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视频喉镜与直接喉镜用于新生儿气管插管的比较。

Videolaryngoscopy versus direct laryngoscopy for tracheal intubation in neonates.

机构信息

Division of Neonatology, Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.

Department of Pediatrics, Section of Neonatology, Baylor College of Medicine, Houston, Texas, USA.

出版信息

Cochrane Database Syst Rev. 2023 May 12;5(5):CD009975. doi: 10.1002/14651858.CD009975.pub4.

Abstract

BACKGROUND

Establishment of a secure airway is a critical part of neonatal resuscitation in the delivery room and the neonatal intensive care unit. Videolaryngoscopy has the potential to facilitate successful endotracheal intubation, and decrease adverse consequences of a delay in airway stabilization. Videolaryngoscopy may enhance visualization of the glottis and intubation success in neonates. This is an update of a review first published in 2015, and updated in 2018.

OBJECTIVES

To determine the effectiveness and safety of videolaryngoscopy compared to direct laryngoscopy in decreasing the time and attempts required for endotracheal intubation and increasing the success rate on first intubation attempt in neonates (0 to 28 days of age).

SEARCH METHODS

In November 2022, we updated the search for trials evaluating videolaryngoscopy for neonatal endotracheal intubation in CENTRAL, MEDLINE, Embase, CINAHL, and BIOSIS. We also searched abstracts of the Pediatric Academic Societies, clinical trials registries (www.

CLINICALTRIALS

gov; www.controlled-trials.com), and reference lists of relevant studies.

SELECTION CRITERIA

Randomized controlled trials (RCTs), quasi-RCTs, cluster-RCTs, or cross-over trials, in neonates (0 to 28 days of age), evaluating videolaryngoscopy with any device used for endotracheal intubation compared with direct laryngoscopy.

DATA COLLECTION AND ANALYSIS

Three review authors performed data collection and analysis, as recommended by Cochrane Neonatal. Two review authors independently assessed studies identified by the search strategy for inclusion. We used the GRADE approach to assess the certainty of the evidence.

MAIN RESULTS

The updated search yielded 7786 references, from which we identified five additional RCTs for inclusion, seven ongoing trials, and five studies awaiting classification. Three studies were included in the previous version of the review. For this update, we included eight studies, which provided data on 759 intubation attempts in neonates. We included neonates of either sex, who were undergoing endotracheal intubation in international hospitals. Different videolaryngoscopy devices (including C-MAC, Airtraq, and Glidescope) were used in the studies. For the primary outcomes; videolaryngoscopy may not reduce the time required for successful intubation when compared with direct laryngoscopy (mean difference [MD] 0.74, 95% confidence interval [CI] -0.19 to 1.67; 5 studies; 505 intubations; low-certainty evidence). Videolaryngoscopy may result in fewer intubation attempts (MD -0.08, 95% CI -0.15 to 0.00; 6 studies; 659 intubations; low-certainty evidence). Videolaryngoscopy may increase the success of intubation at the first attempt (risk ratio [RR] 1.24, 95% CI 1.13 to 1.37; risk difference [RD] 0.14, 95% CI 0.08 to 0.20; number needed to treat for an additional beneficial outcome [NNTB] 7, 95% CI 5 to 13; 8 studies; 759 intubation attempts; low-certainty evidence).  For the secondary outcomes; the evidence is very uncertain about the effect of videolaryngoscopy on desaturation or bradycardia episodes, or both, during intubation (RR 0.94, 95% CI 0.38 to 2.30; 3 studies; 343 intubations; very-low certainty evidence). Videolaryngoscopy may result in little to no difference in the lowest oxygen saturations during intubation compared with direct laryngoscopy (MD -0.76, 95% CI -5.74 to 4.23; 2 studies; 359 intubations; low-certainty evidence). Videolaryngoscopy likely results in a slight reduction in the incidence of airway trauma during intubation attempts compared with direct laryngoscopy (RR 0.21, 95% CI 0.05 to 0.79; RD -0.04, 95% CI -0.07 to -0.01; NNTB 25, 95% CI 14 to 100; 5 studies; 467 intubations; moderate-certainty evidence). There were no data available on other adverse effects of videolaryngoscopy. We found a high risk of bias in areas of allocation concealment and performance bias in the included studies.

