Taboada M, Estany-Gestal A, Rama-Maceiras P, Orallo M A, Bermúdez M, Barreiro C, Gómez L, Amor M, Otero F, Fernández J, Molins N, Amate J J, Bascuas B, Rey R, Alonso M C, Castro M J, Sarmiento A, Dos Santos L, Nieto C, Paredes S, Velasco A, Taboada C, Martín L, Campaña D, Mosquera E, Novoa C, Varela S, da Silva L, Domínguez E, Bedoya A, Gómez A I, Estévez M, Martínez P, Sotojove R, Naveiro A, Díaz C, Ruido R, Mirón P, González M, Francisco C, Regueira J, Peiteado M, Eiras M, Paz E
Department of Anaesthesiology, University Clinical Hospital of Santiago, Santiago de Compostela, A Coruña, Spain.
Research Methodology Unit, Fundación Instituto de Investigaciones Sanitarias (FIDIS), Santiago de Compostela, A Coruña, Spain.
Rev Esp Anestesiol Reanim (Engl Ed). 2025 Jan;72(1):101649. doi: 10.1016/j.redare.2024.101649. Epub 2024 Nov 12.
Standard tracheal intubation performed in the operating room is based on direct laryngoscopy using a standard Macintosh laryngoscope. Several authors recommend the universal use of a video laryngoscope as the first option for all intubations, regardless of whether the patient has predictors of a difficult airway or not. We hypothesize that using the McGrath video laryngoscope as the first intubation option increases the frequency of patients with easy intubation, and decreases intubation-related complications.
The VIDEOLAR-SURGERY trial is a prospective, multicentre, open-label, interventional, before-after study. In the pre-implementation period (non-interventional phase, 6-9 months [2600 intubations]), 35 anaesthesiologists from 8 hospitals perform all tracheal intubations for an elective or urgent surgical procedure using the standard Macintosh direct laryngoscope as the first intubation option. During the implementation period (2 months), each anaesthesiologist is given a McGrath Mac video laryngoscope and trained in its use. During the post-implementation period (interventional-phase, 6-9 months [2600 intubations]), the 35 anaesthesiologists perform all tracheal intubations using a McGrath Mac video laryngoscope as the first intubation option. The main objective of this study is to evaluate whether the use of a McGrath Mac video laryngoscope as the first intubation option increases the percentage of patients with easy intubation compared with the standard Macintosh laryngoscope.
The study protocol was approved on 2 May 2023 by the Ethics Committee of Galicia, Spain (CEI-SL, code No. 2023-177), and was registered on the Clinicaltrials.gov clinical trials registry under No. NCT NCT05850260. Informed consent is required. The results will be submitted for publication in a peer-reviewed journal and presented at one or more scientific conferences. If video laryngoscopy improves easy intubation compared with Macintosh direct laryngoscopy in all operating room intubations, its use may well become standard practice, thereby decreasing the risks of intubation-related complications.
手术室中进行的标准气管插管是基于使用标准麦金托什喉镜的直接喉镜检查。几位作者建议,无论患者是否有困难气道的预测因素,都应普遍将视频喉镜作为所有插管的首选。我们假设,将麦格拉斯视频喉镜作为首次插管选择会增加容易插管患者的比例,并减少与插管相关的并发症。
VIDEOLAR - 手术试验是一项前瞻性、多中心、开放标签、干预性、前后对照研究。在实施前阶段(非干预期,6 - 9个月[2600次插管]),来自8家医院的35名麻醉医生使用标准麦金托什直接喉镜作为首次插管选择,为择期或急诊手术进行所有气管插管。在实施期(2个月),为每位麻醉医生提供一台麦格拉斯Mac视频喉镜并进行使用培训。在实施后阶段(干预期,6 - 9个月[2600次插管]),35名麻醉医生使用麦格拉斯Mac视频喉镜作为首次插管选择进行所有气管插管。本研究的主要目的是评估与标准麦金托什喉镜相比,将麦格拉斯Mac视频喉镜作为首次插管选择是否会增加容易插管患者的百分比。
该研究方案于2023年5月2日获得西班牙加利西亚伦理委员会(CEI - SL,编号2023 - 177)批准,并在Clinicaltrials.gov临床试验注册中心注册,编号为NCT05850260。需要获得知情同意。研究结果将提交至同行评审期刊发表,并在一个或多个科学会议上展示。如果与麦金托什直接喉镜相比,视频喉镜在所有手术室插管中都能改善容易插管的情况,那么其使用很可能会成为标准操作,从而降低与插管相关并发症的风险。