Efficacy and Safety of a New Protocol for Fast Intubation in Patients With Covid-19 (Sars-Cov-2)

Ricardo Eliud Cisneros Becerra
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Abstract

Introduction: Severe COVID-19 illness is characterized by the development of Acute Respiratory Distress Syndrome (ARDS), for which the mainstay of treatment is represented by mechanical ventilation. Mortality associated with ARDS due to other causes is in the range of 40-60% but currently available data are not yet sufficient to draw safe conclusions on the prognosis of COVID-19 patients who require mechanical ventilation. Materials and Methods: This is a Cross-sectional and retrospective study in which we want to determine if the new intubation protocol developed in our center is safe and efficient to achieve effective intubation in patients with COVID-19 as well as to avoid the transmission of the virus in anesthesiology specialists. Results: The average time to achieve an effective intubation was 49 seconds (range: 35-75 seconds). The number of patients in whom it was possible to achieve intubation on the first attempt was 55 (92.45%). The number of patients who failed to intubate on the first attempt was 4, corresponding to 7.55%. Conclusion: The protocol for intubation of patients COVID19 that we used demonstrated effective results at the time of its application, ensuring the safety of the participating health personnel, as well as all the intubation procedures that were carried out in an effective way.
新方案快速插管治疗新冠肺炎(Sars-Cov-2)的有效性和安全性
简介:COVID-19重症以急性呼吸窘迫综合征(ARDS)为特征,其主要治疗手段为机械通气。由于其他原因导致的与ARDS相关的死亡率在40-60%之间,但目前可用的数据尚不足以对需要机械通气的COVID-19患者的预后得出安全结论。材料和方法:这是一项横断面和回顾性研究,我们想要确定我们中心制定的新插管方案是否安全有效,以实现COVID-19患者的有效插管,并避免病毒在麻醉专家中的传播。结果:实现有效插管的平均时间为49秒(范围:35-75秒)。第一次插管成功的患者55例(92.45%)。第一次插管失败4例,占7.55%。结论:我们采用的新冠肺炎患者插管方案在应用时就显示了有效的效果,确保了参与的卫生人员的安全,确保了所有插管程序的有效实施。
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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