Evaluation of endotracheal intubations in the emergency department of a tertiary care facility.

IF 1.1 Q3 EMERGENCY MEDICINE Turkish Journal of Emergency Medicine Pub Date : 2023-04-01 DOI:10.4103/tjem.tjem_268_22
Mustafa Koray Yildirim, Erkan Göksu, Mohamad El Warea
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Abstract

Objective: In this study, we aimed to evaluate the performance of emergency department intubations for 1 year.

Methods: This was a retrospective analysis of prospectively collected data. The collected variables were patient demographics, indication for intubation, preintubation hemodynamics, preoxygenation methods, medications used for premedication, induction and paralysis, type of laryngoscope used, Cormack-Lehane (C-L) grades, number of intubation attempts, and peri-intubation adverse events.

Results: A total of 194 patients were included. The median age of the population was 66.5 years (53.75-79); 61.9% of the patients were male. The majority of the patients were intubated due to medical conditions. The main indication for endotracheal intubation was respiratory failure in 38.6% of the patients. Preoxygenation before intubation was performed in 87.2% of the patients. Fifty-eight percent of the population were hemodynamically stable before the intubation. Fentanyl was the agent used for premedication, induction agents of choice were ketamine and midazolam, and rocuronium was the neuromuscular blocking agent. The C-L grades 1 and 2 were detected in 87.6% of the patients. The first-pass success rate was 72.8%. The peri-intubation adverse events were mainly hypotension and desaturation observed in 82 (42%) patients. The patients with higher C-L grades needed more intubation attempts (P < 0.001). Peri-intubation adverse events were associated with the increased number of intubation attempts (P < 0.001).

Conclusion: This and similar studies or an airway registry on a national level may help improve the quality of service given and delineate the deficiencies of the airway-related procedures in the emergency department.

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评估气管插管在三级护理机构的急诊科。
目的:在本研究中,我们旨在评估急诊科插管1年的表现。方法:回顾性分析前瞻性收集的资料。收集的变量包括患者人口统计学、插管指征、插管前血流动力学、预充氧方法、用药前使用的药物、诱导和麻痹、使用的喉镜类型、Cormack-Lehane (C-L)分级、插管尝试次数和插管周围不良事件。结果:共纳入194例患者。人口年龄中位数为66.5岁(53.75 ~ 79);男性占61.9%。大多数患者由于医疗条件而插管。38.6%的患者气管插管的主要适应症为呼吸衰竭。插管前预充氧率为87.2%。58%的人在插管前血液动力学稳定。芬太尼为预用药,氯胺酮和咪达唑仑为诱导剂,罗库溴铵为神经肌肉阻滞剂。87.6%的患者有1级和2级C-L。一次通过率为72.8%。82例(42%)患者的插管期不良事件主要为低血压和去血饱和度。C-L分级高的患者需要更多的插管次数(P < 0.001)。插管期不良事件与插管次数增加相关(P < 0.001)。结论:本研究和类似的研究或在全国范围内建立气道登记有助于提高所提供服务的质量,并描述急诊科气道相关程序的不足。
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来源期刊
CiteScore
1.70
自引率
0.00%
发文量
30
审稿时长
22 weeks
期刊介绍: The Turkish Journal of Emergency Medicine (Turk J Emerg Med) is an International, peer-reviewed, open-access journal that publishes clinical and experimental trials, case reports, invited reviews, case images, letters to the Editor, and interesting research conducted in all fields of Emergency Medicine. The Journal is the official scientific publication of the Emergency Medicine Association of Turkey (EMAT) and is printed four times a year, in January, April, July and October. The language of the journal is English. The Journal is based on independent and unbiased double-blinded peer-reviewed principles. Only unpublished papers that are not under review for publication elsewhere can be submitted. The authors are responsible for the scientific content of the material to be published. The Turkish Journal of Emergency Medicine reserves the right to request any research materials on which the paper is based. The Editorial Board of the Turkish Journal of Emergency Medicine and the Publisher adheres to the principles of the International Council of Medical Journal Editors, the World Association of Medical Editors, the Council of Science Editors, the Committee on Publication Ethics, the US National Library of Medicine, the US Office of Research Integrity, the European Association of Science Editors, and the International Society of Managing and Technical Editors.
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