Tube-first Technique as a Conduit for Easy and Fast Nasal Fiberoptic Intubation

A. Shoukry, A. Sharaf
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Abstract

Classical nasal fiberoptic bronchoscope intubation may be a challenging and lengthy procedure with a 1-10% failure rate. This study aimed to compare among patients with difficult airway intubation undergoing general anesthesia, the safety, and efficacy of Tube-First (TF) nasal fiberoptic bronchoscope intubation against the Classic (CL) procedure. This single-blinded, parallel-group, randomized trial enrolled 40 adult patients with known difficult airways and scheduled for surgery under general anesthesia. The patients were randomly allocated into two (n=20 each) patient groups. In the CL group, the endotracheal tube and fiberoptic bronchoscope were inserted together through the nostril; in the TF group, the endotracheal tube insertion preceded the fiberoptic bronchoscope. In both groups, the bronchoscope was used to visualize the vocal cords and removed after ensuring the endotracheal tube position. The primary (efficacy) outcomes were the time elapsing from the bronchoscope insertion and visualizing the vocal cords (T1) and the time elapsing from the bronchoscope advancing initiation to its removal (T2). The secondary (safety) outcomes included oxygen saturation and hemodynamic parameters during the procedure. The TF group showed a significant T1 and T2 mean reduction compared to those of the CL group (37.15 ± 3.87 and 64.25 ± 8.28 vs. 55.05±4.52 and 88.25±5.49 seconds, respectively; p < 0.0001). The oxygen saturation was comparable in both groups with no desaturation (SpO2 < 90%) cases. The heart rate and mean arterial blood pressure changes were significantly lower in the TF group compared to the CL group. Among patients with difficult airway intubation undergoing general anesthesia, we found the Tube-First intubation approach was quicker and safer compared to the classical intubation technique.
导管优先技术作为一种简便快速的鼻腔纤维插管
经典的鼻纤维支气管镜插管可能是一个具有挑战性和漫长的过程,失败率为1-10%。本研究旨在比较在全麻下气道插管困难的患者中,气管插管优先(TF)鼻纤维支气管镜插管与经典(CL)插管的安全性和有效性。这项单盲、平行组、随机试验招募了40名已知气道困难并计划在全身麻醉下进行手术的成年患者。将患者随机分为两组,每组20例。CL组气管插管与纤维支气管镜经鼻孔同时置入;TF组气管内插管先于纤维支气管镜。两组均采用支气管镜观察声带,确认气管内插管位置后取出。主要疗效指标为从支气管镜插入到声带显影的时间(T1)和从支气管镜启动到取出声带的时间(T2)。次要(安全性)结果包括手术过程中的血氧饱和度和血流动力学参数。TF组T1、T2平均较CL组明显缩短(分别为37.15±3.87、64.25±8.28秒比55.05±4.52、88.25±5.49秒);P < 0.0001)。两组的血氧饱和度相当,无去饱和(SpO2 < 90%)病例。与CL组相比,TF组的心率和平均动脉血压变化明显降低。在全麻气管插管困难的患者中,我们发现与传统插管技术相比,管首插管方法更快、更安全。
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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