The Department of Emergency Medicine, Tucson, AZ.
Acad Emerg Med. 2014 Apr;21(4):408-15. doi: 10.1111/acem.12351.
The objective was to compare the first-pass success and clinical performance characteristics of the reusable standard GlideScope® video laryngoscope (sGVL) and the disposable Cobalt GlideScope® video laryngoscope (cGVL).
This was a retrospective analysis of prospectively collected data recorded into a continuous quality improvement database at an urban academic emergency department (ED). The intent of the database is to evaluate operator performance and to track practice patterns used for intubation in the ED. Between July 1, 2007, and June 30, 2013, operators recorded all consecutive intubations performed in the ED. The database included patient demographics and detailed information about each intubation, such as device(s) used, reason for device selection, method of intubation, difficult airway characteristics, number of intubation attempts, and outcome of each attempt. The operator also evaluated the presence of lens fogging and extent of lens contamination. The primary outcome measure was first-pass success. Secondary outcome measures were ultimate success, Cormack-Lehane (CL) view of the airway, presence of lens fogging, and extent of lens contamination. Only adult patients age 18 years or older intubated with the sGVL or cGVL using a stylet, and who had data forms completed at the time of intubation, were included in this study.
A total of 583 intubations were included in the study, 504 with the sGVL and 79 with cGVL. First pass success was achieved in 81.0% (95% confidence interval [CI]=77.3% to 84.3%) of patients in the sGVL group and in 58.2% (95% CI=46.6% to 69.2%) of patients in the cGVL group. In a multivariate logistic regression analysis, the sGVL was associated with a higher first pass success than the cGVL (odds ratio [OR]=3.3, 95% CI=1.9 to 5.8). The ultimate success of the sGVL was 92.1% (95% CI=89.4% to 94.3%) and the cGVL was 72.2% (95% CI=60.9% to 81.7%). A CL grade I or II view was obtained in 93.2% (95% CI=90.7% to 95.3%) in the sGVL group and 86.1% (95% CI=76.5% to 92.8%) in the cGVL group. Lens fogging occurred in 33.3% (95% CI=29.2% to 37.6%) of the cases in the sGVL group and 59.5% (95% CI=47.9% to 70.4%) of the cases in the cGVL group. Significant lens contamination occurred in 5.0% (95% CI=3.2% to 7.2%) of the sGVL group and 21.5% (95% CI=13.1% to 32.2%) of the cGVL group.
In this observational study, the sGVL had higher first pass and overall success than the disposable cGVL. The cGVL had significantly higher incidence of lens fogging and contamination, which may partially account for its lower success. A prospective randomized trial is needed to confirm these findings.
比较可重复使用的标准 GlideScope®视频喉镜(sGVL)和一次性 Cobalt GlideScope®视频喉镜(cGVL)的首次通过成功率和临床性能特征。
这是对城市急诊室(ED)前瞻性收集的数据进行的回顾性分析,记录在持续质量改进数据库中。该数据库的目的是评估操作者的性能,并跟踪 ED 中插管的实践模式。2007 年 7 月 1 日至 2013 年 6 月 30 日期间,操作人员记录了 ED 中进行的所有连续插管。数据库包括患者人口统计学数据和每个插管的详细信息,例如使用的设备、设备选择的原因、插管方法、困难气道特征、插管尝试次数以及每次尝试的结果。操作者还评估了镜头起雾和镜头污染的程度。主要观察指标是首次通过成功率。次要观察指标为最终成功率、气道 Cormack-Lehane(CL)视图、镜头起雾、镜头污染程度。仅纳入使用 sGVL 或 cGVL 插管且使用管芯、并在插管时填写了数据表格的 18 岁及以上的成年患者进行本研究。
共纳入 583 例插管患者,sGVL 组 504 例,cGVL 组 79 例。sGVL 组首次通过成功率为 81.0%(95%置信区间[CI]为 77.3%至 84.3%),cGVL 组为 58.2%(95% CI 为 46.6%至 69.2%)。多变量逻辑回归分析显示,sGVL 与首次通过成功率高于 cGVL 相关(比值比[OR]=3.3,95%CI=1.9 至 5.8)。sGVL 的最终成功率为 92.1%(95% CI=89.4%至 94.3%),cGVL 为 72.2%(95% CI=60.9%至 81.7%)。sGVL 组获得 CL 分级 I 或 II 级视图的比例为 93.2%(95% CI=90.7%至 95.3%),cGVL 组为 86.1%(95% CI=76.5%至 92.8%)。sGVL 组镜头起雾发生率为 33.3%(95% CI=29.2%至 37.6%),cGVL 组为 59.5%(95% CI=47.9%至 70.4%)。sGVL 组明显的镜头污染发生率为 5.0%(95% CI=3.2%至 7.2%),cGVL 组为 21.5%(95% CI=13.1%至 32.2%)。
在这项观察性研究中,sGVL 的首次通过和总体成功率高于一次性 cGVL。cGVL 的镜头起雾和污染发生率明显较高,这可能部分解释了其较低的成功率。需要前瞻性随机试验来证实这些发现。