Department of Anesthesiology, Chi Mei Medical Center, Tainan, Taiwan.
Department of Anesthesiology, Kaohsiung Chang Gung Memorial Hospital, Chang Gung University and College of Medicine, 123 Ta-Pei Road, Niao-Song District, Kaohsiung, 833, Taiwan.
Can J Anaesth. 2021 Jan;68(1):137-147. doi: 10.1007/s12630-020-01830-1. Epub 2020 Oct 21.
This meta-analysis aimed to assess the impact of cricoid pressure (CP) application on intubation outcomes.
Electronic databases (i.e., MEDLINE, PubMed, Embase, and Cochrane review) were searched from inception to 2 June 2020 for randomized-controlled trials that assessed the intubation outcomes in adult patients using laryngoscopic approaches with and without the application of CP (i.e., CP vs non-CP group). The primary outcome was the successful first-attempt intubation rate (SFAIR), and the secondary outcomes were intubation time, incidences of poor laryngoscopic views (i.e., Cormack and Lehane grade 3-4), airway complications, and pulmonary aspiration.
A total of five trials (published from 2005 to 2018) were included, and all tracheal intubations were performed by anesthesiologists or nurse anesthetists with a video (n = 3) or Macintosh laryngoscope (n = 2) in the operating room. We found no significant difference in SFAIR (risk ratio [RR], 0.98; P = 0.37), incidence of poor laryngoscopic views (RR, 1.49; P = 0.21), and risk of sore throat (RR, 1.17; P = 0.73) between the two groups. Nevertheless, the intubation time on the first successful attempt was slightly longer (weighted mean difference = 4.40 sec, P = 0.002) and risk of hoarseness was higher (RR, 1.70; P = 0.03) in the CP group compared with in the non-CP group. The secondary outcome "pulmonary aspiration" was not analyzed because only one trial was available.
The application of CP did not have a negative impact on the SFAIR or laryngoscopic view. Nevertheless, this maneuver may slightly prolong intubation time and increase the risk of postoperative hoarseness.
本荟萃分析旨在评估环状软骨施压(CP)应用对插管结果的影响。
从建库至 2020 年 6 月 2 日,电子数据库(即 MEDLINE、PubMed、Embase 和 Cochrane 评价)检索了评估成人经喉镜插管时应用和不应用 CP(CP 组与非 CP 组)的插管结局的随机对照试验。主要结局是首次尝试插管成功率(SFAIR),次要结局是插管时间、喉镜显露不佳的发生率(即 Cormack 和 Lehane 分级 3-4)、气道并发症和肺误吸。
共纳入 5 项试验(发表于 2005 年至 2018 年),所有气管插管均由麻醉医师或麻醉护士在手术室使用视频喉镜(n = 3)或 Macintosh 喉镜(n = 2)进行。我们发现两组间 SFAIR(风险比 [RR],0.98;P = 0.37)、喉镜显露不佳的发生率(RR,1.49;P = 0.21)和咽痛风险(RR,1.17;P = 0.73)无显著差异。然而,CP 组首次成功尝试的插管时间略长(加权均数差=4.40 秒,P = 0.002),且 CP 组声音嘶哑的风险更高(RR,1.70;P = 0.03)。由于仅有 1 项试验,故未对次要结局“肺误吸”进行分析。
CP 的应用对 SFAIR 或喉镜显露没有负面影响。然而,该操作可能会略微延长插管时间并增加术后声音嘶哑的风险。