Cibotto Cédric, Pasquier Mathieu, Beysard Nicolas, Rouyer Frédéric, Grosgurin Olivier, Bourgeois Laurent, Erriquez Elio, Braun Ely, Gartner Birgit Andrea, Desmettre Thibaut, Suppan Laurent
Division of Anaesthesiology, Department of Acute Care Medicine, Geneva University Hospitals, Rue Gabrielle-Perret-Gentil 4, Geneva, 1205, Switzerland.
Department of Anaesthesiology, Pharmacology, Intensive Care and Emergency Medicine, Faculty of Medicine, University of Geneva, Geneva, Switzerland.
BMC Emerg Med. 2025 Jul 1;25(1):112. doi: 10.1186/s12873-025-01266-0.
In critically ill patients, tracheal intubation may be required in the prehospital setting, where airway management presents unique technical and logistical challenges. While videolaryngoscopy has emerged as a potential alternative to direct laryngoscopy by providing a better and easier visualization of the glottis, the improved view of anatomical structures does not necessarily correlate with successful tracheal tube placement. Intubation may be harder because novice providers performing videolaryngoscopy may only look at the screen and only obtain a two-dimensional representation of the patient's airways. By directly visualizing the airways, these providers may obtain a better 3D apprehension and an improved mental visualization of the patient's anatomy. We compared the impact of an unrestricted videolaryngoscopy use with a sequence consisting in direct visualization of the airway followed by videolaryngoscopy ("Direct Laryngoscopy-to-VideoLaryngoscopy sequence" or "DL-VL sequence") on time to intubation among novice providers.
This was a parallel group simulated randomized controlled superiority trial. Participants were medical students or junior residents with an experience of less than 10 intubations. After a presentation and workshop on direct laryngoscopy and videolaryngoscopy, participants were randomized in two groups. In the control group, participants were free to use of the videolaryngoscope as they intended. In the other group (DL-VL sequence), participants were told to perform an initial direct laryngoscopy without looking at the video screen until they reached the epiglottis. All intubations were conducted in a simulated prehospital environment, with a high-fidelity manikin placed supine on the floor. Each participant performed three intubations of increasing levels of difficulty. The primary outcome was the time to intubation. Secondary outcomes included first-pass success, time to ventilation, and number of intubation attempts. The chi-squared test was used to compare categorical variables while the t-test was used to compare continuous variables.
Time to intubation was shorter in the control group (22±8 s vs. 27±11 s, p < 0.001). This difference was consistent in all levels of difficulties. First-pass success rates were similar (99/111, 89% in the control group vs. 85/105, 81%, p = 0.089). Time to ventilation was significantly shorter in the control group (37±9 vs. 41±11 s, p = 0.008). The mean number of intubation attempts was similar between groups (p = 0.231).
In this simulated study among novice providers, direct airway visualization prior to videolaryngoscopy did not improve time to intubation or to ventilation.
ClinicalTrials.gov, Registration Number: NCT06918717, registered on April 8th, 2025. Retrospectively registered.
在危重症患者中,院前环境可能需要气管插管,而气道管理存在独特的技术和后勤挑战。虽然视频喉镜已成为直接喉镜的一种潜在替代方法,可更好、更轻松地观察声门,但解剖结构的改善视野并不一定与气管导管成功置入相关。插管可能更困难,因为进行视频喉镜检查的新手可能只看屏幕,只能获得患者气道的二维图像。通过直接观察气道,这些医护人员可能会对患者的解剖结构有更好的三维认知和更清晰的心理图像。我们比较了新手医护人员中无限制使用视频喉镜与先直接观察气道再使用视频喉镜的顺序(“直接喉镜-视频喉镜顺序”或“DL-VL顺序”)对插管时间的影响。
这是一项平行组模拟随机对照优势试验。参与者为插管经验少于10次的医学生或初级住院医师。在进行直接喉镜和视频喉镜的演示及培训后,参与者被随机分为两组。在对照组中,参与者可按自己的意愿自由使用视频喉镜。在另一组(DL-VL顺序组)中,参与者被告知在到达会厌之前先进行直接喉镜检查,不看视频屏幕。所有插管均在模拟的院前环境中进行,使用高仿真人体模型仰卧在地板上。每位参与者进行三次难度递增的插管。主要结局是插管时间。次要结局包括首次通过成功率、通气时间和插管尝试次数。采用卡方检验比较分类变量,采用t检验比较连续变量。
对照组的插管时间更短(22±8秒 vs. 27±11秒,p < 0.001)。在所有难度水平上,这种差异都是一致的。首次通过成功率相似(对照组99/111,89% vs. 85/105,81%,p = 0.089)。对照组的通气时间明显更短(37±9秒 vs. 41±11秒,p = 0.008)。两组间的平均插管尝试次数相似(p = 0.231)。
在这项针对新手医护人员的模拟研究中,在视频喉镜检查前直接观察气道并未改善插管时间或通气时间。
ClinicalTrials.gov,注册号:NCT06918717,于2025年4月8日注册。回顾性注册。