AUTHORS' CONCLUSIONS: Videolaryngoscopy may increase the success of intubation on the first attempt and may result in fewer intubation attempts, but may not reduce the time required for successful intubation (low-certainty evidence). Videolaryngoscopy likely results in a reduced incidence of airway-related adverse effects (moderate-certainty evidence). These results suggest that videolaryngoscopy may be more effective and potentially reduce harm when compared to direct laryngoscopy for endotracheal intubation in neonates. Well-designed, adequately powered RCTS are necessary to confirm the efficacy and safety of videolaryngoscopy in neonatal intubation.

摘要

背景

在产房和新生儿重症监护病房中,建立安全气道是新生儿复苏的关键部分。视频喉镜有潜力促进气管内插管的成功,并减少气道稳定延迟的不良后果。视频喉镜可增强对声门的可视化效果,并提高新生儿插管的成功率。这是 2015 年首次发表的一篇综述的更新版本,于 2018 年进行了更新。

目的

确定视频喉镜与直接喉镜相比,在减少气管内插管所需的时间和尝试次数,以及提高首次插管尝试成功率方面的有效性和安全性,即在新生儿(0 至 28 天龄)中。

检索方法

2022 年 11 月,我们更新了对评估视频喉镜用于新生儿气管内插管的试验的检索,检索了 CENTRAL、MEDLINE、Embase、CINAHL 和 BIOSIS。我们还检索了儿科学术协会的摘要、临床试验注册处(www.clinicaltrials.gov;www.controlled-trials.com)和相关研究的参考文献列表。

选择标准

随机对照试验(RCTs)、半随机对照试验、整群随机对照试验或交叉试验,纳入 0 至 28 天龄的新生儿,评估任何用于气管内插管的视频喉镜设备与直接喉镜的比较。

数据收集和分析

三位综述作者按照 Cochrane 新生儿的建议进行了数据收集和分析。两位综述作者独立评估了搜索策略确定的研究是否符合纳入标准。我们使用 GRADE 方法评估证据的确定性。

主要结果

更新后的搜索产生了 7786 条参考文献,从中我们确定了另外 5 项 RCT 纳入研究,7 项正在进行的试验和 5 项有待分类的研究。之前的版本综述纳入了 3 项研究。对于本次更新,我们纳入了 8 项研究,这些研究提供了 759 次新生儿插管尝试的数据。我们纳入了男性和女性新生儿,他们在国际医院接受气管内插管。研究中使用了不同的视频喉镜设备(包括 C-MAC、Airtraq 和 Glidescope)。对于主要结局,与直接喉镜相比,视频喉镜可能不会减少成功插管所需的时间(平均差值 [MD] 0.74,95%置信区间 [CI] -0.19 至 1.67;5 项研究;505 次插管;低确定性证据)。视频喉镜可能会减少插管尝试次数(MD -0.08,95%置信区间 -0.15 至 0.00;6 项研究;659 次插管;低确定性证据)。视频喉镜可能会增加首次尝试插管的成功率(风险比 [RR] 1.24,95%置信区间 1.13 至 1.37;差异风险 [RD] 0.14,95%置信区间 0.08 至 0.20;需要治疗的人数增加一个有益结果 [NNTB] 7,95%置信区间 5 至 13;8 项研究;759 次插管尝试;低确定性证据)。对于次要结局,关于视频喉镜对插管期间缺氧或心动过缓发作或两者同时发生的影响的证据非常不确定(RR 0.94,95%置信区间 0.38 至 2.30;3 项研究;343 次插管;极低确定性证据)。与直接喉镜相比,视频喉镜可能不会对插管期间的最低氧饱和度产生显著差异(MD -0.76,95%置信区间 -5.74 至 4.23;2 项研究;359 次插管;低确定性证据)。与直接喉镜相比,视频喉镜可能会略微降低插管尝试时气道损伤的发生率(RR 0.21,95%置信区间 0.05 至 0.79;差异风险 [RD] -0.04,95%置信区间 -0.07 至 -0.01;NNTB 25,95%置信区间 14 至 100;5 项研究;467 次插管;中等确定性证据)。没有关于视频喉镜其他不良影响的数据。我们发现纳入研究在分配隐藏和实施偏倚方面存在高偏倚风险。

作者结论

与直接喉镜相比,视频喉镜可能会增加首次插管的成功率,并可能减少插管尝试次数,但可能不会减少成功插管所需的时间(低确定性证据)。视频喉镜可能会降低与气道相关的不良事件的发生率(中等确定性证据)。这些结果表明,与直接喉镜相比,视频喉镜可能在新生儿气管内插管中更有效,并可能降低危害。需要设计良好、充分有力的 RCT 来证实视频喉镜在新生儿插管中的疗效和安全性。

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