Comparison of Clinical Performance of I-gel and Fastrach Laryngeal Mask Airway as an Intubating Device in Adults: A Systematic Review and Meta-Analysis.

Maria Luisa Machado Assis,Fabricio Batistella Zasso,Matheus Pedrotti Chavez,Eduardo Cirne Toledo,Gabriel Motta,Leonardo Duarte Moraes,Eric Pasqualotto,Rafael Oliva Morgado Ferreira,Naveed Siddiqui,Kong Eric You-Ten
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Abstract

BACKGROUND The supraglottic airway device (SGD) was introduced as a breakthrough in airway management. The Fastrach emerged as the first commercially available intubating SGD, drawing extensive investigation. I-gel is a more recent device that has gained popularity, can be used as an intubating SGD, and replaced Fastrach in many institutions. However, there is uncertainty regarding the comparison between these devices in terms of efficacy for intubation and ventilation, and safety in an airway rescue situation. METHODS PubMed, EMBASE, Scopus, and Cochrane databases were searched for randomized controlled trials (RCTs) comparing I-gel and Fastrach SGD in adult patients undergoing intubation. The primary outcome was the first-pass success rate for tracheal intubation. Secondary outcomes were tracheal intubation time, SGD insertion time and success, and complications. We computed risk ratios (RRs) to assess binary end points and weighted mean differences (WMDs) for continuous outcomes, with corresponding 95% confidence intervals (CIs) for the primary outcome and its subgroup analysis (P < .05 was considered statistically significant) and 99% CI after Bonferroni correction for the secondary outcomes (P < .01 was considered statistically significant). RESULTS This study included a total of 14 RCTs encompassing 1340 patients. The results indicated a significant difference in the first-pass success rate favoring Fastrach (RR, 0.81; 95% CI, 0.67-0.98; P = .03; I² = 91%). In the subgroup analysis, when a flexible scope was utilized through I-gel, providers achieved a better tracheal intubation first-pass success rate (RR, 1.05; 95% CI, 1.01-1.11; P = .03; I² = 0%), compared with the Fastrach. Overall intubation success rates (RR, 0.92; 99% CI, 0.82-1.04; P = .08, I² = 92%) and time (WMD - 1.03 seconds; 99% CI, -4.75 to 2.69; P = .48; I² = 84%) showed no significant difference irrespective of the device used. There was no significant difference regarding device insertion time by the providers (WMD -6.48 seconds; 99% CI, -13.23 to 0.27; P = .01; I2 = 98%). Success rates of the providers' initial SGD insertion and complications such as sore throat (RR, 1.01; 99% CI, 0.65-1.57; P = .95, I² = 33%) and blood presence post-SGD removal (RR, 0.89; 99% CI, 0.42-1.86; P = .68, I² = 0%) showed no significant difference. CONCLUSIONS Based on our findings, a higher first-pass success rate was observed with the use of Fastrach when compared to I-gel. However, the use of I-gel might result in a better intubation success rate with the flexible scope-guided intubation. There are no significant differences in performance in terms of the success rate for intubation overall, time for device insertion, or time to intubation or complications regardless of the device used.
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I-gel 和 Fastrach 喉罩气道作为成人插管设备的临床性能比较:系统回顾与元分析》。
背景声门上气道装置(SGD)作为气道管理的一项突破而问世。Fastrach 是第一款商用插管 SGD,引起了广泛的研究。I-gel 是最近才流行起来的一种设备,可用作插管式 SGD,并在许多机构中取代了 Fastrach。方法检索了 SpubMed、EMBASE、Scopus 和 Cochrane 数据库中的随机对照试验 (RCT),比较了 I-gel 和 Fastrach SGD 在成人插管患者中的应用。主要结果是气管插管的首次成功率。次要结果是气管插管时间、SGD 插入时间和成功率以及并发症。我们计算了风险比(RRs)以评估二元终点,并计算了连续结果的加权平均差(WMDs),对主要结果及其亚组分析计算了相应的 95% 置信区间(CIs)(P < .05 为有统计学意义),对次要结果计算了 Bonferroni 校正后的 99% CI(P < .01 为有统计学意义)。结果表明,法斯拉赫的首次通过成功率与其他疗法有显著差异(RR,0.81;95% CI,0.67-0.98;P = .03;I² = 91%)。在亚组分析中,与 Fastrach 相比,当通过 I-gel 使用柔性探头时,医护人员的气管插管一次成功率更高(RR,1.05;95% CI,1.01-1.11;P = .03;I² = 0%)。总体插管成功率(RR,0.92;99% CI,0.82-1.04;P = .08;I² = 92%)和时间(WMD - 1.03 秒;99% CI,-4.75 至 2.69;P = .48;I² = 84%)显示,无论使用哪种设备,均无显著差异。医疗服务提供者插入器械的时间也无明显差异(WMD -6.48 秒;99% CI,-13.23 至 0.27;P = .01;I2 = 98%)。医疗服务提供者初次插入 SGD 的成功率以及咽喉痛(RR,1.01;99% CI,0.65-1.57;P = .95,I² = 33%)和取出 SGD 后出现血迹(RR,0.89;99% CI,0.42-1.86;P = .68,I² = 0%)等并发症无显著差异。然而,使用 I-gel 可能会使柔性镜引导下的插管成功率更高。无论使用哪种器械,在总体插管成功率、器械插入时间、插管时间或并发症方面都没有明显差异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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