in five hospitals in Hunan Province, China. Approximately 164 patients undergoing major spine surgery lasting >3 hours will be randomly assigned to two groups in a 1:1 ratio. In the remimazolam-flumazenil group, remimazolam will be administered for anaesthesia induction and maintenance, followed by flumazenil for reversal after surgery, whereas propofol will be administered in the propofol group. The primary outcome is the incidence of DE from anaesthesia. The secondary outcomes include the time to obey verbal command, time to bispectral index over 80, time to extubation, length of stay in the post-anaesthesia care unit (PACU), Richmond Agitation-Sedation Scale scores and Modified Aldrete scores on arrival at PACU, at 30 and 60 min, as well as adverse events throughout recovery. All statistical tests will be conducted using SPSS version 27.0 (IBM Corp., Armonk, NY, USA). A -value<0.05 will be considered significant.

ETHICS AND DISSEMINATION

This randomised controlled trial protocol has received ethical approval from the Second Xiangya Hospital, Central South University (Approval number: LYEC2024-0357). All participants will be required to provide written informed consent before study enrolment. The findings will be disseminated at academic conferences and published in a peer-reviewed journal.

TRIAL REGISTRATION NUMBER

ChiCTR2400092451.

摘要

引言

由于残留药物效应,长时间输注麻醉剂与全身麻醉后苏醒延迟(DE)相关。新型超短效苯二氮䓬类药物苯磺酸瑞马唑仑蓄积极少,其镇静作用可用氟马西尼逆转。本研究旨在评估接受脊柱大手术的患者使用瑞马唑仑-氟马西尼或丙泊酚麻醉后苏醒延迟的发生率。

方法与分析

本多中心随机对照试验将在中国湖南省的五家医院进行。约164例接受持续时间超过3小时的脊柱大手术的患者将按1:1比例随机分为两组。在瑞马唑仑-氟马西尼组,瑞马唑仑用于麻醉诱导和维持,术后用氟马西尼进行逆转,而丙泊酚组将使用丙泊酚。主要结局是麻醉后苏醒延迟的发生率。次要结局包括对口头指令有反应的时间、脑电双频指数超过80的时间、拔管时间、在麻醉后监护病房(PACU)的停留时间、到达PACU时、30分钟和60分钟时的里士满躁动-镇静量表评分和改良Aldrete评分,以及整个恢复过程中的不良事件。所有统计检验将使用SPSS 27.0版(美国纽约州阿蒙克市IBM公司)进行。P值<0.05将被视为具有统计学意义。

伦理与传播

本随机对照试验方案已获得中南大学湘雅二医院伦理批准(批准号:LYEC2024-0357)。所有参与者在研究入组前均需提供书面知情同意书。研究结果将在学术会议上公布,并发表在同行评审期刊上。

试验注册号

ChiCTR2400092451。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c83/12336592/cdf56e38a494/bmjopen-15-8-g001.jpg

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